Active, not recruitingPhase 3NCT05456191
A Study to Investigate Tolerability and Efficacy of Asciminib (Oral) Versus Nilotinib (Oral) in Adult Participants (≥18 Years of Age) With Newly Diagnosed Philadelphia Chromosome Positive Chronic Myelogenous Leukemia in Chronic Phase (Ph+ CML-CP)
Studying Chronic myeloid leukemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Novartis Pharmaceuticals
- Principal Investigator
- Novartis PharmaceuticalsNovartis Pharmaceuticals
- Intervention
- Asciminib(drug)
- Enrollment
- 568 enrolled
- Eligibility
- 18-100 years · All sexes
- Timeline
- 2022 – 2031
Study locations (30)
- Rocky Mountain Cancer Centers, Denver, Colorado, United States
- Illinois Cancer Care, Peoria, Illinois, United States
- Regions Hospital, Saint Paul, Minnesota, United States
- Messino Cancer Centers, Asheville, North Carolina, United States
- Oncology Hematology Care Inc, Cincinnati, Ohio, United States
- Williamette Cancer Center, Eugene, Oregon, United States
- Texas Oncology P A, Bedford, Texas, United States
- Texas Oncology PA Bedford, Bedford, Texas, United States
- Virginia Oncology Associates, Norfolk, Virginia, United States
- Novartis Investigative Site, CABA, Buenos Aires, Argentina
- Novartis Investigative Site, Buenos Aires, Argentina
- Novartis Investigative Site, Caba, Argentina
- Novartis Investigative Site, CABA, Argentina
- Novartis Investigative Site, Pleven, Bulgaria
- Novartis Investigative Site, Plovdiv, Bulgaria
- +15 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.
Open NCT05456191 on ClinicalTrials.govOther trials for Chronic myeloid leukemia
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