Dose De-escalation Study of the PI3k Alpha/Delta Inhibitor, Copanlisib Given in Combination With the Immunotherapeutic Agents, Nivolumab and Rituximab in Patients With Relapsed/Refractory Indolent Lymphoma

PHASE1TerminatedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

June 15, 2020

Primary Completion Date

November 14, 2023

Study Completion Date

November 14, 2023

Conditions
Indolent Lymphoma
Interventions
DRUG

Copanlisib

Copanlisib IV: day 1, 8, 15 every 28 days

DRUG

Nivolumab

Nivolumab IV: Cycle 1 days 1 and 15; then day 1 only

DRUG

Rituximab

Rituximab IV: Cycle 1 days 1, 8, 15, 22; then day 1 (C2-6); then Q2 cycles (8-12)

Trial Locations (5)

48109

University of Michigan Comprehensive Cancer Center, Ann Arbor

University of Michigan Health System, Ann Arbor

60612

University of Illinois Cancer Center, Chicago

68198

University of Nebraska Medical Center, Omaha

08903

Rutgers Cancer Institute of New Jersey, New Brunswick

Sponsors

Collaborators (2)

All Listed Sponsors
collaborator

Bayer

INDUSTRY

collaborator

Bristol-Myers Squibb

INDUSTRY

collaborator

University of Michigan

OTHER

collaborator

Big Ten Cancer Research Consortium

OTHER

lead

University of Michigan Rogel Cancer Center

OTHER