Longevity Blogs

Discover insightful articles on health, wellness, and the habits that support a longer, stronger life.

Showing 25 to 36 of 38 articles

2026 regulatory–payer blueprint for geroscience therapies: biomarkers, CMC, and Medicare coverage

Why 2026 is a turning point for getting geroscience therapies to older adults As of May 12, 2026, developers of therapies aimed at aging biology face a regulato...

May 12, 2026
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The doxycycline ‘on’ switch: practical safety and monitoring questions for ER‑100’s first human doses

Why the induction method matters Life Biosciences’ ER‑100, the first partial‑reprogramming therapy to receive an FDA IND, uses a doxycycline‑inducible system to...

May 11, 2026
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Inside ER‑100’s eye‑first strategy: intravitreal tradeoffs, monitoring, and what to watch in the Phase 1 protocol

Summary In early 2026 Life Biosciences received FDA clearance of an IND for ER‑100, opening a Phase 1, first‑in‑human, single‑dose safety trial in open‑angle gl...

May 9, 2026
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Designing trial endpoints and biomarkers for ER‑100 versus D+Q and rapamycin: matching measures to mechanism

Why different geroscience tools demand different trials The partial epigenetic reprogramming approach represented by ER‑100 (AAV2‑delivered OSK) and two classes...

May 9, 2026
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How ER-100’s design reflects the science: OSK, doxycycline control, and the translational safeguards guiding the first human trial

A focused look at why ER-100’s clinical protocol looks the way it does Life Biosciences’ ER-100 program—cleared by the FDA to begin a Phase 1 study in early 202...

May 9, 2026
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ER‑100 IND Cleared: What Glaucoma Patients Should Know About the New Partial Reprogramming Trial

What happened and why it matters now Life Biosciences announced U.S. Food and Drug Administration (FDA) clearance of an investigational new drug (IND) applicati...

May 9, 2026
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Longevity Clinics at a Crossroads: Teleprescribing, Privacy Risks, and the Push for Standards

Why 2026 feels like a turning point for longevity clinics Growth in private longevity clinics, expanded telemedicine prescribing flexibilities, and a simultaneo...

May 9, 2026
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Staged‑Evidence Pathways: How Bayesian Tools and Conditional Approvals Are Creating New Translational Templates for Geroscience

Why the idea of a “staged” evidence pathway matters now Over the past 18 months regulators and sponsors have produced a set of operational precedents that, take...

May 8, 2026
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FDA’s Bayesian and RWE Push: Practical next steps for geroscience trials

Regulatory momentum: two complementary shifts In the first four months of 2026 the FDA published a draft guidance that explicitly endorses practical use of Baye...

May 6, 2026
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How 2025–2026 Funding and a Canine Drug Pathway Are Rewiring Geroscience Translation

Summary In the last 12–18 months U.S. geroscience has moved from isolated pilot projects toward a coordinated translational stack: new center grants and cores,...

May 6, 2026
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Mixed Signals from Early Human Rapamycin Trials: What the 2025–2026 Data Actually Show

Where the human data stand Over the past two years a small but growing set of randomized and pilot human trials has begun to test whether rapamycin or related "...

May 6, 2026
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Tissue-Targeted Senolytics Meet Better Biomarkers: A Practical Roadmap for Near-Term Geroscience Trials

Why tissue delivery and better biomarkers matter now Over the past 18 months a distinct translational pathway for geroscience has gained momentum: local deliver...

May 4, 2026
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