drugset / Trial / NCT02190747

An Efficacy and Safety Study of Palovarotene to Treat Preosseous Flare-ups in FOP Subjects

NCT02190747 ↗

Phase 2 Completed 40 enrolled Ipsen
RandomizedParallel-groupTriple-blindTreatment

Summary

Fibrodysplasia ossificans progressiva (FOP) is a rare, severely disabling disease characterized by painful, recurrent episodes of soft tissue swelling (flare-ups) that result in abnormal bone formation in muscles, tendons, and ligaments. Flare-ups begin early in life and may occur spontaneously or after soft tissue trauma, vaccinations, or influenza infections. Recurrent flare-ups progressively restrict movement by locking joints leading to cumulative loss of function and disability. Mouse models of FOP have demonstrated the ability of retinoic acid receptor (RAR) gamma agonists to prevent heterotopic ossification (HO) following injury. The purpose of the study is to evaluate whether palovarotene, an RAR gamma agonist, will prevent HO during and following a flare-up in subjects with FOP.

Timeline

Start
2014-07-14
Primary completion
2016-05-23
Completion
2016-05-23

Outcome

Missed primary endpoint

registry analysis (other test); Palovarotene 10/5 mg vs Palovarotene 5/2.5 mg vs Placebo; p = 0.1664; Cochran-Armitage test of trend NCT02190747 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Palovarotene Small molecule 2.5 mg Oral
Subject Palovarotene Small molecule 5 mg Oral