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Novartis scores phase III wins for two ianalumab indications

European Pharmaceutical Review

In addition to Sjögren’s disease, the candidate is also being investigated as a treatment for a number of B cell-driven autoimmune diseases, including immune thrombocytopenia (ITP) , systemic lupus erythematosus and lupus nephritis.

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From ECHELON-3 to Clinical Practice: Newly Approved Brentuximab Vedotin With Lenalidomide and Rituximab for R/R DLBCL

Pharmacy Times

Zyanya Rizzo is a class of 2027 PharmD candidate at the University of Southern California Alfred E. 2 Len enhances immune response and promotes antibody-dependent cellular cytotoxicity, whereas R targets CD20-expressing B cells. Martina Nasralla is a class of 2026 PharmD candidate at the University of Southern California Alfred E.

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FDA Approves Immunoglobulin Formulation With Low IgA Content for Primary Immunodeficiency

Pharmacy Times

Takeda will discontinue Gammagard S/D by December 2027, transitioning to the new low IgA formulation. Pharmacists are essential in evaluating patient suitability for Gammagard Liquid ERC, considering IgA levels and potential hypersensitivity reactions.

FDA
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Taletrectinib Gains FDA Approval for Locally Advanced or Metastatic ROS1+ NSCLC

Pharmacy Times

Completion Date (Estimated): June 2027 “For people living with advanced ROS1+ lung cancer, who tend to be diagnosed at a younger age, having another treatment option can make a real difference for them and their loved ones,” Janet Freeman-Daily, cofounder and president of The ROS1ders, said in a news release.

FDA
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FDA approves Takeda’s Gammagard liquid ERC for primary immunodeficiency

Pharmaceutical Technology

The US Food and Drug Administration (FDA) has approved Takeda’s new immunoglobulin (IG) therapy, Gammagard liquid ERC [immune globulin infusion (human)], to treat primary immunodeficiency (PI) in individuals aged two years and above. Credit: HenadziPechan/Shutterstock. Don’t let policy changes catch you off guard.

FDA
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AbbVie expands North Chicago API production with $195m investment

Pharmaceutical Technology

By GlobalData Learn more about Strategic Intelligence The construction on the new API facility in North Chicago is set to commence in autumn 2025, with the site fully operational by 2027. This development will enlarge AbbVie’s current manufacturing presence in the US.

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Subcutaneous Biologics Market Analysis: Current Trends and Future Outlook

Roots Analysis

Moreover, protein-based drugs are also well tolerated inside the body, thereby reducing the chances of causing any immune response in the body. Currently, antibodies segment is likely to occupy the largest share in the overall market.