Dabrafenib and Pazopanib Hydrochloride in Treating Patients With Advanced Malignant Tumors
- Disease/Condition
- Unspecified Adult Solid Tumor, Protocol Specific
- Drug/Device/Intervention
- dabrafenib
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Manisha Shah
- Funder
- Ohio State University Comprehensive Cancer Center
- Location
- Columbus,Houston, United States of America
- Phase
- Phase 1
- Start date
- Nov 19, 2012
- End date
- Dec 26, 2018
- Enrollment
- 23 participants
Incidence of adverse events using Common Terminology Criteria for Adverse Events (CTCAE) v4,Maximum tolerated dose, defined as the dose below the dose where at least 2 dose limiting toxicities (DLTs) are observed, graded using CTCAE v4
This phase I trial studies the side effects and best dose of dabrafenib and pazopanib
 hydrochloride when given together in treating patients with advanced malignant tumors.
 Dabrafenib and pazopanib hydrochloride may stop the growth of tumor cells by blocking some of
 the enzymes needed for cell growth
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT01713972
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT01713972 through Pure Global AI's free database. This Phase 1 trial is sponsored by Manisha Shah and is currently Completed. The study focuses on Unspecified Adult Solid Tumor, Protocol Specific. Target enrollment is 23 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.