Safety and Efficacy of (PN-152,243)/PN-196,444 in the Prevention of Thrombocytopenia
Completed · Phase 3
Conditions studied: Neoplasms, Thrombocytopenia, Multiple Myeloma, Lymphoma, Malignant
In brief
Intensive chemotherapy is associated with significant thrombocytopenia, often requiring platelet transfusion to maintain platelet counts. This investigational drug has demonstrated the ability to increase platelet counts. This study will test the safety and efficacy of this investigational drug in the prevention of thrombocytopenia in patients with solid tumors, lymphomas or multiple myeloma who are receiving myelosuppressive treatment regimens requiring platelet transfusion support.
Key facts
- Study ID
- NCT00037791
- Run by
- Pfizer
- People needed
- 180
- Starts
- 1999-12-01
- Expected to finish
- 2002-09-01
- Last updated by the study team
- 2006-11-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients must have solid tumors, lymphomas or multiple myeloma who are receiving myelosuppressive treatment regimens requiring platelet transfusion support
You may not qualify if…
- Patients must not have active bleeding (exclusions do apply) or history of platelet disorder
Where it is running
- Pfizer Investigational Site — Berkeley, California, United States
- Pfizer Investigational Site — La Jolla, California, United States
- Pfizer Investigational Site — Los Angeles, California, United States
- Pfizer Investigational Site — Los Angeles, California, United States
- Pfizer Investigational Site — New Orleans, Louisiana, United States
- Pfizer Investigational Site — Houston, Texas, United States
- Pfizer Investigational Site — Buenos Aires, Buenos Aires F.D., Argentina
- Pfizer Investigational Site — Buenos Aires, Buenos Aires F.D., Argentina
- Pfizer Investigational Site — Mexico City, Mexico City, Mexico
Full record on ClinicalTrials.gov
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