A Study to Evaluate the Effect of Rifampin on the Pharmacokinetics of Divarasib in Healthy Participants
Completed · Phase 1
Conditions studied: Healthy Participants
In brief
This is a phase 1, open-label, two-period, fixed sequence drug-drug interaction study to evaluate the impact of multiple doses of rifampin on the pharmacokinetics (PK) and safety of divarasib in healthy participants.
Key facts
- Study ID
- NCT06835465
- Run by
- Genentech, Inc.
- People needed
- 18
- Starts
- 2025-02-21
- Expected to finish
- 2025-05-06
- Last updated by the study team
- 2025-05-13
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Males or females of non-childbearing potential
- Within body mass index (BMI) range of 18.0 to 32.0 kg/m2, inclusive
You may not qualify if…
- Significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal (GI), neurological, or psychiatric disorder
- History of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, unless approved by the investigator
- Poor peripheral venous access
Where it is running
- Fortrea Dallas CRU — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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