CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


TERN-101Wiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug1822 Placebo Wiki 0.06

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
D065626 Non-alcoholic Fatty Liver Disease NIH 1.00
D005234 Fatty Liver NIH 1.00

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0001397 Hepatic steatosis HPO 1.00

There is one clinical trial.

Clinical Trials


1 A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2a Clinical Trial to Evaluate the Safety, Tolerability, Efficacy, and Pharmacokinetics of Orally Administered TERN-101 Tablets in Adult Patients With Presumed Non-Cirrhotic Non-Alcoholic Steatohepatitis (NASH)

This is a Phase 2, randomized, double-blind, placebo-controlled study designed to evaluate the safety, tolerability, efficacy, and pharmacokinetics (PK) of TERN-101 in non-cirrhotic NASH patients.

NCT04328077 NASH - Nonalcoholic Steatohepatitis Drug: TERN-101 Other: Placebo
MeSH:Fatty Liver Non-alcoholic Fatty Liver Disease
HPO:Hepatic steatosis

Primary Outcomes

Measure: Subject incidence of adverse events for TERN-101 versus placebo

Time: 16 weeks

Secondary Outcomes

Measure: Percent change from baseline in ALT for TERN-101 versus placebo at 12 weeks

Time: 12 weeks

Description: Area under the curve

Measure: Plasma concentration of TERN-101 - AUC

Time: 12 weeks

Description: Maximum observed concentration

Measure: Plasma concentration of TERN-101 - Cmax

Time: 12 weeks

Description: Time to reach maximum measured plasma concentration

Measure: Plasma concentration of TERN-101 - Tmax

Time: 12 weeks

Description: Determination of half-life

Measure: Plasma concentration of TERN-101 - t1/2

Time: 12 weeks


Related HPO nodes (Using clinical trials)