Last reviewed · How we verify
Zolgensma
At a glance
| Generic name | Zolgensma |
|---|---|
| Sponsor | Novartis Pharmaceuticals |
| Modality | Small molecule |
| Therapeutic area | Other |
| Phase | FDA-approved |
| Annual revenue | 925 |
Approved indications
- Spinal muscular atrophy
Common side effects
- Elevated aminotransferases
- ALT > 3 X ULN
- ALT > 20 X ULN
- Vomiting
Serious adverse events
- Thrombocytopenia
- Platelet count < 50,000 per µL
- Leukoencephalopathy
- Respiratory insufficiency
- Serious hypotension
- Seizures
- Death
Key clinical trials
- Single-Dose Gene Replacement Therapy Using for Patients With Spinal Muscular Atrophy Type 1 With One or Two SMN2 Copies (PHASE3)
- Gene Replacement Therapy Clinical Trial for Participants With Spinal Muscular Atrophy Type 1 (PHASE3)
- Pre-Symptomatic Study of Intravenous Onasemnogene Abeparvovec-xioi in Spinal Muscular Atrophy (SMA) for Patients With Multiple Copies of SMN2 (PHASE3)
- Single-Dose Gene Replacement Therapy Clinical Trial for Participants With Spinal Muscular Atrophy Type 1 (PHASE3)
- Study of Intrathecal Administration of Onasemnogene Abeparvovec-xioi for Spinal Muscular Atrophy (PHASE1)
- Long-term Follow-up of Patients With Spinal Muscular Atrophy Treated With OAV101 in Clinical Trials (PHASE3)
- Phase IIIb, Open-label, Multi-center Study to Evaluate Safety, Tolerability and Efficacy of OAV101 Administered Intrathecally to Participants With SMA Who Discontinued Treatment With Nusinersen or Risdiplam (PHASE3)
- Efficacy and Safety of Intrathecal OAV101 (AVXS-101) in Pediatric Patients With Type 2 Spinal Muscular Atrophy (SMA) (PHASE3)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
| SEC EDGAR | Revenue + earnings |