Tularik Compound Library definition

Tularik Compound Library means that collection of natural extracts, natural compounds and synthetic compounds which Tularik owns or has the right to license or sublicense as of the Effective Date or from time to time during the period of the Research Program.
Tularik Compound Library means the library consisting of Tularik Substances.

Examples of Tularik Compound Library in a sentence

  • Each party agrees and acknowledges that use of the substances contained in the Taisho Compound Library or the Tularik Compound Library, as the case may be, is limited solely to those activities contemplated by the Research Program, unless otherwise provided for in this Agreement, and are for research use only and shall not be administered to humans in any manner or form, except in accordance with the terms of this Agreement, subject to appropriate governmental approval.

  • Taisho acknowledges and agrees that Tularik is and shall remain the sole owner (or licensee with right to sublicense) of the Tularik Patents, the Tularik Know-How, the Tularik Assays and the materials and compounds in the Tularik Compound Library and that Taisho has no rights in or to any of them other than the rights specifically granted herein.

  • The Tularik Compound Library shall be treated as Tularik's Confidential Information.

  • The Tularik Compound Library shall be used in HTS against the Current Program Targets.

  • Except for the research license granted to Knoll contained in Section 2.9.1, Xxxxx shall have no rights to make, use or sell Tularik Substances in the Knoll Territory unless a Tularik Substance becomes a Program Product and the Parties execute a License Agreement therefor following a Commercialization Notice pursuant to Section 5.1. Tularik shall provide structural information to Knoll on Validated Hits from the Tularik Compound Library within [ * ].

  • Except for the research license granted to Xxxxx contained in Section 2.9.1, Xxxxx shall have no rights to make, use or sell Tularik Substances in the Xxxxx Territory unless a Tularik Substance becomes a Program Product and the Parties execute a License Agreement therefor following a Commercialization Notice pursuant to Section 5.1. Tularik shall provide structural information to Xxxxx on Validated Hits from the Tularik Compound Library within [ * ].

Related to Tularik Compound Library

  • 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 [***].

  • 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.

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

  • Collaboration Know-How means all Know-How and Materials discovered, created, conceived, developed or reduced to practice in the course of performing activities under the Collaboration Program (whether solely by one Party or jointly by the Parties, in each case with their Affiliates or any Third Parties or any employees, consultants or agents of any of the foregoing which perform activities under the Collaboration Program).

  • Program Technology means Program Know-How and Program Patents.

  • 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.

  • Compounds means a small molecule HMT inhibitor.

  • 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.

  • Manufacturing Know-How means, with respect to the Product or any Variant thereof, the technology, data, designs, processes, methods, specifications and other know-how used in connection with the formulation, manufacture, labeling, packaging, quality control, release testing, and production of the Product, and all ingredients used therein and portions thereof.

  • 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.

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

  • Collaboration Patent Rights means Patent Rights claiming Collaboration Know-How.

  • Library means a code module that cannot be installed or executed separately from an Application and that is developed by You in compliance with the Documentation and Program Requirements only for use with iOS Products, Apple Watch, or Apple TV.

  • Collaboration Patents means any and all Patents that claim or cover any of the Collaboration Know-How.

  • Phase I Clinical Study means, as to a particular Licensed Product, an initial clinical study in humans with the purpose of assessing the Licensed Product’s safety, tolerability, toxicity, pharmacokinetics or other pharmacological properties.

  • 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.

  • Phase I Clinical Trial means a human clinical trial that is intended to initially evaluate the safety and/or pharmacological effect of a Product in subjects or that would otherwise satisfy requirements of 21 C.F.R. 312.21(a), or its foreign equivalent.

  • 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.

  • Phase II Clinical Study means a human clinical study of a product initiated to determine the safety and efficacy in the target patient population, as described 21 C.F.R. 312.21(b).

  • Collaboration IP means Collaboration Know-How and Collaboration Patents.

  • Development Site means any parcel or lot on which exists or which is intended for building development other than the following:

  • 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.

  • Program Patent Rights means any Patent Rights that are Controlled by one or both parties and that Cover any Program Technology or Program Materials. For clarification, such Program Patent Rights include the entire scope of all of the claims contained in such Patent Rights.

  • Development Application means the development application identified in Item 5 of Schedule 1 and includes all plans, reports models, photomontages, material boards (as amended supplemented) submitted to the consent authority before the determination of that Development Application.