drugset / Trial / NCT03439761

An Open-label Phase I/II Clinical Trial of PT-112 Injection for Advanced Solid Tumors and Advanced Hepatocellular Carcinoma

NCT03439761

Phase 1/2 Unknown 125 enrolled SciClone Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
Subject IMIFOPLATIN Other / unclassified 200 mg/m2 Intravenous
Subject IMIFOPLATIN Other / unclassified 250 mg/m2 Intravenous
Subject IMIFOPLATIN Other / unclassified 300 mg/m2 Intravenous

Indications