Research and Development Collaboration and License agreement
Exhibit 10.13
CONFIDENTIAL
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Gryphon Therapeutics, Inc. |
Phylos, Inc. |
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000 Xxxxxxx Xxxx. |
000 Xxxxxx Xx. |
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Xx. Xxx Xxxxxxxxx, XX 00000 |
Xxxxxxxxx, XX 00000 |
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(“Gryphon”) |
(“Phylos”) |
Research and Development Collaboration and License agreement
1 Scope and Field.
1.1 Set forth below is the agreement of Gryphon and Phylos, each sometimes referred to herein as a “Party” or collectively as the “Parties”, which hereby acknowledge that they have received adequate and sufficient consideration for entering into their respective and mutual agreements below.
1.2 Gryphon wishes to apply Phylos’ PROfusion™ Technology in developing high affinity peptides.
1.3 The Parties wish to establish a collaboration which will allow Gryphon to evaluate the PROfusion Technology in conjunction with its Cosmix Technology.
1.4 Phylos wishes to grant Gryphon a nonexclusive license for the use of PROfusion Technology.
2 Definitions.
2.1 “Affiliate” means any corporation or non-corporate business entity which controls, is controlled by, or is under common control with a party to this Agreement. A corporation or non-corporate business entity shall be regarded as in control of another corporation if it owns or directly or indirectly controls at least fifty percent (50%) of the voting stock of the other corporation, or (a) in the absence of the ownership of at least fifty percent (50%) of the voting stock of a corporation, or (b) in the case of a non-corporate business entity, if it possesses, directly or indirectly, the power to direct or cause the direction of the management and policies of the corporation or non-corporate business entity, as applicable, whether through the ownership or control of voting securities, by contract or otherwise.
2.2 “Cosmix Technology” means (a) all present and future patents, patent applications, reissued patents, re-examined patents, divisions, renewals, continuations and continuations-in-part, substitutions, extensions and foreign counterparts thereof owned, controlled by or licensed to Gryphon that relate to Cosmix-plexing® technology, as described in Exhibit A attached hereto and (b) all present and future techniques, inventions, discoveries, practices, methods, know-how, technical data and information (other than described in clause (a) of this Section 2.1) that are necessary or useful to practice the Cosmix-plexing® technology, that are not generally known and that are within the Control of Cosmix or its affiliates, “Control” meaning the right and ability to grant sublicenses.
2.3 “Effective Date” means the date of execution of this Agreement by the last of the three signatories hereto.
2.4 “D-Target” means a protein composed of D amino acids.
2.5 “Gryphon Patent Rights” means those patents, patent applications, reissued patents, reexamined patents, divisions, renewals, continuations and continuations-in-part, substitutions, extensions and foreign counterparts thereof, relating to Gryphon’s D-screening technology set forth on Exhibit B hereto, and arising after the Effective Date but before completion of performance by Phylos under this Agreement or such earlier expiration or termination of this Agreement and agreed by the parties to be added to Exhibit B, but in all instances excluding Cosmix Technology).
2.6 “Gryphon Know-How” means techniques, inventions and/or discoveries, practices, methods, knowledge, know-how, skill, technical data and information, and materials that are necessary or useful to the practice of Gryphon Patent Rights, that are not generally known and that are within the Control of Gryphon or its Affiliates as of the Effective Date or come into the Control of Gryphon or its Affiliates before completion of performance by Phylos under this Agreement or such earlier expiration or termination of this Agreement, but in all instances excluding know how related to Cosmix Technology and Gryphon Patent Rights.
2.7 “Gryphon Technology” means the Gryphon Know-How and the Gryphon Patent Rights, collectively.
2.8 “Gryphon” means Gryphon Therapeutics, Inc, a California corporation and its Affiliates
2.9 “Major Market” means any of: the United States, Japan, Germany, France, the United Kingdom, Italy or Spain.
2.10 “Owner” means the Party having rights to the Product.
2.11 “PROfusion™ Technology” means compositions of matter (including, but not limited to reagents) and methods, whether or not patented or patentable, and know-how for in vitro protein evolution wherein peptide-encoding messenger RNA (“mRNA”) molecules are generated with a modification linking a peptide acceptor such as a puromycin molecule to the 3’ terminus of the mRNA molecule so that in vitro translation results in a peptide or protein covalently linked to its encoding nucleic acid via the 3’ terminus of the mRNA and the carboxyl terminus of the peptide or protein via a peptide acceptor such as a puromycin molecule and wherein peptides or proteins having a desired binding affinity are selected from libraries of these RNA-protein fusion molecules. The PROfusion™ Technology, including a description of peptide acceptors such as a puromycin molecule, includes, without limitation, the following family of patents: US 6,261,804; 6,258,558; 6,214,553; 6,281,344; and 6,207,446, and others listed on Exhibit E, and all reissues, reexaminations, renewals, divisionals, continuations, continuations-in-part and foreign counterparts of any of the foregoing.
2.12 “Product” means any peptides or their derivatives identified during PROfusion Technology screening pursuant to this Agreement.
3 Licenses and Intellectual Property.
3.1 Gryphon hereby grants and will grant to Phylos and its Affiliates, a nonexclusive license under Gryphon Patent Rights solely for the purpose of conducting research and development activities in the performance of it obligations under this Agreement until the earlier of (i) completion of such activities hereunder or (ii) the earlier of expiration or termination of this Agreement.
3.2 Phylos hereby grants and will grant to Gryphon and its Affiliates a worldwide, nonexclusive license under PROfusion Technology including future improvements and enhancements thereto, specifically for use with Peptide Libraries (as defined in Appendix C) to screen, make, have made, improve, have improved, use, market, offer for sale, sell, have sold, distribute, have distributed, export and import (i) peptides and their derivatives isolated during use of PROfusion Technology, including but not limited to, screening of D-Targets provided to Phylos hereunder, and (ii) Products resulting from the application of PROfusion Technology using Peptide Libraries, with or without the additional application of Cosmix Technology. The foregoing licenses to Gryphon and Affiliates to use the PROfusion Technology shall be sublicensable solely for the purpose of enabling manufacturers to produce Products, if necessary or advisable. Nothing in this Agreement shall be construed to limit Gryphon’s or its Affiliates right or ability to grant licenses in respect of Products.
3.3 Gryphon shall xxxxx Xxxxxx and its Affiliates a fully paid up worldwide, non-exclusive license, with the right to sublicense, for any patented improvements and enhancements to Profusion Technology made by Gryphon or its Affiliates.
3.4 All inventions, data, and reports resulting from the activities of Phylos under this Agreement, with the exception of improvements or enhancements to the PROfusion Technology, will be assigned to Gryphon.
3.5 If a third party asserts that a patent or other right owned or controlled by it is infringed by PROfusion Technology, Phylos shall have the first right, but not the obligation, to defend against any such third party allegation of infringement by PROfusion Technology, and Phylos shall bear the costs of any such action, including attorneys’ fees. Gryphon shall also have the right to defend against such third party allegation of infringement at its own cost, if Phylos does not undertake such defense within forty-five (45) days after receiving notice of such third party allegation of infringement by the PROfusion Technology. Each Party shall promptly notify the other of its receipt from a third party of an allegation of infringement based upon the practice of any of the PROfusion Technology. For purposes of this section, the “right to defend” includes the right to commence an action for declaratory relief.
3.6 If there shall be declared an interference pertaining to any part of the PROfusion Technology, Phylos shall diligently pursue such interference to conclusion and shall bear the costs thereof, including attorneys’ fees.
