U:  P:        Forgot Password? Username?
Gastrointestinal


A Study of the Safety and Efficacy of Infliximab(REMICADE ) in Pediatric Subjects With ULC Colitis PDF Print E-mail
  • The purpose of the study is to evaluate the effectiveness and safety of infliximab (Remicade) in children with moderately to severely active ulcerative colitis.
 
Efficacy and Long Term Safety of Adalimumab in Pediatric Subjects Who Have Demonstrated Clinical Response in M06-806 PDF Print E-mail
  • Efficacy and Long Term Safety of Adalimumab in Pediatric Subjects Who Have Demonstrated Clinical Response in M06-806
 
Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe Crohn's Disease PDF Print E-mail
  • Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe Crohn's Disease
 
Efficacy and Safety of Budesonide Foam for Patients With Active Mild to Moderate Ulcerative Proctitis or Proctosigmoiditis PDF Print E-mail

This is a Phase 3, randomized, double-blind, placebo-controlled, multi-center study to assess the efficacy and safety of budesonide foam in subjects with active mild to moderate proctitis or proctosigmoiditis.

 
NURTURE, the Use of Certolizumab Pegol for Treatment of Active Crohn's Disease in Children and Adolescents PDF Print E-mail
  • The purpose of this study is to evaluate the safety, efficacy, pharmacokinetics, and immunogenicity of certolizumab pegol treatment in pediatric patients, aged 6 to 17, with moderately to severe active Crohn's disease. The target enrollment is 160 patients.

 

 
Phase II Study of HMPL-004 in Subjects With Crohn's Disease PDF Print E-mail
  • Double-blind, randomized, multicenter, placebo-controlled study The purpose of this study is to evaluate the efficacy and safety of HMPL-004 in patients with active moderate Crohn's Disease,compared with placebo.
 
Prevention of Recurrence of Diverticulitis (PREVENT 2) PDF Print E-mail

Adult patients that have had at least one episode of a diverticulitus attack in the last 36 months will be placed on a drug that may help patient symptoms.

The purpose of this study is to determine whether SPD476 is effective in reducing recurrence of diverticulitis

 
A Multi-Center, Double-Blind, Parallel-Group Study to Evaluate Short-Term PDF Print E-mail

This study consists of 2 parts. A multi-center, short-term, double-blind, randomized, parallel group

study (Part 1), and a long-term, double-blind, maintenance study (Part 2) in pediatric subjects 1 to

11 years of age with endoscopically proven GERD. In Part 1, the study will consist of 3 phases: a

14-day screening phase, a double-blind treatment phase of 12 weeks, and an end-of-study or early

withdrawal phase followed by Part 2, which consists a of double-blind treatment continuation for

subjects who achieved healing

 

(grade 0 on the Hetzel and Dent classification or grade 0 on the

Histological Features of Reflux Esophagitis scale) during the short-term double-blind treatment phase

 
A Pharmacokinetic, Pharmacodynamic and Safety Study of Single and Multiple Doses of Rabreprazole in Pediatric Patients With Gastroesophageal Reflux Disease (GERD) 1 to 11 Months Old, Inclusive PDF Print E-mail
  • The purpose of the study is to evaluate the pharmacokinetics, pharmacodynamics and safety of rabeprazole after single and multiple daily administration in infants between the ages of 1 and 11 months, inclusive, with GERD.
 
A Study of the Safety and Effectiveness of Rabeprazole for the Treatment of Gastroesophageal Reflux PDF Print E-mail
  •  The purpose of the study is to access the effectiveness and safety of oral rabeprazole in the treatment of acid-related disorders in pediatric patients, focusing specifically on the manifestation of GERD (symptomatic and erosive types).
 
<< Start < Prev 1 2 Next > End >>

Page 1 of 2