Ipsen to Present Results From MOVE, the First Global Phase III Trial in Fibrodysplasia Ossificans Progressiva (FOP), at ASBMR 2020 Annual Meeting
Retrieved on:
Tuesday, August 25, 2020
Health, Clinical trials, Research, Pharmaceutical, Science, Biotechnology, Health, Chemical compounds, Rare diseases, Palovarotene, Pyrazoles, Retinoids, Fibrodysplasia ossificans progressiva, FOP, Fibrodysplasia, Clinical trial, International FOP Association, the FOP clinical program, palovarotene, fibrodysplasia ossificans progressiva (FOP), Ipsen
Dosing of palovarotene in the MOVE clinical trial was paused when futility criteria were met at a pre-specified interim analysis.
Key Points:
- Dosing of palovarotene in the MOVE clinical trial was paused when futility criteria were met at a pre-specified interim analysis.
- We are pleased to present the third interim analysis results of the Phase III MOVE trial in FOP, evaluating Ipsens oral investigational therapy palovarotene, to the global community at the ASBMR annual meeting, said Jim Roach, M.D., Senior Vice President and Global Head of Rare Diseases Therapeutic Area at Ipsen.
- Dosing for eligible study patients 14 years of age has resumed across the Phase II and Phase III programs for palovarotene in FOP.
- Palovarotene (PVO) for fibrodysplasia ossificans progressiva (FOP): Data from the phase III MOVE trial.