Study of ARRY-614 Plus Either Nivolumab or Nivolumab+Ipilimumab

PHASE1/PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

June 11, 2020

Primary Completion Date

December 27, 2024

Study Completion Date

October 1, 2025

Conditions
Renal Cell CarcinomaMelanomaSolid TumorNon-small Cell Lung CancerHead and Neck Squamous Cell Carcinoma
Interventions
DRUG

Phase Ib ARRY-614 + nivolumab

ARRY-614 continuously in 4-week cycles (± 3 days). Nivolumab will be dosed according to FDA-approved dosing schedule.

DRUG

Phase Ib ARRY-614 + nivolumab+ipilimumab

ARRY-614 continuously in 4-week cycles (± 3 days). Nivolumab will be dosed according to FDA-approved dosing schedule. Ipilimumab therapy will be dosed according to FDA-approved dosing schedule.

DRUG

Phase II ARRY-614 + nivolumab

"Recommended Phase II dose of ARRY-614 (to be determined) daily in 4-week cycles (± 3 days).~Nivolumab will be dosed according to FDA-approved dosing schedule."

DRUG

Phase II ARRY-614 + nivolumab+ipilimumab (melanoma)

"Recommended Phase II dose of ARRY-614 (to be determined) daily in 4-week cycles (± 3 days).~Nivolumab will be dosed according to FDA-approved dosing schedule. Ipilimumab therapy will be dosed according to FDA-approved dosing schedule."

DRUG

Phase II ARRY-614 + nivolumab+ipilimumab (RCC)

"Recommended Phase II dose of ARRY-614 (to be determined) daily in 4-week cycles (± 3 days).~Nivolumab will be dosed according to FDA-approved dosing schedule. Ipilimumab therapy will be dosed according to FDA-approved dosing schedule."

Trial Locations (1)

15232

UPMC Hillman Cancer Center, Pittsburgh

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Array BioPharma

INDUSTRY

lead

Dan Zandberg

OTHER