Study of ACTR707 in Combination With Rituximab in Subjects With Relapsed or Refractory B Cell Lymphoma
Part of paid clinical trials in Gilbert, Arizona.
- Sponsor
- Cogent Biosciences, Inc.
- Study ID
- NCT03189836
- Phase
- PHASE1
- Status
- Terminated
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- ACTR707 — BIOLOGICALautologous T cell product
- rituximab — BIOLOGICALCD20-directed cytolytic antibody
Study Details
This is a phase 1, multi-center, single-arm, open-label study evaluating the safety and anti-lymphoma activity of an autologous T cell product (ACTR707) in combination with rituximab in subjects with refractory or relapsed CD20+ B cell lymphoma.
Key Dates
- Start date
- Oct 4, 2017
- Status verified
- Oct 2021
- Primary completion
- Sep 21, 2020
- Completion
- Sep 21, 2020
Study Design
- Enrollment
- 26 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: ACTR707 in combination with rituximab
Primary Outcome Measure
Safety as assessed by dose limiting toxicities (DLTs) [ Time Frame: 28 days ]
Locations (11)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Banner MD Anderson Cancer Center | Gilbert | Arizona | 85234 | - |
| Yale University | New Haven | Connecticut | 06520 | - |
| Emory University, Winship Cancer Institute | Atlanta | Georgia | 30322 | - |
| Loyola University | Maywood | Illinois | 60153 | - |
| Indiana Bone and Marrow Transplantation | Indianapolis | Indiana | 46327 | - |
| University of Maryland | Baltimore | Maryland | 21201 | - |
| University of Minnesota | Minneapolis | Minnesota | 55455 | - |
| Ohio State University | Columbus | Ohio | 43210 | - |
| Tennessee Oncology - Nashville | Nashville | Tennessee | 37203 | - |
| The University of Texas MD Anderson Cancer Center | Houston | Texas | 77030 | - |
| Medical College of Wisconsin | Milwaukee | Wisconsin | 53226 | - |
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