drugset / Trial / NCT01677741

A Study to Determine Safety, Tolerability and Pharmacokinetics of Oral Dabrafenib In Children and Adolescent Subjects

NCT01677741

Phase 1/2 Completed 85 enrolled Novartis Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This was a 2-part, Phase I/IIa, multi-center, open label, study in pediatric and adolescent patients with advanced BRAF V600 mutation-positive solid tumors. Part 1 was a dose escalation study in patients with any BRAF V600 mutation-positive solid tumor using a modified Rolling 6 Design (RSD). Part 2 was an expansion study to further evaluate the safety, tolerability, and clinical activity of dabrafenib in 4 tumor-specific pediatric populations. Patients participated in only either part 1 or part 2 of the study.

Timeline

Start
2013-05-23
Primary completion
2020-12-04
Completion
2020-12-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dabrafenib Small molecule 1.5 mg/kg Oral
Subject Dabrafenib Small molecule 2.25 mg/kg Oral
Subject Dabrafenib Small molecule 3 mg/kg Oral
Subject Dabrafenib Small molecule 3.75 mg/kg Oral
Subject Dabrafenib Small molecule 4.5 mg/kg Oral
Subject Dabrafenib Small molecule 5.25 mg/kg Oral

Indications