3.7 Phylos shall obtain Gryphon’s written consent (not to be unreasonably withheld) prior to entering into any settlement or other transaction (i) with any third party to resolve such third party infringement action or assertions or (ii) to settle an interference, if such settlement or transaction does not contain a full and unconditional release of Gryphon for past infringements, if any, and a grant to Gryphon of such rights to practice third party intellectual property as shall have been granted to Phylos in such settlement., provided .however, that such consent shall not be required if such settlement or transaction contains a full and unconditional release of Gryphon for past infringement and a grant to Gryphon of such rights to practice such third party intellectual property as have been granted to Phylos in such settlement; provided, however, such consent shall not be required if such settlement or transaction contains a full and unconditional release of Gryphon for past infringement and a grant to Gryphon of such rights to practice such third party intellectual property as have been granted to Phylos in such settlement.
4 Screening of Targets.
4.1 Gryphon will supply at least two D-Targets to Phylos for screening , the first within 30 days and the second within 6 months of the Effective Date.
4.2 Phylos will screen its PROfusion Technology peptide libraries against each D-Target, and identify the sequence of any peptides showing better than 50 nanomolar affinity for the D-Target. The Parities shall jointly agree to the libraries’ composition as part of an overall workplan to be established by the parties within 14 days of the Effective Date.
4.3 Phylos will notify Gryphon of the amino acid sequences of not less than 15 and not more than 25 peptides identified pursuant to Section 4.2 above during the screening of each D-Target within ten days of their identification.
4.4 The Phylos screening of the two initial D-Targets shall be deemed successful, if Phylos identifies five Products for each of the two D-Targets with affinities better than 50 nanomolar for their respective D-Targets, each Product with less than 25% sequence identity with any of the other Products relating to the same D-Target.
4.5 If the Phylos screening of the two initial D-Targets is successful, then for each additional target Gryphon wishes to screen under this Agreement, it will offer the opportunity to Phylos to perform PROfusion Technology screening of Phylos Peptide Libraries against such additional targets under the same terms and conditions as pertained to the initial two D-Targets.
4.6 Phylos may, in its sole discretion, accept or decline any request of Gryphon to screen more than the initial two D-Targets. Phylos must accept, if at all, in writing, any Gryphon
proposal of Phylos to perform additional screening within thirty days of its being sent by Gryphon to Phylos.
4.7 Phylos and Gryphon will develop a work plan for each target accepted under 4.6, including project goals and timelines. Gryphon shall be precluded from applying PCT (as hereinafter defined) to any target which has been accepted for screening using PROfusion Technology by Phylos, until such time as such screening has failed to meet the goals within the timeline set forth in the work plan agreed to by the Parties.
4.8 Gryphon shall compensate Phylos for its activities pursuant to Article 4 and 5 hereof at Phylos’ prevailing fully burdened FTE rate (not to exceed $ 250,000 per year for the calendar year starting January 1, 2003). In future years, but not earlier than for the calendar year starting January 1, 2005, such FTE rate can increase on Phylos’ request, but not in excess of the annual rate of inflation as measured by the Consumer Price Index for all urban areas. Such FTE charges shall not exceed by more than 20% the charges allotted therefore in the applicable mutually agreed upon work plan. Such payments shall be in addition to any sums earned by Phylos pursuant to Article 6 herein and such monthly payments shall be due at the start of each work month..
5 Research Collaboration.
5.1 Phylos and Gryphon will design PROfusion Technology peptide libraries adapted to the application of Cosmix Technology.
5.2 The characteristics of such PROfusion Technology peptide libraries, including, but not limited to diversity, sustainability, sequence length and cloning strategies of the PROfusion library shall be agreed to by the parties and attached hereto as Exhibit C within 30 days of the Effective Date.
5.3 Phylos will use its best efforts to construct the designed library according to the Work Plan and timelines agreed to by the parties and attached hereto as part of Exhibit C within 30 days following agreement of the parties pursuant to Section 5.2 above.
5.4 Phylos will conduct a selection against a D-Target specified by Gryphon using the constructed libraries and will supply Gryphon with the sequence information and the appropriate DNA samples representing those selected pools. Gryphon will be free to attempt to apply Cosmix Technology to the selected pools and demonstrate the enhanced diversity contained within and increased affinity of Products developed from the resulting Cosmix Technology, if any.
6 Consideration.
6.1 Within 48 hours of notice of the Effective Date, Gryphon shall pay to Phylos as a license fee.
6.2 Within 48 hours of receipt of a License Approval Order (as defined below) from the U.S. Bankruptcy Court for the District of Delaware conforming to the requirements set forth below and signifying approval of this Agreement, Gryphon shall pay to Phylos the sum of as an additional license fee. Such approval shall be by entry of a final Court order (“License Approval Order”) which is not subject to an appeal or a stay pending appeal. The inability or failure of Phylos to obtain a License Approval Order shall not affect the rights of Gryphon under this Agreement, but shall relieve Gryphon of any obligation to make payment pursuant to this Section 6.2. The License Approval Order must specifically provide that:
i. The License Approval Order will be binding upon Phylos or any successor of Phylos or its bankruptcy estate, including but not limited to any Chapter 7 or 11 Trustee appointed in the Phylos case; and shall constitute without variation the treatment of Gryphon’s administrative claim in the Phylos case or any successor case, binding upon all parties in interest, including but not limited to in any liquidation or in any Plan of Reorganization to be confirmed by the Court or proposed by Phylos.
ii. The License Approval Order shall provide that Gryphon will receive immediate and unconditional relief from the automatic stay to pursue its foreclosure rights without further order of the Court to enforce post-petition any of its rights under the License, including but not limited to: 1) the ability to terminate the License Agreement; 2) the ability to commence suit against Phylos or others to enforce its rights under the License Agreement; and 3) to take any other action even against property of the estate to enforce Gryphon’s rights under the license.
iii. The rights and interests granted to Gryphon under the License Agreement shall be free and clear of all liens, security and other interests, mortgages, trust deeds, encumbrances, pledges, and claims of any kind of any party (“License Encumbrances”) whether arising on, before or after the Petition Date. All such License Encumbrances shall be terminated and released as to the License Agreement and underlying licenses and shall attach to the proceeds of the transaction in the order of priority and with the same validity, force, and effect possessed by such License Encumbrances, if any, prior to the effectiveness of the License Agreement.
6.3 Upon filing of an IND or equivalent for the first indication for a Product, Gryphon will pay Phylos $50,000. If Gryphon has partnered the Product prior to filing the IND, Gryphon will pay Phylos the lesser of $250,000 or 20% of the applicable license milestone payments received to such time.
6.4 Upon the start of Phase II trials (commencement of drug administration) for the first indication of a Product, Gryphon will pay Phylos $150,000. If Gryphon has partnered the Product prior to such time, Gryphon will pay Phylos the lesser of $300,000 or 20% of the applicable license milestone payments.
6.5 The greater of (i) 20% of any milestones received by Gryphon from a sublicensee of a Product as a result of entry of such Product into its first pre-registration clinical trial in any Major Market (Phase III, Phase ll/lll, or an equivalent, whichever first occurs) or (ii) $2.0 million upon such event.
6.6 The greater of (i) 20% of any applicable licensing milestones received by Gryphon from a sublicensee as a result of filing for the first registration (NDA or equivalent) of each Product in any Major Market, or (ii) $3.0 million upon such event.
6.7 The greater of (i) 20% of any applicable licensing milestones received by Gryphon from a sublicensee as a result of the first commercial sale of each Product in any Major Market, or (ii) $5.0 million upon such event.
