Promising antibody trial aims to halt rare bone disease in kids
NCT ID NCT07559513
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This Phase 3 trial tests garetosmab, an antibody that blocks activin A, in 18 children and teens with fibrodysplasia ossificans progressiva (FOP), a rare disease where muscle and tissue turn into bone. The study will check safety, side effects, and whether the drug reduces new abnormal bone growth and flare-ups. Participants receive the drug by infusion, and the trial is not yet recruiting.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- garetosmab (a lab-made antibody that blocks activin A)
- What this could lead to
- If it works, this could slow or prevent the formation of extra bone in children with FOP, reducing painful flare-ups and preserving mobility.
- What could go wrong
- This is an early Phase 3 trial with only 18 participants, so results may not apply to everyone. The drug may cause side effects or fail to show benefit.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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