drugset / Trial / NCT04106492

Phase 1/2a Study of SQ3370 in Patients With Advanced Solid Tumors

NCT04106492 ↗

Phase 1/2 Terminated 53 enrolled Shasqi, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and preliminary activity of SQ3370 in patients with advanced solid tumors.

Timeline

Start
2020-08-01
Primary completion
2023-09-07
Completion
2023-09-07

Outcome

Outcome not reported

Stopped: “Sponsor's decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject SQL70 Other / unclassified 10 ml Other
Subject SQL70 Other / unclassified 20 ml Other
Subject SQP33 Other / unclassified 8 mg/m2 Intravenous
Subject SQP33 Other / unclassified 16 mg/m2 Intravenous
Subject SQP33 Other / unclassified 32 mg/m2 Intravenous
Subject SQP33 Other / unclassified 58 mg/m2 Intravenous
Subject SQP33 Other / unclassified 85 mg/m2 Intravenous
Subject SQP33 Other / unclassified 125 mg/m2 Intravenous
Subject SQP33 Other / unclassified 185 mg/m2 Intravenous
Subject SQP33 Other / unclassified 250 mg/m2 Intravenous
Subject SQP33 Other / unclassified 315 mg/m2 Intravenous
Subject SQP33 Other / unclassified 500 mg/m2 Intravenous

Indications