Evidence & record

The record, stated plainly.

Granted patents in three jurisdictions, the published research beneath them, and an honest account of what that record establishes and what it does not.

Granted patents

Five grants, three jurisdictions.

Each of these is a granted patent held by ReeLabs, not an application. Every number below links to the public register, so you can read the claims rather than take our description of them.

US 10,745,664 B2United States

Method of progenitor cell isolation from different organs by natural destruction of extracellular matrix

Bopardikar, Kulkarni, Pophale, A. Kukharchuk, O. Kukharchuk and Anand Baskaran. Filed October 2016.

Granted
18 August 2020
US 11,072,776 B2United States

Foetal polymix of mesenchymal stem cells under hypoxic conditions for the treatment of clinical disorders and diseases

Bopardikar, Kulkarni and Pophale. Priority May 2014. This is the preparation at the centre of the Golden Vial protocol.

Core to the protocol
Granted
27 July 2021
EP 3 140 417 B1Europe

Foetal polymix of mesenchymal stem cells under hypoxic conditions for the treatment of clinical disorders

The European grant of the same invention, held by ReeLabs Private Limited, Mumbai. Filed May 2015.

Core to the protocol
Granted
21 April 2021
US 12,234,478 B2United States

Method of autologous primary hair follicles preparation in 3D culture

A proprietary three-dimensional culture system for cultivating and multiplying autologous human hair follicles.

Granted
25 February 2025
IN 442695India

The method of autologous primary hair follicles preparation in 3D culture

Application 201821017071, filed 7 May 2018. Granted for a term of twenty years by the Patent Office, Government of India.

Granted
3 August 2023
Trials

Seven completed. Three running.

SevenCompleted clinical trials behind the underlying cell science
ThreeTrials currently ongoing
EighteenProprietary technologies developed in-house
TenSources from which stem cells are isolated and banked
Published research

Nineteen papers, and what they cover.

The published work of the laboratory behind the protocol. Each entry links to the paper itself.

Clinical studies

Work carried out in patients, published in peer-reviewed journals.

01

Fetal progenitor cells for treatment of chronic limb ischemia

American Journal of Stem Cells
Read
02

Phase 1 clinical trial for intravenous administration of mesenchymal stem cells derived from umbilical cord and placenta in patients with moderate Covid-19 virus pneumonia

American Journal of Stem Cells
PDF
03

Convalescent plasma to limit coronavirus associated complications: a proof of concept phase-2 clinical study

Journal of Current Medical Research and Opinion
PDF
04

Safety and efficacy of a combination therapy in Duchenne muscular dystrophy patients

Journal of Embryology & Stem Cell Research
PDF
05

Retrospective analysis of autologous bone marrow derived mononuclear stem cells in degenerative arthritis of the knee

Journal of Stem Cell Research & Therapeutics
PDF
Laboratory research

Cell characterisation, expansion and banking method.

06

A mixture of mesenchymal stem cells from perinatal sources supports consistent ex-vivo CD34+ haematopoietic stem cell expansion

International Journal of Life Sciences Research
PDF
07

Human adult stem cells maintain a constant phenotype profile irrespective of their origin, basal media, and long term cultures

Hindawi Publishing Corporation
PDF
08

Strategies to make cord blood banking more meaningful

International Journal for Scientific Research & Development
PDF
Volunteer studies

Conducted at PGIMER, Chandigarh.

09

Successful volunteer study helps Airlite back claims

PGIMER, Chandigarh
PDF
10

Successful volunteer study helps Hormonice back claims

PGIMER, Chandigarh
PDF
11

Successful volunteer study helps OPOA back claims

PGIMER, Chandigarh
PDF
Book chapters and conference papers

Contributions to the regenerative medicine literature.

12

Promises of stem cell research and therapeutics

Somasundaram, Anandan & Marappagounder
PDF
13

Bone marrow versus dental pulp stem cells in osteogenesis

Kanafi, Ganneru, Marappagounder, Behera & Bhonde
PDF
14

Adipose-derived stem cells in musculoskeletal disorders

Marappagounder, Kotturu, Behera, Ajumeera & Rajappa
PDF
15

Stem cells of human endometrium: trash to treasure

Somasundaram, Marappagounder, Venkatesan, Behera & Bhonde
PDF
16

Identity of human endometrial tissue: potent source of stem cells

Indumathi & Dhanasekaran
PDF
17

Redundant human omentum fat: a leap towards regenerative medicine

Indumathi, Harikrishnan & Dhanasekaran
PDF
18

Subcutaneous adipose tissue-derived stem cells: advancement and applications in regenerative medicine

Indumathi, Mishra, Harikrishnan & Dhanasekaran
PDF
19

Behaviour of human mesenchymal stem cells on calcium phosphosilicate scaffolds for bone tissue engineering

European Federation of Periodontology
PDF

Read this part

What this record establishes — and what it does not.

The patents cover the cell-processing methods the Golden Vial protocol is built on. Two of them — the foetal polymix of mesenchymal stem cells under hypoxic conditions, granted in both the United States and Europe — describe the preparation at the centre of the programme. Those are the strongest documents on this page, and they are public.

The published papers are a different thing, and we would rather say so than let the length of the list do the arguing. They document two decades of ReeLabs work in regenerative medicine: limb ischaemia, Covid-19 pneumonia, muscular dystrophy, degenerative arthritis of the knee, cell characterisation and banking method. None of them is a trial of the Golden Vial programme, and none should be read as evidence that it reverses biological age.

What the record does establish is who stands behind the protocol: a laboratory with granted patents in three jurisdictions, published clinical work in peer-reviewed journals, and standing in the field the programme draws on. That is a reason to take the science seriously. It is not the same as proof, and we are not going to present it as such.

Evidence for the programme itself is the thing we build with you, and it is the reason nothing starts before a measurement: your baseline panel, and the same panel run again afterwards. The distance between those two reports is yours — not a brochure’s.