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SYNT001-103 is an ongoing, multi-center, open-label Phase 1b study evaluating the safety and clinical effect of SYNT001 in patients with active pemphigus vulgaris (PV) or pemphigus foliaceus (PF).

“We are very pleased to receive FDA Orphan Drug Designation as we advance our clinical development of SYNT001 in pemphigus,” said Jean-Paul Kress, M.D., president and CEO of Syntimmune.

Correspondence Published: 22 February 2018 Authors' reply: Paraneoplastic autoimmune multiorgan syndrome and paraneoplastic pemphigus describe the same spectrum of disease pathology Aimee S. Payne ...

We studied 21 patients with pemphigus whose disease had not responded to an 8-week course of 1.5 mg of prednisone per kilogram of body weight per day (corticosteroid-refractory disease), who had ...

Researchers conducted a multicenter cohort study across France from September 2018 to June 2023, which included 87 adults (mean age, 55.3 years; 50.6% women) with newly diagnosed pemphigus ...