Possible Treatment for Rare Lymphomas Withdrawn from FDA Consideration
source: pixabay.com

Possible Treatment for Rare Lymphomas Withdrawn from FDA Consideration

According to a story from AJMC, the drug developer Incyte has made the decision to withdraw its New Drug Application (NDA) for its investigational therapy parsaclisib. This therapy was submitted…

Continue Reading Possible Treatment for Rare Lymphomas Withdrawn from FDA Consideration
INFILTR8: A New and Rare Genetic Disease
source: pixabay.com

INFILTR8: A New and Rare Genetic Disease

  Pursuing an education can be difficult enough without any other extraneous factors. But what if you were also battling frequent infections, gastrointestinal problems, and recurrent hospitalizations? For Evan Brandon,…

Continue Reading INFILTR8: A New and Rare Genetic Disease
Walmart Aromatherapy Linked to Deadly Melioidosis
https://unsplash.com/photos/r40EYKVyutI

Walmart Aromatherapy Linked to Deadly Melioidosis

Also known as Whitmore's disease, melioidosis is a rare and deadly infectious disease. While rare in the United States, melioidosis is considered a public health crisis in northern Australia, Southeast…

Continue Reading Walmart Aromatherapy Linked to Deadly Melioidosis
Crizanlizumab for SCD is Coming to England
https://pixabay.com/en/heart-red-blood-cells-erythrocyte-2176218/

Crizanlizumab for SCD is Coming to England

According to The Guardian, England’s National Health Service (NHS) has announced that a new therapeutic option will be available for patients with sickle cell disease (SCD). This treatment, called crizanlizumab,…

Continue Reading Crizanlizumab for SCD is Coming to England
Abecma for MM Approved by European Commission
source: pixabay.com

Abecma for MM Approved by European Commission

According to Pharmaceutical Business Review, Abecma (idecabtagene vicleucel), a CAR T-cell therapy designed to treat patients with relapsed and refractory (R/R) multiple myeloma (MM), received conditional marketing authorization from the…

Continue Reading Abecma for MM Approved by European Commission