Clin2
NCT04901702Possibly a fitRecruiting

Onivyde plus talazoparib or temozolomide for resistant solid tumors

Recurrent Solid TumorRecurrent Ewing SarcomaRecurrent HepatoblastomaRecurrent Malignant Germ Cell TumorRecurrent Malignant Solid NeoplasmRecurrent NeuroblastomaRecurrent OsteosarcomaRecurrent Peripheral Primitive Neuroectodermal Tumor

Treatments studied

Part of Cancer, Genetic & congenital, Kidney & urinary, Women’s health & pregnancy clinical trials.

This trial tests whether adding Onivyde to either talazoparib or temozolomide can shrink or control hard-to-treat (refractory or recurring) cancers in children and young adults. It aims to find safer dosing first, then look at how well the treatment works—especially for Ewing sarcoma.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
90 people
Ages
1 year to 30 years
Study type
Interventional

Who can take part

  • Your age at enrollment must be over 12 months and under 30 years.
  • You must have a hard-to-cure (refractory or recurrent) cancer that cannot be treated with curative surgery/therapy.
  • For Ewing sarcoma studies: your tumor must have an EWSR1-FLI1 fusion or another EWS gene rearrangement.
  • You must have cancer that can be measured or at least evaluated on scans/tests (bone-only disease may not count for some outcome goals).
  • You must be recovered from prior treatments and have adequate blood counts, kidney function, liver function, and oxygen/breathing status.
  • If you could become pregnant: you must have a negative pregnancy test and use effective birth control during treatment and for months after the last dose; pregnancy or breastfeeding is not allowed.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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