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

PHASE1CompletedINTERVENTIONAL
Enrollment

33

Participants

Timeline

Start Date

August 30, 2023

Primary Completion Date

October 22, 2024

Study Completion Date

October 22, 2024

Conditions
Chronic Inducible Urticaria
Interventions
DRUG

Oral EP262

Once daily

Trial Locations (15)

12203

Institut fur Allergieforschung Charite - Universitatsmedizin Berlin, Berlin

15241

Allergy and Clinical Immunology Associates, Pittsburgh

21224

Johns Hopkins University, Baltimore

29420

National Allergy and Asthma Research, LLC., North Charleston

30625

Medizinische Hochschule Hannover, Hanover

33607

Advanced Clinical Research Institute, Tampa

42301

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

45236

Bernstein Clinical Research Center, LLC, Cincinnati

46015

Hospital Arnau de Vilanova, Valencia

83706

Treasure Valley Medical Research, Boise

H2X 2V1

Innovaderm Research Inc., Montreal

M3B 3S6

Gordon Sussman Clinical Research Inc., North York

01307

Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden, Dresden

2333 CL

Centre for Human Drug Research (CHDR), Leiden

08003

Hospital del Mar, Barcelona

Sponsors
All Listed Sponsors
lead

Escient Pharmaceuticals, Inc

INDUSTRY

NCT06050928 - Phase 1b, Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacodynamics of EP262 in Subjects With Chronic Inducible Urticaria | Biotech Hunter | Biotech Hunter