6.8 For each Product developed hereunder by Gryphon using both PROfusion Technology and Cosmix Technology, Gryphon will pay amounts due to Phylos under Sections 6.3, 6.4, 6.5, and 6.6 at one-half the rates set forth therein in substitution of the amounts and * rates se| forth therein. Payments due Phylos under Sections 6.2 shall remain unaffected by the use of Cosmix Technology.
7 Termination.
7.1 Gryphon may terminate this Agreement without cause upon 60 days’ notice to Phylos.
7.2 In the event of a termination of this Agreement pursuant to Section 7.1 Gryphon shall remain responsible to pay to Phylos any sums thereafter due pursuant to Article 6 above.
7.3 As between Gryphon and Phylos, Gryphon shall be the sole owner of all peptides delivered hereunder and resulting Products, and its right, title, and ownership therein shall survive termination of this Agreement. Gryphon, in its sole discretion, shall be responsible for the pursuit, if any, maintenance and enforcement of any patents or other intellectual property protection relating to any such peptides or Products.
7.4 The licenses granted by Phylos to Gryphon under this Agreement in respect of Products shall survive termination of this Agreement. All licenses granted hereunder by Phylos to Gryphon shall be deemed to be the grant of licenses of “Intellectual Property” under Section 365(n) of the United States Bankruptcy Code, as amended.
8 Publicity.
Neither Party may publicize the existence of this Agreement or the participation of the other Party in the development of its Products without the express written permission of the other Party.
9 Additional.
9.1 Representations and Warranties. Except as disclosed on the Schedule of Exceptions attached hereto as Exhibit D, each Party represents and warrants to the other Party as of the Effective Date as follows:
9.1.1 that it is duly organized, validly existing and in good standing under the laws of the jurisdiction where it is organized;
9.1.2 that it is in compliance with all requirements of applicable law, except to the extent that any noncompliance would not have a material adverse effect on the properties, business, financial or other condition of such Party and would not materially adversely affect such Party’s ability to perform its obligations under this Agreement;
9.1.3 that it has the lawful right to execute and perform this Agreement and to accept this grant of rights from the other Party, and that this Agreement does not violate or conflict with any other agreement to which the Party is a Party or any law or regulation applicable to it;
9.1.4 that it will use the Confidential Information, Know-How, Intellectual Property, Technology, and other property of the other Party only as authorized under this Agreement, and will follow all applicable standards, specifications, laws, regulations, guidelines and rules;
9.1.5 that no claim has been asserted or threatened by any person that the practice of such Party’s Technology constitutes, and to such Party’s knowledge, the practice of its Technology does not constitute, an infringement, misappropriation or violation of any intellectual property rights of any other person or constitutes unfair competition;
9.1.6 that such Party shall not knowingly infringe, misappropriate or violate the intellectual property rights of any person in carrying out it obligations hereunder;
9.1.7 to such Party’s knowledge, no third Party has materially infringed, misappropriated or violated, or is materially infringing, misappropriating or violating, its Technology; and
9.1.8 to such Party’s knowledge, exercise by the other Party of its rights under this Agreement will not result in any infringement, misappropriation or violation of any intellectual property rights of any Third Party.
9.2 Limitation. EXCEPT AS PROVIDED IN THIS ARTICLE 9, EACH PARTY, ITS DIRECTORS, OFFICERS, EMPLOYEES AND AFFILIATES MAKE NO OTHER REPRESENTATIONS OR WARRANTIES OF ANY KIND, EITHER EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, VALUE, SAFETY, RELIABILITY, EFFICACY, NONTOXICITY, PATENTABILITY OF PATENTS OR VALID CLAIMS, ISSUED OR PENDING, NON-INFRINGEMENT, OR THE ABSENCE OF LATENT OR OTHER DEFECTS, WHETHER OR NOT DISCOVERABLE, IN THE TECHNOLOGY, PRODUCTS OR IN ANY INTANGIBLE OR TANGIBLE ITEM GENERATED UNDER OR USED WITHIN THIS AGREEMENT;
9.3 Limited Liability. IN NO EVENT SHALL EITHER PARTY TO THIS AGREEMENT BE LIABLE FOR ANY LOST PROFITS OR FOR ANY INDIRECT, SPECIAL, INCIDENTAL, CONSEQUENTIAL OR PUNITIVE DAMAGES ARISING OUT OF THIS AGREEMENT, THE BREACH OF THIS AGREEMENT OR THE EXERCISE OF RIGHTS HEREUNDER WHETHER UNDER ANY CONTRACT, NEGLIGENCE, STRICT LIABILITY OR OTHER LEGAL OR EQUITABLE THEORY.
10 Confidentiality.
10.1 Definitions. In this Section 10, the following terms shall have the following meanings whenever such terms are used in their capitalized form:
10.1.1 “Confidential Information” means any proprietary or confidential information of the Disclosing Party, except such information falling within an exception recited below, which is communicated in any way or form by the Disclosing Party to the recipient, either before or after the Effective Date of this Agreement, and whether or not such information is identified as confidential. Confidential Information includes any data or reports provided by one Party to the other Party pursuant to this Agreement, as well as the terms and conditions of this Agreement. Confidential Information shall not include any information that:
a) is or later becomes a part of the public domain through no fault of Recipient;
or
b) recipient can demonstrate was in its rightful possession, without a restriction on use or disclosure, prior to receipt of the information from the disclosing Party or an entity acting on its behalf; or
c) Recipient can demonstrate was rightfully received from a third party without a restriction on use or disclosure; or
d) recipient can demonstrate by written evidence was independently developed by Recipient without use, directly or indirectly, of Confidential Information of the Disclosing Party.
10.1.2 “Disclosing Party” means the Party making disclosure of or otherwise communicating its Confidential Information to the other Party.
10.1.3 “Recipient” means the Party receiving or otherwise obtaining Confidential Information from the Disclosing Party.
10.1.4 “Third Party” means any party other than Gryphon, Phylos, and their respective Affiliates.
10.2 Restrictions on Use. In consideration of disclosure by either of the Parties to the other Party of Confidential Information in written, oral, graphic or electronic form pursuant to the terms of this Agreement, the Recipient undertakes, unless otherwise stipulated herein, (a) to treat such Confidential Information received from the Disclosing Party with the same degree of care to maintain the secrecy of the Confidential Information as it uses to maintain the secrecy of its own information of like kind; and (b) to use the Confidential Information only to accomplish the purposes of this Agreement. Recipient will not disclose Confidential Information received from the Disclosing Party except to its employees, agents, consultants, independent contractors who have a need to know the Confidential Information in furtherance of the purposes of this Agreement (collectively, the “Representatives”), and such Representatives will be bound to Recipient by obligations of non-use and non-disclosure that are similar to or more stringent than those imposed on Recipient pursuant to this Agreement.
11 Indemnification.
11.1 Obligation to Indemnify. Each of the Parties hereto shall defend, indemnify and hold harmless the other Party and its Affiliates, successors and assigns, and their respective directors, officers, shareholders, partners, employees, and agents (collectively, the
“Indemnitees”) from and against all losses, damages, costs and expenses (including legal fees) incurred thereby or caused thereto which arise out of claims against the Indemnitees brought by Third Parties after the Effective Date of this Agreement which arise out of or relate to (i) any material breach or violation of, or failure to properly perform, any covenant or agreement made by the Indemnifying Party in this Agreement; or (ii) any material breach of any of the representations or warranties made by the Indemnifying Party in this Agreement. The Indemnifying Party shall have no obligation to indemnify any Indemnitee hereunder to the extent any such losses, damages, costs and expenses arise out of the negligence or willful misconduct of Indemnitee.
