- Vor Bio dosed first patient in UPSTREAM SjD, a global Phase 3 registrational trial of telitacicept in adults with active primary Sjögren’s disease.
- Trial targets enrollment of about 250 patients, testing subcutaneous telitacicept versus placebo.
- Primary endpoint measures change in ESSDAI score at Week 48.
- RemeGen presented Phase 3 China data in late 2025, reporting statistically significant, clinically meaningful improvements in ESSDAI and ESSPRI.
- Vor Bio positioned telitacicept as only BAFF/APRIL inhibitor in Phase 3 development for Sjögren’s disease.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Vor Biopharma Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603300800PRIMZONEFULLFEED9680185) on March 30, 2026, and is solely responsible for the information contained therein.
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