News Releases

News Releases

Date Title and Summary Additional Formats
Toggle Summary Clementia Pharmaceuticals Raises $10 Million in Extension of Series A Financing to Support Development of Palovarotene for FOP
Company Opens New Subsidiary to Serve U.S. Market MONTREAL, CANADA, January 5, 2015  –  Clementia Pharmaceuticals Inc.  today announced that it has secured an additional $10 million from current investors to support development of the company’s lead compound palovarotene for the
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Toggle Summary Clementia Pharmaceuticals Initiates First Prospective Natural History Study in Patients with Fibrodysplasia Ossificans Progressiva (FOP)
MONTREAL, CANADA, DECEMBER 17, 2014  –  Clementia Pharmaceuticals Inc.  announced today the initiation of a natural history study in patients with fibrodysplasia ossificans progressiva (FOP), a rare, severely disabling genetic disease characterized by painful, recurrent episodes of
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Toggle Summary Clementia Pharmaceuticals Receives Fast Track Designation for Palovarotene for Treatment of Fibrodysplasia Ossificans Progressiva (FOP)
MONTREAL, CANADA, December 1, 2014  –  Clementia Pharmaceuticals Inc.  announced today that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to palovarotene, which is being developed for the treatment of fibrodysplasia ossificans progressiva (FOP).
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Toggle Summary Clementia Pharmaceuticals Receives EMA Orphan Medicinal Product Designation for Palovarotene for the Treatment of Fibrodysplasia Ossificans Progressiva
MONTREAL, CANADA, NOVEMBER 21, 2014  –  Clementia Pharmaceuticals Inc.  announced today that the European Medicines Agency (EMA) has granted Orphan Medicinal Product Designation for palovarotene, the company’s lead product candidate, for the treatment of fibrodysplasia ossificans
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Toggle Summary Phase 2 Clinical Trial Milestone
Clementia Completes Enrollment Of First Cohort In Phase 2 Clinical Trial! February 5, 2015: Clementia is pleased to announce the enrollment of the 8th patient in Cohort 1 of its Phase 2 clinical trial of palovarotene for the treatment of FOP! This important milestone triggers the Data Monitoring
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Toggle Summary Clementia Pharmaceuticals Announces Open-Label Phase 2 Extension Study of Palovarotene in Patients with Fibrodysplasia Ossificans Progressiva
MONTREAL, CANADA, OCTOBER 27, 2014  –  Clementia Pharmaceuticals Inc.  announced today the initiation of a Phase 2 extension study of palovarotene in patients with fibrodysplasia ossificans progressiva (FOP), a rare, severely disabling genetic disease characterized by painful,
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Toggle Summary Clementia Pharmaceuticals Receives U.S. Orphan Drug Designation for Palovarotene for the Treatment of Fibrodysplasia Ossificans Progressiva
MONTREAL, CANADA and BOSTON, MA, July 24, 2014  (Marketwired) —  Clementia Pharmaceuticals Inc. , announced today that the U.S. Food and Drug Administration (FDA) has granted the Company’s lead product candidate, palovarotene, Orphan Drug Designation for the treatment of Fibrodysplasia
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Toggle Summary Clementia Pharmaceuticals Initiates Phase 2 Study of Palovarotene in Patients with Fibrodysplasia Ossificans Progressiva (FOP)
MONTREAL, CANADA and BOSTON, MA, July 14, 2014 (Marketwired)  —  Clementia Pharmaceuticals Inc.  announced today the initiation of a Phase 2 clinical trial of palovarotene for the treatment of Fibrodysplasia Ossificans Progressiva (FOP).
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Toggle Summary Clementia Pharmaceuticals Marks Fibrodysplasia Ossificans Progressiva (FOP) Awareness Day
MONTREAL, CANADA, April 23, 2014  —  Clementia Pharmaceuticals Inc. , a privately held clinical stage biotechnology company dedicated to serving those afflicted with severe and rare diseases through the development and commercialization of innovative treatments, observes the 2014
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Toggle Summary Clementia Pharmaceuticals Inc. Appoints Francois Nader, M.D. to Board of Directors
Healthcare Industry Veteran Brings Deep Expertise in Developing Innovative Therapies for Patients with Rare Diseases MONTREAL, CANADA, March 26, 2014 (Marketwired)  —  Clementia Pharmaceuticals Inc. , a privately held clinical-stage biotechnology company dedicated to serving those
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