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A long-term extension study of AG-1749 in patients on concomitant long-term low-dose aspirin therapy

Phase 3
Conditions
Prevention of onset of low dose aspirin related gastric ulcer
Registration Number
JPRN-jRCT2080220830
Lead Sponsor
Takeda Pharmaceutical Company Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1. Patients who have finished the preceding confirmatory anti-ulcer efficacy study
2. Patients who are on oral low-dose aspirin at the time of consent and who require continued long-term use of low-dose aspirin even after the start of study treatment in this study

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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