Clinical trials

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Condition / disease
Location
Status: Recruiting

Study of Safety, Tolerability and Efficacy of GB221 in Infants With Spinal Muscular Atrophy Type 1

GB221 is a gene therapy that delivers a working SMN1 gene to the motor neurons of people with spinal muscular atrophy (SMA) Type 1. This study will evaluate the safety, tolerability and efficacy of GB221 in two groups: 1. participants aged from 2 weeks to younger than 12 months presenting with symptoms of SMA Type 1 who have never received a treatment OR are receiving the drug risdiplam 2. participants aged from 2 weeks to younger than 5 months who are at risk of developing SMA Type 1 (presymptomatic) and have never received treatment OR are receiving the drug risdiplam.

Participants needed: 22
Trial details
Phase: Phase 1, Phase 2Age: 2-12Biological sex: AllType: InterventionalSponsor: Gemma BiotherapeuticsUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Symptomatic Participants [+5]

Any suspected or confirmed active viral infection at screening baseline (includi... [+6]