Fibrodysplasia Ossificans Progressiva (FOP): Clinical Trials

6 trials for Fibrodysplasia Ossificans Progressiva (FOP), newest first

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3 recruiting, 2 completed, 1 temporarily not available. 1 Phase 2, 1 Phase 3.

By phase and status

PhaseTrialsStatus
Phase 21Recruiting 1
Phase 31Completed 1

Follow Fibrodysplasia Ossificans Progressiva (FOP): new trials by email Literature Review of Fibrodysplasia Ossificans Progressiva (FOP) trials Research Report on Fibrodysplasia Ossificans Progressiva (FOP)

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
IL1 Inhibition in FOP
Anti-IL1 Therapy - Fibrodysplasia Ossificans Progressiva (FOP)
RecruitingUniversity of California, San Francisco112025-04-012026-08-06
A Non-Interventional Study of Clinical Characteristics and Mortality of US Patients With Fibrodysplasia Ossificans Progressiva (FOP)
Non-Interventional - Fibrodysplasia Ossificans Progressiva (FOP)
CompletedRegeneron Pharmaceuticals1312023-06-292025-07-03
To Assess the Efficacy, Safety, and Tolerability of INCB000928 in Participants With Fibrodysplasia Ossificans Progressiva
INCB000928, Placebo - Fibrodysplasia Ossificans Progressiva (FOP)
Phase 2RecruitingIncyte Corporation982022-05-052026-10-22
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.
Palovarotene - Fibrodysplasia Ossificans Progressiva (FOP)
Phase 3CompletedIpsen612022-03-142025-06-22
The Fibrodysplasia Ossificans Progressiva (FOP) Registry
Fibrodysplasia Ossificans Progressiva (FOP)
RecruitingThe International FOP Association8002015-07-012026-04-08
An Expanded Access Program of Garetosmab in Adult Patients With Fibrodysplasia Ossificans Progressiva (FOP)
Garetosmab - Fibrodysplasia Ossificans Progressiva (FOP)
Temporarily not availableRegeneron Pharmaceuticals2025-12-24

Narrower conditions

Myositis Ossificans (6)  ·  Ossification, Heterotopic (4)  ·  Genetic Diseases, Inborn (1)  ·  Hallux Valgus (1)  ·  Mucopolysaccharidosis IV (1)  ·  Osteochondroma (1)

Broader conditions

Muscular Diseases (6)  ·  Musculoskeletal Diseases (6)  ·  Myositis (6)  ·  Pathologic Processes (4)  ·  Pathological Conditions, Signs and Symptoms (4)  ·  Bone Diseases (1)  ·  Bone Diseases, Developmental (1)  ·  Carbohydrate Metabolism, Inborn Errors (1)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1)  ·  Connective Tissue Diseases (1)  ·  Foot Deformities (1)  ·  Lysosomal Storage Diseases (1)  ·  Metabolic Diseases (1)  ·  Metabolism, Inborn Errors (1)  ·  Mucinoses (1)

Interventions

Interleukin 1 Receptor Antagonist Protein (1)  ·  Palovarotene (1)  ·  canakinumab (1)

Sponsors

Regeneron Pharmaceuticals (2)  ·  Incyte Corporation (1)  ·  Ipsen (1)  ·  The International FOP Association (1)  ·  University of California, San Francisco (1)

Countries

United States (5)  ·  Argentina (2)  ·  Australia (2)  ·  Brazil (2)  ·  Canada (2)  ·  France (2)  ·  Italy (2)  ·  Spain (2)  ·  United Kingdom (2)  ·  Chile (1)  ·  China (1)  ·  Germany (1)  ·  Mexico (1)  ·  Netherlands (1)  ·  New Zealand (1)

Top investigators

Amanda McBride, MD (1)  ·  Edward Hsiao, MD, PhD (1)  ·  Mark Hamilton, PhD (1)

Results publications

PMID 36526263, PMID 41360500

NIH funding

2023 (1), R01AR083628 (1)