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Enrolling by invitationPhase 3

Long-term safety of dapirolizumab pegol in people with lupus

Tests dapirolizumab pegol's long-term safety in people with systemic lupus erythematosus.

Plain-language title generated from the registry record
Registry title: A Study to Evaluate the Safety and Tolerability of Dapirolizumab Pegol in Study Participants With Systemic Lupus Erythematosus

Key facts

Where
Davao City and Makati, PhilippinesSee the 2 sites
Phase
Phase 3

Where in Philippines

  • Sl0046 20182Davao City, PhilippinesNo longer taking part
  • Sl0046 20181Makati, PhilippinesNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
UCB Biopharma SRL
Trial code
NCT04976322EU 2023-506368-14-00
Record updated
15 October 2026
Original description
The purpose of this study is to evaluate long-term safety and tolerability of dapirolizumab pegol treatment.Read full original descriptionShow less

A Multicenter, Open-Label Extension Study to Assess the Long-Term Safety and Tolerability of Dapirolizumab Pegol Treatment in Study Participants With Systemic Lupus Erythematosus

The purpose of this study is to evaluate long-term safety and tolerability of dapirolizumab pegol treatment.

Inclusion: The participant could, in the opinion of the Investigator, benefit from long-term dapirolizumab pegol (DZP) treatment; The participant completed one of the parent studies within 4 weeks prior to entry to this study.

Exclusion: Study participant has any medical or psychiatric condition (including conditions due to neuropsychiatric systemic lupus erythematosus (SLE)) that, in the opinion of the Investigator, could jeopardize or would compromise the study participant's ability to participate in this study. This includes study participants with a life-threatening condition or ongoing malignancies at the start of the study.

ClinicalTrials.gov NCT04976322 · EU CTIS 2023-506368-14-00