drugset / Trial / NCT04237649

KAZ954 Alone and With PDR001, NZV930 and NIR178 in Advanced Solid Tumors

NCT04237649

Phase 0 Terminated 77 enrolled Novartis Pharmaceuticals
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary objective of the trial was to characterize the safety, tolerability, and maximum tolerated dose (MTD)/recommended dose (RD) for expansion of single agent KAZ954 and KAZ954 in combination with PDR001, NIR178 and NZV930.

Timeline

Start
2020-02-20
Primary completion
2023-09-15
Completion
2023-09-15

Drugs

EvaluationDrugModalityDoseRoute
Subject KAZ954 Unknown
Subject NIR178 Unknown
Subject NZV930 Unknown
Subject Spartalizumab Monoclonal antibody

Indications