๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-12-02

A Study to Investigate the Long-term Safety and Efficacy of Belimumab in Adults With Interstitial Lung Disease (ILD) Associated With Systemic Sclerosis (SSc) and Other Connective Tissue Diseases (CTD) (BLISSconneCTD-OLE) (NCT06716606)

An Open Label Study to Investigate the Long-term Safety and Efficacy of Belimumab in Adults With Interstitial Lung Disease (ILD) Associated With Systemic Sclerosis (SSc) and Other Connective Tissue Diseases (CTD)

๐ŸŸข Recruiting Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: GlaxoSmithKline

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This is an open label extension (OLE) study of an ongoing randomized controlled parent clinical studies 218224 (NCT05878717) and 221672 (NCT06572384) which aim to assess the efficacy and safety of belimumab on reducing the decline in lung function in participants with interstitial lung disease associated with diffuse cutaneous systemic sclerosis (dcSSc-ILD) and interstitial lung disease associated with other connective tissue diseases (CTD-ILD), respectively. The OLE study will describe how well tolerated belimumab will be long term, and whether it might continue to slow progression of lung function decline, slow overall disease progression and improve quality of life.

Who can join: Review the eligibility criteria below.

Location: GSK Investigational Site โ€” Philadelphia, Pennsylvania

Age range: 18 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (10 Sites)

  • GSK Investigational Site โ€” Philadelphia, Pennsylvania
  • GSK Investigational Site โ€” Ciudad Autonoma Buenos Aires,
  • GSK Investigational Site โ€” Ciudad Autonoma de Buenos Aire,
  • GSK Investigational Site โ€” Beijing,
  • GSK Investigational Site โ€” Zhuzhou,
  • GSK Investigational Site โ€” Larissa,
  • GSK Investigational Site โ€” Hokkaido,
  • GSK Investigational Site โ€” Tokyo,
  • GSK Investigational Site โ€” Yongsan-Ku Seoul,
  • GSK Investigational Site โ€” London,

๐Ÿ“ž Contact the Study Coordinator

Phone: (877) 379-3718

Email: GSKClinicalSupportHD@gsk.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—