TIME: Rapa, SGLT2i and GLPa chosen for first Phase 3 clinical trial in aging!

Wow

Partnership between ARPA-H and the FDA:

To validate this score, PROSPR will run the first Phase 3 clinical trial targeting aging in people not yet diagnosed with a specific disease, evaluating three drug targets already approved by the FDA for other conditions: rapamycin, which acts on cellular pathways linked to aging; newer obesity and diabetes medications known as GLP-1 agonists; and diabetes drugs called SGLT-2 inhibitors that also benefit the heart and kidneys.

And as a second step

The program will then test whether novel compounds designed specifically to target aging biology can be evaluated the same way.

And can provide a valuable toolkit for biohackers too:

If the score proves accurate, it won’t just be a research tool; individuals could use a home testing kit to determine whether their lifestyle choices or treatments are actually making a difference. Our goal is to have that testing kit cost less than $100 by 2031.

@RapAdmin @adssx @DrFraser @A_User @Agetron @Beth @DeStrider @desertshores @Joseph_Lavelle @John_Hemming

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Yes - it’s great news. Finally! some good human trials with good medications.

Posted about it yesterday here, with details on other compounds:

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Seems like the near term, first trial with rapa, dapa and sema (not the new novel drug candidates like the new Cambrian mTOR one) is as follows

  1. The VITAL-H Trial Overview

Backed by up to $38 million in ARPA-H funding, UT Health San Antonio is launching the first nationwide clinical study focused on healthy longevity. Instead of targeting a specific disease, the trial aims to see if midlife interventions can delay age-related physical and cognitive decline in generally healthy adults aged 60 to 65.

To do this, they are repurposing three FDA-approved medications that have shown strong preclinical and early human data for targeting the biological hallmarks of aging:

• Rapamycin (mTOR inhibitor)

• Dapagliflozin (SGLT2 inhibitor)

• Semaglutide (GLP-1 receptor agonist)

This effort targets generally healthy adults ~60–65, with endpoints framed around Intrinsic Capacity plus decentralized/wearable measurement

  1. A Stanford/Buck/Methuselah-linked team (“THRIVE”) is building an FDA-grade Intrinsic Capacity score (PROSPR-IC) intended to predict long-term outcomes and enable shorter trials.

https://www.eurekalert.org/news-releases/1117997

And

  1. A Columbia-led effort (“FAST”) will mine completed trials/biospecimens to find biomarkers that respond to interventions—including rapamycin, SGLT-2 inhibitors, GLP-1 agonists—to support PROSPR’s shorter trial model.
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Yes, this is great news. Great drug selection. It seems like they’re listening to the scientific community when they selected these 3. Honestly, though, I would have added a lipid-lowering medication just to help prevent CVD deaths, which will skew the results due to death by heart attack/stroke. Dapagliflozin will help, but add a direct lipid-lowering med like BA and Ezetimibe, and I think the results will be better!