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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