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We will realize our vision of a cure only with the help of first-class external partners

Vor Bio is working on a new platform for treating and curing blood cancers.

Combining expertise in Hematopoietic Stem Cell (HSC) biology, genome engineering, and the development of Chimeric Antigen Receptor T (CAR-T) cell therapies, we will realize our vision of a cure only with the help of first-class external partners.

Acute Myeloid Leukemia (AML) is a blood cancer that still lacks highly effective treatment options. While many patients receive Hematopoietic Cell Transplants (HCTs), around 40% will relapse following their transplant with two-year survival rates of less than 20%.

Now, working with partners and across disciplines, Vor Bio is developing a new approach. Based upon a deep understanding of HSC biology and using recent advances in genome engineering, we are editing HSCs to protect them from the damaging effects of targeted therapies post-transplant. This potentially allows treatment with powerful targeted therapies such as CAR-Ts soon after transplant. Preclinical data shows that our approach can protect healthy cells without compromising blood cell populations or function. Vor Bio is now working with top transplant centers to recruit patients into a clinical trial evaluating this approach.

In collaboration with industry partners like you, we have the potential to expand our proprietary platform to address some of the most challenging cancers and other serious medical conditions.

We know that without quality partners, none of this is possible. It is our experience that the best working relationships are based upon open communication, with both parties responding to the needs of the other. We are interested in exploring how we can work collaboratively with you to build a long-term relationship that will ultimately benefit cancer patients who need better treatment options.

We look forward to exploring how we can work with you.

Contact us about partnership opportunities


We have built a proprietary technology platform by leveraging our scientific expertise and recent advances in stem cell biology and genome engineering.