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Spots Global Cancer Trial Database for Study to Investigate the Efficacy, Safety and Tolerability of AZD1152 Alone and in Combination With Low Dose Cytosine Arabinoside (LDAC)in Acute Myeloid Leukaemia (AML) Patients

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Trial Identification

Brief Title: Study to Investigate the Efficacy, Safety and Tolerability of AZD1152 Alone and in Combination With Low Dose Cytosine Arabinoside (LDAC)in Acute Myeloid Leukaemia (AML) Patients

Official Title: A Randomised, Open-label, Multi-centre, 2-stage, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of AZD1152 Alone and in Combination With Low Dose Cytosine Arabinoside (LDAC) in Comparison With LDAC Alone in Patients Aged ≥ 60 With Newly Diagnosed Acute Myeloid Leukaemia (AML)

Study ID: NCT00952588

Interventions

AZD1152
LDAC

Study Description

Brief Summary: The purpose of this study is to assess the efficacy, safety and tolerability of AZD1152 alone and in combination with low dose cytosine arabinoside (LDAC) in comparison with LDAC alone in AML patients.

Detailed Description:

Eligibility

Minimum Age: 60 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Research Site, Atlanta, Georgia, United States

Research Site, Chicago, Illinois, United States

Research Site, New York, New York, United States

Research Site, Cleveland, Ohio, United States

Research Site, Portland, Oregon, United States

Research Site, Greenville, South Carolina, United States

Research Site, Nashville, Tennessee, United States

Research Site, Houston, Texas, United States

Research Site, Westmead, New South Wales, Australia

Research Site, Herston, Queensland, Australia

Research Site, Melbourne, Victoria, Australia

Research Site, Parkville, Victoria, Australia

Research Site, Angers Cedex 01, , France

Research Site, Clermont-ferrand, , France

Research Site, Grenoble Cedex 09, , France

Research Site, Lyon Cedex 03, , France

Research Site, Marseille Cedex 09, , France

Research Site, Nantes, , France

Research Site, Duisburg, , Germany

Research Site, Erlangen, , Germany

Research Site, Frankfurt, , Germany

Research Site, Munster, , Germany

Research Site, Villingen-schwenningen, , Germany

Research Site, Bologna, BO, Italy

Research Site, Genova, GE, Italy

Research Site, Orbassano, TO, Italy

Research Site, Udine, UD, Italy

Research Site, Roma, , Italy

Research Site, Nagoya, Aichi, Japan

Research Site, Yoshida-gun, Fukui, Japan

Research Site, Maebashi, Gunma, Japan

Research Site, Isehara, Kanagawa, Japan

Research Site, Yokohama, Kanagawa, Japan

Research Site, Chuo, Tokyo, Japan

Research Site, Fukuoka, , Japan

Research Site, Brasov, , Romania

Research Site, TG Mures, , Romania

Research Site, Oviedo, Asturias, Spain

Research Site, Badalona(barcelona), Cataluna, Spain

Research Site, Barcelona, Cataluna, Spain

Research Site, Madrid, Comunidad DE Madrid, Spain

Research Site, Valencia, Comunidad Valenciana, Spain

Research Site, Majadahonda, Madrid, Spain

Research Site, Brighton, , United Kingdom

Research Site, London, , United Kingdom

Contact Details

Name: Paul Stockman

Affiliation: AstraZeneca

Role: STUDY_DIRECTOR

Name: Hagop Kantarjian

Affiliation: M.D. Anderson Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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