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

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Key facts

Sponsor
Geron Corporation
Principal Investigator
Michelle Mudge-Riley, DO
Geron Corporation
Intervention
Imetelstat sodium(drug)
Enrollment
36 target
Eligibility
18 years · All sexes
Timeline
20222028

Study locations (8)

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.gov

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