Evaluating the Pharmacokinetics and Safety of Miricorilant

Recruiting Phase 1 Interventional Study
Nonalcoholic Steatohepatitis (NASH) Metabolic Dysfunction-Associated Steatohepatitis (MASH) / Nonalcoholic Steatohepatitis (NASH) With Compensated Cirrhosis Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) Non-alcoholic Fatty Liver Disease (NAFLD)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
15 (estimated)
Sponsor
Corcept Therapeutics · Industry
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About This Trial

A Phase 1b, Open-Label Study Evaluating the Pharmacokinetics and Safety of Miricorilant in Adult Patients With Presumed Metabolic Dysfunction-Associated Steatohepatitis (MASH)

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Evidence of presumed MASH with either FibroScan liver stiffness measurement ≥ 8 kPa and controlled attenuation parameter (CAP) ≥ 280 dB/m OR historical biopsy within 12 months of screening that meets the following criteria: 1. Nonalcoholic fatty liver disease (NAFLD) activi…
Contacts

Eric Lawitz, MD

210-253-3426

lawitz@txliver.com

CONTACT

Toluwalase Okubote, MBBS, MPH, PMP

210-253-3426

tokubote@txliver.com

CONTACT