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Clinical Trials/EUCTR2020-000082-16-NL
EUCTR2020-000082-16-NL
Active, not recruiting
Phase 1

A randomized, placebo-controlled, double-blind trial evaluating the efficacy, tolerability and safety of ESO-101 in adult patients with active eosinophilic esophagitis

EsoCap AG0 sites42 target enrollmentSeptember 3, 2020

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Active eosinophilic esophagitis
Sponsor
EsoCap AG
Enrollment
42
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 3, 2020
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
EsoCap AG

Eligibility Criteria

Inclusion Criteria

  • 1\. Adult patients aged 18\-70 years;
  • 2\. Confirmed clinicopathological diagnosis of EoE;
  • 3\. Active and symptomatic EoE, defined as:
  • a. peak eosinophil count \=15 eosinophils/hpf at 2 levels of the esophagus at the
  • screening endoscopy (Visit 2\) as measured in a total of 6 hpfs derived from 6 biopsies,
  • 2 each from the proximal, mid, and distal segment of the esophagus;
  • b. either a dysphagia or odynophagia severity sore of \=4 on a 11\-point numeric rating scale (NRS) for \=1 day during the 7 days before Screening (Visit 1\);
  • 4\. Written informed consent;
  • 5\. Willingness and ability to comply with the protocol for the duration of the trial;
  • 6\. Negative pregnancy test at Screening (Visit 1\) and Day 0 (Visit 3\) in women of

Exclusion Criteria

  • General criteria
  • 1\. Women who are pregnant, lactating, possibly pregnant or planning a pregnancy during the trial period;
  • 2\. Current or past (within the last 3 months) alcohol or drug abuse;
  • 3\. Initiation of a diet\-modifying food restriction within 4 weeks before the screening endoscopy (Visit 2\) until the EOT;
  • 4\. Use of systemic corticosteroids or biologic immunomodulators within 3 months before the screening endoscopy (Visit 2\) until the EOT;
  • 5\. History of non\-response to treatment of EoE with topical corticosteroid drugs (defined as no improvement of clinical symptoms of EoE after a minimum of 4 weeks corticosteroid therapy used at appropriate doses according to the investigator’s judgment) or requirement of cessation of corticosteroid therapy for EoE treatment due to oral candidiasis or systemic corticosteroid side effects;
  • 6\. Use of corticosteroids for treatment of EoE within 4 weeks before the screening endoscopy (Visit 2\) until the EOT;
  • 7\. Use of inhalable (pulmonary or nasal) corticosteroids within 4 weeks before the screening endoscopy (Visit 2\) until the EOT;
  • 8\. Asthma requiring corticosteroid therapy in the seasonal allergy period according to the investigator’s judgment based on anamnesis until the EOT;
  • 9\. Change in proton pump inhibitor (PPI) dosing regimen within 4 weeks before the screening endoscopy (Visit 2\) until the EOT;

Outcomes

Primary Outcomes

Not specified

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