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Brief Title: Study to Assess the Safety of AZD1480 in Patients With Myeloproliferative Diseases
Official Title: A PhaseI/II, Open Label Multi-Centre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of the JAK2 Inhibitor AZD1480 Administered Orally to Patients With Primary Myelofibrosis (PMF) and Post-Polycythaemia Vera/Essential Thrombocythaemia Myelofibrosis (Post-PV/ET MF
Study ID: NCT00910728
Brief Summary: This study is being conducted to test study drug AZD1480 to see how it may work to treat myeloproliferative diseases. The main purpose of this study is to determine the safety and tolerability of AZD1480. This is the first time the drug has been given to humans and is classed as a first time in man study. Its main purpose is to establish a safe dosage of the drug and provide additional information on any potential side effects this drug may cause. The study will also assess the blood levels and action of AZD1480 in the body over a period of time and will indicate whether the drug has a therapeutic effect on myeloproliferative diseases.
Detailed Description:
Minimum Age: 25 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Research Site, New York, New York, United States
Research Site, Houston, Texas, United States
Research Site, Villejuif Cedex, , France
Name: Srdan Verstovsek, MD
Affiliation: MDACC
Role: PRINCIPAL_INVESTIGATOR
Name: Ronald Hoffman, MD
Affiliation: Mt. Sinai
Role: PRINCIPAL_INVESTIGATOR
Name: Vincent Ribrag, MD
Affiliation: Gustave Roussy, Cancer Campus, Grand Paris
Role: PRINCIPAL_INVESTIGATOR
Name: Becker Hewes, MD
Affiliation: AstraZeneca
Role: STUDY_DIRECTOR