Spots Global Cancer Trial Database for Study Evaluating Orally Administered AMG 900 in Adult Subjects With Acute Myeloid Leukemia
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Trial Identification
Brief Title: Study Evaluating Orally Administered AMG 900 in Adult Subjects With Acute Myeloid Leukemia
Official Title: A Phase 1 Study Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Orally Administered AMG 900 in Adult Subjects With Acute Myeloid Leukemia
Study ID: NCT01380756
Study Description
Brief Summary: This study of AMG 900 will be conducted in two parts: dose escalation and dose expansion. The dose escalation part of the study is aimed at evaluating the safety, tolerability and PK (pharmacokinetics) of oral AMG 900 in subjects with acute myeloid leukemia. Up to 93 subjects may be enrolled in dose escalation. The dose expansion part of the study will consist of 20 subjects with acute myeloid leukemia. The dose of AMG 900 will be dependent upon data from the dose escalation part of the study.
Detailed Description:
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
Research Site, Stony Brook, New York, United States
Research Site, Cleveland, Ohio, United States
Research Site, Houston, Texas, United States
Contact Details
Name: MD
Affiliation: Amgen
Role: STUDY_DIRECTOR
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