A Long-term Extension Study of Dazodalibep in Participants With Sjögren's Syndrome (SS)

NCT06747949 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 844

Last updated 2026-04-28

No results posted yet for this study

Summary

The primary objective of this study is to evaluate the long-term safety and tolerability of dazodalibep.

Conditions

  • Sjögren's Syndrome

Interventions

DRUG

Dazodalibep

Dazodalibep will be given intravenously (IV).

Sponsors & Collaborators

Principal Investigators

  • MD · Amgen

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-25
Primary Completion
2029-12-11
Completion
2029-12-11
FDA Drug
Yes

Countries

  • United States
  • Argentina
  • Australia
  • Belgium
  • Brazil
  • Canada
  • Chile
  • Croatia
  • France
  • Germany
  • Greece
  • Hungary
  • Israel
  • Italy
  • Japan
  • Mexico
  • New Zealand
  • Peru
  • Poland
  • Portugal
  • Serbia
  • Slovenia
  • South Korea
  • Spain
  • Taiwan
  • United Kingdom

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 NCT06747949 on ClinicalTrials.gov