🇺🇸 FDA
Pipeline program

A Phase 1/2, Multicenter, Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Exploratory Efficacy of Intrathecally Administered Gene Therapy AMT-162 in Adult Participants with SOD1 Amyotrophic Lateral Sclerosis (SOD1-ALS)

AMT-162-001

Phase 2 other active

Quick answer

A Phase 1/2, Multicenter, Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Exploratory Efficacy of Intrathecally Administered Gene Therapy AMT-162 in Adult Participants with SOD1 Amyotrophic Lateral Sclerosis (SOD1-ALS) for Amyotrophic Lateral Sclerosis (ALS) is a Phase 2 program (other) at uniQure biopharma B.V. with 1 ClinicalTrials.gov record(s).

Program details

Company
uniQure biopharma B.V.
Indication
Amyotrophic Lateral Sclerosis (ALS)
Phase
Phase 2
Modality
other
Status
active

Clinical trials