Small Genes, Big Impact
What does AIconic Bio do?
We are unlocking the true potential of gene therapy by enabling AAV vectors to access previously undruggable targets. In turn, offering hope to the millions of neglected and devastated families in the rare disease community.
Our Vision
AIconic Bio envisions a future where life-changing genetic therapies are within reach for all patients, regardless of rarity or technical challenge.
Our Mission
To unlock the full potential of gene therapy by engineering functionally precise, deliverable gene isoforms using our AI-powered ArtSplice™ platform, bridging evolutionary biology, synthetic design, and therapeutic delivery for diseases once thought untreatable.
ArtSplice
TM
Transforming Limits into Therapies.
1
Evolution-Guided Design
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AI-Powered Candidate Selection
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In Vivo Validation
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Intelligent Feedback Loop
By integrating AI and conservation biology, ArtSplice crafts novel gene isoforms tailored for delivery, bringing previously untreatable diseases into therapeutic reach.
Cochlear Gene Therapy
From snail shell to sound, our pipeline speeds up breakthroughs in cochlear gene therapy, crafting precise treatments to restore hearing.
Ocular Gene Therapy
With eagle-eyed precision, our platform targets the genetic roots of blindness, advancing ocular gene therapies that aim to bring clarity to millions.
Join Us
Be part of the founding team at AIconic, where we are redefining what’s possible in gene therapy. Help build a platform that merges AI, synthetic biology, and evolutionary insights to unlock cures once thought unreachable.