Status:
COMPLETED
Efficacy and Safety of TAK-438 for the Prevention of Recurrent Gastric or Duodenal Ulcers During Therapy of Low-dose Aspirin
Lead Sponsor:
Takeda
Conditions:
Gastric Ulcers
Duodenal Ulcers
Eligibility:
All Genders
20+ years
Phase:
PHASE3
Brief Summary
The purpose of this study is to evaluate the efficacy of TAK-438, once daily (QD) compared to AG-1749 (Lansoprazole) in patients with a history of gastric or duodenal ulcer who require long-term thera...
Eligibility Criteria
Inclusion
- Participants who require continuous low-dose aspirin therapy during the treatment period with the study drug
- Participants who have a history of ulcer in stomach or duodenum, endoscopically confirmed
- Outpatient (including inpatient for examinations)
Exclusion
- Participants scheduled to change the type and dosage regimen of low-dose aspirin
- Participants with ulcers or bleeding in stomach or duodenum, endoscopically confirmed
- Participants with small intestine bleeding, large intestine bleeding, or gastrointestinal bleeding of unknown etiology
- Participants who have a history of surgery which affects gastric acid secretion (e.g., resection of upper gastrointestinal tract, vagotomy) or who are scheduled to undergo such surgery
- Participants with a previous or current history of Zollinger-Ellison syndrome, or other gastric acid hypersecretion disorders
- Participants with a previous or current history of aspirin-induced asthma
Key Trial Info
Start Date :
October 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2013
Estimated Enrollment :
621 Patients enrolled
Trial Details
Trial ID
NCT01452763
Start Date
October 1 2011
End Date
April 1 2013
Last Update
January 20 2014
Active Locations (76)
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1
Komaki-shi, Aichi-ken, Japan
2
Seto-shi, Aichi-ken, Japan
3
Akita, Akita, Japan
4
Ichikawa-shi, Chiba, Japan