Study Evaluating Orally Administered AMG 900 in Adult Subjects With Acute Myeloid Leukemia

PHASE1CompletedINTERVENTIONAL
Enrollment

35

Participants

Timeline

Start Date

October 4, 2011

Primary Completion Date

September 4, 2014

Study Completion Date

September 4, 2014

Conditions
CancerHematologic MalignanciesLeukemiaMyeloid Leukemia
Interventions
DRUG

Arm 1- Dose Escalation

AMG 900 is a small molecule aurora kinase inhibitor. AMG 900 will be administered daily for 4 days every 2 weeks or daily 7 days every 2 weeks (ie.g., 4 consecutive days of dosing followed by 10 consecutive days off treatment).

DRUG

Arm 2- Dose Expansion

AMG 900 is a small molecule aurora kinases inhibitor. The dose expansion phase would be conducted to gain further clinical experience with AMG 900 in AML at the optimal dose schedule.

Trial Locations (3)

11794

Research Site, Stony Brook

44195

Research Site, Cleveland

77030

Research Site, Houston

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY

NCT01380756 - Study Evaluating Orally Administered AMG 900 in Adult Subjects With Acute Myeloid Leukemia | Biotech Hunter | Biotech Hunter