NCT01452763

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 therapy of low-dose aspirin.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
621

participants targeted

Target at P75+ for phase_3

Timeline
Completed

Started Oct 2011

Geographic Reach
1 country

76 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 16, 2011

Completed
15 days until next milestone

Study Start

First participant enrolled

October 1, 2011

Completed
16 days until next milestone

First Posted

Study publicly available on registry

October 17, 2011

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2013

Completed
Last Updated

January 20, 2014

Status Verified

January 1, 2014

Enrollment Period

1.5 years

First QC Date

September 16, 2011

Last Update Submit

January 17, 2014

Conditions

Keywords

Drug Therapy

Outcome Measures

Primary Outcomes (1)

  • Recurrence rate of gastric or duodenal ulcer within 24 weeks

    Mucosal defects with a white coating of 3 mm or larger will be determined as ulcers. Recurrence rate of gastric or duodenal ulcer within 24 weeks will be calculated for each treatment group.

    24 weeks

Secondary Outcomes (5)

  • Recurrence rate of gastric or duodenal ulcer within 12 weeks

    12 weeks

  • Gastric mucosal injury

    24 Weeks

  • Duodenal mucosal injury

    24 weeks

  • Occurrence rate of hemorrhagic lesion in stomach or duodenum

    24 weeks

  • Time to recurrence of gastric or duodenal ulcer

    24 weeks

Study Arms (3)

TAK-438 10 mg QD

EXPERIMENTAL
Drug: TAK-438Drug: Placebo

TAK-438 20 mg QD

EXPERIMENTAL
Drug: TAK-438Drug: Placebo

Lansoprazole 15 mg QD

ACTIVE COMPARATOR
Drug: LansoprazoleDrug: Placebo

Interventions

TAK-438 10 mg tablets, orally, once daily for up to 24 weeks.

TAK-438 10 mg QD

Lansoprazole placebo-matching capsules, orally, once daily for up to 24 weeks.

TAK-438 10 mg QD

Lansoprazole 15 mg capsules, orally, once daily for up to 24 weeks.

Also known as: AG-1749
Lansoprazole 15 mg QD

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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)

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (76)

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Komaki-shi, Aichi-ken, Japan

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Seto-shi, Aichi-ken, Japan

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Akita, Akita, Japan

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Ichikawa-shi, Chiba, Japan

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Kisarazu-shi, Chiba, Japan

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Matsudo-shi, Chiba, Japan

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Imabari, Ehime, Japan

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Matsuyama, Ehime, Japan

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Niihama-shi, Ehime, Japan

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Fukui-shi, Fukui, Japan

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Chikushino-shi, Fukuoka, Japan

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Fukuoka, Fukuoka, Japan

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Kasuya-gun, Fukuoka, Japan

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Kitakyushu-shi, Fukuoka, Japan

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Miyako-gun, Fukuoka, Japan

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Onga-gun, Fukuoka, Japan

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Yanagawa-shi, Fukuoka, Japan

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Yukuhashi-shi, Fukuoka, Japan

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Koriyama-shi, Fukushima, Japan

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Gifu, Gifu, Japan

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Takasaki-shi, Gunma, Japan

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Fukuyama-shi, Hiroshima, Japan

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Hatsukaichi-shi, Hiroshima, Japan

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Hiroshima, Hiroshima, Japan

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Asahikawa-shi, Hokkaido, Japan

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Obihiro-shi, Hokkaido, Japan

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Sapporo, Hokkaido, Japan

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Tomakomaki-shi, Hokkaido, Japan

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Kobe, Hyōgo, Japan

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Nishinomiya-shi, Hyōgo, Japan

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Takarazuka-shi, Hyōgo, Japan

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Koga-shi, Ibaragi, Japan

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Tsuchiura-shi, Ibaragi, Japan

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Kanazawa, Ishikawa-ken, Japan

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Komatsu-shi, Ishikawa-ken, Japan

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Nomi-shi, Ishikawa-ken, Japan

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Shiroyama-shi, Ishikawa-ken, Japan

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Takamatsu, Kagawa-ken, Japan

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Ibusuki-shi, Kagoshima-ken, Japan

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Ichikikushikino-shi, Kagoshima-ken, Japan

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Izumi-shi, Kagoshima-ken, Japan

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Atsugi-shi, Kanagawa, Japan

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Kawasaki-shi, Kanagawa, Japan

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Sagamihara-shi, Kanagawa, Japan

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Yokohama, Kanagawa, Japan

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Kochi, Kochi, Japan

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Kumamoto, Kumamoto, Japan

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Kyoto, Kyoto, Japan

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Uji-shi, Kyoto, Japan

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Tsu, Mie-ken, Japan

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Sendai, Miyagi, Japan

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Nagasaki, Nagasaki, Japan

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Nara, Nara, Japan

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Niigata, Niigata, Japan

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Ōita, Oita Prefecture, Japan

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Osaka, Osaka, Japan

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Sakai-shi, Osaka, Japan

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Tondabayashi-shi, Osaka, Japan

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Ageo-shi, Saitama, Japan

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Hiki-gun, Saitama, Japan

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Kumagaya-shi, Saitama, Japan

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Saitama-shi, Saitama, Japan

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Sayama-shi, Saitama, Japan

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Tokorozawa-shi, Saitama, Japan

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Ōtsu, Shiga, Japan

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Utsunomiya, Tochigi, Japan

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Adachi-ku, Tokyo, Japan

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Hachioji-shi, Tokyo, Japan

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Koto-ku, Tokyo, Japan

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Meguro-ku, Tokyo, Japan

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Minato-ku, Tokyo, Japan

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Shinjuku-ku, Tokyo, Japan

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Tonami-shi, Toyama, Japan

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Toyama, Toyama, Japan

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Iwakuni-shi, Yamaguchi, Japan

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Shimonoseki-shi, Yamaguchi, Japan

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Related Publications (1)

  • Kawai T, Oda K, Funao N, Nishimura A, Matsumoto Y, Mizokami Y, Ashida K, Sugano K. Vonoprazan prevents low-dose aspirin-associated ulcer recurrence: randomised phase 3 study. Gut. 2018 Jun;67(6):1033-1041. doi: 10.1136/gutjnl-2017-314852. Epub 2017 Dec 1.

MeSH Terms

Conditions

Stomach UlcerDuodenal Ulcer

Interventions

1-(5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamineLansoprazole

Condition Hierarchy (Ancestors)

Peptic UlcerDuodenal DiseasesIntestinal DiseasesGastrointestinal DiseasesDigestive System DiseasesStomach Diseases

Intervention Hierarchy (Ancestors)

2-PyridinylmethylsulfinylbenzimidazolesSulfoxidesSulfur CompoundsOrganic ChemicalsPyridinesHeterocyclic Compounds, 1-RingHeterocyclic CompoundsBenzimidazolesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-Ring

Study Officials

  • Senior Manager

    Takeda

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 16, 2011

First Posted

October 17, 2011

Study Start

October 1, 2011

Primary Completion

April 1, 2013

Study Completion

April 1, 2013

Last Updated

January 20, 2014

Record last verified: 2014-01

Locations