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NCT06050928 · ClinicalTrials.gov registry record · Phase 1

Phase 1b, Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacodynamics of EP262 in Subjects With Chronic Inducible Urticaria

A Phase 1 study of Chronic Inducible Urticaria, sponsored by Escient Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
33
Enrollment target
15
Study locations

NCT06050928 is a Phase 1 study of Chronic Inducible Urticaria that has completed, run by Escient Pharmaceuticals. The registered enrollment target is 33 participants, below the 226-participant average among 4 other Chronic Inducible Urticaria trials with a reported enrollment target (85% lower). The trial reports 15 study locations across 11 states.

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The verdict

NCT06050928, a Phase 1 study of Chronic Inducible Urticaria, has completed, sponsored by Escient Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
33 participants
Enrollment target
15
Study locations

Study Summary

This phase 1b trial will evaluate the effects of EP262 in subjects with Chronic Inducible Urticaria (CIndU), including symptomatic dermographism and cold urticaria.

Interventions

  • DRUG Oral EP262

Study Locations (15)

Other

  • Innovaderm Research Inc. - Montreal
  • Gordon Sussman Clinical Research Inc. - North York
  • Institut fur Allergieforschung Charite - Universitatsmedizin Berlin - Berlin
  • Hospital del Mar - Barcelona
  • Hospital Arnau de Vilanova - Valencia

Florida

  • Advanced Clinical Research Institute - Tampa

Idaho

  • Treasure Valley Medical Research - Boise

Kentucky

  • Allergy & Asthma Specialists, P.S.C. - Owensboro

Maryland

  • Johns Hopkins University - Baltimore

Ohio

  • Bernstein Clinical Research Center, LLC - Cincinnati

Pennsylvania

  • Allergy and Clinical Immunology Associates - Pittsburgh

South Carolina

  • National Allergy and Asthma Research, LLC. - North Charleston

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2023-08-30
Est. Completion 2024-10-22
Phase Phase 1

Sponsor

Escient Pharmaceuticals

5 total trials

What the Registry Record Tells You About NCT06050928

The ClinicalTrials.gov registry entry for NCT06050928 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 226-participant average among 4 other Chronic Inducible Urticaria trials with a reported enrollment target (85% lower). The listed sponsor is Escient Pharmaceuticals, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Chronic Inducible Urticaria appearing as the primary indexed condition, and to 1 intervention - of which Oral EP262 is the first listed.

NCT06050928 reports 15 study locations spanning 11 distinct geographic areas - top geographies include Other, Florida, Idaho.

Frequently Asked Questions

What is clinical trial NCT06050928 about?

NCT06050928 is a clinical study titled "Phase 1b, Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacodynamics of EP262 in Subjects With Chronic Inducible Urticaria". This phase 1b trial will evaluate the effects of EP262 in subjects with Chronic Inducible Urticaria (CIndU), including symptomatic dermographism and cold urticaria.

What is the current status of trial NCT06050928?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 33 participants. The study started on 2023-08-30. Estimated completion is 2024-10-22.

What conditions does trial NCT06050928 study?

This clinical trial studies the following conditions: Chronic Inducible Urticaria.

What interventions are being tested in trial NCT06050928?

The interventions under investigation include: Oral EP262 (DRUG).

Who is sponsoring clinical trial NCT06050928?

This trial is sponsored by Escient Pharmaceuticals, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06050928 being conducted?

This trial has 15 study locations across Florida, Idaho, Kentucky, Maryland, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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