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Helex Bio
Accelerating Gene-Editing Based Next-Generation Therapies
Funding to Date*
Poulami Chuadhuri, Ph.D., CEO
The moment we have a database with a significant amount of data correlating guide RNA, its on-target efficiency and the off-target effects, we are definitely going to fast track the entire development process of CRISPR based therapies.
It costs $2 billion to develop a new gene-editing therapy, and $2 million to treat one patient.

Helex Bio enables gene therapy companies to design gRNAs & simulate outcomes of CRISPR edits to bring effective therapies to market faster with our Helex Platform™. The Helex Platform™ guides gene therapy companies in target identification, design and validation of efficient and safe gRNAs for creating functional impact with minimal significant off-targets. Additionally, the platform simulates edit outcomes to reliably develop therapy protocols.

The Helex Platform™ is powered by intelligent data driven deep-learning modeling using extensive high throughput next generation sequencing data derived from CRISPR edits on human cell lines. Helex not only gives reliable predictions through the Helex Platform™, but validate them in-house using cell-based assays and next generation sequencing to support with proven experimental data for high degree of reliability.