drugset / Trial / NCT02189174

Study of CLR457 Administered Orally in Adult Patients With Advanced Solid Malignancies

NCT02189174 ↗

Phase 1 Terminated 31 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

To estimate the maximum tolerated dose (MTD) or recommended dose for phase II (RP2D) of CLR457 and to investigate the anti-tumor activity of CLR457

Timeline

Start
2014-08-07
Primary completion
2015-11-12
Completion
2015-11-12

Outcome

Outcome not reported

Stopped: “Novartis decided to terminate the study considering safety and tolerability concerns and limited clinical activity with CLR457 study drug administered once daily (qd).”

Drugs

EvaluationDrugModalityDoseRoute
Subject CLR457 Unknown — Oral

Indications