
IP-NFT
A VITADAO PROJECT
Aubrai
Funding
$75,000
Initiated
25.08.2025
AT A GLANCE
Stage: Research
Area: Longevity AI / Rejuvenation
Status: Active
Patent Status: N/A

Funding
$75,000
Initiated
25.08.2025
AT A GLANCE
Stage: Research
Area: Longevity AI / Rejuvenation
Status: Active
Patent Status: N/A
Aubrai is a decentralized scientific BioAgent co-developed by VitaDAO and BIO, built to accelerate longevity R&D with private LEV knowledge, a Longevist-backed knowledge graph, and OpenScholar-based retrieval to support the RMR2 robust rejuvenation program.
Background
Aubrai is presented as a decentralized scientific agent focused on longevity research. It is co-developed by VitaDAO and BIO to support hypothesis generation, validation, and experiment planning in high-complexity aging biology programs.
RMR2 Objective
The RMR2 target is robust mouse rejuvenation: identify an intervention program that materially extends remaining lifespan in wild-type adult mice by combining therapies across multiple aging hallmarks rather than relying on single-pathway effects.
Study Design Highlights
- Interventions begin in mid-late life (about 18 to 20 months).
- The protocol plans 10 treatment groups to evaluate both single interventions and higher-order interaction effects.
- Primary endpoint focuses on treatment-group interaction effects on overall lifespan, with secondary tracking of morbidity trajectories, causes of death, and functional decline.
- Control design includes both mock and naive controls to separate administration/vehicle effects from active treatment effects.
- Scale target is approximately 500 male and 500 female mice to preserve statistical power in a multiplexed design.
Intervention Selection Framework
RMR2 selection criteria prioritize evidence of damage-reversal potential, mechanistic divergence across interventions, durability of benefit, translatability, technical feasibility at large scale, and financial practicality.
Top-Line Intervention Set in RMR2 Docs
- Deuterated fatty acids (D-PUFAs)
- Mouse serum albumin (rMSA)
- Mesenchymal stem cells or exosome-oriented alternatives
- Partial cellular reprogramming
- Anti-IL-11
- CDC42 inhibition (CASIN)
- Senolysis (Rockfish track)
- Oxytocin therapy
Docs also describe interaction hypotheses (for example D-PUFAs with senolytic and mTOR-pathway contexts) and baseline context choices such as broad rapamycin exposure and voluntary wheel access to reduce inactivity confounding.
Latest Project Updates
25 August
2025
Project Initiated