article thumbnail

AbbVie Invests $195 Million to Expand Stateside API Manufacturing

Pharmaceutical Commerce

The new North Chicago facility, slated to open in 2027, will boost domestic production of key drug ingredients for immunology, neuroscience, and oncology therapies, reinforcing US pharmaceutical capacity amid industry reshoring and tariff concerns.

article thumbnail

Action required over ‘precautionary’ recall of UK tamoxifen batch

Hospital Pharmacy Europe

Wockhardt UK Limited has recalled batch number HZ10030 (expiry date: 30/04/2027), distributed in packs of 30 tablets. A batch of tamoxifen 20mg film-coated tablets has been recalled as a precautionary measure following the identification of a ‘dissolution failure’ during stability testing, its manufacturer has announced.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

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. Martina Nasralla is a class of 2026 PharmD candidate at the University of Southern California Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences in Los Angeles. Mann School of Pharmacy and Pharmaceutical Sciences in Los Angeles.

article thumbnail

BEAM-101 Receives RMAT for the Treatment of Sickle Cell Disease

Pharmacy Times

Completion Date (Estimated): February 1, 2027 BEAM-101 is an investigational, genetically modified cell therapy that consists of autologous CD34+ hematopoietic stem and progenitor cells that have been base-edited in the promoter regions of the HBG1/2 genes.

article thumbnail

AbbVie invests $195m to expand API manufacturing in the US

European Pharmaceutical Review

The investment will go into expanding the pharma company’s existing North Chicago, Illinois manufacturing plant, with construction beginning in the autumn and its new capabilities coming online in 2027.

FDA
article thumbnail

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. Takeda has informed the FDA that the manufacturing of Gammagard S/D will cease in December 2027.

FDA
article thumbnail

Novartis scores phase III wins for two ianalumab indications

European Pharmaceutical Review

The trial data will be presented at an upcoming medical meeting and be included, alongside results from the ongoing first-line ITP trial VAYHIT1, in regulatory submissions that are expected to be made in 2027. The post Novartis scores phase III wins for two ianalumab indications appeared first on European Pharmaceutical Review.