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Single-arm, Open Label, Phase II Study of MBG453 (Sabatolimab) Added to FDA Approved Hypomethylating Agents of Investigator's Choice (IV/SC/Oral) for Patients With Intermediate, High or Very High Risk Myelodysplastic Syndrome (MDS) as Per IPSS-R Criteria (US Multi-center) (STIMULUS MDS-US)

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Trial Profile

Single-arm, Open Label, Phase II Study of MBG453 (Sabatolimab) Added to FDA Approved Hypomethylating Agents of Investigator's Choice (IV/SC/Oral) for Patients With Intermediate, High or Very High Risk Myelodysplastic Syndrome (MDS) as Per IPSS-R Criteria (US Multi-center) (STIMULUS MDS-US)

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 13 Aug 2025

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At a glance

  • Drugs Sabatolimab (Primary) ; Azacitidine; Azacitidine; Cedazuridine/decitabine; Decitabine
  • Indications Myelodysplastic syndromes
  • Focus Adverse reactions
  • Acronyms STIMULUS MDS-US
  • Sponsors Novartis Pharmaceuticals

Most Recent Events

  • 31 Jul 2025 Status changed from completed to discontinued.
  • 03 Oct 2024 Status changed from active, no longer recruiting to completed.
  • 21 Aug 2024 Planned End Date changed from 14 Jun 2024 to 25 Oct 2024.

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