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Sunday, February 23, 2014 4:41:25 PM
This is the cut/paste from the referenced study (it is 55 months duration) if it is the correct one.
Overview
Research Study Summary
A clinical research study of RO5429083 and cytarabine for the treatment of Myelogenous Leukemia, Acute
Research Study Title
Open Label, Multicenter, Dose Escalation Phase 1a/b Study of RO5429083, Administered as Intravenous Infusion Alone or in Combination With Cytarabine in Patients With Acute Myelogenous Leukemia (AML).
Purpose
This multi-center, open-label study will evaluate the safety, pharmacokinetics, pharmacodynamics and efficacy of RO5429083 alone and in combination with cytarabine in patients with acute myelogenous leukemia. In Part A, patients will receive multiple escalating doses of RO5429083 intravenously. In Part B, patients will receive RO5429083 plus up to 4 cycles of cytarabine (1000 mg/m2 iv daily for 5 consecutive days). Anticipated time on study treatment is until disease progression or unacceptable toxicity occurs.
Phase
1
Gender
Both Male and Female
Age
18 and up
Overall Status
Recruiting
Lead Sponsor
Hoffmann-La Roche
Duration
55 Months
Facility Type
N/A
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