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Archive for the 'Irritable-Bowel Syndrome' Category

IBS Symptoms Relieved By Home-Based Cognitive Behavioral Therapy

Persons with irritable bowel syndrome (IBS) can relieve their symptoms as effectively by following a self-administered, at-home cognitive behavioral program as they can by undergoing a 10-week in-office program administered by a trained therapist, a new pilot study has shown.

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Choice Of Hospital Impacts Outcomes For Inflammatory Bowel Disease Surgery

Hospitals with higher annual volumes of patients with inflammatory bowel disease (IBD) who undergo surgery have lower in-hospital mortality rates than hospitals with lower volumes of IBD patients, according to a new study by researchers at the Medical College of Wisconsin in Milwaukee.The study also found a trend toward shorter post-operative hospital stays for patients who undergo surgery for Crohn’s Disease, a form of IBD, at high-volume centers.

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Tioga Pharmaceuticals’ Asimadoline Demonstrates Positive Results In A Phase 2b Clinical Trial For The Treatment Of Irritable Bowel Syndrome

Tioga Pharmaceuticals, Inc. announced the results of a recent Phase 2b study of its oral kappa opioid receptor agonist, asimadoline, which demonstrated statistically significant results in the treatment of Irritable Bowel Syndrome (IBS).

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Dynogen Presents Results Of Its Positive Phase 2a IBS-c Study With DDP733

Dynogen Pharmaceuticals, Inc. announced the presentation of positive results from its Phase 2a clinical trial for DDP733 (pumosetrag) as a treatment for irritable bowel syndrome with constipation (IBS-c) at the Digestive Disease Week 2008 (DDW) scientific meeting.

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Salix Presents New Rifaximin Phase IIb Data Demonstrating Significant And Sustained Improvement In Diarrhea-Associated Irritable Bowel Syndrome

Salix Pharmaceuticals, Ltd. (NASDAQ:SLXP) announced findings from two analyses of the Phase IIb clinical trial of rifaximin, its non-absorbed, gut-selective antibiotic for the treatment of patients with diarrhea-associated irritable bowel syndrome (d-IBS).

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Sucampo Pharmaceuticals Obtains FDA Approval For AMITIZA(R) For The Treatment Of Irritable Bowel Syndrome With Constipation In Adult Women

Sucampo Pharmaceuticals, Inc., (NASDAQ: SCMP, Sucampo Pharmaceuticals) and Takeda Pharmaceutical Company Limited (TSE: 4502, Takeda) and its wholly owned subsidiary, Takeda Pharmaceuticals North America, Inc., announced that the U.S.

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Invivodata’s EPRO Solution Captures Primary Efficacy Data Supporting Supplemental Approval Of Sucampo’s AMITIZA For A New Indication

invivodata inc., the industry leader in electronic patient reported outcomes (ePRO) solutions and services for global clinical research, announced that its ePRO solutions - DiaryPROŽ and SitePROŽ- captured primary efficacy data that supported the recent U.S. Food and Drug Administration’s (FDA) supplemental approval of Sucampo Pharmaceutical Inc.

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Antidepressant Found To Alleviate Symptoms Of Irritable Bowel Syndrome In Adolescents

Researchers at Mattel Children’s Hospital UCLA have found that low-dose antidepressant therapy can significantly improve the overall quality of life for adolescents suffering from irritable bowel syndrome, or IBS.The syndrome affects 6 percent of middle school students and 14 percent of high school kids in the United States.

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FDA Approves Amitiza For IBS-C - Only Drug Available In USA For Irritable Bowel Syndrome With Constipation

The U.S. Food and Drug Administration approved Amitiza (lubiprostone) for the treatment of Irritable Bowel Syndrome with Constipation (IBS-C) in adult women aged 18 and over. There is currently no prescription drug therapy for IBS-C. With this approval, Amitiza becomes the only FDA-approved medical treatment for IBS-C available in the United States. Irritable bowel syndrome is a disorder characterized by cramping, abdominal pain, bloating, constipation, and diarrhea.

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Callisto Pharmaceuticals Files IND For SP-304 (Guanilib) In Chronic Constipation And Irritable Bowel Syndrome

Callisto Pharmaceuticals, Inc. (AMEX: KAL; FWB: CA4) announced that through its wholly-owned subsidiary, Synergy Pharmaceuticals, Inc. it filed an IND on April 2, 2008 with the FDA for SP-304 (also called Guanilib) for the treatment of chronic constipation and constipation-predominant irritable bowel syndrome. SP-304 is an analog of uroguanylin, a natural hormone produced in the gastro-intestinal (GI) tract that is a key regulator of intestinal function.

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