Tepotinib Hepatic Impairment Trial
Part of paid clinical trials in Miami, Florida.
- Sponsor
- EMD Serono Research & Development Institute, Inc.
- Study ID
- NCT03546608
- Phase
- PHASE1
- Status
- Completed
Conditions
- Hepatic Impairment
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Accepted
Interventions
- Tepotinib — DRUGParticipants received a single oral dose of tepotinib in Part 1.
Study Details
The study investigated the effect of various degrees of hepatic impairment on the pharmacokinetics (PK), safety and tolerability of tepotinib.
Key Dates
- Start date
- Jun 13, 2018
- Status verified
- Mar 2024
- Primary completion
- Feb 5, 2019
- Completion
- Feb 5, 2019
Study Design
- Enrollment
- 18 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Experimental: Healthy Participants (Control)Participants with normal hepatic function matched to moderate hepatic impairment received single oral dose of 500 milligrams (mg) of tepotinib film-coated tablet on Day 1 after a standard breakfast.
- Experimental: Mild Hepatic Impairment (Child-Pugh Class A)Participants with mild hepatic impairment (Child-Pugh Class A, score 5 to 6) received single oral dose of 500 mg tepotinib film-coated tablet on Day 1 after a standard breakfast.
- Experimental: Moderate Hepatic Impairment (Child-Pugh Class B)Participants with moderate hepatic impairment (Child-Pugh Class B, score 7 to 9) received single oral dose of 500 mg tepotinib film-coated tablet on Day 1 after a standard breakfast.
Primary Outcome Measure
Area Under the Plasma Concentration Time Curve From Time Zero to Infinity ( AUC0-inf ) of Tepotinib [ Time Frame: Pre-dose and 0.25, 0.5, 0.75, 1.0, 1.5, 2, 3, 4, 6, 8, 10, 12, 16, 24, 30, 36, 48, 54, 60, 72, 96, 120, 144, 168, 216, 288, 336 and 504 hours (for hepatic impaired participants only) post-dose on Day 1 ]
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Qps Mra, Llc | Miami | Florida | 33143 | - |
| Orlando Clinical Research Center | Orlando | Florida | 32809 | - |
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