drugset / Trial / NCT02508441

Phase 1 Safety and Tolerability Study of Andes-1537 for Injection in Patients With Advanced Unresectable Solid Tumors

NCT02508441 ↗

Phase 1 Terminated 22 enrolled Andes Biotechnologies
NaSingle-groupOpen-labelTreatment

Summary

This is a first-in-human, open-label, dose escalation and expansion, 2-part study to determine the safety, tolerability, and maximum tolerated dose of Andes-1537 for Injection in patients with advanced unresectable solid tumors that are refractory to standard therapy or for which no standard therapy is available.

Timeline

Start
2015-12-08
Primary completion
2017-11-13
Completion
2017-11-13

Outcome

Outcome not reported

Stopped: “Part 1 of the study was completed and the maximum tolerated dose determined. Part 2 of the study was terminated and will be conducted under a new protocol.”

Drugs

EvaluationDrugModalityDoseRoute
Subject MULNITORSEN Unknown 100 mg Subcutaneous
Subject MULNITORSEN Unknown 1000 mg Subcutaneous

Indications

No indication recorded.