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Spots Global Cancer Trial Database for Study to Assess the Safety and Tolerability of AZD1152 in Combination With Low Dose Cytosine Arabinoside (LDAC)

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Trial Identification

Brief Title: Study to Assess the Safety and Tolerability of AZD1152 in Combination With Low Dose Cytosine Arabinoside (LDAC)

Official Title: A Phase I, Open-label, Multi-centre, Multiple Ascending Dose Study to Assess the Safety and Tolerability of AZD1152 in Combination With Low Dose Cytosine Arabinoside (LDAC) in Patients With Acute Myeloid Leukaemia (AML)

Study ID: NCT00926731

Study Description

Brief Summary: A study to assess the safety and tolerability of AZD1152 in combination with low dose cytosine arabinoside (LDAC) in patients with acute myeloid leukaemia (AML). The first three patients to complete a 28 day cycle in the cohort, before the second three patients start treatment.

Detailed Description:

Eligibility

Minimum Age: 60 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Research Site, Cleveland, Ohio, United States

Research Site, Houston, Texas, United States

Research Site, Le Chesnay Cedex, , France

Research Site, Villejuif Cedex, , France

Contact Details

Name: Paul Stockman

Affiliation: AstraZeneca

Role: STUDY_DIRECTOR

Name: Hagop Kantarjian

Affiliation: M. D. Anderson, (University of Texas)

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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