drugset / Trial / NCT03439761
An Open-label Phase I/II Clinical Trial of PT-112 Injection for Advanced Solid Tumors and Advanced Hepatocellular Carcinoma
NaSingle-groupOpen-labelTreatment
Summary
Use PT-112 alone for Phase I dose escalation stage: advanced solid tumors, Phase I dose confirmation stage: advanced solid tumors. Phase II hepatocellular carcinoma (HCC). To evaluate the safety and tolerability of PT-112 injection from 250mg/m2 dose level with 3+3 dose escalation design, find Maximum tolerated dose (MTD), Recommended Phase II Dose(RP2D) and evaluate the Pharmacokinetic (PK) profile of PT-112 through Phase I dose escalation stage. Phase I dose confirmation stage: evaluate the safety and tolerability of PT-112 with RP2D, evaluate the anti-tumor effect of PT-112 at RP2D. Phase II stage: evaluate the anti-tumor effect of PT-112 at RP2D in advanced HCC
Timeline
- Start
- 2018-03-07
- Primary completion
- 2020-05
- Completion
- 2020-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IMIFOPLATIN | Other / unclassified | 200 mg/m2 | Intravenous |
| Subject | IMIFOPLATIN | Other / unclassified | 250 mg/m2 | Intravenous |
| Subject | IMIFOPLATIN | Other / unclassified | 300 mg/m2 | Intravenous |