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
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- University of Michigan Rogel Cancer Center
- Study ID
- NCT04431635
- Phase
- PHASE1
- Status
- Terminated
Conditions
- Indolent Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
Study Details
Patients with relapsed or refractory follicular or marginal zone lymphoma who have received at least one prior line of therapy will receive * Copanlisib IV: day 1, 8, 15 every 28 days * Nivolumab IV: Cycle 1 days 1 and 15; then day 1 only * Rituximab IV: Cycle 1 days 1, 8, 15, 22; then day 1 (C2-6); then Q2 cycles (8-12)
Key Dates
- Start date
- Jun 15, 2020
- Status verified
- Sep 2024
- Primary completion
- Nov 14, 2023
- Completion
- Nov 14, 2023
Study Design
- Enrollment
- 6 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm A: Copanlisib, Nivolumab & RituximabCopanlisib IV: day 1, 8, 15 every 28 days Nivolumab IV: Cycle 1 days 1 and 15; then day 1 only Rituximab IV: Cycle 1 days 1, 8, 15, 22; then day 1 (C2-6); then Q2 cycles (8-12)
Primary Outcome Measure
MTD (Maximum Tolerated Dose) of copanlisib given in combination with nivolumab and rituximab [ Time Frame: 28 days ]
Locations (5)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Illinois Cancer Center | Chicago | Illinois | 60612 | - |
| University of Michigan Comprehensive Cancer Center | Ann Arbor | Michigan | 48109 | - |
| University of Michigan Health System | Ann Arbor | Michigan | 48109 | - |
| University of Nebraska Medical Center | Omaha | Nebraska | 68198 | - |
| Rutgers Cancer Institute of New Jersey | New Brunswick | New Jersey | 08903 | - |
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