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OpenTrials
Completed

NCT Number: NCT00548574

Efficacy and Safety of Two Doses of SPD476 (Mesalazine) 2.4g and 4.8g Once Daily, With Reference to Asacol 0.8g Three Times Daily in Subjects With Acute, Mild to Moderate Ulcerative Colitis

The primary objective of the study was to compare the percentage of subjects in remission after 8 weeks of treatment with SPD476, 2.4 g/day once daily vs placebo and SPD476 4.8 g/day once daily versus placebo

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Imelda General Hospital Dept of Gastroenterology

Bonheiden, Belgium

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • newly diagnosed or relapsing mild to moderate UC (score of 4-10 (inclusive) on the UC-DAI scale, with a sigmoidoscopy score of => 1 and a PGA <=2) with compatible histology
  • females eligible if post--menopausal, surgically sterile or if they had a negative urine pregnancy test at screening and were on adequate contraception

Exclusion criteria

  • subjects with relapsing UC who were in relapse for > 6 weeks prior to baseline
  • subjects who relapsed on maintenace therapy with doses of mesalazine => 2g/day
  • subjects who had unsuccessfully treated their current relapse with steroids or a mesalazine dose of > 2g/day
  • subjects with Crohn's disease, proctitis, bleeding disorders, active peptic ulcer disease, previous colonic surgery, or those at an immediate risk of toxic megacolon or a stool culture positive for enteric pathogens
  • subjects who had used systemic or rectal steroids within the last 4 weeks, immunosuppressants wihtin the last 6 weeks or anti-inflammatory drugs on a repeat basis within 7 days prior to the baseline visit
  • subjects with hypersensitivity to salicylates and subjects with moderate/severe renal impairment

Treatment and study plan

SPD476 is a polymeric matrix formulation that displays both delayed- and extended-release of mesalazine

Drug

Other names: LIALDA

Mesalazine

Drug

Other names: ASACOL

Primary outcomes

  1. Percentage of subjects in remission (UC-DAI score <=1, with scores of 0 for rectal bleeding and stool frequency and a sigmoidoscopy score reduction of 1 point or more from baseline)

    Time frame: 8 weeks

Secondary outcomes

  1. Clinical improvement as defined by a drop of => 3 points from baseline in the overall UC-DAI score

    Time frame: 8 weeks

  2. Change from baseine in UC-DAI score, symptoms, sigmoidscopy score, and PGA

    Time frame: 8 weeks

  3. Clinical remission defined as subjects who scored 0 for both the total stool frequency and the total rectal bleeding score

    Time frame: 8 weeks

  4. Treatment failure defined as unchanged, worsened missing or imcomplete UC-DAI score

    Time frame: 8 weeks

Sponsors and collaborators

Lead sponsor

Shire

Industry

Registry information

Official study title

A Phase III, Randomized, Multi-Centre, Double-blind, Double Dummy, Parallel Group, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Two Doses of SPD476 (Mesalazine) 2.4g and 4.8g Once Daily, With Reference to ASACOL 0.8g Three Times Daily, in Subjects With Mild to Moderate Ulcerative Colitis

Important dates

Study start
2003
Primary completion
2004
Study completion
2004
First posted
Oct 24, 2007
Registry last updated
Jun 11, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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