Sunovion discontinues dasotraline program

13 May 2020 - Sunovion Pharmaceuticals today announced that it has withdrawn the new drug applications for dasotraline, a novel ...

Read more →

Russia says search for a coronavirus treatment should not be a medical ‘arms race’

14 May 2020 - Russia’s sovereign wealth fund has been funding Russian development and production of the drug favipiravir, an anti-influenza ...

Read more →

FDA grants priority review of sutimlimab, potential first approved treatment of haemolysis in adult patients with cold agglutinin disease

14 May 2020 - Sutimlimab targets C1-activated haemolysis in cold agglutinin disease. ...

Read more →

Gilead’s remdesivir tested with other drugs to fight COVID-19

13 May 2020 - Researchers are looking to find a more potent coronavirus-fighting cocktail. ...

Read more →

Arbor Pharmaceuticals announces FDA filing acceptance of new drug application for AR19, an investigational ADHD prescription stimulant treatment specifically designed to resist physical manipulation for non-medical misuse or abuse

13 May 2020 - If approved, AR19 would be the first-ever FDA approved ADHD stimulant medication designed to resist manipulation for ...

Read more →

Vanda Pharmaceuticals announces agreement with FDA on resubmission of the application for Hetlioz for the treatment of patients with Smith-Magenis syndrome

13 May 2020 - Vanda Pharmaceuticals today announced that following the completion of a Type A meeting with the U.S. FDA ...

Read more →

Rhythm Pharmaceuticals announces FDA acceptance of new drug application for setmelanotide for the treatment of POMC and LEPR deficiency obesities

13 May 2020 - FDA grants priority review of application and sets PDUFA goal date of 27 November 2020. ...

Read more →

Bristol Myers Squibb and bluebird bio provide regulatory update on idecabtagene vicleucel (ide-cel, bb2121) for the treatment of patients with multiple myeloma

Bristol Myers Squibb and bluebird bio today announced that the companies received a Refusal to File letter from the U.S. ...

Read more →

Gilead strikes deal to make remdesivir coronavirus treatment in 127 countries

12 May 2020 - Gilead Sciences has struck a licensing agreement with five generic drugmakers to make anti-viral drug remdesivir in ...

Read more →

Investigators propose different measures for biosimilar equivalence

12 May 2020 - Investigators use the HERITAGE trial findings to argue for a more precise way of measuring clinical equivalence ...

Read more →

Doctors face 'nearly an impossible situation' as they ration remdesivir

11 May 2020 - As coronavirus cases surged across the United States earlier this year, doctors faced a harrowing prospect. ...

Read more →

Moderna receives FDA fast track designation for mRNA vaccine (mRNA-1273) against novel voronavirus

12 May 2020 - Finalizing protocol for Phase 3 study of mRNA-1273, expected to begin in early summer of 2020. ...

Read more →

COVID-19 update: FDA takes new actions to accelerate development of novel prevention, treatment options for COVID-19

11 May 2020 - Today, the U.S. FDA took important actions to help accelerate the development of prevention and treatment options ...

Read more →

FDA's drug approval system is more open than Australia's

11 May 2020 - Australia’s secretive drug approval system gives what some believe is an unfair advantage to rival drug companies. ...

Read more →

CRISPR Therapeutics and Vertex Pharmaceuticals announce FDA regenerative medicine advanced therapy designation granted to CTX001 for the treatment of severe hemoglobinopathies

11 May 2020 - CTX001 has received orphan drug designation from the U.S. FDA for transfusion-dependent beta thalassemia and from the ...

Read more →