Diabetic Gastroparesis Efficacy/Safety Study of TZP-102
Status: | Completed |
---|---|
Conditions: | Gastrointestinal |
Therapuetic Areas: | Gastroenterology |
Healthy: | No |
Age Range: | Any |
Updated: | 11/18/2012 |
Start Date: | August 2012 |
End Date: | April 2013 |
Contact: | Beth Chamblin, B.S. |
Email: | BChamblin@tranzyme.com |
Phone: | 919-328-1132 |
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Evaluation of the Efficacy and Safety of TZP-102 Given Orally Three Times a Day for the Treatment of Symptoms Associated With Diabetic Gastroparesis
The purpose of this study is to test the safety and effectiveness of 10 mg TZP-102 given
prior to meals three times a day compared to placebo (capsule that looks like active study
drug but contains no active drug), administered for 12 weeks, in diabetic subjects with
symptoms associated with gastroparesis.
Inclusion Criteria:
- 18 to 80 years of age inclusive
- Type 1 or type 2 diabetes mellitus
- History of symptoms of gastroparesis for at least 3 months leading up to the
Screening Visit
- Documented delayed gastric emptying
- Upper gastrointestinal obstruction ruled out by endoscopy or barium scan
- Concomitant medications must be stable for at least 2 weeks leading up to the
Screening visit and must be maintained during the study.
- Females of child-bearing potential must have a negative serum pregnancy test and use
(and agree to continue to use throughout the study) an acceptable form of
contraception
Exclusion Criteria:
- Gastrectomy, bariatric surgery, fundoplication or vagotomy/pyloroplasty
- Has had or plans to have endoscopic pyloric injections of botulinum toxin within 6
months prior to the Screening Visit or during the study
- NG, PEG or PEJ feeding tube or inpatient hospitalization for gastroparesis within 2
weeks prior to the Screening Visit
- Required parenteral nutrition for treatment of gastroparesis within 2 months prior to
the Screening Visit
- Active gastric pacemaker within 3 months prior to the Screening Visit
We found this trial at
14
sites
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