CRISPR Therapeutics
Pioneering CRISPR-based medicines
Explore the leading gene editing and longevity companies shaping the future of medicine. Detailed profiles with pipeline data, funding, key people, and technologies.
34 companies
Pioneering CRISPR-based medicines
In vivo CRISPR gene editing
Precision base editing medicines
Gene editing for heart disease
Editing genes to treat disease
Search-and-replace gene editing
Next-gen CRISPR for cell therapy
Restoring cell health to reverse disease
Reversing aging through partial epigenetic reprogramming — first in humans
Adding 10 years to healthy human lifespan
Epigenome editing — gene control without cutting
Programmable RNA editing
Zinc finger pioneers
AI-powered drug discovery for aging
Epigenetic reprogramming for human rejuvenation
mRNA epigenetic reprogramming
De-extinction and species preservation through gene editing
AI-first drug discovery from DeepMind
China's CRISPR and RNA editing leader
Next-gen CRISPR for neurological diseases
Transformer base editing from China
TALEN pioneers for off-the-shelf CAR-T
mRNA giant expanding into gene editing
Tuning genes without cutting DNA
Epigenome editing from Japan
Korea's CRISPR pioneer
Coding biology to reprogram human cells
Shielded cell therapy via gene editing
India's stem cell and gene therapy pioneer
Multi-approach anti-aging therapeutics
Precision AAV gene therapy for the eye, brain, and salivary glands
Gene silencing with DNA-directed RNA interference (ddRNAi)
A portfolio approach to drug aging itself
Precision gene editing with prime editing technology