CONSULTING AGREEMENT
Exhibit
10.10
THIS
CONSULTING AGREEMENT
(this
“Agreement”)
is
made and entered into as of January 1, 2007 (the
“Effective Date”),
by and
between MODIGENETECH
LTD.,
an
Israeli corporation (the “Company”)
and
Dr. Fuad Fares (the “Consultant”)
operating through his privately owned company _________________ Ltd.
(“FCO”)
through which the Consultant services to the Company will be
rendered.
RECITALS
WHEREAS,
the
Company desires the expertise the Consultant can provide in connection with
the
business of the Company and in connection with certain scientific areas;
and
WHEREAS,
the
Consultant has agreed to provide his services to the Company on the terms
and
conditions hereinafter set forth; and
WHEREAS,
the
parties also desire to terminate certain prior agreements;
NOW,
THEREFORE,
the
parties hereby agree as follows:
AGREEMENTS
1. Engagement,
Period of Engagement.
(a) The
Company offers to engage the Consultant and the Consultant hereby accepts
such
engagement, to provide services to the Company as a consultant for the period
established under this Section 1
(the
“Period
of Engagement”).
The
Period of Engagement commences on the Effective Date, and shall end on the
date
that is 24 months after the Effective Date. The Period of Engagement may
be
extended for subsequent 12-month periods upon the written agreement of the
Consultant and the Company.
(b) Notwithstanding
anything contained herein to the contrary, the Period of Engagement shall
end
upon any termination of this Agreement pursuant to Section 5.
2. Services.
During
the Period of Engagement, the Consultant shall provide the following
services:
(a) Serving
in the capacity as the Chief Scientific Officer of the Company and, together
with the CEO of the Company, advise on all of the scientific affairs and
operations of the Company, subject to the direction and control of the CEO
of
the Company;
(b) Invent,
improve and design new technologies related with the Company’s business, as
detailed in the work plan in Schedule A, which shall start upon approval
of the
Company’s Board of Directors; and
(c) make
such
presentations and reports to the Board of Directors of the Company (the
“Board”)
as and
when the Board may request.
(d) All
services listed in Section 2(b) - (d) will be provided by the Consultant
on part
time basis of two business days per week.
3. Compensation. In
consideration for any services to be provided under Section 2,
the
Company shall pay to the Consultant a monthly consulting fee of Two Thousand
U.S. Dollars ($3,000.00) plus V.A.T (if applicable); payable on the first
of
each month upon providing the Company with an invoice. In addition, the Company
shall pay the consultant milestone payments in accordance with the successful
completion of the milestones as determined by the Company, all as detailed
in
Schedule A. Payments will be in Israeli Shekels (IS) according to the official
IS-US$ exchange rate as published by the Bank of Israel on the date of payment
in (xxx.xxxxxxxxxx.xxx.xx).
4. Expenses.
If
in
connection with the performance of services hereunder at the request of the
Company, the Consultant incurs reasonable out-of-pocket costs for expenses
for
travel abroad, meals and lodging or other reasonable expenses of a type for
which other providers of professional services to the Company would be
reimbursed by the Company, the Consultant shall be entitled to reimbursement
therefor by the Company in accordance with the reasonable standards and
procedures established by the Company and communicated to the
Consultant.
5. Termination
of Agreement. This
Agreement and the Period of Engagement established hereunder shall terminate
immediately upon the occurrence of any of the following events: (i) the
Consultant’s death; (ii) the Consultant’s material breach of the Consultant’s
obligations under Section 2
and
subsequent failure to substantially cure such breach after notice of such
breach; (iii) the Consultant’s voluntary termination of this Agreement for any
reason, upon thirty (30) days written notice to the Company; or (iv) in the
event of no material breach of the Consultant’s obligations under Section 2 and
subsequent failure to cure the same, the Company’s voluntary termination of this
Agreement for any reason, upon thirty (30) days written notice to the
Consultant. In the event of a termination of this Agreement in accordance
with
clause (iv) of the previous sentence, the Company shall pay to the Consultant
a
lump sum equal $18,000. Following the termination of this Agreement, the
Company
shall have no further obligations hereunder, except as specified in the prior
sentence. The provisions of Sections 6,
7,
16 and
17 shall survive the termination of this Agreement.
