drugset / Trial / NCT06215755

A Study of VRG50635 in Participants With Amyotrophic Lateral Sclerosis (ALS)

NCT06215755 ↗

Phase 1 Terminated 54 enrolled Verge Genomics
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to evaluate the safety and tolerability of VRG50635 in participants with ALS.

Timeline

Start
2024-01-15
Primary completion
2025-07-07
Completion
2025-07-07

Outcome

Outcome not reported

Stopped: “Study terminated by Sponsor due to lack of risk-benefit data.”

Drugs

EvaluationDrugModalityDoseRoute
Subject VRG50635 Small molecule 400 mg Oral
Subject VRG50635 Small molecule 600 mg Oral
Subject VRG50635 Small molecule 800 mg Oral