Study of Intravenous (IV) Methylnaltrexone Bromide (MNTX) in the Treatment of Post-Operative Ileus (POI)
Completed
Wyeth is now a wholly owned subsidiary of Pfizer
Phase 3
2006-10-31
To evaluate the safety and efficacy of MNTX in participants who have undergone segmental
colectomy and to assess if the time between the end of surgery and the first bowel movement
is significantly shorter in the MNTX regimen than the equivalent assessment using a placebo
regimen.
Study of Intravenous (IV) Methylnaltrexone Bromide (MNTX) in the Treatment of Post-Operative Ileus (POI)
Completed
Bausch Health Americas, Inc.
Phase 3
2006-10-31
To evaluate the safety and efficacy of MNTX in participants who have undergone segmental
colectomy and to assess if the time between the end of surgery and the first bowel movement
is significantly shorter in the MNTX regimen than the equivalent assessment using a placebo
regimen.
Study of Intravenous (IV) Methylnaltrexone Bromide (MNTX) in the Treatment of Post-Operative Ileus (POI)
Completed
Valeant Pharmaceuticals International, Inc.
Phase 3
2006-10-31
To evaluate the safety and efficacy of MNTX in participants who have undergone segmental
colectomy and to assess if the time between the end of surgery and the first bowel movement
is significantly shorter in the MNTX regimen than the equivalent assessment using a placebo
regimen.
Study Evaluating Oral MOA-728 For The Treatment Of OIBD In Subjects With Chronic Non-Malignant Pain
Completed
Progenics Pharmaceuticals, Inc.
Phase 2
2007-10-01
The primary purpose of this study is to evaluate the safety and dose-response relationship of
N-methylnaltrexone bromide (MOA-728) by observing spontaneous bowel movements in subjects
with chronic pain, which is not due to malignant cancer, and who have opioid-induced bowel
dysfunction (OIBD).
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