Active, not recruitingPhase 2NCT05201066
Roll-over Study for Patients Who Have Completed a Prior Novartis-sponsored Sabatolimab (MBG453) Study and Are Judged by the Investigator to Benefit From Continued Treatment With Sabatolimab.
Studying Myelodysplastic syndrome
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Novartis Pharmaceuticals
- Principal Investigator
- Novartis PharmaceuticalsNovartis Pharmaceuticals
- Intervention
- decitabine(drug)
- Enrollment
- 33 enrolled
- Eligibility
- 12-99 years · All sexes
- Timeline
- 2023 – 2028
Study locations (20)
- Oregon Health Sciences University, Portland, Oregon, United States
- Huntsman Cancer Institute Univ of Utah, Salt Lake City, Utah, United States
- Novartis Investigative Site, Clayton, Victoria, Australia
- Novartis Investigative Site, Florianópolis, Santa Catarina, Brazil
- Novartis Investigative Site, Vancouver, British Columbia, Canada
- Novartis Investigative Site, Changchun, Jilin, China
- Novartis Investigative Site, Tianjin, China
- Novartis Investigative Site, Prague, Czechia
- Novartis Investigative Site, Toulouse, France
- Novartis Investigative Site, Freiburg im Breisgau, Baden-Wurttemberg, Germany
- Novartis Investigative Site, Alexandroupoli, Greece
- Novartis Investigative Site, Pátrai, Greece
- Novartis Investigative Site, Brescia, BS, Italy
- Novartis Investigative Site, Florence, FI, Italy
- Novartis Investigative Site, Genova, GE, Italy
- +5 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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