drugset / Trial / NCT02500199
Phase I Study of Pyrotinib in Patients With HER2-positive Solid Tumors
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |