Study of the Efficacy and Safety of RPH-104 in Adult Subjects With Schnitzler Syndrome

PHASE2WithdrawnINTERVENTIONAL
0
Timeline

Start Date

May 31, 2023

Primary Completion Date

August 31, 2023

Study Completion Date

January 31, 2024

Conditions
Schnitzler SyndromeUrticarial Vasculitis With Monoclonal Immunoglobulin M Component, Schnitzler (Disorder)
Interventions
BIOLOGICAL

80 mg RPH-104

solution for subcutaneous administration 40 mg/mL, 2 mL in the 4-mL glass vial

DRUG

Placebo

Normal Saline (0.9% Sodium Chloride solution for Injection), 2 mL in the 4 mL-glass vial

Trial Locations (4)

17033

Penn State Health Hersey Medical Center, Hershey

55905

Mayo Clinic, Rochester

80206

National Jewish Health, Denver

97239-3098

Oregon Health & Science University, Portland

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Worldwide Clinical Trials

OTHER

lead

R-Pharm Overseas, Inc.

INDUSTRY