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OncoMatch/Clinical Trials/NCT04570423

A Study to Evaluate the Safety and Pharmacokinetics of Eflapegrastim in Pediatric Participants With Solid Tumors or Lymphomas and Treated With Myelosuppressive Chemotherapy

Is NCT04570423 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Eflapegrastim and Chemotherapy for solid tumors.

Phase 2RecruitingSpectrum Pharmaceuticals, IncNCT04570423Data as of May 2026

Treatment: Eflapegrastim · ChemotherapyThe 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.

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Non-Hodgkin Lymphoma

Prior therapy

Cannot have received: filgrastim (filgrastim)

previous exposure to filgrastim (within 7 days)

Cannot have received: pegfilgrastim (pegfilgrastim)

pegfilgrastim (within 14 days)

Cannot have received: granulocyte colony stimulating factor

other granulocyte colony stimulating factor (G-CSF) products in clinical development within 2 weeks prior to the administration of study drug (eflapegrastim)

Cannot have received: bone marrow or hematopoietic stem cell transplant

prior bone marrow or hematopoietic stem cell transplant

Cannot have received: spinal radiation therapy

spinal radiation therapy within 30 days prior to study enrollment

Cannot have received: investigational drugs, biologics or devices

used any investigational drugs, biologics or devices within 30 days prior to study treatment or plans to use any of these during the study

Lab requirements

Blood counts

adequate hematological function

Kidney function

adequate renal function

Liver function

adequate hepatic function

Cardiac function

ECHO or MUGA within 14 days of Screening if receiving a cardiotoxic therapy and have a cardiac ejection fraction of >50%

adequate hematological, renal, and hepatic function; echocardiogram (ECHO) or multigated acquisition (MUGA) within 14 days of Screening if receiving a cardiotoxic therapy and have a cardiac ejection fraction of >50%

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • New York Medical College · Valhalla, New York
  • Carolinas Medical Center/ Levine Children's Hospital · Charlotte, North Carolina
  • Levine Children's Health · Charlotte, North Carolina
  • University Hospitals Cleveland Medical Center · Cleveland, Ohio
  • UT MD Anderson Cancer Center · Houston, Texas

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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