12 Miscellaneous.
12.1 Severability. If any court of competent jurisdiction determines that any provision of this Agreement is partially or wholly unenforceable under applicable law, such provision shall be enforced to the maximum extent permitted by applicable law, and the remaining provisions of this Agreement shall remain in full force and effect.
12.2 Force Majeure. In the event that any strike, epidemic, natural disaster, fire, other act of God, war, civil disturbance, act of terrorism, explosion, or act or decision of any governmental authority renders impossible the performance of any of the obligations of the Parties or either of them under this Agreement, the Party or Parties affected shall be excused the performance of the relevant obligation or obligations upon notifying the other Party in writing, giving a detailed explanation of the occurrence in question. Upon the giving of such a notice, the performance of the Party giving notice shall be excused only to the extent and for so long as performance remains impossible. Notwithstanding the foregoing, in the event that a force majeure event declared by a Party persists for more than 180 days, the other Party shall have the right to terminate this Agreement pursuant to Section 7.1 hereof.
12.3 No Assignment. Neither Party may assign this Agreement without the prior written permission of the other Party, which permission shall not be unreasonably withheld or delayed; provided, however, this Agreement may be assigned without such permission to an Affiliate or to a successor to or purchaser of all or substantially all of the business or assets of the assigning Party, or as part of a reorganization, merger, or change of control of the assigning Party.
12.4 Independent Contractors. In entering into and carrying out their respective rights and obligations under this Agreement, the Parties are independent contractors and shall have no power or authority, express or implied, to bind the other Party, act on the other Party’s behalf, or in any way enter into or incur any liability for or on behalf of the other Party, and nothing in this Agreement shall be construed as giving rise to a relation of partnership or agency between the Parties.
12.5 Dispute Resolution. In any disagreement or dispute that may arise between the Parties in relation to, resulting from, or arising out of this Agreement, the Parties shall attempt to settle such disagreement or dispute amicably and expeditiously by good faith negotiation. Any such dispute which cannot be so settled within ninety (90) days after the commencement of negotiations shall be referred to binding arbitration by a single, independent arbitrator who is experienced in dealing with disputes of the sort in question and with business relations of the type under this Agreement, to be appointed by mutual agreement of the Parties. If the Parties are not able to agree upon an arbitrator within thirty (30) days, each Party shall appoint one arbitrator who shall mutually agree upon a third arbitrator to serve as the arbitrator for the dispute. The arbitration will be conducted in the vicinity of the non-triggering Party in accordance with the terms and conditions of this Agreement. The arbitration shall be conducted in accordance with the Commercial Arbitration Rules of the American Arbitration Association. The decision of the arbitrator shall be final and shall be fully and irrevocably accepted by the Parties. Judgment upon the award rendered by the arbitrator may be entered in any court having jurisdiction thereof. The arbitrator is not empowered to award treble, punitive or any other damages
in excess of compensatory damages, and each Party irrevocably waives any claim to recover such damages. The Parties shall use their reasonable efforts to conduct all dispute resolution procedures under this Agreement as expeditiously, efficiently and cost-effectively as possible. Notwithstanding the foregoing, any dispute relating to intellectual property or Confidential Information of either or both Parties shall not be subject to this Section 12.5 dispute resolution provision.
12.6 Governing Law. This Agreement shall be governed by and construed in accordance with the laws of the State of Massachusetts, U.S.A. in respect of all matters, including the execution, interpretation, performance and enforcement of this Agreement.
12.7 Notices. All notices and payments required or permitted by this Agreement shall be in writing and shall be sent by reliable overnight commercial courier (e.g., Federal Express, DHL, Airborne or the like), or hand delivered or mailed by registered or certified mail, postage prepaid and return receipt requested, to the relevant Party at the appropriate address, as noted below, and either Party may, in writing, change the address to which notices may be given.
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If to Gryphon: |
If to PHYLOS: |
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Gryphon Therapeutics, Inc. |
PHYLOS |
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Gateway Boulevard |
000 Xxxxxx Xxxxxx |
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Xxxxx Xxx Xxxxxxxxx, XX 00000-0000 |
Xxxxxxxxx, XX 00000 |
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Attn: Chief Financial Officer |
Attn: CEO |
12.8 Entire Agreement; Amendment. This Agreement constitutes the entire agreement between the Parties concerning the subject matter of this Agreement, and any representation, promise or condition not incorporated in this Agreement shall not be binding upon either Party. No amendment, modification or addition to this Agreement shall be binding on the Parties unless made in writing and executed by both Parties.
IN WITNESS WHEREOF the Parties, by and through their authorized officers, have executed this Agreement as of the Effective Date.
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GRYPHON THERAPEUTICS, INC. |
PHYLOS, INC. | |||
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By: |
/s/ X. Xxxxxx |
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By: |
/s/ Xxxxxx X. Xxxxxxxxxxx |
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Xxxxxxxxx Xxxxxx, Ph.D. |
Name: Xxxxxx X. Xxxxxxxxxxx | ||
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President and CEO |
Title: C.E.O. | ||
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Date: |
8/26/03 |
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Date: |
8/27/03 |
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Acknowledged and agreed to: |
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/s/ B. Seed |
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Xxxxx Xxxx |
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Date: |
8/28/03 |
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Exhibits:
A — Cosmix Technology Patents and Patent Applications
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Matter No. / |
