Study of Efficacy and Safety of Ligelizumab in Adolescents and Adults With Chronic Inducible Urticaria Who Remain Symptomatic Despite Treatment With H1- Antihistamines

Stopped early · Phase 3 · Has a placebo group

Conditions studied: Chronic Inducible Urticaria

In brief

This was a placebo controlled, phase 3 study designed to evaluate the efficacy and safety of ligelizumab in participants with chronic inducible urticaria who are inadequately controlled with H1-antihistamines

Key facts

Study ID

NCT05024058

Run by

Novartis Pharmaceuticals

People needed

39

Starts

2021-11-16

Expected to finish

2022-08-09

Last updated by the study team

2024-06-18

Who can join

Age: 12 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Confirmed CINDU diagnosis (as per guidelines) for symptomatic dermographism, cold urticaria or cholinergic urticaria for ≥ 4 months.
• Diagnosis of CINDU (symptomatic dermographism, cold urticaria or cholinergic urticaria) inadequately controlled with H1-AH at local label approved doses at the time of randomization, as defined by all of the following:
• Positive response (i.e development of symptoms) to triggers despite treatment with H1-AH
• Positive response (i.e. development of symptoms) to provocation test on day of randomization
• Participants must be able to physically perform the protocol defined provocation test specific to the participant's CINDU.
• Cholinergic urticaria participants must show sweating in performing the pulse-controlled ergometry test on day of randomization. Participants with anhidrosis must not be included.
• Willing and able to complete a daily symptom eDiary as per protocol requirement and adhere to the study visit schedules

You may not qualify if…

• History of hypersensitivity to any of the study drugs or its components or to drugs of similar chemical classes or to the provocation test or items used in provocation tests
• Participants who have concomitant CSU at screening
• Participants who have a familial form of the target CINDU that is being considered for the participant's inclusion in this study
• Participants having a more defined other form of inducible urticaria than the target CINDU that is being considered for the participant's inclusion in this study
• Diseases, other than chronic inducible urticaria, with urticarial or angioedema symptoms such as urticarial vasculitis, erythema multiforme, cutaneous mastocytosis (urticaria pigmentosa) and hereditary or acquired angioedema (eg, due to C1 inhibitor deficiency).
• Any other skin disease associated with chronic itching that might influence, in the investigator's opinion, the study evaluations and results (eg, atopic dermatitis, bullous pemphigoid, dermatitis herpetiformis, senile pruritus, etc.) or skin diseases associated with only wheals and no itch e.g asymptomatic dermographism
• Prior exposure to ligelizumab, omalizumab and or other anti-IgE therapies

Where it is running

• Novartis Investigative Site — Evansville, Indiana, United States
• Novartis Investigative Site — North Charleston, South Carolina, United States
• Novartis Investigative Site — El Paso, Texas, United States
• Novartis Investigative Site — Murray, Utah, United States
• Novartis Investigative Site — East Melbourne, Victoria, Australia
• Novartis Investigative Site — Parkville, Victoria, Australia
• Novartis Investigative Site — Athens, Greece
• Novartis Investigative Site — Debrecen, Hajdú-Bihar, Hungary
• Novartis Investigative Site — Pécs, Hungary
• Novartis Investigative Site — Szeged, Hungary
• Novartis Investigative Site — Izhevsk, Russia
• Novartis Investigative Site — Rostov-on-Don, Russia
• Novartis Investigative Site — Saint Petersburg, Russia
• Novartis Investigative Site — Saint Petersburg, Russia
• Novartis Investigative Site — Saint Petersburg, Russia
• Novartis Investigative Site — Stavropol, Russia
• Novartis Investigative Site — Kežmarok, Slovakia
• Novartis Investigative Site — Svidník, Slovakia
• Novartis Investigative Site — Córdoba, Andalusia, Spain
• Novartis Investigative Site — Barcelona, Catalonia, Spain
• Novartis Investigative Site — Valencia, Valencia, Spain
• Novartis Investigative Site — Taipei, Taiwan
• Novartis Investigative Site — Ankara, Turkey (Türkiye)
• Novartis Investigative Site — Istanbul, Turkey (Türkiye)

Full record on ClinicalTrials.gov

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