A 52-WEEK MULTI-CENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED PHASE 3 STUDY TO EVALUATE THE EFFICACY, SAFETY AND TOLERABILITY OF REMIBRUTINIB IN ADULT PARTICIPANTS WITH SEVERE CHRONIC PRURITUS OF UNKNOWN ORIGIN (CPUO)

Registry ID

CLOU064R12301

Source registry

HEALTH_CANADA

Status

Pending

Phase

PHASE3

Study type

INTERVENTIONAL

Sponsor

NOVARTIS PHARMACEUTICALS CANADA INC

Last update

2026-07-09

Conditions

• PRURITIS

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