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Toggle Summary Clementia Pharmaceuticals to Participate in Upcoming Investor Conferences
MONTREAL , Sept. 06, 2017 (GLOBE NEWSWIRE) -- Clementia Pharmaceuticals Inc. (NASDAQ:CMTA), a clinical stage biopharmaceutical company, today announced that Dr. Clarissa Desjardins , CEO of Clementia Pharmaceuticals , will participate in two upcoming investor conferences: Morgan Stanley 15 th
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Toggle Summary Clementia Announces Data Presentations at Upcoming Medical Conferences in September
MONTREAL , Aug. 31, 2017 (GLOBE NEWSWIRE) -- Clementia Pharmaceuticals Inc. (NASDAQ:CMTA), a clinical stage biopharmaceutical company, today announced upcoming data presentations highlighting our palovarotene development efforts at the 2017 American Society for Bone and Mineral Research (ASBMR)
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Toggle Summary Clementia Announces Closing of Over-Allotment Option in its Initial Public Offering
MONTREAL , Aug. 21, 2017 (GLOBE NEWSWIRE) -- Clementia Pharmaceuticals Inc. (NASDAQ:CMTA) (the “Company” or “Clementia”), a clinical stage biopharmaceutical company, today announced that the underwriters of its previously announced initial public offering exercised their option to purchase an
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Toggle Summary Clementia Announces Pricing of Initial Public Offering
MONTREAL , Aug. 2, 2017 /PRNewswire/ --  Clementia Pharmaceuticals Inc. (NASDAQ: CMTA) (the "Company" or "Clementia"), a clinical stage biopharmaceutical company, today announced the pricing of its initial public offering of 8,000,000 common shares at an initial public offering price of $15 .00 per
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Toggle Summary Phase 2 Part A Open Label Extension Trial of Palovarotene for Treatment of Patients with Fibrodysplasia Ossificans Progressiva Continues Positive Trends
MONTREAL, CANADA, March 28, 2017  – Clementia Pharmaceuticals Inc. today announced the preliminary results of its Phase 2 Part A Open Label Extension (OLE) palovarotene trial in the treatment of fibrodysplasia ossificans progressiva (FOP). All 40 subjects who enrolled into the double-blind,
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Toggle Summary Clementia Clinical Program: Queensland University of Technology (QUT) Institute of Health and Biomedical Innovation (IHBI) Begins Enrolling Patients in Palovarotene 2B Extension Study
MONTREAL, CANADA, November, 18, 2016  – Clementia is pleased to announce that the Queensland University of Technology (QUT) Institute of Health and Biomedical Innovation (IHBI) is treating FOP patients in Part B of the Phase 2 Open-label Extension Trial (PVO-1A-202). Prof. Dr.
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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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