Active, not recruitingPhase 2NCT04626024
Safety And Efficacy Of TKI Cessation For CML Patients With Stable Molecular Response In A Real World Population
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
- Baylor College of Medicine
- Principal Investigator
- Martha P. Mims, MD, PhDBaylor College of Medicine
- Intervention
- Imatinib Mesylate, Dasatinib, Nilotinib or Bosutinib Withdrawal(other)
- Enrollment
- 17 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2028
Study locations (4)
- Baylor College of Medicine- McNair Campus, Houston, Texas, United States
- Ben Taub General Hospital, Houston, Texas, United States
- CHI St. Luke's Health Baylor College of Medicine Medical Center, Houston, Texas, United States
- Harris Health System- Smith Clinic, Houston, Texas, United States
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 NCT04626024 on ClinicalTrials.govOther trials for Congenital generalized lipodystrophy
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