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Application No. / |
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Title |
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Country |
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Patent No. |
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Status |
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GRFN-055 |
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AUSTRALIA |
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749249 |
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Issued -10/3/2002 |
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GENERATION OF DIVERSITY IN COMBINATORIAL LIBRARIES |
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CANADA |
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2279341 |
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Pending |
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CHINA |
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98802184.6 |
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Pending | |
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EPO |
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97101539.1 |
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Pending |
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EPO |
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968283 |
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Issued - 5/2/2003 |
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EPO |
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02021507.5 |
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Pending |
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HONG KONG |
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00102476.9 |
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Pending |
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ISRAEL |
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000000 |
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Xxxxxxx |
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XXXXX |
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10.532545 |
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Pending |
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SINGAPORE |
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9903327-6 |
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Issued - 7/19/2002 |
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UNITED STATES |
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6,310,191 |
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Issued -10/30/2001 |
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UNITED STATES |
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09/912,165 |
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Pending |
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per |
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PCT/EP98/00533 |
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National Stage Filed |
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GRFN-056 |
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EPO |
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02020639.7 |
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Pending |
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RECOMBINATION PROCESS FOR RECOMBINING FRAGMENTS OF VARIANT POLYNUCLEOTIDES |
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EPO |
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02021514.1 |
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Pending |
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GRFN-057 |
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|
|
EPO |
|
02016743.3 |
|
Pending |
|
METHOD FOR GENERATING MOLECULES WITH SPECIFIC PROPERTIES BY RECOMBINATION AND SELECTION |
|
EPO |
|
02027002.1 |
|
Pending |
|
|
|
|
|
|
| |
|
|
|
|
|
|
| |
|
|
|
|
|
|
| |
|
|
|
|
|
|
|
|
|
GRFN-058 |
|
|
|
|
|
|
|
|
|
EPO |
|
02023588.3 |
|
Pending |
|
METHOD FOR MODULATING THE SURFACE CHARACTERISTICS OF A DEVICE |
|
|
|
|
|
|
|
|
|
|
|
|
| |
|
|
|
|
|
|
|
B. - Gryphon Patent Rights
D-ENZYME COMPOSITIONS AND METHODS OF THEIR USE
|
COUNTRY |
|
REFERENCE# |
|
TYPE |
|
FILED |
|
SERIAL# |
|
ISSUED |
|
PATENT# |
|
STATUS |
|
XXXXXXXXX |
|
000/00XX |
|
XXX |
|
6/7/1993 |
|
45996/93 |
|
10/2/1997 |
|
678768 |
|
ISSUED |
|
AUSTRALIA |
|
008/01AU |
|
DIV |
|
6/7/1993 |
|
37564/97 |
|
6/29/2000 |
|
721228 |
|
ISSUED |
|
CANADA |
|
008/00CA |
|
DCA |
|
6/7/1993 |
|
2,137,378 |
|
|
|
|
|
PENDING |
|
EUROPEAN PATENT |
|
008/00EP |
|
DCA |
|
6/7/1993 |
|
93916447.1 |
|
4/7/1999 |
|
0647266 |
|
ISSUED |
|
EUROPEAN PATENT |
|
008/02EP |
|
DIV |
|
6/7/1993 |
|
98108855.2 |
|
|
|
|
|
PENDING |
|
JAPAN |
|
008/00J X |
|
XXX |
|
0/0/0000 |
|
0-000000 |
|
|
|
|
|
XXXXXXX |
|
XXXXXX XXXXXX |
|
008/01 US |
|
DCA |
|
12/2/1994 |
|
08/343,585 |
|
4/15/2003 |
|
6,548,279 |
|
ISSUED |
|
UNITED STATES |
|
008/02US1 |
|
DIV |
|
5/22/1996 |
|
08/651,144 |
|
3/21/2000 |
|
6,040,133 |
|
ISSUED |
|
UNITED STATES |
|
008/03US |
|
CON |
|
5/22/1996 |
|
08/651,303 |
|
6/8/1999 |
|
5,910.437 |
|
ISSUED |
|
UNITED STATES |
|
008/04US |
|
CON |
|
8/17/2002 |
|
10/223,103 |
|
|
|
|
|
PENDING |
|
UNITED STATES |
|
008/05US |
|
CON |
|
8/27/2002 |
|
10/229,553 |
|
|
|
|
|
PENDING |
C. — PROfusion Technology Peptide Library Characteristics
Peptide Libraries, for the purposes of this agreement, are defined as nucleic acid libraries comprising, on each molecule:
· two fixed regions containing all necessary nucleic acid and amino acid encoding regions necessary for the practice of PROfusion (including but not limited to PCR primer-binding regions, a linker binding region, Transcription and Translation initiating regions, nucleic acid sequence tags, 4-8 amino acid peptide purification tags) and, optionally may include fixed amino acids, which may be cysteine, that allow the formation of a disulfide constrained loop containing the variable region, and;
· a variable region encoding 5-50 amino acids where at least 90%* of the amino acids encoded at each position are randomly selected from a group of at least 15 amino acids.
Specifically excluded from Peptide Libraries are libraries based on a naturally occurring protein or domain(s) of a protein or an de novo engineered protein designed based on the tertiary structure of naturally occurring domains, with the deliberate insertion of amino acid variability in one or more exposed portions of that molecule (Scaffolded Libraries) and libraries derived from cellular mRNA (Proteomic Libraries). Examples of scaffolded proteins already practiced are antibody VH or VL domains, the 10th Type III repeat of Fibronectin (TRINECTINTM binding proteins), Titin and Gurmarin.* Individual clones or pools for affinity maturation are exempted from the “at least 90%” restriction as long as all invariant sequences in the variable region are derived from a pre-existing clone from a peptide library.
