RecruitingPhase 1NCT05371964
A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Imetelstat in Combination With Ruxolitinib in Participants With Myelofibrosis
Studying Primary myelofibrosis
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
- Geron Corporation
- Principal Investigator
- Michelle Mudge-Riley, DOGeron Corporation
- Intervention
- Imetelstat sodium(drug)
- Enrollment
- 36 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2028
Study locations (8)
- City of Hope, Duarte, California, United States
- City of Hope, Irvine, California, United States
- University of Miami, Coral Gables, Florida, United States
- H. Lee Moffitt Cancer Center and Research Institute, Inc., Tampa, Florida, United States
- Icahn School of Medicine at Mount Sinai, New York, New York, United States
- Texas Oncology, Denison, Texas, United States
- Texas Oncology, Tyler, Texas, United States
- Fred Hutchinson Cancer Center, Seattle, Washington, 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 NCT05371964 on ClinicalTrials.govOther trials for Primary myelofibrosis
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