RecruitingPHASE1, PHASE2NCT04925479
Study to Determine the Dose and Safety of Asciminib in Pediatric Patients With Chronic Myeloid Leukemia
Studying Congenital generalized lipodystrophy
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 Pediatric formulation group(drug)
- Enrollment
- 34 target
- Eligibility
- 1-17 years · All sexes
- Timeline
- 2021 – 2031
Study locations (30)
- Indiana UH Riley H for CIU, Indianapolis, Indiana, United States
- Dana Farber Cancer Institute, Boston, Massachusetts, United States
- University of Mississippi Medical Center, Jackson, Mississippi, United States
- Columbia University Medical Center New York Presbyterian, New York, New York, United States
- Cinn Children Hosp Medical Center, Cincinnati, Ohio, United States
- Childrens Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
- Uni Of Texas MD Anderson Cancer Ctr, Houston, Texas, United States
- University Of Utah, Salt Lake City, Utah, United States
- Novartis Investigative Site, Hangzhou, Zhejiang, China
- Novartis Investigative Site, Beijing, China
- Novartis Investigative Site, Shanghai, China
- Novartis Investigative Site, Tianjin, China
- Novartis Investigative Site, Bordeaux, France
- Novartis Investigative Site, Lille, France
- Novartis Investigative Site, Paris, France
- +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 NCT04925479 on ClinicalTrials.govOther trials for Congenital generalized lipodystrophy
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