Exhibit D
Schedule of Exceptions
In connection with the execution and delivery by Phylos, Inc. (“Phylos”) of that certain Research and Development Collaboration and License Agreement with Gryphon Therapeutics, Inc. (the “Agreement”), Phylos hereby provides this Schedule of Exceptions on Exhibit D. The disclosure contained herein shall qualify the Re presentations and Warranties made by Phylos in Section 9 of the Agreement.
United States Patent 6,361,943, Yanagawa, et al. March 26,2002. No agreement is currently in place between Phylos and Mitsubishi Chemical Corp. Phylos has filed an interference with the US Patent Office.
German Patent DE19646372. Pschorr, June 19, 1997. Phylos filed a brief in 5 German courts including Frankfurt and Munich.
Xxxxxxx Patent Estate currently held by Advanced Molecular Evolution. Phylos has a license, but it is not transferable and may apply to the Gryphon applications if they were to take a license.
AME PATENT RIGHTS
|
Country |
|
Application No. |
|
Filing Date |
|
Patent No. |
|
Issue Date |
|
United States |
|
|
|
|
|
|
|
|
|
U.S. |
|
08/349,510 |
|
12/2/94 |
|
5,723,323 |
|
3/3/98 |
|
U.S. |
|
08/464,142 |
|
6/5/95 |
|
5,824,514 |
|
10/20/98 |
|
U.S. |
|
08/464,327 |
|
6/5/95 |
|
5,976,862 |
|
11/2/99 |
|
U.S. |
|
08/464,141 |
|
6/5/95 |
|
5,817,483 |
|
10/6/98 |
|
U.S. |
|
08/468,468 |
|
6/5/95 |
|
|
|
|
|
U.S. |
|
08/462,637 |
|
6/5/95 |
|
5,763,192 |
|
6/9/98 |
|
U.S. |
|
08/468,477 |
|
6/5/95 |
|
5,814,476 |
|
9/29/98 |
|
U.S. |
|
08/464,569 |
|
6/5/95 |
|
|
|
|
|
Non-U.S. |
|
|
|
|
|
|
|
|
|
Switzerland |
|
1379/85 |
|
3/14/86 |
|
EP 8603683 |
|
12/24/87 |
|
Switzerland |
|
85902946.4 |
|
6/17/85 |
|
EP 229,046 |
|
5/4/94 |
|
Germany |
|
85902946.4 |
|
6/17/85 |
|
DE 3,587,814 |
|
5/4/94 |
|
Germany |
|
P 3546806.8 |
|
6/17/85 |
|
3,546,806 |
|
3/28/91 |
|
Germany |
|
P 3546807.6 |
|
6/17/85 |
|
3,546,807 |
|
3/28/91 |
|
Germany |
|
P 3590766.5 |
|
6/17/85 |
|
3,590,766 |
|
1/10/91 |
|
England |
|
8628313.2 |
|
6/17/85 |
|
2,183,661 |
|
6/28/89 |
|
Hong Kong |
|
9,200,202 |
|
6/17/85 |
|
# 200 of 1992 |
|
6/28/95 |
|
Singapore |
|
P 79/92 |
|
6/17/85 |
|
9290079.4 |
|
6/28/95 |
|
EPO |
|
93116225.9 |
|
6/17/85 |
|
|
|
|
|
Japan |
|
60-502625 |
|
6/17/85 |
|
2,584,613 |
|
Published 2/26/97 |
|
Japan |
|
7-243853 |
|
8/3/95 |
|
|
|
|
|
EPO |
|
85902946.4 |
|
6/17/85 |
|
229,046 |
|
5/04/94 |
|
Canada |
|
504,653 |
|
3/20/86 |
|
1,339,937 |
|
6/30/98 |
|
Canada |
|
617,095 |
|
4/28/98 |
|
|
|
|
EXHIBIT E - Profusion Technology
EXHIBIT E
Phylos, Inc. Patents
|
Country/Type |
|
Title |
|
Registration/ |
|
Registration/ |
|
Status |
|
US Provisional |
|
IN VITRO SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
60/035,963 |
|
1/21/1997 |
|
|
|
US Provisional |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
60/064,491 |
|
11/6/1997 |
|
|
|
US |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
09/007,005 |
|
1/14/1998 |
|
Issued |
|
PCT |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
US98/00807 |
|
1/14/1998 |
|
|
|
AU |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
62419/98 |
|
8/4/1999 |
|
Issued |
|
CA |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
2278786 |
|
7/21/1999 |
|
|
|
CN |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
98803511.1 |
|
9/21/1999 |
|
|
|
EP |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
98904574.5 |
|
9/21/1999 |
|
|
|
HK |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
106756.1 |
|
9/21/1999 |
|
|
|
IL |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
131016 |
|
7/21/1999 |
|
|
|
IN |
|
A PROCESS FOR THE MANUFACTURE OF A PROTEIN |
|
158/DEL/1998 |
|
1/20/1998 |
|
|
|
JP |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
10-534534 |
|
7/21/1999 |
|
|
|
KR |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
00-0000000 |
|
7/21/1999 |
|
|
|
RU |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
99118585 |
|
8/20/1998 |
|
|
|
TH |
|
SELECTIONS OF PROTEINS USING RNA-PROTEINS FUSIONS |
|
41800 |
|
1/15/1998 |
|
|
|
TW |
|
SELECTIONS OF PROTEINS USING RNA-PROTEINS FUSIONS |
|
87100513 |
|
1/15/1998 |
|
|
|
ZA |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
98/0489 |
|
1/21/1998 |
|
|
|
AU |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
97069/01 |
|
8/4/1999 |
|
|
|
US |
|
RNA-ANTIBODY FUSIONS AND THEIR SELECTION |
|
09/238,710 |
|
1/28/1999 |
|
Issued |
|
US |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
09/244,794 |
|
2/5/1999 |
|
Issued |
|
US |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
09/244,796 |
|
2/5/1999 |
|
Issued |
|
US |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
09/247,190 |
|
2/9/1999 |
|
Issued |
|
PCT |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
US00/02589 |
|
2/1/2000 |
|
|
|
AU |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
34793/00 |
|
2/1/2000 |
|
|
|
CA |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
2361725 |
|
2/1/2000 |
|
|
|
EP |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
913326.5 |
|
2/1/2000 |
|
|
|
HK |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
02 103 482.7 |
|
2/1/2000 |
|
|
|
IL |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
247,190 |
|
2/1/2000 |
|
|
|
JP |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
2000-598669 |
|
2/1/2000 |
|
|
|
KR |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
2001-7009987 |
|
2/1/2000 |
|
|
|
NO |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
2001 3842 |
|
2/1/2000 |
|
|
|
NZ |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
513153 |
|
2/1/2000 |
|
|
|
RU |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
2001 124810 |
|
2/1/2000 |
|
|
|
US |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
09/430,049 |
|
10/29/1999 |
|
Issued |
|
US |
|
SELECTION OF PROTEINS USING RNA-PROTEIN FUSIONS |
|
09/876,235 |
|
6/6/2001 |
|
|
|
US Provisional |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
60/090,970 |
|
6/29/1998 |
|
|
|
US |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
09/342.980 |
|
6/29/1999 |
|
|
|
PCT |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
US99/14776 |
|
6/29/1999 |
|
|
|
AU |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
48470/99 |
|
6/29/1999 |
|
|
|
CA |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
2,331,92 |
|
6/29/1999 |
|
|
|
CN |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
99807977.4 |
|
6/29/1999 |
|
|
|
CZ |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
PV200-4564 |
|
6/29/1999 |
|
|
|
EP |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
99,932,082 |
|
6/29/1999 |
|
|
|
HK |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
01107096.7 |
|
6/29/1999 |
|
|
|
IN |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
684 |
|
6/29/1999 |
|
|
|
IL |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