6. Nonsolicitation. In
consideration of the compensation to be paid to the Consultant pursuant to
Section 3,
the
Consultant hereby covenants and agrees that for a period of twelve (12) months
following the termination of this Agreement for any reason, the Consultant
will
not directly or indirectly (including, without limitation, any action by
any
corporation, partnership or other entity for which the Consultant acts as
officer, employer, or consultant or in which the Consultant directly or
indirectly holds a shareholder or other ownership position greater than five
percent (5%)) offer employment to, hire, engage or assist another in offering
employment to, hiring or engaging (without regard to whether it would be
in
competition with the Company’s business) a person who is or was an employee or
who performed similar services of or for the Company at any time during the
then
preceding twelve (12) month period or undertake any business with or solicit
the
business of any person, firm or company who shall have been a customer of
the
Company during the then preceding twelve (12) month period, in any such case
without the prior written consent of the Company.
2
7. Confidential
Information.
The
Consultant shall maintain Confidential Information (as defined below) in
strict
confidence and secrecy and shall not at any time, directly or indirectly,
use,
publish, make lists of, communicate, divulge or disclose to any person or
business entity or use for any purpose any Confidential Information or assist
any third parties in doing so, except on behalf of and for the benefit of
the
Company. The Consultant agrees, upon demand by the Company, to promptly return
all Confidential Information (including any copies, extracts thereof or
materials reflecting any such information) which is in the Consultant’s
possession.
For
purposes of this Agreement, “Confidential
Information”
shall
include, but not be limited to, materials, records, data or trade secrets
regarding the assets, condition, business, financial information, business
affairs, business matters or other matters related to the Company and to
its
direct and indirect subsidiaries and affiliates which the Consultant has
knowledge of as a result of the Consultant’s services for the Company.
Confidential Information shall not include information that becomes generally
available to the public other than as a result of disclosure by the Consultant.
Nothing in this Agreement modifies or reduces the Consultant’s obligations to
comply with applicable laws related to trade secrets, confidential information
or unfair competition.
8. No
Employment Relationship Created.
The
relationship between the Company and the Consultant shall be that of client
and
independent contractor. The Company shall not assume, and specifically
disclaims, any obligations of an employer to an employee which may exist
under
applicable law. The Consultant shall be treated as an independent contractor
for
all purposes of federal, state and local income taxes and payroll taxes and
the
Company shall report on the appropriate IRS Form 1099 all compensation paid
to
the Consultant. The Consultant shall be responsible for payment of all taxes,
including federal, state and local taxes, arising out of the Consultant’s
activities in accordance with this Agreement, including by way of illustration,
but not limitation, federal and state personal income tax and social security
tax, all as may be required by applicable law or regulation. The Consultant
shall have the full authority to select the means, manner and method of
performing the services to be performed under this Agreement. The Consultant
shall not be considered by reason of the provisions of this Agreement or
otherwise as being an employee of the Company. The Consultant shall not be
eligible to participate in any employee benefit plans offered by the Company
or
any of its subsidiaries to their respective employees.
9. Successors
and Assigns.
This
Agreement will inure to the benefit of and be binding upon the Consultant,
the
Consultant’s legal representatives and testate or intestate distributees, and
the Company, and its successors and assigns, including, in the case of the
Company, any successor by merger or consolidation or a statutory receiver
or any
other person or firm or corporation to which all or substantially all of
the
respective assets and business of the Company may be sold or otherwise
transferred. The Consultant may not assign any of his rights under this
Agreement without the prior written consent of the Company. Except as expressly
provided herein, nothing in this Agreement shall be construed to give any
person
other than the parties to this Agreement any legal or equitable right, remedy
or
claim under or with respect to this Agreement or any provision of this
Agreement.
