Overcoming delivery barriers
to unlock novel therapies
Our novel, non-viral platform enables efficient
delivery of gene editors, proteins, and RNA
We engineer ARMMs by appending a therapeutic payload to the protein ARRDC1, encapsulating it within the vesicle for efficient and non-immunogenic delivery.
Express ARRDC1 and payload as transgene
Producer cell buds engineered ARMMs containing payload
Isolate engineered ARMMs
Administer as therapeutic