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Phase I/Ib Study of NIS793 in Combination With PDR001 in Patients With Advanced Malignancies.

NCT02947165 PHASE1 COMPLETED

To characterize the safety and tolerability of NIS793 as single agent and in combination with PDR001 and to identify recommended doses for future studies.

Details

Lead sponsorNovartis Pharmaceuticals
PhasePHASE1
StatusCOMPLETED
Enrolment120
Start dateTue Apr 25 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionFri Jun 18 2021 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Hong Kong, Italy, Japan, Austria, Taiwan, Germany, Canada, Switzerland, United States