Pilot Study of the Safety/Efficacy of Combination Checkpoint Blockade + External Beam Radiotherapy in Stage IV Melanoma

PHASE1CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

October 13, 2016

Primary Completion Date

May 9, 2019

Study Completion Date

July 27, 2020

Conditions
Melanoma
Interventions
DRUG

Nivolumab

Nivolumab was administered as an intravenous (IV) infusion over approximately 30 or 90 minutes, with dosing calculated using body weight.

DRUG

Ipilimumab

Ipilimumab was administered as an IV infusion over approximately 30 or 90 minutes, with dosing calculated using body weight. The ipilimumab infusion was initiated approximately 30 minutes after the end of the nivolumab infusion on applicable dosing days.

RADIATION

Radiotherapy

RT was delivered in accordance with cohort assignment and institutional practices.

Trial Locations (2)

10065

Memorial Sloan Kettering Cancer Center, New York

94304

Stanford Cancer Institute, Stanford

All Listed Sponsors
collaborator

Bristol-Myers Squibb

INDUSTRY

collaborator

Conquer Cancer Foundation

OTHER

lead

Ludwig Institute for Cancer Research

OTHER