
A new variant of coronavirus found in South Africa is feared to be more transmissible than other strains, and poses …
Allorion Therapeutics has announced that they have gained $40 million in Series A financing. The funding was led by Chinese …

The Biden administration has expanded COVID-19 booster eligibility, and millions of Americans have received their booster shots at a near …
A combination of two targeted cancer drugs have shown unprecedented activity in patients with highly malignant brain tumours carrying a …

Aadi Bioscience announced that the FDA have approved the intravenous drug Fyarro (sirolimus protein-bound particles for injectable suspension) for the …
Ocuphire Pharma, a clinical-stage ophthalmic biopharmaceutical company, announced that the first subjects have been enrolled in the MIRA-3 Phase III …

The FDA have approved Livtencity (maribavir) as the first drug for treating adults and pediatric patients with a common type …

HUTCHMED Limited and AstraZeneca have initiated SACHI, a China Phase III study of Savolitinib (ORPATHYS®), an oral, potent, and highly …

Santhera Pharmaceuticals and ReveraGen BioPharma have announced new topline results after completion of the VISION-DMD study at week 48.

Contract development and manufacturing organisation Sterling Pharma Solutions has announced a £10m multi-year investment strategy for its site in Dudley, …

Johnson & Johnson have announced the approval of the long-acting atypical antipsychotic therapy BYANNLI® by the European Commission (EC), for …

The Centre for Cancer and Immunology Research, Children’s National Research Institute, have developed a new approach that identifies unique proteins …

The FDA and CDC have cleared the Pfizer and Moderna booster jabs for adults, after reviewing new data supporting the …

Obseva, a biopharmaceutical company developing and commercialising novel therapies to improve reproductive health, have announced that the NDA for linzagolix …
Leading science and technology company, Merck KGaA, Darmstadt, Germany have identified five mid- to late-stage assets with first-in-class potential for …
Scientists have discovered multiple factors influencing declining immunity over time with the Pfizer COVID-19 vaccine, according to News Medical.

Pfizer is seeking FDA Emergency Use Authorisation (EUA) for the novel oral antiviral, Paxlovid. The pill, if authorised, will help …

Clinical-stage immunotherapy company, ImmunityBio Inc, has announced the expansion of the company’s cancer and infectious disease vaccine programmes to include …

The FDA has approved Keytruda® for the treatment of patients with early renal cell carcinoma at high or intermediate-high risk …

NICE has recommended risdiplam as treatment for the rare genetic disorder, spinal muscular atrophy, as part of a managed access …