140,100 |
|
6/29/1999 |
|
|
|
JP |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
2000-557385 |
|
6/29/1999 |
|
|
|
KR |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
2000-7014838 |
|
6/29/1999 |
|
|
|
NO |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
20006675 |
|
6/29/1999 |
|
|
|
NZ |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
508287 |
|
6/29/1999 |
|
|
|
RU |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
2001102509 |
|
6/29/1999 |
|
|
|
ZA |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
2000/7261 |
|
6/29/1999 |
|
|
|
US |
|
METHODS FOR GENERATING HIGHLY DIVERSE LIBRARIES |
|
09/434,834 |
|
11/5/1999 |
|
|
|
US Provisional |
|
METHODS FOR PRODUCING NUCLEIC ACIDS LACKING 3’-UNTRANSLATED REGIONS AND OPTIMIZING CELLULAR RNA-PROTEIN FUSION FORMATION |
|
60/096,818 |
|
8/17/1998 |
|
|
|
US |
|
METHODS FOR PRODUCING NUCLEIC ACIDS LACKING 3’-UNTRANSLATED REGIONS AND OPTIMIZING CELLULAR RNA-PROTEIN FUSION FORMATION |
|
09/374,962 |
|
8/16/1999 |
|
Issued |
|
PCT |
|
METHODS FOR PRODUCING NUCLEIC ACIDS LACKING 3’-UNTRANSLATED REGIONS AND OPTIMIZING CELLULAR RNA-PROTEIN FUSION FORMATION |
|
US99/18603 |
|
8/16/1999 |
|
|
|
AU |
|
METHODS FOR PRODUCING NUCLEIC ACIDS LACKING 3’-UNTRANSLATED REGIONS AND OPTIMIZING CELLULAR RNA-PROTEIN FUSION FORMATION |
|
54883/99 |
|
8/16/1999 |
|
|
|
EP |
|
METHODS FOR PRODUCING NUCLEIC ACIDS LACKING 3’-UNTRANSLATED REGIONS AND OPTIMIZING CELLULAR RNA-PROTEIN FUSION FORMATION |
|
99941179.6 |
|
8/16/1999 |
|
|
|
JP |
|
METHODS FOR PRODUCING NUCLEIC ACIDS LACKING 3’-UNTRANSLATED REGIONS AND OPTIMIZING CELLULAR RNA-PROTEIN FUSION FORMATION |
|
2000-565171 |
|
8/16/1999 |
|
|
|
CA |
|
METHODS FOR PRODUCING NUCLEIC ACIDS LACKING 3’-UNTRANSLATED REGIONS AND OPTIMIZING CELLULAR RNA PROTEIN FUSION FORNATION |
|
2,334,946 |
|
8/16/1999 |
|
|
|
US |
|
METHODS FOR PRODUCING NUCLEIC ACIDS LACKING 3’-UNTRANSLATED REGIONS AND OPTIMIZING CELLULAR RNA-PROTEIN FUSION FORMATION |
|
09/910,518 |
|
7/20/2001 |
|
|
|
US Provisional |
|
IDENTIFICATION OF COMPOUND-PROTEIN INTERACTIONS USING LIBRARIES OF PROTEIN-NUCLEIC ACID FUSION MOLECULES |
|
60/096,820 |
|
8/17/1998 |
|
|
|
US |
|
IDENTIFICATION OF COMPOUND-PROTEIN INTERACTIONS USING LIBRARIES OF PROTEIN-NUCLEIC ACID FUSION MOLECULES |
|
09/374,964 |
|
8/16/1999 |
|
|
|
PCT |
|
IDENTIFICATION OF COMPOUND-PROTEIN INTERACTIONS USING LIBRARIES OF PROTEIN-NUCLEIC ACID FUSION MOLECULES |
|
US99/18600 |
|
8/16/1999 |
|
|
|
AU |
|
IDENTIFICATION OF COMPOUND-PROTEIN INTERACTIONS USING LIBRARIES OF PROTEIN-NUCLEIC ACID FUSION MOLECULES |
|
61296/99 |
|
8/16/1999 |
|
|
|
CA |
|
IDENTIFICATION OF COMPOUND-PROTEIN INTERACTIONS USING LIBRARIES OF PROTEIN-NUCLEIC ACID FUSION MOLECULES |
|
2,337,490 |
|
8/16/1999 |
|
|
|
EP |
|
IDENTIFICATION OF COMPOUND-PROTEIN INTERACTIONS USING LIBRARIES OF PROTEIN-NUCLEIC ACID FUSION MOLECULES |
|
999480.42.9 |
|
8/16/1999 |
|
|
|
JP |
|
IDENTIFICATION OF COMPOUND-PROTEIN INTERACTIONS USING LIBRARIES OF PROTEIN-NUCLEIC ACID FUSION MOLECULES |
|
2000-564919 |
|
8/16/1999 |
|
|
|
US Provisional |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
60/110,549 |
|
12/2/1998 |
|
|
|
US |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
09/453,190 |
|
12/2/1999 |
|
Issued |
|
PCT |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
US99/28472 |
|
12/2/1999 |
|
|
|
AU |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
23509/00 |
|
12/2/1999 |
|
|
|
CA |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
2350417 |
|
12/2/1999 |
|
|
|
EP |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
99967171.2 |
|
12/2/1999 |
|
|
|
HK |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
02100680.3 |
|
1/29/2002 |
|
|
|
IL |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
143236 |
|
12/2/1999 |
|
|
|
IN |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
|
|
12/2/1999 |
|
|
|
JP |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
2000-585,454 |
|
12/2/1999 |
|
|
|
KR |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
2001-7006742 |
|
12/2/1999 |
|
|
|
NO |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
2001-2735 |
|
12/2/1999 |
|
|
|
NZ |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
511699 |
|
12/2/1999 |
|
|
|
US |
|
DNA-PROTEIN FUSIONS AND USES THEREOF |
|
10/180,819 |
|
6/26/2002 |
|
|
|
US Provisional |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
60/137,032 |
|
6/1/1999 |
|
|
|
US |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
09/585,207 |
|
6/1/2000 |
|
|
|
PCT |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
US00/15077 |
|
6/1/2000 |
|
|
|
AU |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
54555/00 |
|
6/1/2000 |
|
|
|
CA |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
2,373,047 |
|
6/1/2000 |
|
|
|
EP |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
939 474.3 |
|
6/1/2000 |
|
|
|
HK |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
02105898.0 |
|
6/1/2000 |
|
|
|
JP |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
2000-620978 |
|
6/1/2000 |
|
|
|
NO |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
2001 5828 |
|
6/1/2000 |
|
|
|
NZ |
|
METHODS OF PRODUCING 5’-NUCLEIC ACID-PROTEIN CONJUGATES |
|
514772 |
|
6/1/2000 |
|
|
|
US Provisional |
|
C-TERMINAL PROTEIN TAGGING |
|
60/143,339 |
|
7/12/1999 |
|
|
|
US |
|
C-TERMINAL PROTEIN TAGGING |
|
09/614,264 |
|
7/12/2000 |
|
|
|
PCT |
|
C-TERMINAL PROTEIN TAGGING |
|
US00/40347 |
|
7/11/2000 |
|
|
|
AU |
|
C-TERMINAL PROTEIN TAGGING |
|
71338/00 |
|
7/11/2000 |
|
|
|
CA |
|
C-TERMINAL PROTEIN TAGGING |
|
2,372,795 |
|
7/11/2000 |
|
|
|
EP |
|
C-TERMINAL PROTEIN TAGGING |
|
960 132.S |
|
7/11/2000 |
|
|
|
HK |
|
C-TERMINAL PROTEIN TAGGING |
|
02106434.S |
|
7/11/2000 |
|
|
|
IL |
|
C-TERMINAL PROTEIN TAGGING |
|
146451 |
|
7/11/2000 |
|
|
|
NZ |
|
C-TERMINAL PROTEIN TAGGING |
|
515292 |
|
7/11/2000 |
|
|
|
US Provisional |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
60/145,834 |
|
7/27/1999 |
|
|
|
US |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
09/619,103 |
|
7/19/2000 |
|
Issued |
|
PCT |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
US00/19653 |
|
7/19/2000 |
|
|
|
AU |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
61112/00 |
|
7/19/2000 |
|
|
|
CA |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
2,377,468 |
|
7/19/2000 |
|
|
|
EP |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
947 524.5 |
|
7/19/2000 |
|
|
|
HK |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
2106728.4 |
|
7/19/2000 |
|
|
|
IL |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
147037 |
|
7/19/2000 |
|
|
|
JP |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
2001-512922 |
|
7/19/2000 |
|
|
|
KR |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
2002-7001058 |
|
7/19/2000 |
|
|
|
NO |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
2002 0348 |
|
7/19/2000 |
|
|
|
