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A RAndomised Placebo Controlled Trial - to Explore the Efficacy and Mechanism of Action of Tezepelumab in EGPA- RACE-MATE

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-514794-22-01
Enrollment
10
Registered
2025-05-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eosinophilic granulomatosis with polyangiitis (EGPA)

Brief summary

The primary endpoint is the proportion of patients, who achieve remission at week 24 (defined as a Birmingham Vasculitis Score (BVAS) version 3 score of 0 and receipt of prednisolone of ≤ 4mg daily and no receipt of oral steroids above baseline dose in the 4 weeks prior to week 24).

Detailed description

(I) Time to first EGPA flare. (II) Total accrued weeks of remission defined as defined as a Birmingham Vasculitis Activity Score (BVAS) – version 3(11), score of 0 with mOCS dose of prednisolone/prednisolone ≤ 4mg/day and BVAS of 0.

Interventions

Sponsors

Imperial College London Limited
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the proportion of patients, who achieve remission at week 24 (defined as a Birmingham Vasculitis Score (BVAS) version 3 score of 0 and receipt of prednisolone of ≤ 4mg daily and no receipt of oral steroids above baseline dose in the 4 weeks prior to week 24).

Secondary

MeasureTime frame
(I) Time to first EGPA flare. (II) Total accrued weeks of remission defined as defined as a Birmingham Vasculitis Activity Score (BVAS) – version 3(11), score of 0 with mOCS dose of prednisolone/prednisolone ≤ 4mg/day and BVAS of 0.

Countries

Italy

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026