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Autoimmune-Summaries: Daily Autoimmune Updates at a Glance
20/05/2026 Savara presented biomarker data from the Phase 3 trial of molgramostim inhalation solution in aPAP at the ATS International Conference 2026 Savara presented biomarker data from the Phase 3 trial of molgramostim inhalation solution in aPAP at the ATS International Conference 2026 (Ref) Savara presented a poster at American Thoracic Society (ATS) International Conference 2026. The poster reported new biomarker data from the Phase 3, IMPALA-2, double blind study which
decodeMR Team
May 211 min read


Autoimmune-Summaries: Daily Autoimmune Updates at a Glance
19/05/2026 UCB announced week 16 data from the BE BOLD study in PsA Zenas BioPharma announced the upcoming presentation of results from the Phase 3 trial of Obexelimab in IgG4-RD at EULAR 2026 Congress Savara presented long-term data from the Phase 3 OLE study of molgramostim inhalation solution in aPAP Tiziana announced positive data for intranasal foralumab in non-active secondary progressive multiple sclerosis ImmuneOnco announced first patient dosed in Phase 2 trial of mo
decodeMR Team
May 193 min read


Autoimmune-Summaries: Daily Autoimmune Updates at a Glance
15/04/2026 Savara announced that the US FDA had extended the review period for molgramostim BLA in autoimmune PAP Savara announced that the US FDA had extended the review period for molgramostim BLA in autoimmune PAP ( Ref ) Savara announced that the FDA had extended the review period for the malgramostim ( Molgramostim Inhalation Solution ) BLA in autoimmune pulmonary alveolar proteinosis (Autoimmune PAP) by three months The Agency was reviewing the molgramostim BLA under Pr
decodeMR Team
Apr 171 min read


Autoimmune-Summaries: Daily Autoimmune Updates at a Glance
20/02/2026 Dr. Reddy’s announced that the US FDA had accepted for review its BLA for a proposed interchangeable biosimilar of ORENCIA® Savara announced that the US FDA had filed for review the BLA for MOLBREEVI for the treatment of autoimmune PAP Dr. Reddy’s announced that the US FDA had accepted for review its BLA for a proposed interchangeable biosimilar of ORENCIA® ( Ref ) Dr. Reddy’s Laboratories announced that the US FDA had accepted for review its Biologics License Appl
decodeMR Team
Feb 231 min read
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