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Two-arm Study to Assess Efficacy and Safety of Ianalumab (VAY736) in Patients With Active Sjogren's Syndrome

NCT05350072 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 275

Last updated 2026-05-14

No results posted yet for this study

Summary

A randomized, double-blind, placebo controlled, 2-arm multicenter phase 3 study to assess the efficacy and safety of ianalumab in patients with active Sjogren's syndrome (NEPTUNUS-1)

Conditions

  • Sjogren Syndrome

Interventions

BIOLOGICAL

VAY736

ianalumab s.c.

OTHER

Placebo

placebo s.c.

Sponsors & Collaborators

Principal Investigators

  • Novartis Pharmaceuticals · Novartis Pharmaceuticals

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-28
Primary Completion
2025-05-07
Completion
2026-06-02
FDA Drug
Yes

Countries

  • United States
  • Austria
  • Belgium
  • Brazil
  • Chile
  • China
  • Czechia
  • France
  • Germany
  • Guatemala
  • Lithuania
  • Mexico
  • Poland
  • Portugal
  • Singapore
  • South Korea
  • Spain
  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05350072 on ClinicalTrials.gov