A Study of Participants With Lymphoma Who Take R-CHOP and Enzastaurin Compared to Participants Who Take R-CHOP Only
Part of paid clinical trials in Huntsville, Alabama.
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT00451178
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- enzastaurin — DRUG1125 milligrams (mg) then 500 mg, oral, daily, six 21-day cycles or up to 3 years
- rituximab — DRUG375 milligrams per square meter (mg/m\^2), intravenous (IV), Day 1 every 21 days, six 21-day cycles
- cyclophosphamide — DRUG750 mg/m\^2, IV, Day 1 every 21 days, six 21-day cycles
- doxorubicin — DRUG50 mg/m\^2, IV, Day 1 every 21 days, six 21-day cycles
- vincristine — DRUG1.4 mg/m\^2, IV, Day 1 every 21 days, six 21-day cycles
- prednisone — DRUG100 mg, oral, Days 1-5, six 21-day cycles
Study Details
To compare R-CHOP plus enzastaurin versus R-CHOP for progression-free survival (PFS) time measured in participants with intermediate and/or high risk for diffuse large B-cell lymphoma (DLBCL) receiving first-line treatment.
Key Dates
- Start date
- May 31, 2007
- Status verified
- Jul 2020
- Primary completion
- Feb 29, 2012
- Completion
- Jan 31, 2013
Study Design
- Enrollment
- 101 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: R-CHOP and EnzastaurinR-CHOP includes rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone treatment therapies.
- Active Comparator: R-CHOPR-CHOP includes rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone treatment therapies.
Primary Outcome Measure
Progression-Free Survival (PFS) Time [ Time Frame: Randomization to measured PD or death from any cause (up to 55 months) ]
Locations (25)
Find similar trials in Huntsville, AL
By research site
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.· Huntsville, ALFor additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.· Beverly Hills, CAFor additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.· Greenbrae, CAFor additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.· Palm Springs, CAFor additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.· Fort Myers, FLFor additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.· Jacksonville, FL
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