Vor Bio is working to transform treatment and ultimately cure Acute Myeloid Leukemia (AML) and other blood cancers.
Combining proven technologies in new ways, our unique approach aims to protect your healthy blood cells while enabling the use of powerful targeted therapies against cancer cells that may remain following your Hematopoietic Stem Cell Transplant (HSCT).
For some types of AML, HSCT is the only potentially curative option. However, in many cases, AML can relapse even after transplant. A major challenge following transplant is that many of the current therapies that are intended to kill the cancer cells can also target and destroy healthy blood cells. Our approach is based on an elegant idea: make HSCTs resistant to cancer-directed therapies so that healthy blood cells are protected, but cancer cells can be directly targeted for destruction. Healthy donor HSCs are first edited to remove a marker on the outside of the cells so that they can no longer be recognized by targeted therapies.
Once you recover from your HSCT with the modified healthy donor cells, you may now be able to receive a targeted therapy to kill any remaining cancer cells and to decrease the chance that the cancer can come back—only possible because your healthy cells are now “invisible” to the targeted therapy.
