LivingGLP1
Study S002155

A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Trial Evaluating the Safety, Efficacy, and Pharmacokinetic Characteristics of TP04HN106 in the Treatment of Patients With Amyotrophic Lateral Sclerosis

Registration

Registration
NCT06726577
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1; PHASE2
Masking
TRIPLE
Status
RECRUITING
Enrollment
60
Start
2026-06-04
Primary completion
2027-01
Lead sponsor
Talengen Institute of Life Sciences, Shenzhen, P.R. China.
Conditions
Amyotrophic Lateral Sclerosis
Interventions
DRUG:TP04HN106; DRUG:Saline
Results posted
FALSE

Registered primary outcomes

  • Amyotrophic Lateral Sclerosis Rating Scale (ALSFRS-R) [Baseline, 10th week]

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