3
10. Waiver.
The
rights and remedies of the parties to this Agreement are cumulative and not
alternative. Neither the failure nor any delay by any party in exercising
any
right, power or privilege under this Agreement or the documents referred
to in
this Agreement will operate as a waiver of such right, power or privilege,
and
no single or partial exercise of any such right, power or privilege will
preclude any other or further exercise of such right, power or privilege
or the
exercise of any other right, power or privilege.
11. Modification.
This
Agreement may only be amended by a written agreement executed by both
parties.
12. Notices.
All
notices and other communications under this Agreement must be in writing
and
will be deemed to have been duly given if delivered by hand or by nationally
recognized overnight delivery service (receipt requested) or mailed by certified
mail (return receipt requested) with first class postage prepaid:
(a) |
if
to the Company, to:
|
ModigeneTech
Ltd.
0
Xxxxx
Xxxxxx
Weizmann
Science Park
Nes
Ziona
Attention:
CEO
with
a
copy to:
Xxxxxxxx
Xxxx Xxxxx, Esq.
Barack
Xxxxxxxxxx Xxxxxxxxxx Xxxxxxx & Xxxxxxxxx LLP
000
X.
Xxxxxx Xxxxx, Xxxxx 0000
Xxxxxxx,
Xxxxxxxx 00000
(b) |
if
to Consultant, to:
|
_______________
_______________
_______________
or
to
such other person or place as either party shall furnish to the other in
writing. Except as otherwise provided herein, all such notices and other
communications shall be effective: (x) if delivered by hand, when
delivered; (y) if mailed in the manner provided in this Section, five (5)
business days after deposit with the United States Postal Service; or
(z) if delivered by overnight express delivery service, on the next
business day after deposit with such service.
13. Entire
Agreement.
This
Agreement and any documents executed by the parties pursuant to this Agreement
and referred to herein constitute a complete and exclusive statement of the
entire understanding and agreement of the parties hereto with respect to
their
subject matter and supersede all other prior agreements and understandings,
written or oral, relating to such subject matter between the parties.
4
14. Severability.
Whenever
possible, each provision of this Agreement shall be interpreted in such manner
as to be effective and valid under applicable law, but if any provision of
this
Agreement is held to be prohibited by or invalid under applicable law, such
provision will be ineffective only to the extent of such prohibition or
invalidity, without invalidating the remainder of such provision or the
remaining provisions of this Agreement. Without limiting the generality of
the
foregoing, if the scope of any provision contained in this Agreement is too
broad to permit enforcement to its full extent, but may be made enforceable
by
limitations thereon, such provision shall be enforced to the maximum extent
permitted by law, and the Consultant hereby agrees that such scope may be
judicially modified accordingly.
15. Counterparts.
This
Agreement and any amendments hereto may be executed in any number of
counterparts, each of which shall be deemed an original, but all of which
together shall constitute one and the same agreement.
16. Intellectual
Property.
1. If
Consultant creates, invents, designs, develops, contributes to or improves
any
works that relate to Employer’s business of developing therapeutic proteins,
either alone or with third parties, at any time during Consultant’s employment
by Employer and within the scope of such employment and/or with the use of
any
of Employer resources (“Employer Works”), Consultant shall promptly and fully
disclose same to Employer and hereby irrevocably assigns, transfers and conveys,
to the maximum extent permitted by applicable law, all rights and intellectual
property rights therein (including rights under patent, industrial property,
copyright, trademark, trade secret, unfair competition and related laws)
of the
Employer Works to Employer to the extent ownership of any such rights does
not
vest originally in Employer.
2. Consultant
agrees to keep and maintain adequate and current written records (in the
form of
notes, sketches, drawings, and any other form or media requested by Employer)
of
all Employer Works. The records will be available to and remain the sole
property and intellectual property of Employer at all times.
