drugset / Trial / NCT07412821

A Phase 1b Study of Adenylosuccinic Acid (ASA-001) for Adenylosuccinate Synthase 1 (ADSS1) Deficient Myopathy.

NCT07412821 ↗

Phase 1 Enrolling by invitation 2 enrolled Cure ADSSL1 University of California, Los Angeles · collab
NaSingle-groupOpen-labelTreatment

Summary

The goal of this clinical trial is to evaluate the safety, tolerability and preliminary efficacy of ASA-001 in two adults diagnosed with ADSS1 deficient myopathy. The main questions it aims to answer are: * Whether ASA-001 can be safely administered to ADSS1 deficient myopathy patients; * Whether daily treatment with ASA-001 provides benefit or slows progression of disease. Participants will: * Take ASA-001 every day for 8 months; * Visit the clinic once every 2 weeks for check-ups and tests

Timeline

Start
2026-03-26
Primary completion
2027-12-31
Completion
2027-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject adenylosuccinic acid Unknown 500 mg Subcutaneous
Subject adenylosuccinic acid Unknown 2500 mg Subcutaneous

Indications

No indication recorded.