drugset / Trial / NCT04413227
A Phase Ib Study With Pegylated Recombinant Human Endostatin in Advanced / Metastatic NSCLC or Other Solid Tumors
NaSingle-groupOpen-labelTreatment
Summary
The primary purpose of this study is to examine the safety, tolerability and pharmacokinetics of PEG-ENDO in combination with docetaxel in subjects previously treated or untreated (standard therapy is not suitable or without standard therapy) for advanced or metatatic non-small cell lung cancer (NSCLC) or other solid tumors.
Timeline
- Start
- 2020-04-02
- Primary completion
- 2021-05-31
- Completion
- 2021-09-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Pegylated Recombinant Human Endostatin | Unknown | 1 mg/kg | — |
| Subject | Pegylated Recombinant Human Endostatin | Unknown | 2 mg/kg | — |
| Subject | Pegylated Recombinant Human Endostatin | Unknown | 4 mg/kg | — |
| Subject | Pegylated Recombinant Human Endostatin | Unknown | 6 mg/kg | — |
| Subject | Pegylated Recombinant Human Endostatin | Unknown | 8 mg/kg | — |
| Background | Docetaxel | Small molecule | 75 mg/m2 | — |