Use of UTMDACC’s Cell Processing Facility Sample Clauses

Use of UTMDACC’s Cell Processing Facility. (i) During the TERM, at ZIOPHARM’s request and cost, UTMDACC agrees to produce, at its cell processing facility ([***]) and/or at the cell processing facility funded by ZIOPHARM, any human cellular and tissue based STUDY PRODUCT and/or components used to manufacture the STUDY PRODUCT (“HCT STUDY PRODUCTS”) for any CLINICAL TRIALS under the oversight of the JSC; provided, however, that UTMDACC will only be [***] to manufacture HCT STUDY PRODUCTS for which it determines in its reasonable discretion that it has the existing ability, capacity, facilities, equipment, resources, and expertise to do so, giving [***] (at a minimum no less than any [***] of [***]) to the use of its resources for the manufacturing of HCT STUDY PRODUCTS for use in the TCR-T PROGRAM in such determination. If UTMDACC is unable to manufacture a product for ongoing or planned clinical trial it will promptly provide written notification to ZIOPHARM of such inability, together with an explanation for the reason thereof. In the event there are manufacturing activities ongoing pursuant to this Section 2.4 at the end of the TERM, UTMDACC agrees to, at its election: (A) negotiate with ZIOPHARM the terms and conditions under which UTMDACC will continue to conduct such manufacturing activities on behalf of ZIOPHARM; or (B) cooperate with ZIOPHARM to, at ZIOPHARM’s cost and expense, effect an orderly transition of such manufacturing activities to ZIOPHARM or its designee.
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Related to Use of UTMDACC’s Cell Processing Facility

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