Geneva, Jan. 12 -- International Clinical Trials Registry received information related to the study (ChiCTR2500115074) titled 'A randomised, double-blind, placebo-controlled study of Phase ? was conducted to demonstrate the safety and preliminary efficacy of escalating of ALT001 in patients' on Dec. 22, 2025.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: Beijing Tiantan Hospital, Capital Medical University
Condition:
Amyotrophic lateral sclerosis
Intervention:
Experimental group:Calculate the dosage according to body weight. Dissolve ALT001 in 100ml of normal saline injection and administer it by intravenous once daily.Single-dose administration.
Multiple-dose administration: A treatment cycle consists ...