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ENROLLING BY INVITATION
NCT07850843
PHASE2

Apremilast Added to Antihistamines in Chronic Urticaria

Sponsor: Rashid Latif Medical College

View on ClinicalTrials.gov

Summary

This study evaluates whether adding oral apremilast, a phosphodiesterase-4 inhibitor, to second-generation H1 antihistamines improves disease activity and quality of life in adults with chronic urticaria that is not controlled by antihistamines alone. Patients who chose apremilast plus antihistamines were compared over 12 weeks with patients who continued antihistamines alone. Disease activity was measured with the weekly Urticaria Activity Score (UAS7), quality of life with the Dermatology Life Quality Index (DLQI), and adverse effects were recorded at every visit.

Official title: Evaluating the Therapeutic Potential of Apremilast as Add-on Therapy to Second-Generation H1 Antihistamines in the Management of Chronic Urticaria: A Non-Randomised Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

86

Start Date

2026-09-23

Completion Date

2026-10-31

Last Updated

2026-09-30

Healthy Volunteers

No

Interventions

DRUG

Apremilast

Oral apremilast, 5-day titration (10 mg to 30 mg) then 30 mg twice daily for 12 weeks.

DRUG

Second-generation H1 antihistamine

Oral second-generation H1 antihistamine at the licensed dose or up-dosed up to fourfold, continued throughout the 12-week study.

Locations (1)

Arif Memorial Teaching Hospital, Rashid Latif Medical College

Lahore, Punjab Province, Pakistan