Eisai and Biogen move to bring IV maintenance dosing for Leqembi to the US
As Eli Lilly’s plans for its Alzheimer’s medication donanemab get delayed, Eisai has submitted a supplemental Biologics License Application (sBLA)…
As Eli Lilly’s plans for its Alzheimer’s medication donanemab get delayed, Eisai has submitted a supplemental Biologics License Application (sBLA)…
Soon after GSK gained traction with a US Food and Drug Administration (FDA) fast track designation for its investigational treatment…
Johnson & Johnson (J&J) is allegedly looking to strengthen its presence in the cardiovascular device market with the acquisition of…
Amneal Pharmaceuticals announced that the US Food and Drug Administration (FDA) has approved an abbreviated new drug application (ANDA) for…
With positive preclinical data for its Alzheimer’s disease drug candidate TGR-63, IGC Pharma has announced that it plans to advance…
AmyriAD Therapeutics is looking to evaluate its lead Alzheimer’s disease small molecule candidate AD-101 in three upcoming Phase III studies,…
The US Food and Drug Administration (FDA) has granted a fast track designation to Sellas Life Sciences Group’s SLS009 for…
Allyx Therapeutics is planning a Phase II study to demonstrate proof of concept in Alzheimer’s disease with its lead drug…
The European Commission (EC) has approved Seagen and Takeda Pharmaceuticals’ Adcetris (brentuximab vedotin)/chemotherapy combination as a first-line treatment for patients…
Sexually transmitted diseases (STDs) such as hepatitis B, chlamydia, syphilis, and gonorrhea are currently on the rise in many countries…