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Ewingo sarkoma klinikiniai tyrimai Mičiganas

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Oficialus tyrimo tekstas (anglų kalba)

Metastatic Ewing's Trial Testing Schedule Enhancement to Improve Outcomes

  • Helen DeVos Children's Hospital, Grand Rapids
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)

  • Corewell Health ( Site 1001), Grand Rapids
Renkami dalyviai1/2 fazė
6 Months – 25 Years · Visoms lytims · Atnaujinta 2026-09-17 · NCT06395103

Phase 1 Study of INBRX-109 in Subjects With Locally Advanced or Metastatic Solid Tumors Including Sarcomas

  • University of Michigan, Ann Arbor
  • START Midwest Michigan, PC, Grand Rapids
Renkami dalyviai1 fazė
Amžius nuo 12 iki 85 · Visoms lytims · Atnaujinta 2026-09-08 · NCT03715933

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

  • Children's Hospital of Michigan/Wayne State University, Detroit
Renkami dalyviai1/2 fazė
Iki 30 metų · Visoms lytims · Atnaujinta 2026-09-03 · NCT06541262

Lurbinectedin in FET-Fused Tumors

  • University of Michigan, Ann Arbor
Renkami dalyviai1/2 fazė
Amžius 10 ir vyresni · Visoms lytims · Atnaujinta 2026-09-02 · NCT05918640

Tegavivint for the Treatment of Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors

  • C S Mott Children's Hospital, Ann Arbor
Renkami dalyviai1/2 fazė
12 Months – 30 Years · Visoms lytims · Atnaujinta 2026-08-25 · NCT04851119

A Study to Evaluate the Utilization of 3D Printed Models in Pre-Operative Planning

  • William Beaumont University Hospital, Royal Oak
Renkami dalyviai
Amžius 13 ir vyresni · Visoms lytims · Atnaujinta 2026-02-06 · NCT06387485

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

  • Corewell Health, Grand Rapids
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.