Advertisement Sucampo Completes Lubiprostone Phase 3 Trial - Pharmaceutical Business review
Pharmaceutical Business review is using cookies

ContinueLearn More
Close

Sucampo Completes Lubiprostone Phase 3 Trial

Sucampo Pharmaceuticals has completed Phase 3 double blind trial of Lubiprostone (marketed as Amitiza in the US) for chronic idiopathic constipation (CIC) in Japanese patients.

Sucampo claimed that the trial met its primary endpoint with statistical significance and demonstrated a safety profile consistent with previously reported clinical lubiprostone data.

The primary endpoint of the trial was a change in the number of spontaneous bowel movements (SBMs) at the end of the first week of treatment. The pivotal, double-blinded, placebo-controlled trial evaluated 124 Japanese CIC patients each of whom received one Lubiprostone 24-mcg, or placebo, capsule twice daily for 28 days.

Sucampo said that it would continue to conduct a long-term, open-label, multi-center, confirmatory, safety trial in 209 Japanese CIC patients. Top-line results from the safety trial are expected during the fourth quarter of 2010.

R-Tech Ueno has an agreement with Sucampo Pharma (SPL), a wholly owned subsidiary of Sucampo, under which it has the exclusive right to manufacture and supply Lubiprostone (marketed as Amitiza in the US) in Japan, Asia, Oceania and other regions.