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Starting soon Phase 1

Aleniglipron Hepatic Impairment Study

NCT07872033 · tracked via the Priya Life Science USA tracker
Phase
Phase 1
Started
2026-10
Last updated
2026-10-13

Condition(s) studied

Hepatic Impairment

Investigational drug(s) / intervention(s)

Aleniglipron →

Aleniglipron: administered orally

Study summary

The purpose of this study is to evaluate the PK of aleniglipron in participants with Hepatic Impairment to establish scientifically guided dosing recommendations in these special patient populations.

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: 1. Is an adult, male or female, ≥ 18 to 85 years of age (inclusive), at screening. 2. Female and male participants must follow protocol-specified contraception guidance as described in Section 5.4.2.1 and Section 5.4.2.2. 3. Is a continuous non-smoker or smoker (≤ 10 cigarettes per day or equivalent) for at least 3 months prior to dosing. Participants must agree to maintain the same smoking status (i.e., smoker or non-smoker) from screening and until after the last PK sample collection. 4. BMI ≥ 17.0 and ≤ 40.0 kg/m2 and weight of at least 40.0 kg at screening. 5. Understands the study procedures in the ICF and be willing and able to comply with the protocol and communicate effectively with study personnel. Exclusion Criteria: 1. Is mentally or legally incapacitated or has significant emotional problems at the time of screening or expected during the conduct of the study. 2. History or presence of alcohol or drug abuse (including participants with symptoms of cannabis disorder) within the past 6 months prior to the dosing. 3. History or presence of hypersensitivity or idiosyncratic reaction to the study drug or related compounds. 4. Female participant with a positive serum pregnancy test at screening or at check-in or who is lactating or breastfeeding. 5. Has positive drug results at screening or at check-in, unless the positive drug screen is due to prescription drug use that is approved by the PI or designee. Participants with a positive result for cannabinoids may be enrolled at the discretion of the PI or designee and the Sponsor. 6. Has taken medications intended to promote weight loss within 3 months or 5 half-lives, whichever is longer, prior to screening, including, but not limited to GLP-1 RAs.

Primary outcome measure(s)

  • PK parameters including but not limited to AUC0-t — Baseline to Day 5 (Part 1)
  • PK parameters including but not limited to AUC0-inf — Baseline to Day 5 (Part 1)
  • PK parameters including but not limited to Cmax — Baseline to Day 5 (Part 1)
  • PK parameters including but not limited to AUC0-t — Baseline to Day 5 (Part 2)
  • PK parameters including but not limited to AUC0-inf — Baseline to Day 5 (Part 2)
  • PK parameters including but not limited to Cmax — Baseline to Day 5 (Part 2)

Trial sites (2)

FacilityCityRegionStatus
Research Site Orlando Florida
Research Site San Antonio Texas
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07872033 on ClinicalTrials.gov ↗ ← All trials in the USA