An Extension Study for Patients Previously Treated With ARQ 501
Completed · Phase 1/Phase 2
Conditions studied: Cancer
In brief
To provide ongoing treatment with ARQ 501 for patients who have benefited from prior treatment with ARQ 501
Key facts
- Study ID
- NCT00622063
- Run by
- ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)
- People needed
- 1
- Starts
- 2006-12-01
- Last updated by the study team
- 2013-02-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Signed written informed consent
- Has previous participated in a clinical trial with ARQ 501 and is eligible for continued treatment
You may not qualify if…
- Have not received previous treatment with ARQ 501 under a treatment protocol
- Uncontrolled intercurrent illness, uncontrolled infection or psychiatric illness/social situations that would limit compliance with study requirements
Where it is running
- Mary Crowley Medical Research Center — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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