Overview

Evaluate the Safety and Efficacy of Intrathecal Injection of RJK002 in Patients With Amyotrophic Lateral Sclerosis

Status:
RECRUITING
Trial end date:
2031-05-02
Target enrollment:
Participant gender:
Summary
The goal of the study aims to evaluate the safety and tolerability of a single intrathecal injection of RJK002 in subjects with amyotrophic lateral sclerosis (ALS), and to determine the recommended Phase II dose (RP2D).
Phase:
PHASE1
Details
Lead Sponsor:
RJK Biopharma Ltd
Collaborator:
Peking University Third Hospital