It's been one week since Wanda Lee-Ballou received University of Virginia (UVA) Health's first dose of Ocravus Zunovo – the ...

If the cow conceives during Day 1 to 5, she will not abort when given the prostaglandin injection on Day 5 because the ...

Novo Nordisk’s Alhemo® (concizumab) has been recommended for approval by the European Medicines Agency's (EMA) Committee for ...

Rani Therapeutics Holdings (RANI – Research Report), the Healthcare sector company, was revisited by a Wall Street analyst today. Analyst ...

The global Intradermal Injection Market is expected to exceed an impressive valuation of USD 3,878 Million in 2022, with a ...

The Medicines and Healthcare products Regulatory Agency (MHRA) has approved eplontersen (Wainua) to treat adult ...

Transenteric delivery via the RaniPill yielded 80% relative bioavailability versus SC and differences between PK parameters ...

The FDA granted galinpepimut-S a rare pediatric disease designation for the treatment of pediatric patients with acute ...

This study aims to evaluate the efficacy and safety of picankibart for the treatment of moderately to severely active ulcerative colitis (modified Mayo score of 4 to 9 with an endoscopic subscore of ...

Alnylam Submits Regulatory Application to the European Medicines Agency for Vutrisiran for the Treatment of ATTR Amyloidosis with Cardiomyopathy ...

In people with this disease, small fibres of TTR protein clump together to make deposits called 'amyloid'. Amyloid can build ...