A Pharmacokinetics (PK) Study of the Effects Rabeprazole and Rifampin on Dabrafenib in Subjects With BRAF V600 Mutation Positive Tumors
Part of paid clinical trials in Goodyear, Arizona.
- Sponsor
- GlaxoSmithKline
- Study ID
- NCT01954043
- Phase
- PHASE1
- Status
- Completed
Conditions
- Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Dabrafenib 150 mg twice a day (BID) — DRUGDabrafenib dosed at 150mg twice a day from Day 1 to the morning of Day 29
- Rabeprazole 40 mg once daily (OD) — DRUGRabeprazole dosed at 40mg each morning on Days 16 to 19
- Rifampin 600 mg OD — DRUGRifampin dosed at 600mg each morning on Days 20 to 29
Study Details
The study is being conducted to evaluate the effect of rifampin (a strong CYP3A4 inducer) and rabeprazole (a pH elevating agent) on the PK of dabrafenib (a CYP3A4/CYP2C8 substrate). The study will be conducted in subjects with BRAF V600 mutation-positive tumors. Data collected from this study will be used to inform recommendations regarding use of concomitant medications with dabrafenib and future clinical pharmacologic evaluation of dabrafenib.
Key Dates
- Start date
- Dec 20, 2013
- Status verified
- Nov 2017
- Primary completion
- Feb 29, 2016
- Completion
- Feb 29, 2016
Study Design
- Enrollment
- 23 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm ASubjects will administer Dabrafenib from Day 1 to Day 15, Dabrafenib and Rabeprazole from Day 16 to Day 19, Dabrafenib and Rifampin from Day 20 to Day 29. The serial PK samples will be collected for 12 hours following dosing on Day 15 (Dabrafenib alone), Day 19 (Dabrafenib and Rabeprazole), and Day 29 (Dabrafenib and Rifampin).
Primary Outcome Measure
PK assessment (Cmax) of Dabrafenib with and without Rabeprazole or Rifampin [ Time Frame: Day 15, 19 and Day 29 ]
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| GSK Investigational Site | Goodyear | Arizona | 85338 | - |
| GSK Investigational Site | Dallas | Texas | 75201 | - |
| GSK Investigational Site | Tacoma | Washington | 98405 | - |
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