A Unblinded Study of TAK-438 (20 mg) for Prevention of Recurrence of Gastric or Duodenal Ulcer During Long-Term Non-Steroid Anti-Inflammatory Drug (NSAID) Therapy

NCT ID: NCT01568385

Last Updated: 2014-02-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-04-30
• Study Completion Date: 2013-09-30

Brief Summary

The purpose of this study is to study the safety and efficacy of TAK-438, once daily (QD), in participants with a history of gastric or duodenal ulcer requiring long-term NSAID therapy will be investigated.

Conditions

Gastric Ulcer; Duodenal Ulcer

Study Design

• Primary Study Purpose: TREATMENT

Study Groups

TAK-438 20 mg QD

Group Type: EXPERIMENTAL

TAK-438

Intervention Type: DRUG

Interventions

TAK-438

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Participants who, in the opinion of the principal investigator or subinvestigator, are capable of understanding the details of the study and complying with them.

2. Prior to study commencement, participants who are capable of signing and dating the information/consent form.

3. Participants with a chronic disease (rheumatoid arthritis, osteoarthritis, etc.) which requires continuous NSAID oral therapy for pain control during treatment period.

4. Participants who meet either 1 or 2 below according to gastric or duodenal endoscopy:

• Ulcer scar (defined, in this study, as regenerative mucosa, convergence of mucosal fold, gastric wall transformation, etc) has been confirmed during endoscopy on the study drug initiation day (Visit 2).
• Ulcer (mucosal defects of 3 mm or larger with white moss) or ulcer scar has been endoscopically confirmed before the study drug initiation day (Visit 2).

5. Outpatient participants (inpatients for examinations are acceptable)

6. Women with child-bearing potential must agree to routinely take appropriate contraceptive measures throughout treatment period, from giving consent to the study until 4 weeks after the final dose

Exclusion Criteria

1. Participants who received treatment with another study drug (including approved drugs under post-marketing surveillance) within 84 days prior to commencement of screening

2. Participants who have previously received TAK-438 in a clinical study or as a treatment

3. Participants who are employees of institutions participating in this study and family members of such employees, participants in a dependent relationship with employees of institutions involved in conduct of the study (e.g., spouse, parent, child, sibling), and participants who are under duress in giving their consent

4. Participants who have donated 400 mL or more of blood within 90 days prior to the commencement of screening

5. Participants with a plan to change the type, dosage or administration of NSAID

6. Participants with ulcer (mucosal defects of 3 mm or larger with white moss) or active hemorrhage confirmed during gastric or duodenal endoscopy on the study drug initiation day (Visit 2)

7. Participants with small intestinal hemorrhage, large intestinal hemorrhage, or gastrointestinal hemorrhage of unknown cause

8. Participants with a history of surgery or scheduled surgery influencing gastric acid secretion (resection of upper gastrointestinal tract or vagotomy etc)

9. Participants with a history or complication of Zollinger-Ellison syndrome, or other gastric acid hypersecretion disorders

10. Participants with a history or complication of aspirin asthma

11. Participants who have a history of hypersensitivity or allergy to TAK-438 (including its excipients) or NSAIDs

12. Participants with current use of illicit drug or a history of drug abuse. and/or alcohol dependence within one year prior to the commencement of screening

13. Participants who require treatment with prohibited concomitant drugs or therapies (see 7.3)

14. Female participants who are pregnant or lactating; those who plan to become pregnant or donate ova during treatment period, from giving consent until 4 weeks after final dose

15. Participants with serious central nervous system disorders, cardiovascular disease, pulmonary disease, hepatic disease, renal disease, metabolic disease, gastrointestinal disorders, urinary disorders, endocrine disease, or blood dyscrasia

16. Participants who plan to undergo surgery requiring hospitalization or requires surgery during the study period.

17. Participants with a history of a malignancy (or treatment thereof) within 5 years prior to the commencement of screening; however, participants with completely cured basal cell carcinoma of skin or carcinoma in situ of the cervix may be included in the study.

18. Participants with acquired immune deficiency syndrome (AIDS; including HIV carriers) or hepatitis (including viral hepatitis carriers [HBs antigen or HCV antibody positive]); however, participants who are hepatitis C virus (HCV) antigen negative or HCV-RNA negative may be included in the study.

19. Participants who meet either of the following laboratory test values at the beginning of screening (Visit 1)

• Serum creatinine value: higher than 2 mg/dL
• Alanine transaminase (ALT) or aspartate aminotransferase (AST): higher than 2.5 × the upper limit of normal
• Total bilirubin: higher than 2.0 × the upper limit of normal

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Takeda

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Funabashi-shi, Chiba, Japan

Noda, Chiba, Japan

Fukuoka, Fukuoka, Japan

Annaka-shi, Gunma, Japan

Hiroshima, Hiroshima, Japan

Hakodate-shi, Hokkaido, Japan

Kitahiroshima-shi, Hokkaido, Japan

Sapporo, Hokkaido, Japan

Yubari-gun, Hokkaido, Japan

Kanazawa, Ishikawa-ken, Japan

Sanuki-shi, Kagawa-ken, Japan

Yashiro-shi, Kumamoto, Japan

Nagasaki, Nagasaki, Japan

Sasebo-shi, Nagasaki, Japan

Fuchu-shi, Tokyo, Japan

Katsushika-ku, Tokyo, Japan

Meguro-ku, Tokyo, Japan

Nakano-ku, Tokyo, Japan

Countries

Japan

Other Identifiers

U1111-1128-5905

Identifier Type: REGISTRY

Identifier Source: secondary_id

JapicCTI-121789

Identifier Type: REGISTRY

Identifier Source: secondary_id

TAK-438/OCT-303

Identifier Type: -

Identifier Source: org_study_id