3. Consultant
shall take all requested actions and execute all requested documents (including
any licenses or assignments required by a government contract) at Employer’s
expense (but without further remuneration) to assist Employer in validating,
maintaining, protecting, enforcing, perfecting, recording, patenting or
registering any of Employer’s rights in the Employer Works. If Employer is
unable for any other reason to secure Consultant’s signature on any document for
this purpose, then Consultant hereby irrevocably designates and appoints
Employer and its duly authorized officers and agents as Consultant’s agent and
attorney in fact, to act for and in Consultant’s behalf and stead to execute any
documents and to do all other lawfully permitted acts in connection with
the
foregoing.
5
4. Consultant
shall not improperly use for the benefit of, bring to any premises of, divulge,
disclose, communicate, reveal, transfer or provide access to, or share with
Employer any confidential, proprietary or non-public information or intellectual
property relating to a former employer or third party without the prior written
permission of such third party. Consultant hereby indemnifies, holds harmless
and agrees to defend Employer and its officers, directors, partners, employees,
agents and representatives from any breach of the foregoing covenant. Consultant
shall comply with all relevant policies and guidelines of Employer, including
regarding the protection of confidential information and intellectual property
and potential conflicts of interest. Consultant acknowledges that Employer
may
amend any such policies and guidelines from time to time, and that Consultant
remains at all times bound by their most current version.
5. The
provisions of this Section 16 shall survive the termination of Consultant’s
employment for any reason.
IN
WITNESS WHEREOF, each
of
the parties hereto has caused this Agreement to be executed, all as of the
day
and year first above written.
MODIGENETECH
LTD.
|
|||
By: | |||
|
|||
Its: | |||
|
|||
________________________________, LTD. | |||
By: | |||
|
|||
Its: | |||
|
|||
Dr.
Fuad Fares
|
6
Schedule
A
Work
Plan for developing a new strategy for designing
Long
acting proteins
1.
|
Objective
-
the objective of this work plan is to examine a new strategy of
designing
long acting proteins that have medical importance using a human
peptide
that contain the recognition sequence of O-linked oligosaccharides
(OLP).
|
This
peptide is rich in O-linked oligosaccharide chains and contain more than
12
chains. The CTP that we have used contain 4 O-linked oligosaccharides.
Therefore, it is possible to use the peptide or part of it. Positive results
will enable ModigeneTech to apply for new patents of the technology and of
the
new designed proteins.
2.
|
Scope
of work
|
To
prove
this concept we will use human erythropoietin, because we have in vitro and
in
vivo biological systems. I addition, it will be possible to compare the results
of the new peptide and that of the CTP using the same protein.
In
this
study 4 variants of EPO will be designed.
The
program will include two phases:
Phase
I
- Fusing
the new peptide to the N- or to the C- terminal of EPO
In
this
phase two versions of the intact
authentic human erythropoietin molecule
will be
prepared.
Molecule
|
CTP
type
|
Remarks
|
||
EPO
- (OLP)
|
>12
x O-linked glycosylation sites
|
"Existing
version" with 1 additional OLP containing multi chains of O-linked
oligosaccharides in the C-terminal of EPO
|
||
(OLP)
- EPO
|
>12
x O-linked glycosylation sites
|
Existing
version" with 1 additional OLP containing multi chains of O-linked
oligosaccharides in the N-terminal of
EPO
|
Phase
II
- Fusing
a part of the OLP peptide
In
this
phase two versions of the intact
human erythropoietin molecule
fused to
a part of the OLP in the C- and N- terminals of the molecule.
Molecule
|
CTP
Type
|
Remarks
|
||
EPO-(1/2
OLP)
|
~8
x O-linked glycosylated sites
|
Attaching
a short peptide to the C-terminal
|
||
(1/2
OLP)-E PO
|
~8
x O-linked glycosylated sites
|
Attaching
a short peptide to the N-terminal
|
7
(a) 3.
