drugset / Trial / NCT02500199

Phase I Study of Pyrotinib in Patients With HER2-positive Solid Tumors

NCT02500199

Phase 1 Unknown 50 enrolled Hengrui Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

Part 1: to assess the safety and tolerability of pyrotinib and to define the maximum tolerated dose (MTD) of pyrotinib in patients with Human Epidermal Growth Factor Receptor 2 (HER2)-positive advanced solid tumors (metastatic breast cancer, gastric cancer, or other solid tumors that have no targeted agent as standard of care). Part 2: to estimate the overall response rate (ORR) for patients with HER2-positive metastatic breast cancer (mBC) and HER2 mutant non-small cell lung cancer (NSCLC) treated at the RP2D (or MTD).

Timeline

Start
2015-06
Primary completion
2021-05
Completion
2021-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Pyrotinib Small molecule 320 mg Oral
Subject Pyrotinib Small molecule 400 mg Oral
Subject Pyrotinib Small molecule 480 mg Oral
Subject Pyrotinib Small molecule 560 mg Oral
Subject Pyrotinib Small molecule 640 mg Oral