Best Treatment for Everyone
Extend Life
at the Cellular Level
We discover and develop breakthrough molecules and gene therapies that activate telomerase (hTERT) to lengthen telomeres, potentially slowing or reversing cellular aging.
Innovation Focused
Where Science
Meets Innovation
Pioneering research in biotechnology, chemical analysis, and environmental testing. Your partner for reliable data and groundbreaking discoveries.
Trust & Expertise
Precision You Can Trust
laboratory with cutting-edge equipment and experienced scientists delivering accurate results since 2021.
Compound Discovery
Using our high-throughput GFP reporter system, we screen thousands of molecules to find powerful activators of hTERT and other longevity genes.
Advanced Gene Therapy
We develop AAV-based gene therapies that deliver active hTERT directly into cells to extend telomeres and fight cellular aging.
Partner With Us
Whether you need custom research, licensing of our discoveries, or full technology transfer — we work with you to bring breakthrough longevity solutions to market.
WHAT WE’RE OFFERING
What You Get
At Bio Voyager, we provide three core services that bridge groundbreaking scientific discovery with real-world application.
We identify next-generation telomerase activators through rapid high-throughput screening. Creating AAV-hTERT therapies that can potentially extend healthy human lifespan. From molecule discovery to full technology transfer — your partner in longevity research.
- High-Throughput Compound Discovery
- AAV Gene Therapy Development
- Custom Research Partnerships & Licensing
Our Research
We Have All Type Needs
As Per Your Benefits
There are many variations of passages of available but the majority have suffered alteration.
hTERT / Telomerase Activation
Reactivating this gene allows cells to maintain telomere length → potential cellular immortality and rejuvenation.
Myostatin Inhibition
Follistatin Activation
Myostatin blocks muscle growth. Inhibiting it (or activating its suppressor Follistatin) can significantly increase muscle mass and strength.
15-Lipoxygenase Inhibition
Reduces oxidative stress in mitochondria and improves lipid metabolism.
IL-17A Inhibition
Strongly reduces chronic inflammation.
GSK3 Inhibition
Decreases neuroinflammation and shows promise in Alzheimer’s disease models.
MC1R Activation
Potential to restore natural hair color and reverse graying.
We handle the science — you handle the rest.
We do the lab work
You produce and distribute
Telomere Gene Therapy
is a cutting-edge treatment that delivers the hTERT gene into human cells (usually using AAV virus) to reactivate telomerase production, which extends telomere length, delays cellular aging, and helps restore youthful cell function.
Follistatin gene therapy
uses a harmless virus (typically AAV) to deliver the follistatin gene into muscle cells, where it produces high levels of follistatin protein that blocks myostatin — the natural “brake” on muscle growth — resulting in significantly increased muscle mass, strength, and regeneration.
Digital Surgery
Bacterial plasmid gene therapy (also called non-viral gene therapy) involves introducing a circular piece of DNA called a plasmid that carries a therapeutic gene into human gut then this plasmid serves as a blueprint to produce the desired protein.
High-Throughput Screening (HTS)
is a fast, automated drug discovery technique that allows scientists to rapidly test tens or hundreds of thousands of chemical compounds in laboratory assays to identify which ones actively affect a specific target (such as activating the hTERT gene), dramatically accelerating the discovery of new drug candidates.
Meet our
Dedicated Team
hTertTelomere Creator
FollistatinMyostatin Supressor
Adeno Associate VirusGenetically Engineered Virus
Medical Address
Get in Touch With Us.
Head Office
Tampa
Florida, US
Call Now
312-730-2562
786-307-1256
Email Us
dr.nikolic@ufl.edu
Contact Us
Get In
Touch Whit Us
Our Mission:
Discover and commercialize breakthrough
molecules and gene therapies
that extend healthy human lifespan.
All our work is strictly preclinical.
None of our discoveries or therapies are approved for human use.