Discover how AI-powered tools are transforming rare disease diagnosis, patient care, and clinical decision-making.

How was a new rare disease discovered through Singapore’s Undiagnosed Disease Program? And how will technology allow us to ...

For a child with a rare disease, a doctor’s continuing education can end a years-long diagnostic odyssey and unlock access to ...

Nurses play a vital and multifaceted role in rare disease care, providing consistent patient support, education, and care ...

Montez, Medscape’s Rare Disease Education Lead recently spoke with Dr Lucy McKay, CEO, and Megan Pullein, Strategic Operations Officer from the UK-based charity Medics for Rare Disease (MfRD). We ...

Health equity is an ambitious goal, but the drive to deliver life-changing innovation to all eligible patients is ...

The industry is now entering the next era by embedding AI directly into the software field teams’ use every day. The step ...

AstraZeneca and Daiichi Sankyo’s Enhertu, in combination with pertuzumab, has been approved by the US FDA to treat adult ...

What’s holding pharma back from true digital transformation? At NEXT Pharma 2025, Our CEO Rob Verheul and Roeland van der ...

The US FDA has approved the first ever cell-based gene therapy to treat Wiskott-Aldrich syndrome (WAS).

Follow-up results from the phase 3 EMBER-3 study showed that, as a monotherapy, Inluriyo demonstrated a 38% reduction in the ...

Nektar Therapeutics has announced top-line results from its trial of rezpegaldesleukin to treat severe to very severe ...