Horm Metab Res 2010; 42(1): 23-30
DOI: 10.1055/s-0029-1241195
Humans, Clinical

© Georg Thieme Verlag KG Stuttgart · New York

Long-term Safety and Tolerability of Colesevelam HCl in Subjects with Type 2 Diabetes

A. B. Goldfine1 , V. A. Fonseca2 , M. R. Jones3 , A. C. Wang4 , D. M. Ford4 , K. E. Truitt4
  • 1Joslin Diabetes Center, Boston, MA, USA
  • 2Tulane University Health Sciences Center, New Orleans, LA, USA
  • 3Daiichi Sankyo, Inc., Parsippany, NJ, USA
  • 4Daiichi Sankyo Pharma Development, Edison, NJ, USA
Further Information

Publication History

received 01.05.2009

accepted 09.09.2009

Publication Date:
27 October 2009 (online)

Abstract

The bile acid sequestrant, colesevelam hydrochloride, is approved for glycemic control in adults with type 2 diabetes. In three double-masked, placebo-controlled studies, colesevelam hydrochloride 3.75 g/day demonstrated its glycemic-lowering properties when added to existing metformin-, insulin-, or sulfonylurea-based therapy in adults with inadequately controlled type 2 diabetes. This was a 52-week open-label extension study conducted at 63 sites in the United States and one site in Mexico to further evaluate the safety and tolerability of colesevelam hydrochloride in subjects with type 2 diabetes. All subjects who completed the three double-masked, placebo-controlled studies were eligible to enroll in this open-label extension. In total, 509 subjects enrolled and received open-label colesevelam hydrochloride 3.75 g/day for 52 weeks. Safety and tolerability of colesevelam hydrochloride was evaluated by the incidence and severity of adverse events. In total, 360 subjects (70.7%) completed the extension. Of the safety population, 361 subjects (70.9%) experienced an adverse event, most (88.1%) being mild or moderate in severity. Fifty-six adverse events (11.0%) were drug-related; the most frequent drug-related adverse events were constipation and dyspepsia. Thirty-five subjects (6.9%) discontinued due to an adverse event. Fifty-four subjects (10.6%) experienced a serious adverse event; only one was considered drug-related (diverticulitis). Seventeen subjects (3.3%) experienced hypoglycemia; most episodes were mild or moderate in severity. Glycemic improvements with colesevelam hydrochloride were seen without change in weight over 52 weeks (0.2 kg mean reduction from baseline). Colesevelam hydrochloride was safe and well-tolerated as long-term therapy for patients with type 2 diabetes.

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Correspondence

A. B. GoldfineMD 

Assistant Professor

Harvard Medical School

Assistant Director of Clinical Research

Joslin Diabetes Center One Joslin Place

Boston

MA 02115

USA

Phone: +1/617/732 2643

Fax: +1/617/713 3403

Email: allison.goldfine@joslin.harvard.edu