A Rollover Study to Further Evaluate the Safety and Efficacy of Palovarotene Capsules in Male and Female Participants Aged ≥14 Years With Fibrodysplasia Ossificans Progressiva (FOP) Who Have Completed the Relevant Parent Studies. (PIVOINE)

  • STATUS
    Not Recruiting
  • End date
    Nov 11, 2024
  • participants needed
    87
  • sponsor
    Ipsen
Updated on 25 August 2023

Summary

The main objective of this study is to further evaluate the safety and efficacy of palovarotene in adult and paediatric participants with FOP.

The aim of the study is also to ensure treatment continuity to participants who have completed one of the parent studies (Study PVO-1A-301, Study PVO-1A-202 and Study PVO-1A-204) and who, in the investigator's judgement, may benefit from palovarotene therapy.

Details
Condition Fibrodysplasia Ossificans Progressiva (FOP)
Treatment Palovarotene
Clinical Study IdentifierNCT05027802
SponsorIpsen
Last Modified on25 August 2023

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