NZ |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
516055 |
|
7/19/2000 |
|
|
|
RU |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
2002104938 |
|
7/19/2000 |
|
|
|
US |
|
PEPTIDE ACCEPTOR LIGATION METHODS |
|
10/208,357 |
|
7/30/2002 |
|
|
|
US Provisional |
|
METHODS FOR ENCODING & SORTING IN VITRO TRANSLATED PROTEINS |
|
60/151,261 |
|
8/27/1999 |
|
|
|
US |
|
METHODS FOR ENCODING & SORTING IN VITRO TRANSLATED PROTEINS |
|
09/648,040 |
|
8/25/2000 |
|
Issued |
|
PCT |
|
METHODS FOR ENCODING & SORTING IN VITRO TRANSLATED PROTEINS |
|
US00/23414 |
|
8/25/2000 |
|
|
|
AU |
|
METHODS FOR ENCODING & SORTING IN VITRO TRANSLATED PROTEINS |
|
69387/00 |
|
8/25/2000 |
|
|
|
CA |
|
METHODS FOR ENCODING & SORTING IN VITRO TRANSLATED PROTEINS |
|
2382545 |
|
8/25/2000 |
|
|
|
EP |
|
METHODS FOR ENCODING & SORTING IN VITRO TRANSLATED PROTEINS |
|
00 957 818.8 |
|
8/25/2000 |
|
|
|
JP |
|
METHODS FOR ENCODING & SORTING IN VITRO TRANSLATED PROTEINS |
|
2001-520897 |
|
8/25/2000 |
|
|
|
US |
|
METHODS FOR ENCODING & SORTING IN VITRO TRANSLATED PROTEINS |
|
10/217,914 |
|
8/13/2002 |
|
|
|
US |
|
COUPLED ISOTHERMAL POLYNUCLEOTIDE AMPLIFICATION AND TRANSLATION SYSTEM |
|
07/939,302 |
|
9/2/1992 |
|
|
|
US |
|
COUPLED ISOTHERMAL POLYNUCLEOTIDE AMPLIFICATION AND TRANSLATION SYSTEM |
|
08/231,587 |
|
4/20/1994 |
|
|
|
AT |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
BE |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
CH |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
DE |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
EP |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
ES |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
FR |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
GB |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
GR |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
IT |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
LU |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
NL |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
SE |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
EP0341444 |
|
4/13/1989 |
|
Issued |
|
US |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
07/842,465 |
|
2/27/1992 |
|
Issued |
|
US |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
08/320,663 |
|
10/11/1994 |
|
Issued |
|
US |
|
RAPID MUTATIONAL ANALYSIS METHOD |
|
09/400,207 |
|
9/21/1999 |
|
|
|
US |
|
SYSTEMIC POLYPEPTIDE EVOLUTION BY REVERSE TRANSCRIPTION |
|
07/829,461 |
|
1/31/1992 |
|
Issued |
|
US |
|
SYSTEMIC POLYPEPTIDE EVOLUTION BY REVERSE TRANSCRIPTION |
|
09/197,649 |
|
11/23/1998 |
|
Issued |
|
US |
|
SYSTEMIC POLYPEPTIDE EVOLUTION BY REVERSE TRANSCRIPTION |
|
09/790,399 |
|
2/22/2001 |
|
|
|
US Provisional |
|
SCREENING AND AFFINITY BINDING ASSAYS |
|
60/275,197 |
|
3/12/2001 |
|
|
|
US Provisional |
|
IN VITRO PROTEIN INTERACTION DETECTION SYSTEMS |
|
60/300,267 |
|
6/21/2001 |
|
|
|
US |
|
IN VITRO PROTEIN INTERACTION DETECTION SYSTEMS |
|
10/176,826 |
|
6/20/2002 |
|
|
|
PCT |
|
IN VITRO PROTEIN INTERACTION DETECTION SYSTEMS |
|
US02/19937 |
|
6/20/2002 |
|
|
|
US Provisional |
|
MODULAR ASSEMBLY OF NUCLEIC ACID-PROTEIN FUSION MOLECULES |
|
60/309,231 |
|
7/31/2001 |
|
|
|
US |
|
MODULAR ASSEMBLY OF NUCLEIC ACID-PROTEIN FUSION MOLECULES |
|
10/ |
|
7/31/2002 |
|
|
|
PCT |
|
MODULAR ASSEMBLY OF NUCLEIC ACID-PROTEIN FUSION MOLECULES |
|
US02/24180 |
|
7/31/2002 |
|
|
|
US Provisional |
|
CELLULAR KINASE TARGETS AND INHIBITORS AND METHODS FOR THEIR USE |
|
60/337,990 |
|
11/13/2001 |
|
|
|
US |
|
CELLULAR KINASE TARGETS AND INHIBITORS AND METHODS FOR THEIR USE |
|
10/293,086 |
|
11/13/2002 |
|
|
|
US Provisional |
|
SOLID PHASE IMMOBILIZATION OF PROTEINS AND PEPTIDES |
|
60/333,470 |
|
11/27/2001 |
|
|
|
US |
|
SOLID PHASE IMMOBILIZATION OF PROTEINS AND PEPTIDES |
|
10/302,456 |
|
11/21/2002 |
|
|
|
de |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS, PRODUCTION AND UTILIZATION THEREOF |
|
199 23 966.5 |
|
5/25/1999 |
|
|
|
PCT |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS, PRODUCTION AND UTILIZATION THEREOF |
|
PCT/EP00/04791 |
|
5/25/2000 |
|
|
|
CA |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS. PRODUCTION AND UTILIZATION THEREOF |
|
2,374,438 |
|
5/25/2000 |
|
|
|
CN |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS, PRODUCTION AND UTILIZATION THEREOF |
|
00809231.1 |
|
5/25/2000 |
|
|
|
CZ |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS, PRODUCTION AND UTILIZATION THEREOF |
|
PV2001-4201 |
|
5/25/2000 |
|
|
|
EE |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS, PRODUCTION AND UTILIZATION THEREOF |
|
0616/01 PC |
|
5/25/2000 |
|
|
|
EP |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS, PRODUCTION AND UTILIZATION THEREOF |
|
941987 |
|
5/25/2000 |
|
|
|
IL |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS. PRODUCTION AND UTILIZATION THEREOF |
|
146371 |
|
5/25/2000 |
|
|
|
JP |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS, PRODUCTION AND UTILIZATION THEREOF |
|
2000-620126 |
|
5/25/2000 |
|
|
|
US |
|
DETECTION SYSTEM FOR ANALYZING MOLECULAR INTERACTIONS. PRODUCTION AND UTILIZATION THEREOF |
|
5/25/2000 |
|
|
|
|
|
de |
|
TEST SYSTEM FOR DETECTING ANALYTES, A METHOD FOR THE PRODUCTION THEREOF AND ITS USE |
|
|
|
|
|
|
|
PCT |
|
TEST SYSTEM FOR DETECTING ANALYTES, A METHOD FOR THE PRODUCTION THEREOF AND ITS USE |
|
PCT/EP00/10336 |
|
10/20/2000 |
|
|
|
CA |
|
TEST SYSTEM FOR DETECTING ANALYTES, A METHOD FOR THE PRODUCTION THEREOF AND ITS USE |
|
2393703 |
|
10/20/2000 |
|
|
|
de |
|
BIO-PROBES AND USES THEREOF |
|
100 33 194.7 |
|
6/26/2001 |
|
|
|
PCT |
|
BIO-PROBES AND USES THEREOF |
|
PCT/EP01/07259 |
|
6/26/2001 |
|
|
|
de |
|
METHODS FOR IDENTIFYING SPECIFICALLY CLEAVABLE PEPTIDES AND USE OF SUCH PEPTIDE SEQUENCES |
|
100 41 238 |
|
8/22/2000 |
|
|
|
PCT |
|
METHODS FOR IDENTIFYING SPECIFICALLY CLEAVABLE PEPTIDES AND USE OF SUCH PEPTIDE SEQUENCES |
|
PCT/EP01/0910 |
|
8/7/2001 |
|
|
|
de |
|
METHOD FOR ISOLATING AND IDENTIFYING EFFECTORS |
|
199 59 857 |
|
|
|
|
|
PCT |
|
METHOD FOR ISOLATING AND IDENTIFYING EFFECTORS |
|
PCT/EP01/14337 |
|
12/6/2001 |
|
|
|
de |
|
SECRETION SIGNAL PEPTIDES, DNA SEQUENCES THEREOF, EXPRESSION VECTORS PREPARABLE THEREWITH FOR EUKARYOTIC CELLS AND USE THEREOF FOR BIOTECHNOLOGICAL PREPARATION OF PROTEINS |
|
100 62 302.6 |
|
12/14/2000 |
|
|
|
de |
|
PEPTIDE ACCEPTOR /tRNA-HYBRID MOLECULE AND ITS USE FOR PREPARING CODON-SPECIFICALLY ARRESTED TRANSLATION COMPLEXES |
|
101 16 585.4 |
|
4/3/2001 |
|
|
|
PCT |
|
PEPTIDE ACCEPTOR /tRNA-HYBRID MOLECULE AND ITS USE FOR PREPARING CODON-SPECIFICALLY ARRESTED TRANSLATION COMPLEXES |
|
PCT/EP02/03649 |
|
4/3/2002 |
|
|
|
US Provisional |
|
NOVEL METHOD FOR CLONING VARIABLE DOMAIN SEQUENCES OF IMMUNOLOGICAL GENE REPERTOIRE |
|
60/290,907 |
|
5/14/2001 |
|
|
|
PCT |
|
NOVEL METHOD FOR CLONING VARIABLE DOMAIN SEQUENCES OF IMMUNOLOGICAL GENE REPERTOIRE |
|
US/02/15125 |
|
5/14/2002 |
|
|
