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EP262 for Chronic Hives (CALM-CSU Trial)
Phase 2
Recruiting
Research Sponsored by Escient Pharmaceuticals, Inc
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Must not have
Other active skin diseases associated with chronic pruritus (eg, atopic dermatitis, bullous pemphigoid, prurigo nodularis, dermatitis herpetiformis)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up measured from day 1 to end of study or early termination (up to 10 weeks)
Summary
This trial tests a drug to see if it helps people with long-term hives from unknown causes.
Who is the study for?
This trial is for people with chronic spontaneous urticaria (CSU), also known as hives, who still have symptoms despite taking up to four times the normal dose of H1 antihistamines. Participants must have a documented history of CSU and a UAS7 score of 16 or higher.
What is being tested?
The study is testing EP262, an oral medication, against a placebo to see if it can help with CSU. It's conducted across multiple centers where participants are randomly assigned to receive either EP262 or a placebo without knowing which one they're getting.
What are the potential side effects?
While specific side effects for EP262 aren't provided here, common side effects from treatments in trials like this may include digestive issues, headaches, dizziness, and possible allergic reactions.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have a skin condition that causes long-term itching.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ measured from day 1 to end of study or early termination (up to 10 weeks)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~measured from day 1 to end of study or early termination (up to 10 weeks)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Urticaria Activity Score (UAS) over a 7-day period (UAS7)
Secondary study objectives
Change in Hive Severity Score (HSS) over a 7-day period (HSS7)
Change in Itch Severity Score (ISS) over a 7-day period (ISS7)
Safety and tolerability of EP262
Trial Design
4Treatment groups
Experimental Treatment
Placebo Group
Group I: EP262 50 mgExperimental Treatment1 Intervention
Group II: EP262 25 mgExperimental Treatment1 Intervention
Group III: EP262 150 mgExperimental Treatment1 Intervention
Group IV: PlaceboPlacebo Group1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Oral EP262
2023
Completed Phase 2
~40
Find a Location
Who is running the clinical trial?
Escient Pharmaceuticals, IncLead Sponsor
5 Previous Clinical Trials
226 Total Patients Enrolled
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