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NCT07265232

Real World Clinical Effectiveness & Safety of Vesemnogene Lantuparvovec for Spinal Muscular Atrophy (SMA) in Low-middle Income Countries (LMIC).

Recruiting now Phase 3 Last updated 4 December 2025
What this trial tests

Phase 3 trial testing vesemnogene lantuparvovec in Spinal Muscular Atrophy (SMA) in 15 participants. Currently enrolling.

Timeline
15 October 2025
Primary endpoint
15 October 2030
15 October 2030

Quick facts

Lead sponsorLantu Biopharma
PhasePhase 3
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment15
Start date15 October 2025
Primary completion15 October 2030
Estimated completion15 October 2030
Sites1 location across Indonesia

Drugs / interventions tested

Conditions studied

Sponsor

Lantu Biopharma — full company profile →

Who can join

6 Months and older, any sex, with Spinal Muscular Atrophy (SMA). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study objective is to determine the real-world safety and effectiveness of Vesemnogene lantuparvovec for the treatment of SMA. The specific objectives are: * To determine clinical effectiveness of Vesemnogene lantuparvovec therapy for SMA as evaluated by developmental gross motor milestone and survival. * To describe the safety profile of Vesemnogene therapy for SMA as evaluated by adverse events reporting and laboratory tests, and monitoring of Adverse events of special interest.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of vesemnogene lantuparvovec

Trials testing the same drug.

Other recruiting trials for Spinal Muscular Atrophy (SMA)

Currently open trials in the same condition.

Other Lantu Biopharma trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07265232.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing