Restricted Compounds definition

Restricted Compounds has the meaning set forth in Section 20.4.4(c).
Sample 1
Restricted Compounds means any and all of: (A)(I) (+)-alpha-Methylbenzeneethanamine, also known as “amphetamine”, (II) carbamazepine (5H-Dibenz{b,f}azepine-5-carboxyamide), (III) guanfacine (N-(Aminoiminomethyl)-2,6-dichlorobenzeneacetamide), (IV) lanthanum, and (V) mesalamine (5-Amino-2-hydroxybenzoic acid), (B) any isomers, salts, solvates, hydrates, polymorphs, esters, prodrugs, or metabolites of clause (A), and (C) any compound involving forming or breaking a bond or bonds with any of clause (A) or (B) where at least one prophylactic, therapeutic or diagnostic indication of such compound and/or its metabolite is substantially the same as that of any of clause (A) or (B), but excluding 10,11-Dihydro-10-oxo-5H-debenz[b,f]azepine-5-carboxamide, also known as “oxcarbazepine”.
Sample 1Sample 2
Restricted Compounds has the meaning set forth in Section 2.10.
Sample 1

Examples of Restricted Compounds in a sentence

  • For clarity, and notwithstanding the foregoing, the Company shall be permitted to conduct research using the Collaboration IP and Residuals with respect to any compounds if such compounds are not Restricted Compounds; provided that such compounds have not been created, designed or synthesized by conducting research with respect to (including performing any analoguing of) the Restricted Compounds.

  • From time to time thereafter the RMC may designate additional Active Compounds as "Restricted Compounds", or remove such designation from previously designated Active Compounds, so long as the total number of such Restricted Compounds with respect to a particular Validated Target shall not exceed [ ] at any time.

  • Initially, all such Cortex Compounds shall be Restricted Compounds.

  • The test is not the political correctness of the speech but the possibility to ignite a collective action.

  • At the Port’s option, the Port may require that the Lessee remove some or all improvements at Lessee’s own expense.

  • Restricted Compounds: Paints and coatings shall not contain acrolein, acrylonitrile, antimony, benzene, butyl benzyl phthalate, cadmium, di (2- ethylhexyl) phthalate, di-n-butyl phthalate, di-n-octyl phthalate, 1,2- dichlorobenzene, diethyl phthalate, diethyl phthalate, dimethyl phthalate, ethylbenzene, formaldehyde, hexavalent chromium, isophorone, lead, mercury, methyl ethyl ketone, methyl isobutyl ketone, methylene chloride, naphthalene, toluene (methylbenzene), 1,1,1-trichloroethane, or vinyl chloride.

  • Organon shall own exclusively the Restricted Compounds other than Cortex Compounds.

  • Current plant first and second floor materials flow rate is shown in Figure 3.2 and Figure 3.3. Tecnomatix tool SankeyDiagram visualizes materials flow rate in purple colour.

  • Such compounds which meet the requirements shall remain Restricted Compounds and any screened compounds which do not meet the requirements other than Organon Compounds, shall become Unrestricted Compounds.

  • The tree may be removed even if the total number of trees removed in the harvesting operation concerned will, as a result, exceed the number calculated by applying the principle set out in condition 6.13 (c).


More Definitions of Restricted Compounds

Restricted Compounds shall have the meaning assigned to it in Section 4.4.
Sample 1
Restricted Compounds means: Organon Compounds; compounds which are still under investigation in the Research pursuant to Section 3.3 below; Research Collaboration Compounds that are not AMPAkines; those Research Collaboration Compounds and Cortex Compounds which have entered the Selection Phase and those compounds which are developed and commercialized pursuant to Section 4.5 below.
Sample 1

Related to Restricted Compounds

  • Licensed Compounds means any EZH2 Compound(s) that is:

  • Collaboration Compound means any of the following: (a) FG-4592, (b) any HIF Compound (other than FG-4592) that is added to this Agreement pursuant to Section 3.6, and (c) any salts, esters, complexes, chelates, crystalline and amorphous morphic forms, pegylated forms, enantiomers (excluding regioisomers), prodrugs, solvates, metabolites and catabolites of any of the foregoing ((a) or (b)).

  • Licensed Compound means [***].

  • Compounds means a small molecule HMT inhibitor.

  • Lead Compound means any compound of lead other than galena which, when treated in the manner described below, yields to an aqueous solution of hydrochloric acid a quantity soluble lead compound exceeding, when calculated as lead monoxide, five percent of the dry weight of the portion taken analysis.

  • Product Candidate means each of MYO-101, MYO-102, MYO-103, MYO-201 and MYO-301, as defined on Exhibit B, in each case in any form or formulation.

  • Collaboration Product means any pharmaceutical product in finished form that contains a Collaboration Compound, either as the sole active ingredient or in combination with one or more other active ingredients, and all present and future formulations, dosages and dosage forms thereof.

  • Back-Up Compound means, with reference to any particular Development Candidate or Drug Product Candidate, a Compound which (a) has the same principal mode of action (i.e., Potentiator or Corrector) as that Development Candidate or Drug Product Candidate; and (b) was among the group of Compounds, identified by VERTEX as potential additional lead molecules having the same principal mode of action, from which the Development Candidate was selected.

  • Development Candidate means a Compound that meets the Development Candidate Criteria for the initiation of a Development Program for the treatment of CF, and which is the subject of a notice from Vertex to CFFT that Vertex intends to commence formal pre-clinical development of the Compound in the Field pursuant to the provisions of Section 3.1 hereof.

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Compound means the taking of two or more ingredients and fabricating them into a single

  • Diagnostic Product means any test or assay for diagnosing or detecting a disease, disorder, medical condition, or symptom.

  • Antibody means a molecule or a gene encoding such a molecule comprising or containing one or more immunoglobulin variable domains or parts of such domains or any existing or future fragments, variants, modifications or derivatives thereof.

  • Competing Product means [***].

  • Collaboration Target means the Initial Collaboration Targets set forth on Exhibit F and any Additional Target or Substitute Target that is selected in accordance with Section 3.3 of this Agreement.

  • Competing Products means any product or service in existence or under development that competes with any product or service of the Company Group about which the Participant obtained Confidential Information or for which the Participant provided advisory services or had sales, origination, marketing, production, distribution, research or development responsibilities in the last twenty-four (24) months of employment with the Company Group.

  • Commercialized shall have corresponding meanings.

  • Commercializing means to engage in Commercialization and “Commercialized” has a corresponding meaning.

  • Restricted Territory means any state, county, or locality in the United States in which the Company conducts business and any other country, city, state, jurisdiction, or territory in which the Company does business.

  • Manufacturing Technology means any and all patents, patent applications, Know-How, and all intellectual property rights associated therewith, and including all tangible embodiments thereof, that are necessary or useful for the manufacture of adeno- associated viruses, adeno-associated virus vectors, research or commercial reagents related thereto, Licensed Products, or other products, including manufacturing processes, technical information relating to the methods of manufacture, protocols, standard operating procedures, batch records, assays, formulations, quality control data, specifications, scale up, any and all improvements, modifications, and changes thereto, and any and all activities associated with such manufacture. Any and all chemistry, manufacturing, and controls (CMC), drug master files (DMFs), or similar materials provided to regulatory authorities and the information contained therein are deemed Manufacturing Technology.

  • Restricted Countries shall have the meaning given to it in Clause 26.5.3 (Protection of Personal Data);