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Legal status · United Kingdom

Is OSK Partial Reprogramming legal in the United Kingdom?

Written by Reviewed Sep 2026

Not approvedLongevityHuman studies cited: 1

Direct answer

No. OSK Partial Reprogramming is not approved for any medical use in the United Kingdom; its classification is "Investigational, not licensed". Lawful access is limited to registered clinical trials. "Research use only" labeling on vials sold online does not make human use lawful. On the evidence, 1 human study is cited on its profile.

OSK Partial Reprogramming in the United Kingdom at a glance

ClassificationInvestigational, not licensed
MHRA approval statusNot approved by MHRA; investigational
Human studies cited1 of 6 citations on the profile
ReviewedSep 2026

Classification and note come from the OSK Partial Reprogramming profile, checked against Medicines and Healthcare products Regulatory Agency (MHRA) listings at the reviewed date.

What this means

  • 01

    OSK Partial Reprogramming is being studied in registered clinical trials but has not received MHRA marketing approval in the United Kingdom.

  • 02

    Lawful human access is limited to trial participation or a formal early-access scheme where one exists; there is no pharmacy product to prescribe.

  • 03

    Vials sold online "for research use only" are not trial material, and that label does not make human use lawful.

What OSK Partial Reprogramming is

Three of the four Yamanaka factors, switched on briefly to reset epigenetic marks without erasing cell identity. Every efficacy result is in mice. One phase 1 safety trial is recruiting, in 18 people, in one eye.

Partial reprogramming is the idea that ageing cells keep a readable record of their younger epigenetic state, and that turning on a subset of the Yamanaka factors for a short period can recover it. OSK is that subset: Oct4, Sox2 and Klf4, with c-Myc deliberately left out because c-Myc is an oncogene.

Mechanism: Established in mice. OSK expression drives partial erasure and rewriting of DNA methylation marks, moving the methylation profile of a cell toward a younger pattern without progressing to pluripotency.

Regulatory history: Not approved in any country for any indication. No reprogramming therapy has ever been approved. One investigational product, Life Biosciences ER-100, is in a recruiting phase 1 safety study (NCT07290244).

How MHRA treats this kind of product

Licenses medicines for the UK market. A compound without a marketing authorisation is an unlicensed medicine, which can only lawfully be supplied for human use through a prescriber under the specials scheme, not sold as a research product.

The classification above is the The Longevity Archive reading of Medicines and Healthcare products Regulatory Agency listings for OSK Partial Reprogramming at the reviewed date, not a legal opinion. Rules change, and importing, prescribing and possessing a compound can each be treated differently. Check the regulator directly before acting on anything here.

OSK Partial Reprogramming in other countries

Frequently asked questions

Is OSK Partial Reprogramming legal in the United Kingdom?

No. OSK Partial Reprogramming is not approved for any medical use in the United Kingdom; its classification is "Investigational, not licensed". Lawful access is limited to registered clinical trials. "Research use only" labeling on vials sold online does not make human use lawful. On the evidence, 1 human study is cited on its profile.

Can I buy OSK Partial Reprogramming in the United Kingdom?

No approved product exists to buy. In the United Kingdom OSK Partial Reprogramming is classified as "Investigational, not licensed", so there is no licensed pharmacy product. Vendors selling it "for research use only" are not selling it for human use, and that label does not change its legal status. This site does not list or recommend vendors.

Is OSK Partial Reprogramming MHRA approved?

No. In the United Kingdom OSK Partial Reprogramming is classified as "Investigational, not licensed", which is not a MHRA marketing approval. For comparison, the US FDA status is: Not approved in any country for any indication. No reprogramming therapy has ever been approved. One investigational product, Life Biosciences ER-100, is in a recruiting phase 1 safety study (NCT07290244).. On the evidence, 1 human study is cited on its profile.

Related compounds in the United Kingdom

Full research profile

Mechanism, cited studies, FDA status and the full legal summary for OSK Partial Reprogramming live on its compound profile.

OSK Partial Reprogramming profile

This page is general information about the regulatory status of OSK Partial Reprogramming in the United Kingdom, current as of Sep 2026. It is not legal advice, and classifications change; check Medicines and Healthcare products Regulatory Agency directly or consult a lawyer for a specific situation. Educational use only. This database summarizes published research. It is not medical advice and contains no dosing protocols or recommendations for personal use. The Longevity Archive has no vendor relationships and does not recommend where to buy anything.