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Functional Improvement Seen With C1q Inhibitor in Guillain-Barré Syndrome

ANX005 is a C1q inhibitor that is administered intravenously and works by blocking the activation of classical complement pathway.

International guillain barrDrug administrationResearch councilPeripheral nerve society annual meeting onMedical research councilDouglas loveWestern international guillain barrSyndrome outcomes studyBiologics license applicationNerve society annual meetingFast trackOrphan drug

Annexon Reports Fourth Quarter and Year-End 2023 Financial Results and Key Anticipated Milestones

Pivotal Phase 3 Data for ANX005 in Guillain-Barré Syndrome Expected in Second Quarter 2024 Initiation of Pivotal Phase 3 ANX007 ARCHER II Trial in Geographic Atrophy Expected in mid-2024, a Global.

Joyce allaireSheryl seapyInternational guillain barrSecurities exchangeClinical program updatesEuropean medicines agencyAnnexon incDrug administrationPivotal phaseSecond quarterGeographic atrophyPrimary outcome measureProof of concept dataClassical pathway expectedSecond halfBalance sheet

Annexon Reports Fourth Quarter and Year-End 2023 Financial Results and Key Anticipated Milestones

Annexon Reports Fourth Quarter and Year-End 2023 Financial Results and Key Anticipated Milestones
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Sheryl seapyJoyce allaireAnnexon incSecurities exchangeInternational guillain barrDrug administrationEuropean medicines agencyClinical program updatesReports fourth quarterKey anticipatedSecond quarterPivotal phaseGeographic atrophyPrimary outcome measureProof of concept dataClassical pathway expected

Phase 2 trial data shows safety, tolerability and efficacy of imlifidase in GBS patients

Hansa Biopharma today announced positive high-level data from the 15-HMedIdeS-09 phase 2 trial that demonstrated imlifidase was safe and well tolerated when administered prior to standard of care, including rapid improvement in disease-related efficacy measures.

Shahram attarianHansa biopharmaAchim kaufholdHead of department neuromuscular diseasesInternational coordinating principal investigatorInternational guillain barrChief medical officerNeuromuscular diseasesHopitaux universitaires de marseilleSyndrome outcome studyNervous system

Imlifidase demonstrated positive safety, tolerability, and early efficacy outcomes in 15-HMedIdeS-09 phase 2 trial in Guillain-Barré Syndrome (GBS)

/PRNewswire/ Hansa Biopharma, "Hansa" (NASDAQ Stockholm: HNSA), today announced positive high-level data from the 15-HMedIdeS-09 phase 2 trial that.

United kingdomKlaus sindahlShahram attarianVan doornAchim kaufholdStephanie kenneyHansa biopharmaDrug administrationInternational coordinating principal investigatorVp global corporate affairsInternational guillain barrEuropean medicines agencyHead of department neuromuscular diseasesChief medical officerNeuromuscular diseasesHopitaux universitaires de marseille