Clinical trial
A Multi-center, Randomized, Double-blind, Dose-increasing, Placebo-controlled,Multi-dose, 28-day Continuous Administration Phase Ib/IIa Clinical Trial to Evaluate the Tolerability, Efficacy, and PK of ZSP1601 in Patients With Nonalcoholic Steatohepatitis
NCT04140123 is registered in ClinicalTrials.gov with Guangdong Raynovent Biotech Co., Ltd as lead sponsor.
Search trials, sites, companies and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.
Registry record
As filed in ClinicalTrials.gov.
- Title
- A Multi-center, Randomized, Double-blind, Dose-increasing, Placebo-controlled,Multi-dose, 28-day Continuous Administration Phase Ib/IIa Clinical Trial to Evaluate the Tolerability, Efficacy, and PK of ZSP1601 in Patients With Nonalcoholic Steatohepatitis
- Lead sponsor
- Guangdong Raynovent Biotech Co., Ltd
- Phase
- Phase 1/2
- Overall status
- Completed
- Start date
- June 23, 2020
- Completion date
- August 3, 2021
- Enrollment
- 37 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
non-alcoholic steatohepatitis (nash)