FDA approval of Leqembi subcutaneous formulation charts path to combination therapies for Alzheimer's disease

29 August 2025 - Subcutaneous delivery increases accessibility and introduces potential for at home administration, following model of diabetes and ...

Read more →

Iveric Bio receives US FDA approval for Izervay (avacincaptad pegol intravitreal solution), a new treatment for geographic atrophy

5 August 2023 - Izervay is the only approved GA treatment with a statistically significant reduction in the rate of geographic ...

Read more →

Drug makers brace for list of first 10 drugs for US price negotiations

2 August 2023 - Drug makers are bracing for the US Government's announcement of the 10 prescription medicines that will ...

Read more →

Alarmed by popularity of Ozempic and Wegovy, insurers wage multi-front battle

3 August 2023 - Patients are bracing for “D-Day,” the date their insurance companies will stop covering the drugs. Doctors ...

Read more →

FDA approves first oral treatment for post-partum depression

4 August 2023 - Today, the US FDA approved Zurzuvae (zuranolone), the first oral medication indicated to treat post-partum depression in ...

Read more →

Setmelanotide acetate for the treatment of people with obesity and hyperphagia associated with Bardet-Biedl syndrome

3 August 2023 - The Department of Health and Social Care has asked NICE to produce guidance on the use ...

Read more →

Orchard Therapeutics completes submission of biologics license application for OTL-200 in MLD to US FDA

3 August 2023 - Four MLD patients identified from ~150,000 newborns screened in prospective studies suggests significantly higher incidence than previously ...

Read more →

Mesoblast receives complete response from US FDA for biologics license application for steroid-refractory acute graft versus host disease in children

4 August 2023 - Mesoblast Limited today announced that the US FDA has provided a complete response to its biologics license ...

Read more →

Aardvark Therapeutics announces receipt of FDA rare paediatric disease designation for Prader-Willi syndrome

3 August 2023 - Aardvark's Phase 2 trial of oral ARD-101 in young adults with Prader-Willi syndrome is now open ...

Read more →

US FDA approves Merck’s Ervebo (Ebola Zaire vaccine, live) for use in children 12 months of age and older

3 August 2023 - Merck continues progress in helping to protect people at risk of Zaire ebolavirus disease. ...

Read more →

China’s NMPA accepts and grants priority review designation to the new drug application for Luye Pharma’s rotigotine extended release microspheres

1 August 2023 -  The drug is the world’s first innovative microsphere formulation for treating Parkinson’s disease. ...

Read more →

Jazz Pharmaceuticals enters into letter of intent with the pan-Canadian Pharmaceutical Alliance for Rylaze, helping address the unmet need of acute lymphoblastic leukaemia and lymphoblastic lymphoma patients across Canada

2 August 2023 - Jazz Pharmaceuticals today announced that the Company has entered into a letter of intent with the pan-Canadian ...

Read more →

Health Canada authorises Tecvayli (teclistamab injection), a first in class bispecific antibody for the treatment of patients with relapsed or refractory multiple myeloma

2 August 2023 - Approval for Tecvayli, a subcutaneously administered therapy, is based on results from the Phase 1/2 MajesTEC-1 ...

Read more →

PHARMAC secures supply of vaccines for New Zealanders

3 August 2023 -  PHARMAC has confirmed supply agreements for a range of funded vaccines including those that protect against ...

Read more →

FDA approves trifluridine and tipiracil with bevacizumab for previously treated metastatic colorectal cancer

2 August 2023 - Today, the FDA approved trifluridine and tipiracil (Lonsurf, Taiho Oncology) with bevacizumab, for metastatic colorectal cancer ...

Read more →

Etranacogene dezaparvovec for the treatment of patients with moderately severe or severe haemophilia B

2 August 2023 - The Department of Health and Social Care has asked NICE to produce guidance on the use ...

Read more →