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NCT04570423
A Study to Evaluate the Safety and Pharmacokinetics of Eflapegrastim in Pediatric Participants With Solid Tumors or Lymphomas and Treated With Myelosuppressive Chemotherapy
The purpose of this study is to evaluate the safety and pharmacokinetics of eflapegrastim in pediatric participants with solid tumors or lymphoma and treated with myelosuppressive chemotherapy.
Trial Details
NCT ID NCT04570423
Phase PHASE2
Sponsor Spectrum Pharmaceuticals, Inc
Status RECRUITING
Cancer Type Lymphoma
Interventions Eflapegrastim Chemotherapy
Locations (sample) Valhalla, New York, United States|41.07482,-73.77513 Charlotte, North Carolina, United States|35.22709,-80.84313 Charlotte, North Carolina, United States|35.22709,-80.84313 Cleveland, Ohio, United States|41.4995,-81.69541 Houston, Texas, United States|29.76328,-95.36327
Key Eligibility Criteria
Participant must have a pathologic/histologic confirmed newly diagnosed/relapsed/recurrent solid tumor or lymphoma without bone marrow involvement. Participant must be a candidate to receive myelosuppressive chemotherapy, with a febrile neutropenia rate of at least 20% as outlined in the Nation… Participant has adequate hematological, renal, and hepatic function. Participant must have an echocardiogram (ECHO) or multigated acquisition (MUGA) within 14 days of Screening if receiving a cardiotoxic therapy and …
For full eligibility, visit ClinicalTrials.gov .
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