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Clinical Trials/NCT03137069
NCT03137069
Completed
Phase 2

A Phase II, Multicenter, Randomized, Double-Blind, Placebo-Controlled Pilot and Dose-Ranging Study of GDC-0853 in Patients With Refractory Chronic Spontaneous Urticaria (CSU).

Genentech, Inc.27 sites in 3 countries134 target enrollmentMay 26, 2017
ConditionsUrticaria
InterventionsPlaceboGDC-0853

Overview

Phase
Phase 2
Intervention
Placebo
Conditions
Urticaria
Sponsor
Genentech, Inc.
Enrollment
134
Locations
27
Primary Endpoint
Change From Baseline in the Urticaria Activity Score Over 7 Days (UAS7) at Day 57
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the efficacy, safety and pharmacokinetics of GDC-0853 compared with placebo in participants with Refractory Chronic Spontaneous Urticaria (CSU) already treated with anti-histamines. Participants have the option to enter the Open-Label Extension (OLE) study after completing the 8-week treatment period.

Registry
clinicaltrials.gov
Start Date
May 26, 2017
End Date
October 25, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Aged 18-75 years, inclusive
  • Diagnosis of chronic spontaneous urticaria (CSU) refractory to H1 antihistamines at the time of randomization
  • Willing and able to complete an Urticaria Participant Daily eDiary for the duration of the study
  • No evidence of active or latent or inadequately treated infection with tuberculosis (TB)
  • Partcipants with a history of Bacille Calmette-Guérin (BCG) vaccination should be screened using the QuantiFERON-TB-Gold (QFT) test
  • Only for participants currently receiving proton-pump inhibitors (PPIs) or H2 receptor antagonists (H2RAs): Treatment must be at a stable dose during the 2-week screening period prior to randomization and with a plan to remain at a stable dose for the duration of the study
  • For women of childbearing potential: Agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods that result in a failure rate of \<1% per year during the treatment period and for at least 4 weeks after the last dose of study drug. Women must refrain from donating eggs during this same period.

Exclusion Criteria

  • Treatment with omalizumab or other monoclonal antibody therapies used to treat CSU within 4 months prior to screening or primary nonresponse to omalizumab
  • Use of a non-biologic investigational drug or participation in an investigational study with a non-biologic drug within 30 days prior to study drug administration on Day 1 (or within 5 half-lives of the investigational product, whichever is greater)
  • Use of a biologic investigational therapy or participation in an investigational study involving biologic therapy within 90 days or 5 half-lives, whichever is greater, prior to study drug administration on Day 1
  • Previous treatment with GDC-0853 or other Bruton's tyrosine kinase (BTK) inhibitors
  • Participants whose urticaria is solely due to physical urticaria
  • Other diseases with symptoms of urticaria or angioedema, including urticarial vasculitis, urticaria pigmentosa, erythema multiforme, mastocytosis, hereditary or acquired angioedema, lymphoma, or leukemia
  • Atopic dermatitis, bullous pemphigoid, dermatitis herpetiformis, or other skin disease associated with itch such as psoriasis
  • Routine doses of the following medications within 30 days prior to screening: systemic or cutaneous (topical) corticosteroids (prescription or over the counter), hydroxychloroquine, methotrexate, cyclosporine, or cyclophosphamide
  • Prior utilization of intravenous (IV) steroids for treatment of laryngeal angioedema
  • Intravenous immunoglobulin G (IV IG) or plasmapheresis within 30 days prior to screening

Arms & Interventions

Cohort 1: Placebo

Participants received matching placebo twice daily from Day 1 to 56.

Intervention: Placebo

Cohort 1: GDC-0853 200mg BID

Participants received GDC-0853 200mg twice daily from Day 1 to 56.

Intervention: GDC-0853

Cohort 2: Placebo

Participants received matching placebo up to twice daily from Day 1 to 56.

Intervention: Placebo

Cohort 2: GDC-0853 50mg QD

Participants received GDC-0853 50mg once daily from Day 1 to 56.

Intervention: GDC-0853

Cohort 2: GDC-0853 150mg QD

Participants received GDC-0853 150mg once daily from Day 1 to 56.

Intervention: GDC-0853

Cohort 2: GDC-0853 200mg BID

Participants received GDC-0853 200mg twice daily from Day 1 to 56.

Intervention: GDC-0853

Outcomes

Primary Outcomes

Change From Baseline in the Urticaria Activity Score Over 7 Days (UAS7) at Day 57

Time Frame: Baseline and Day 57

The Urticaria Activity Score (UAS) is a composite, diary-recorded score with numeric severity intensity ratings (0=none to 3=intense/severe) for the number of wheals (hives) and the intensity of the pruritus (itch) over the past 12 hours (twice daily). The daily UAS is calculated as the average of the morning and evening scores. The UAS7 is the weekly sum of the daily UAS, which is the composite score of the intensity of pruritus and the number of wheals. The maximum UAS7 value is 42. A higher score indicates worse disease. A negative change score (Day 57 score minus Baseline score) indicates improvement.

Secondary Outcomes

  • Change From Baseline in the UAS7 at Day 29(Baseline and Day 29)
  • Plasma Concentrations of Fenebrutinib (GDC-0853) at Specified Timepoints(Days 1, 8 and 57.)
  • Percentage of Participants With Adverse Events (AEs)(Baseline up until 4 weeks after the last dose of study drug (up to 2 years, 5 months).)
  • Percentage of Participants Who Are Well-Controlled (UAS7 ≤ 6)(Day 57)

Study Sites (27)

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