Named Patient and Compassionate Use Sample Clauses

Named Patient and Compassionate Use. Not later than the Completion of Technology Transfer and the transfer of the applicable IND(s) to Pharming, Pharming will assume responsibility, at its sole cost and expense, for the supply of Licensed Products for any post-trial access, compassionate use, named patient, or similar programs involving Licensed Product existing as of the Effective Date or arising in connection with the Ongoing Trial or Extension Study; provided, that Pharming shall be responsible, at its sole cost and expense, for the supply of Licensed Products for any such programs initiated following the Effective Date at Pharming’s request. Prior to the Final Transfer Date, Pharming may not initiate any such program without the prior written consent of Novartis, not to be unreasonably withheld. To the extent reasonably requested by Novartis and set forth in the Transition Plan, or otherwise mutually agreed by the Parties, any agreements between Novartis or its Affiliate and one or more Third Parties relating to such managed access programs (“MAP Agreements”) shall be assigned or transferred to Pharming or its designee pursuant to the Ancillary Agreement.
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