TerminatedPhase 1NCT03935555

Assess the Safety, Tolerability Oral PU-H71 in Subjects Taking Ruxolitinib

Studying Essential thrombocythemia

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Samus Therapeutics, Inc.
Principal Investigator
Michael Silverman, M.D., MD
Samus Therapeutics
Intervention
PU-H71(drug)
Enrollment
11 enrolled
Eligibility
18 years · All sexes
Timeline
20192022

Study locations (3)

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 NCT03935555 on ClinicalTrials.gov

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