News Releases

News Releases

Date Title and Summary Additional Formats
Toggle Summary Clementia Clinical Program: Necker Begins Enrolling Patients in Palovarotene 2B Extension Study
MONTREAL, CANADA, November, 18, 2016  – Clementia is pleased to announce that the Hôpital Necker of Paris is ready to enroll FOP patients into Part B of its Phase 2 Open-label Extension Trial, which is a new study in France called PVO-1A-204. Dr Geneviève Baujat is principal investigator at
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Toggle Summary Clementia Clinical Program: Clinical Trial Site for Palovarotene Study Opened in Argentina
MONTREAL, CANADA, November, 14, 2016  – Clementia is pleased to announce to the FOP community that Hospital Italiano in Buenos Aires is ready to enroll FOP patients into Part B of its Phase 2 Open-label Extension Trial (PVO-1A-202). Dra Carmen L De Cunto, MD, Pediatric Rheumatologist at the
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Toggle Summary Clementia Announces Top-line Results from Phase 2 Trial of Palovarotene for Treatment of Patients with Fibrodysplasia Ossificans Progressiva
MONTREAL, CANADA, October, 14, 2016  – Clementia Pharmaceuticals Inc. today announced top-line results from its Phase 2 clinical trial investigating palovarotene for the treatment of fibrodysplasia ossificans progressiva (FOP). FOP is an extremely rare, serious disease in which an accumulation
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Toggle Summary Clementia Clinical Program: Opportunity for New Adult and Older Adolescent Subjects to Enroll in Palovarotene Study
MONTREAL, CANADA, August 8, 2016  – Clementia is pleased to announce to the FOP community that the implementation of Part B of its Phase 2 Open-label Extension Trial (PVO-1A-202) is progressing well and enrollment of adult or older adolescent subjects who have not previously participated in
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Toggle Summary Clementia Clinical Program: Next Step in Clementia’s Clinical Program for Fibrodysplasia Ossificans Progressiva (FOP)
MONTREAL, CANADA, June 13, 2016  – Clementia is pleased to announce that the Phase 2 Open-label Extension Trial (PVO-1A-202) has been modified to enroll up to 20 new participants and to investigate new palovarotene dosing regimens in participants with fibrodysplasia ossificans progressiva
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Toggle Summary Clementia Pharmaceuticals Joins Global FOP Community in Recognizing Fibrodysplasia Ossificans Progressiva (FOP) Awareness Day
10 Year Anniversary of the Discovery of the Gene that Causes FOP MONTREAL, CANADA, April 23, 2016  – Clementia Pharmaceuticals Inc. today joins the FOP community in recognizing and supporting FOP Awareness Day 2016. FOP is a rare, severely disabling myopathy characterized by extra-skeletal
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Toggle Summary Positive Effects of Palovarotene on Spontaneous Heterotopic Ossification, Mobility, and Skeletal Growth in Mouse Models of FOP Reported in Journal of Bone and Mineral Research
MONTREAL, CANADA, April 14, 2016  – Clementia Pharmaceuticals Inc. today reports that the Journal of Bone and Mineral Research has published online a non-Clementia sponsored study describing palovarotene’s novel, beneficial effects on spontaneous heterotopic ossification, mobility, and
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Toggle Summary Clementia Announces Last Patient Enrolled in Phase 2 trial of Palovarotene in Patients with Fibrodysplasia Ossificans Progressiva
Joins Global Rare Disease Community in Recognizing Rare Disease Day 2016 MONTREAL, CANADA, February, 29, 2016  – Clementia Pharmaceuticals Inc. today announced that the 40th and last study participant has enrolled into its Phase 2 clinical trial that is investigating palovarotene for the
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Toggle Summary Clementia Clinical Program: Clementia Natural History Study and Phase 2 Clinical Trial Enrollment Update
MONTREAL, CANADA, DECEMBER 9, 2015  – Clementia is pleased to announce the recent enrollment of the 50th subject in its Natural History Study of fibrodysplasia ossificans progressiva (FOP). Due to the rapid pace with which this important milestone was reached, enrollment continues for eligible
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Toggle Summary Clementia Phase 2 Clinical Trial Site in London, UK Now Enrolling Children
Clementia is pleased to announce that its clinical trial site at The Royal National Orthopaedic Hospital in London, England is now ready to enroll children age 6 to 14 who meet the study eligibility criteria. This site joins the University of California San Francisco (UCSF) and the Necker
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