Omacetaxine + Azacitidine in Untreated Patients With High Grade MDS

PHASE1/PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

September 17, 2018

Primary Completion Date

August 16, 2026

Study Completion Date

June 30, 2027

Conditions
High Grade Myelodysplastic Syndromes
Interventions
DRUG

Omacetaxine

Phase I is a dose escalation phase. Patients will be enrolled into one of three cohorts to receive omacetaxine subcutaneously (0.5, 0.75, 1.0, or 1.25 mg/m2) twice daily on days 1 to 7.

DRUG

Azacitidine

Azacitidine will be given at the standard dose and schedule, 75 mg/m2 once daily, on days 1 to 7. The patients will then be monitored for 21 more days ( to complete one 28 day cycle) but no more medication will be administered during those 21 days.

DRUG

Omacetaxine

Phase II is a maximum tolerated dose phase. Phase I will determine the maximum tolerated dose (highest amount that can be safely administered). Patients will receive omacetaxine subcutaneously at the maximum tolerated dose (0.5, 0.75, 1.0, or 1.25 mg/m2) twice daily on days 1 to 7.

DRUG

Azacitidine

Azacitidine will be given at the standard dose and schedule, 75 mg/m2 once daily, on days 1 to 7. The patients will then be monitored for 21 more days ( to complete one 28 day cycle) but no more medication will be administered during those 21 days.

Trial Locations (1)

80045

Universtiy of Colorado Denver, Aurora

All Listed Sponsors
lead

University of Colorado, Denver

OTHER

NCT03564873 - Omacetaxine + Azacitidine in Untreated Patients With High Grade MDS | Biotech Hunter | Biotech Hunter