Regenfactor

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About Regen Factor

    • ReGen Factor Pty Ltd is an Australian proprietary company limited by shares.

    • The company owns and controls all medical and medical-aesthetic intellectual property, including patents originally developed under the VivoVac platform and subsequently assigned to ReGen Factor Pty Ltd.

    • Our core scientific focus is bio-identical basic fibroblast growth factor (bFGF)—a master regulator of tissue repair, angiogenesis, collagen synthesis, and cellular regeneration.

    • ReGen Factor is also developing next-generation synthetic blood replacement technologies designed to improve oxygen delivery, vascular stability, and emergency and surgical outcomes.

    • Our commercial strategy prioritises medical aesthetics and regenerative medicine as initial deployment pathways, with expansion into regulated therapeutic indications.

Latest Company Announcement

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Fibroblast Growth Factors Simple Explanation

Scientists have discovered something called Fibroblast Growth Factors (FGFs)

Our PepFactor Science | ReGen Factor

CORE TECHNOLOGY: BIO-IDENTICAL bFGF

ReGen Factor has developed proprietary methods to manufacture authentic, tag-free, bio-identical recombinant human bFGF, structurally identical to the native 146-amino-acid protein produced in the human body. Why Bio-Identical bFGF Matters Basic Fibroblast Growth Factor (bFGF / FGF-2) is a primary signalling molecule responsible for: Fibroblast activation Collagen and elastin synthesis Angiogenesis and micro-vascular repair Tissue regeneration and wound healing Hair follicle cycling and stem-cell signalling If bFGF is not bio-identical, signalling is incomplete, unpredictable, or biologically compromised. ReGen Factor’s platform ensures correct folding, receptor specificity, and full biological activity.

WHY NOT EXOSOMES OR MIXED BIOLOGICS?

Many products marketed as “regenerative” rely on exosomes or undefined biological mixtures. From a medical and regulatory standpoint, these approaches have fundamental limitations: Exosomes are heterogeneous vesicles with variable and undefined cargo. Composition varies by donor source, culture conditions, and isolation method. Dosing and signalling are inconsistent and difficult to reproduce. Nano-scale size allows uncontrolled systemic distribution. Long-term safety and regulatory pathways remain uncertain. In contrast, ReGen Factor’s bio-identical bFGF is: A single, fully defined molecule Structurally identical to native human bFGF Locally active at the treatment site Rapidly degraded after signalling Fully characterisable and reproducible Regeneration requires precision, not biological noise.

SYNTHETIC BLOOD & BLOOD REPLACEMENT TECHNOLOGY

ReGen Factor is advancing synthetic blood replacement systems designed to address limitations in donor-derived blood, including availability, storage constraints, and compatibility risks. Our blood replacement technologies are intended to support: Emergency and trauma care Surgical blood substitution Vascular stabilisation Oxygen delivery optimisation These systems are being developed as part of ReGen Factor’s broader vascular and regenerative medicine platform, complementing our bFGF technologies.

INTELLECTUAL PROPERTY POSITION

ReGen Factor controls a consolidated and defensible medical IP portfolio, including:

  • Bio-identical bFGF production and delivery methods

  • Two-phase FGF therapeutic systems for vascular prevention and repair (International PCT filing: PCT/AU2025/050158)

  • Synthetic blood and blood replacement compositions

  • Medical-aesthetic and regenerative medicine patents, including those originally developed under VivoVac and formally assigned to ReGen Factor Pty Ltd

All referenced intellectual property relates exclusively to medical, regenerative, and medical-aesthetic applications.

WHY INVEST IN REGEN FACTOR

ReGen Factor offers a rare combination of:

  • Defined, bio-identical biological technology

  • Clear differentiation from exosome-based competitors

  • Scalable, cost-effective manufacturing

  • Early revenue via medical aesthetics

  • Strong clinical and therapeutic expansion potential

  • A consolidated medical IP estate under a single entity

Our focus is not cosmetic illusion, but true biological regeneration—built on precision molecular science and defensible intellectual property.

OUR SCIENCE (Tech and Stats)

ReGen Factor uses our proprietary production method to create the world’s first authentic bio-identical fibroblast growth factor for use in our products.

With an amino acid sequence identical to our natural Basic Fibroblast Growth Factor (bFGF) structure, PepFactor is 98% pure and encourages the body’s natural stimulation of biological functions.

ReGen Factor uses its novel production technology to ensure its growth factors are affordable and have high efficacy, purity, and stability for the best results at an affordable price.

PepFactor | ReGen Factor

WHY INVEST

ReGen Factor is an Australia-based progressive R&D skin biology company with a global reach. ReGen Factor has developed first-to-market technology to produce bio-identical and cost-effective Fibroblast growth factors (FGFs), which regulate a broad spectrum of biological functions, including cellular proliferation, survival, migration, and differentiation.

We are making a global impact in the cosmetic, cosmeceutical, and pharmaceutical industries with a firm commitment to technology and innovation and our expertise in bio-identical, cost-effective fibroblast growth factors.

DO YOU HAVE ANY QUESTIONS?

We help our patients feel their best, look their best and rediscover theiryouth. Contact us today to get started!

PepFactor GROWTH PIPELINES

PepFactor SALES PIPELINE

PEPFACTOR COSMETIC SALES

Maximise sales of PepFactor as a cosmetic product in the scalp and skin markets: sales currently US$90k per month

PEPFACTOR DISTRIBUTION

Sales and distrIbution are rapidly expanding.

TRADEMARK REGISTRATIONS

Trademarks have neen submitted

DEVELOPMENT PATENT

Patent for ReGen Factors uniguee development method have been processed

CE MARK

CE Mark to be submitted for registration of PepFactor for sale in the European Union and the UK

PepFactor FDA APPROVAL PIPELINE

FDA CONSULTANTS

FOA consultants have been appointed to navigate the FDA approval process

PRIMARY INVESTIGATOR

A primary investigator for the phase 1 trial has been appointed

TRIAL DESIGN AND PLANNING

Trial design and planning is underway

PRE-IND MEETING

Preparations are being made for a Pre-IND meeting to be held H2 2021

PHASE 1 TRIAL

Phase1 Clinical Trial to Commence 2022

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