RecruitingPhase 2NCT06851559

A Study in Adult Participants With EoE to Evaluate Vonoprazan 20 mg Compared to Placebo After 12 Weeks and to Evaluate Vonoprazan 20 mg Up to 24 Weeks

Studying Primary eosinophilic gastrointestinal disease

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Key facts

Sponsor
Phathom Pharmaceuticals, Inc.
Principal Investigator
Medical Director
Phathom Pharmaceuticals
Intervention
Vonoprazan(drug)
Enrollment
80 enrolled
Eligibility
18 years · All sexes
Timeline
20252027

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06851559 on ClinicalTrials.gov

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