A Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Cancer-related Pain
Completed · Phase 2 · Has a placebo group
Conditions studied: Pain, Burning, Pain, Crushing, Pain, Migratory, Pain, Radiating, Pain, Splitting
In brief
The purpose of this study is to compare the safety and effectiveness of JNJ-42160443 with placebo in the treatment of chronic, moderate to severe cancer-related pain in terminally ill patients with a diagnosis of active cancer.
Key facts
- Study ID
- NCT00929188
- Run by
- Janssen Research & Development, LLC
- People needed
- 100
- Starts
- 2009-10-01
- Expected to finish
- 2015-01-01
- Last updated by the study team
- 2016-01-22
Who can join
Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Terminally ill cancer patients as per judgment of the investigator (eg, patients who are in or who are candidates for hospice or palliative care for end-of-life management); Diagnosis of moderate to severe pain directly related to an active cancer that is not controlled by standard pain treatments.
- Exclusion Criteria:Planned major surgical procedures during the double-blind treatment phase that may affect study outcomes; Prior treatment with any other investigational NGF inhibitor therapy; Known allergies, hypersensitivity, or intolerance to JNJ-42160443 or its excipients; Enrolled in any investigational study within the previous 4 weeks or 5 half-lives of the investigational drug (whichever is longer), or are currently enrolled in another investigational study at the time of screening
Where it is running
- Study site — Birmingham, Alabama, United States
- Study site — Tucson, Arizona, United States
- Study site — Laguna Hills, California, United States
- Study site — Montebello, California, United States
- Study site — San Diego, California, United States
- Study site — Miami, Florida, United States
- Study site — Orlando, Florida, United States
- Study site — Stockbridge, Georgia, United States
- Study site — Anderson, Indiana, United States
- Study site — Lexington, Kentucky, United States
- Study site — Marrero, Louisiana, United States
- Study site — Shreveport, Louisiana, United States
- Study site — Farmington Hills, Michigan, United States
- Study site — Flat Rock, North Carolina, United States
- Study site — Cleveland, Ohio, United States
- Study site — Orem, Utah, United States
- Study site — Falls Church, Virginia, United States
- Study site — Lille, France
- Study site — Lyon, France
- Study site — Suresnes, France
- Study site — Toulouse, France
- Study site — Villejuif, France
- Study site — Bygdoszcz, Poland
- Study site — Gdansk, Poland
- Study site — Gdansk-Zaspa, Poland
Full record on ClinicalTrials.gov
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