drugset / Trial / NCT04462471

Vemurafenib Plus Copanlisib in Radioiodine-Refractory (RAIR) Thyroid Cancers

NCT04462471

Phase 1 Completed 8 enrolled Memorial Sloan Kettering Cancer Center
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to develop a new drug treatment to reverse tumor resistance to radioiodine in BRAF mutant tumors so that radioiodine can be given to shrink tumors. This study is also being done to find out the highest doses of copanlisib and vemurafenib that, when given in combination, do not cause serious side effects, and whether the study treatment will make radioiodine therapy work better in patients with BRAF-mutant thyroid cancers.

Timeline

Start
2020-06-26
Primary completion
2023-09-29
Completion
2023-09-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Copanlisib Small molecule 45 mg Intravenous
Subject Copanlisib Small molecule 60 mg Intravenous
Subject Vemurafenib Small molecule 480 mg Oral
Subject Vemurafenib Small molecule 720 mg Oral
Subject Vemurafenib Small molecule 960 mg Oral