General considerations and responsibilities
This
plan
is based on sharing the responsibilities for the preparation of the required
EPO-OLP versions
between ModigeneTech and Dr. Fares laboratory:
3.1
|
Dr.
Fares Lab - Upstream activities for preparing non-formulated crude
concentrated EPO-OLP from
the CHO cells growth medium including in-process control to determine
concentration and activity of the secreted molecule. .Dr. Fares
Lab in
collaboration with ModigeneTech will also perform animal studies
in animal
models to measure the biological activity and biological half-life
time of
the EPO-OLP.
|
3.2
|
ModigeneTech
will decide whether to developer outsource the purification processes
for
those candidate molecules which will demonstrate promising potential
in
the early studies.
|
3.2. |
Subcontracting
- ModigeneTech will use subcontractors for the experimental parts
of the
work which require animal studies.
|
3.3. |
ModigeneTech
will apply the results for a patent where Dr. Fuad Fares is the
inventor.
|
4. |
Basic
plan of action
|
4.2.
|
EPO
variants will be prepared using overlapping PCR technique
|
4.3.
|
Cloning
and expression vectors of the 4 candidate molecules can be done
in Dr.
Fares Laboratory
|
4.4.
|
CHO
cells will be used to express the various versions of EPO-OLP.
Different
CHO cell lines and vectors may be used for doing so.
|
4.5.
|
EPO-OLP molecules
will be tested for in vitro and in vivo biological
activity
|
5. |
Material
requirements
|
5.1 |
It
is estimated that a quantity of micrograms of each EPO-OLP will
be required to carry out the animal
experiments.
|
5.2.
|
It
is estimated that a quantity of ~500µg of each EPO-OLP will
be required to carry out the animal
experiments
|
8
5.3.
|
Level
of purity of the EPO-CTP
experimental material - crude sterile filtered aqueous solution
(in buffer
to
be determined)
following dialysis and concentration using tangential ultrafiltration.
|
5.4.
|
Target
concentration: to
be determined
|
6. |
Schedule
of time in months
|
Months
|
||||||||||||||||||
Step
|
Activity
|
3
|
6
|
9
|
12
|
15
|
18
|
21
|
24
|
|||||||||
I
|
Gene
fusion, Cloning into expression vectors, sequencing of EPO-OLP
variants.
|
|||||||||||||||||
II
|
Transfection
into CHO cells and stable clone selection
|
|||||||||||||||||
Collection
media, concentration and measuring the concentration of EPO variants
by
RIA
|
||||||||||||||||||
III
|
In
vitro biological activity and receptor binding studies
|
|||||||||||||||||
IV
|
Animal
studies in rodents -2 first candidate molecules
|
|||||||||||||||||
V
|
Animal
studies in rodents- 2 second candidate molecules
|
7. |
Budget
|
7.1
|
Oligonucleotides,
PCR reagents, enzymes, DNA sequences
|
$
|
10000
|
||||
7.2.
|
Materials
(medium, chemicals and disposables)
|
|
$
|
35,000
|
|||
7.3.
|
Animals
+ CRO costs
|
$
|
35,000
|
||||
7.4.
|
Technician
(100%) for 24 months
|
$
|
36,000
|
||||
|
|||||||
7.5.
|
Total
budget:
|
$
|
116,000
|
9
8. |
Milestones
& Payments
|
Step
|
Milestone
|
Payment
|
|||||
I
|
In
vitro biological activity and receptor binding studies
|
$
|
7,000
|
||||
II
|
Receipt
of report by the Company detailing the results of in vitro biological
activity and receptor binding assays
|
$
|
20,000
|
||||
III
|
Receipt
of report by the Company detailing the results of animal studies
in
rodents with first pair of candidate molecules
|
$
|
37,500
|
||||
IV
|
Receipt
of report by the Company detailing the results of animal studies
in
rodents with second pair of candidate molecules
|
$
|
37,500
|
10