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Long-Term Safety & Efficacy of Apitegromab in Patients With SMA Who Completed Previous Trials of Apitegromab

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NCT05626855 · readout in 74 d

Sponsored by Scholar Rock, Inc. (industry) · SRRK — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
238actual
Sites
49
Countries
Belgium, France, Germany +6

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-04-17actualWhen the study began enrolling
Primary completion2026-11-01estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-05-02estimatedThe whole study's end, after follow-up
First posted2022-11-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-05-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Spinal Muscular Atrophy
  • Spinal Muscular Atrophy Type 3
  • Spinal Muscular Atrophy Type 2
  • SMA
  • Neuromuscular Diseases
  • Muscular Atrophy
  • Atrophy
  • Muscular Atrophy, Spinal
  • Neuromuscular Manifestations
  • Anti-myostatin

Intervention

  • Drug: Apitegromab

Primary outcome

what the primary-completion date above is the date OF
Evaluate the long-term safety and tolerability of apitegromab in patients with Type 2 and Type 3 SMA
measured Up to 6 years

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