INST Phase II Trial of Gemcitabine and Irinotecan in Patients With Relapsed or Refractory Lymphoma.
Completed · Phase 2
Conditions studied: Non-Hodgkin's Lymphoma, Cancer
In brief
Primary objectives * Assess the response rate in patients with recurrent or refractory B-cell NHL or Hodgkins disease, treated with the combination of the gemcitabine and irinotecan. Secondary objectives * Assess progression free survival in these patients treated with this regimen. * Assess toxicity of this regimen in this group of patients.
Key facts
- Study ID
- NCT00276003
- Run by
- University of New Mexico
- People needed
- 22
- Starts
- 2002-08-01
- Expected to finish
- 2005-08-01
- Last updated by the study team
- 2010-01-07
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with a histologic diagnosis of non-HIV related B-cell NHL or Hodgkins disease are eligible.
- Patients should have documented evidence of refractory or relapsed NHL or Hodgkins disease for inclusion.
- Patient should have received 1 or more prior chemotherapeutic regimens for relapse, and should have completed last course of treatment at least 3 weeks prior to enrollment.
- The patient must have bidimensionally measurable or evaluable disease.
- Age > 18 years.
- ECOG Performance status < 2
- Informed consent.
- ANC > 1.5, platelet count > 100K, creatinine< 2.0, bilirubin < 3
- Female patients must have a negative pregnancy test.
Where it is running
- Lovelace Sandia Health Systems Dept of Hematology — Albuquerque, New Mexico, United States
- University of New Mexico — Albuquerque, New Mexico, United States
Full record on ClinicalTrials.gov
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