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Ewingo sarkoma klinikiniai tyrimai Florida

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Oficialus tyrimo tekstas (anglų kalba)

Metastatic Ewing's Trial Testing Schedule Enhancement to Improve Outcomes

  • University of Florida, Gainesville
  • Nemours Jacksonville, Jacksonville
  • University of Miami, Miami
  • ir dar 2
Renkami dalyviai1 fazė
Amžius 1 ir vyresni · Visoms lytims · Atnaujinta 2026-09-25 · NCT07194044

Substudy 01A: Zilovertamab Vedotin in Pediatric and Young Adult Participants With Hematologic Malignancies or Solid Tumors (MK-9999-01A/LIGHTBEAM-U01)

  • Johns Hopkins All Children's Hospital ( Site 1025), St. Petersburg
Renkami dalyviai1/2 fazė
6 Months – 25 Years · Visoms lytims · Atnaujinta 2026-09-17 · NCT06395103

Eflornithine (DFMO) and AMXT 1501 for Neuroblastoma, CNS Tumors, and Sarcomas

  • University of Florida, Gainesville
  • Nicklaus Children's Hospital, Miami
  • Arnold Palmer Hospital for Children, Orlando
  • ir dar 1
Renkami dalyviai1/2 fazė
Iki 26 metų · Visoms lytims · Atnaujinta 2026-09-03 · NCT06465199

Silmitasertib (CX-4945) in Combination With Chemotherapy for Relapsed Refractory Solid Tumors

  • University of Florida, Gainesville
  • Nicklaus Children's Hospital, Miami
  • Arnold Palmer Hospital for Children, Orlando
  • ir dar 2
Renkami dalyviai1/2 fazė
Iki 30 metų · Visoms lytims · Atnaujinta 2026-09-03 · NCT06541262

Eflornithine (DFMO) for Ewing Sarcoma and Osteosarcoma

  • St. Joseph's Children's Hospital, Tampa
Renkami dalyviai2 fazė
Amžius nuo 0 iki 50 · Visoms lytims · Atnaujinta 2026-07-09 · NCT07321912

Alpha/Beta T and B Cell Depletion With Zoledronic Acid for Solid Tumors

  • University of Florida, Gainesville
Renkami dalyviai1/2 fazė
6 Months – 25 Years · Visoms lytims · Atnaujinta 2026-06-30 · NCT06625190

Study of Lurbinectedin Monotherapy in Pediatric and Young Adult Participants With Relapsed/Refractory Ewing Sarcoma

  • Johns Hopkins All Children's Hospital, St. Petersburg
Renkami dalyviai1/2 fazė
Amžius nuo 2 iki 30 · Visoms lytims · Atnaujinta 2026-02-03 · NCT05734066

Iš ClinicalTrials.gov, duomenys gauti 2026-10-05. Kiekvienas tyrimas nustato savo tinkamumo kriterijus; tyrimo komanda sprendžia, kas gali dalyvauti.