Organogenesis ReNu receives FDA regenerative medicine advanced therapy designation for osteoarthritis of the knee

11 January 2021 - FDA determines ReNu preliminary clinical evidence indicates potential to address unmet medical needs for the management of ...

Read more →

US FDA accepts supplemental new drug application for Jardiance (empagliflozin) for adults with heart failure with reduced ejection fraction

11 January 2021 - The U.S. FDA has accepted a supplemental new drug application for Jardiance (empagliflozin) which is being ...

Read more →

FDA takes steps to provide clarity on developing new drug products in the age of individualised medicine

4 January 2021 - Advances in scientific knowledge and drug development technology have provided an opportunity for new approaches to drug ...

Read more →

U.S. FDA approves addition of overall survival and other secondary outcome data to Nubeqa (darolutamide) Prescribing Information

8 January 2021 - Phase 3 data showed treatment with Nubeqa resulted in a 31% reduction in risk of death, with ...

Read more →

2020: a strong year for new drug therapy approvals – despite many COVID-19 challenges

8 January 2021 - Throughout 2020, the U.S. Food and Drug Administration’s Center for Drug Evaluation and Research was challenged ...

Read more →

Praxis Precision Medicines receives rare paediatric disease and orphan drug designations for severe paediatric epilepsy programs

7 January 2021 - FDA grants RPD and ODD for PRAX-222 for treatment of SCN2A-DEE. ...

Read more →

FDA statement on following the authorised dosing schedules for COVID-19 vaccines

4 January 2021 - Two different mRNA vaccines have now shown remarkable effectiveness of about 95% in preventing COVID-19 disease ...

Read more →

Inversago Pharma receives rare paediatric disease designation from the FDA for INV-101 for the treatment of Prader-Willi syndrome

7 January 2021 - Inversago Pharma today announced the U.S. FDA granted a rare paediatric disease designation to the Company’s lead ...

Read more →

Gemini Therapeutics announces FDA fast track designation granted for GEM103 for the treatment of dry age-related macular degeneration in patients with complement factor H loss of function gene variants

7 January 2020 - Gemini Therapeutics today announced that GEM103, the Company’s investigational treatment for dry age-related macular degeneration, has been ...

Read more →

Merus granted FDA fast track designation of zenocutuzumab for the treatment of patients with neuregulin 1 fusion cancers

7 January 2021 - NRG1 fusions are rare mutations in many types of solid tumours, including non-small cell lung cancer and ...

Read more →

Warning of shortages, researchers look to stretch vaccine supply

5 January 2021 - The N.I.H. and Moderna are examining whether doses of Moderna’s coronavirus vaccine can be halved to double ...

Read more →

Adalimumab biosimilars face product obsolescence before launch

 6 January 2021 - Product differentiation by concentration is a threat to the multiple adalimumab biosimilars approved but not yet ...

Read more →

RedHill Biopharma's RHB-204 granted FDA fast track designation for non-tuberculous mycobacteria disease

6 January 2021 - FDA Fast Track designation, together with previously granted QIDP designation, provides RHB-204 with eligibility for rolling NDA ...

Read more →

Farxiga granted priority review in the US for the treatment of patients with chronic kidney disease

6 January 2021 - Farxiga could become the first SGLT2 inhibitor approved to treat patients with chronic kidney disease, with ...

Read more →

Marius Pharmaceuticals submits new drug application to U.S. FDA for next generation oral testosterone replacement therapy in male patients with hypogonadism

5 January 2021 - Kyzatrex new drug application includes data demonstrating less than 2 mm Hg mean SBP increase as measured ...

Read more →