Open Label Study to Evaluate the Safety and Efficacy of Lenalidomide With MOR00208 in Patients With R-R DLBCL
Part of paid clinical trials in Bakersfield, California.
- Sponsor
- MorphoSys AG
- Study ID
- NCT02399085
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Tafasitamab — DRUG12 mg/kg
- Lenalidomide — DRUG25 mg
Study Details
This is a Phase II, Single-Arm, Open-Label, Multicentre Study to Evaluate the Safety and Efficacy of Lenalidomide Combined with MOR00208 in Participants with Relapsed or Refractory Diffuse Large B-Cell Lymphoma (R-R DLBCL).
Key Dates
- Start date
- Mar 29, 2016
- Status verified
- Sep 2023
- Primary completion
- Nov 14, 2022
- Completion
- Apr 19, 2023
Study Design
- Enrollment
- 81 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Tafasitamab (MOR00208) + lenalidomide (LEN)MOR00208: MOR00208 was administered via IV infusion at a dose of 12 mg/kg. For the first three cycles (Cycles 1 to 3) of the study each cycle consisted of a MOR00208 infusion on Day 1, Day 8, Day 15 and Day 22 of the cycle. Additionally, a loading dose was administered on Day 4 of Cycle 1. Thereafter MOR00208 was administered on a bi-weekly (every 14 days) basis with infusions on Day 1 and Day 15 of each 28-day cycle. LEN: Participants self-administered a starting dose of 25 mg oral LEN daily on Days 1-21 of each cycle, for up to 12 cycles in total. LEN dose could be modified in a de-escalating fashion or discontinued based upon clinical and laboratory findings. On days when both study drugs were given together, LEN was administered prior to MOR00208.
Primary Outcome Measure
Number of Participants With Best Objective Response Rate (ORR) [ Time Frame: Approximately 4.5 years after first participant enrolled; Approximately 6.5 years after first participant enrolled ]
Locations (10)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| CBCC Global Research, Inc. at Comprehensive Blood and Cancer Center | Bakersfield | California | 93309 | - |
| UCLA - David Geffen School of Medicine | Los Angeles | California | 90095 | - |
| Cancer Care - Torrance Memorial Physician Network | Redondo Beach | California | 90277 | - |
| Central Coast Medical Oncology Corporation | Santa Maria | California | 93454 | - |
| St. Mary's Hospital And Regional Medical Center | Grand Junction | Colorado | 81501 | - |
| Norwalk Hospital | Norwalk | Connecticut | 06856 | - |
| St. Joseph Mercy Hospital Cancer Care Center | Ypsilanti | Michigan | 48179 | - |
| Ohio State University Medical Center | Columbus | Ohio | 43210 | - |
| Charleston Hematology Oncology Associates | Charleston | South Carolina | 29414 | - |
| Tyler Hematology-Oncology | Tyler | Texas | 75701 | - |
Find similar trials in Bakersfield, CA
By research site
CBCC Global Research, Inc. at Comprehensive Blood and Cancer Center· Bakersfield, CAUCLA - David Geffen School of Medicine· Los Angeles, CACancer Care - Torrance Memorial Physician Network· Redondo Beach, CACentral Coast Medical Oncology Corporation· Santa Maria, CASt. Mary's Hospital And Regional Medical Center· Grand Junction, CONorwalk Hospital· Norwalk, CT
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