There are currently no FDA- or EMA-approved treatment options available for any form of frontotemporal dementia.

The relationship between climate change and infectious disease is raising questions around therapeutic innovation, logistical ...

The US Food and Drug Administration has declined to approve Applied Therapeutics’ govorestat for classic galactosemia.

The EC has granted approval for presentation of GSK's Menveo vaccine (MenACWY) for invasive meningococcal disease (IMD).

The Norse Eight trial was part of the data requested by the FDA after the agency rejected the BLA for the company’s Lytenava ...

The EC has approved BeiGene’s PD-1 inhibitor Tevimbra in combination with chemotherapy to treat ESCC and G/GEJ adenocarcinoma ...

Pharmaceutical professionals expect digital solutions to solve drug development headaches, with AI already proving disruptive ...

In recent years, the evolution of biologic therapies for severe asthma has paralleled advancements in other chronic ...

Idorsia has extended its cash runway into 2025 via an exclusivity fee for global rights negotiations for Tryvio.

In an advancement for diabetes management, the US Food and Drug Administration (FDA) has granted clearance to Medtronic’s new ...

With expected sales for GLP1Rs in obesity estimated to surpass $126 billion by 2030, this drug category presents a lucrative ...

The EC has granted approval to Novartis' Kisqali (ribociclib) plus an aromatase inhibitor to treat early breast cancer ...