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A Study to Assess the Effectiveness and Safety of 2 Dosage Regimens of Oral Fidrisertib (IPN60130) for the Treatment of Fibrodysplasia Ossificans Progressiva (FOP).

Terminated · Phase 2 · NCT05039515

Conditions: Fibrodysplasia Ossificans Progressiva

At a glance

Research payments reported, 2025
$2.5M
U.S. investigators named
10
Sites paid
7
Planned or actual enrollment
113

About the trial

Sponsor
Clementia Pharmaceuticals Inc. (with Ipsen)
Tested
IPN60130 (drug), IPN60130 (drug), Placebo (drug)
Dates
Started 2021-12-01; completion 2026-03-27
Results posted
Not yet

Fibrodysplasia Ossificans Progressiva (FOP) is a rare, severely disabling disease characterized by the presence of bone in soft tissue where bone normally does not exist, known as Heterotopic Ossification (HO). It is often associated with painful, recurrent episodes of soft tissue swelling (flare-ups) that lead to abnormal stiffening and immobility (ankyloses) of major joints with cumulative and irreversible loss of movement and disability. This study will evaluate the efficacy of 2 dosing regimens of IPN60130 in inhibiting new HO volume compared with placebo (a dummy treatment) in adult and paediatric participants with FOP. It will be assessed by a scan (provides internal images of the b…

From ClinicalTrials.gov, last updated 2026-04-24. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Ipsen Innovation reported $2.5M in research payments for this study in 2025 (293 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.