Health & Science

Biolojic Design's BD200 demonstrated superior tumor uptake compared to marketed antibody-drug conjugates in dual-expressing breast cancer cells, becoming the first AI-designed antibody to reach clinical trials. The dual-targeting approach showed efficacy in patient-derived models resistant to existing ADCs, compressing development timelines that typically span years across global pharmaceutical pipelines.

As AI-powered clinical decision support tools spread across healthcare systems worldwide, the risk of 'hallucinations' — confidently delivered but factually wrong medical guidance — is emerging as a critical patient safety challenge. The case of Epocrates, a tool used by millions of clinicians globally, illustrates how the race to embed generative AI into medical workflows is outpacing regulatory frameworks on every continent.

French-American biotech Cellectis is preparing a landmark FDA filing for its allogeneic CAR-T therapy lasme-cel, targeting a $700M peak sales opportunity across the US and Europe by 2035 — with a potential $1.3B upside if label expansions succeed. The move positions Cellectis at the frontier of a global shift away from costly, patient-specific cell therapies toward scalable, off-the-shelf alternatives. A deepening partnership with AstraZeneca and dual manufacturing facilities on two continents u