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Sanofi stories

Aug 27, 2026

AstraZeneca and Amgen's Tezspire meets Phase 3 goals in eosinophilic esophagitis

Tezspire succeeded in a Phase 3 trial for eosinophilic esophagitis, potentially becoming the drug's third approved indication and positioning it to compete with Sanofi's Dupixent, currently the only approved biologic for the condition.

Aug 27, 2026·2 sources
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Aug 12, 2026

Boulevard Bio launches with $65M to develop targeted autoimmune antibody therapies

Boulevard Bio emerged from stealth with $65 million in funding from Deerfield Management, co-founded by renowned autoimmune researcher Georg Schett and former Sanofi CSO Frank Nestle. The startup is advancing three antibody programs targeting autoimmune diseases, with its lead candidate BLVD101 in early clinical development for IgA nephropathy.

Aug 12, 2026·4 sources
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Jul 9, 2026

FDA Approves First Wearable On-Body Injector for Cancer Drug Delivery with Sanofi's Sarclisa

The FDA has approved Sanofi's Sarclisa (isatuximab) for subcutaneous delivery via a wearable on-body injector, marking the first cancer drug to receive approval for this delivery method. The device offers multiple myeloma patients a less burdensome alternative to intravenous infusions.

Jul 9, 2026·6 sources
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Jun 26, 2026

European Commission Opens Antitrust Investigation Into Sanofi's Flu Vaccine Marketing Practices

The European Commission launched an antitrust probe into Sanofi for allegedly disparaging a rival's flu vaccine in its marketing campaigns, potentially violating competition rules.

Jun 26, 2026·3 sources
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May 7, 2026

Sanofi Withdraws Diabetes Drug from FDA's Expedited Review Program After Political Interference

Sanofi requested the FDA remove its type 1 diabetes drug from Commissioner Marty Makary's new speedy drug review voucher program after a political appointee interfered with the review process.

May 7, 2026·1 source
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Top claims

  • ▪Tezspire is a monoclonal antibody designed to bind to and block thymic stromal lymphopoietin, a signaling protein implicated in epithelial-driven inflammatory conditions
  • ▪Under their collaboration agreement, Amgen holds United States commercialization rights to Tezspire, while AstraZeneca records sales for the rest of the world
  • ▪AstraZeneca and Amgen reported that the safety profile of Tezspire in the Phase 3 CROSSING trial was generally consistent with the drug's previously approved indications

Topics

Biologic therapiesDrug Approval and Clinical TrialsPharmaBiotech startupVenture capital fundingWearables & health trackingCancer treatment breakthroughsFDA drug approvalEuropean UnionRegulatory enforcementVaccine development and innovationAntitrust & competitionHealthcare Policy

Related entities

Eosinophilic esophagitis