Insilico Medicine announced that first-in-human P

Indiana University and Pharmatrophix presented a

Humacyte announced that the U.S.

Six of seven compounds clear a reconstituted com

New six-month data strengthen the case for a one

Breakthroughs in longevity research are accelera

Serotonin Centers opened a new location in Del Ma

NADclinic Group and the Geneva College of Longevi

AnHorn Medicines on 23 July 2026 reported that th

Serina Therapeutics will participate in the BTIG

Collaboration adds multiple potential obesity dr

New data suggest LM11A-31 may help preserve the

HCW Biologics has requested a Type B pre-Investig

Insilico Medicine nominated ISM9528 as a Preclini

Serina Therapeutics announced that it has complet

London event expands as founders, investors and

As personalized nutrition grows, experts argue t

Lausanne-based Vandria presented multiple ascendi

Winona, a physician-led telehealth company focuse

Immorta Bio published a peer-reviewed Perspective

i-Lumen Scientific, a clinical-stage medical tech

i-Lumen Scientific, a clinical-stage medical tech

California-based Frontier Bio was named a Phase 1

D&D Pharmatech reported publication in Lancet Gas

NeuroSense intends to proceed with a New Drug Sub

The Emerald update redesigns the app around acti

Federal court ruling highlights growing pressure

Federal court ruling highlights growing pressure

Wellthspan Advisory’s Nadine Esposito explains

New UAE-backed venture bets future of longevity

Cumulus Neuroscience and Muse bring lab-grade sl

As investment fuels brain diagnostics, Amprion’s expansion highlights growing belief that better tests are just as important as better drugs. The race against neurodegenerative disease has largely focused on finding the next breakthrough drug. However, a growing number of researchers are beginning to ask a different question: what if one of the biggest bottlenecks isn’t the medicine, but knowing exactly who should receive it? That question sits at the heart of two conversations reshaping the field. The first is about de-risking drug development. Every failed clinical trial represents years of work and billions of dollars, but sometimes a promising therapy isn’t what fails. Sometimes the wrong patients are enrolled because diagnosing diseases like Parkinson’s or Lewy body dementia remains remarkably difficult, particularly in their early stages. Companies like Amprion are increasingly becoming the gateway that helps biopharma identify the right patients before a trial even begins. If that’s true, could expanding diagnostic capacity ultimately help speed the arrival of disease-modifying therapies? The second conversation is even broader. As medicine shifts toward detecting disease before symptoms become severe, biomarkers – the measurable biological signs that reveal what’s happening inside the body – have become one of healthcare’s hottest currencies. Companies that…

Swiss-developed system brings longitudinal blood

Debut and Natura team up to develop an AI-discov

True cellular therapeutics require stem cells bu

Report says performance health startup winding d

New platform reflects growing demand for persona

Pilot research suggests Basis may ease menopausa

FDA clearance for all skin types is making regen

New assay could make tracking Alzheimer’s prog

Preventive health platform will use new funding

AIA and BCA are turning preventive longevity int

Funding backs new diagnostics platform as the co

Avaí Bio completes a manufacturing step that co

Dubai’s new longevity authority could reshape

As AI becomes increasingly capable of interpreti

Lighthouse Pharmaceuticals presented new analyses

Biogen and Ionis presented Phase 2 CELIA results

BioAge Labs has dosed the first participant in QU

Halia Therapeutics announced two posters at the A