Study identifier:D1060C00001
ClinicalTrials.gov identifier:NCT00910728
EudraCT identifier:N/A
CTIS identifier:N/A
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
Primary Myelofibrosis (PMF)
Phase 1
No
AZD1480
All
65
Interventional
25 Years - 99 Years
Allocation: N/A
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Other
Verified 01 Mar 2017 by AstraZeneca
AstraZeneca
University of Texas, New York City Hoffman Center, Institut Gustave Roussy
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.
Location
Location
Villejuif Cedex, France
Location
Houston, TX, United States
Location
New York, NY, United States
Arms | Assigned Interventions |
---|---|
Experimental: 1 AZD1480 | Drug: AZD1480 Oral capsule 2.5 mg, 10 mg and 40 mg |
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