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Remibrutinib safe, effective for chronic spontaneous urticaria over 52 weeks

Patients with chronic spontaneous urticaria experienced early symptom improvements that were sustained through 52 weeks with remibrutinib, according to a presentation at the European Academy of Allergy & Clinical Immunology Congress. The safety profile for the Bruton’s tyrosine kinase (BTK) inhibitor was favorable and consistent through 52 weeks as well, the researchers said.

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Markg-lebwohl
Kristen-dowd
Byrichard-gawel
European-academy-of-allergy-clinical-immunology-congress
Novartis
European-academy
Clinical-immunology
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Icahn-school
Mount-sinai
Urticaria-activity-score

Aravax doses first patient in Phase 2 peanut allergy clinical trials

MELBOURNE, Australia, June 1, 2023 /PRNewswire/ The first patient has been dosed in a Phase 2 study (AVX-201) being run by biotechnology company Aravax, which is developing the novel therapy PVX108 for the safe and convenient treatment of peanut allergy. The study is being conducted under a U.S. FDA Investigational New Drug Application. Allergy clinical trial centres across Victoria, South Australia, New South Wales, and Western Australia have invited children and adolescents aged four to 17 years with peanut allergy to take part in the Phase 2 study. Researchers aim to evaluate the efficacy of the novel therapy PVX108. In Phase 1 trials, researchers observed that PVX108 produced relevant changes in the immune response to peanut protein, which continued to develop once dosing had completed. "We're thrilled to have dosed our first patient in Phase 2. In this Phase 2 trial we will evaluate how the immunological changes observed in Phase 1 trials translate to clinical reductions

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Victoria
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Massachusetts
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Kirsten-perrett

Aravax doses first patient in Phase 2 peanut allergy clinical trials

Aravax doses first patient in Phase 2 peanut allergy clinical trials
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