That's fantastic news for the patients and another breakthrough for
#xenoTx!
I remember first discussing with Bob Montgomery
@nyulangone the prospects of applying
#C3 inhibition in Tx with multiple projected benefits! In fact, we had established the potential of C3 inhibition in ex vivo xenoTx models of pig
#kidney and
#heart perfusion with human blood, using the initially discovered compstatin and its third-generation analog Cp40 (see:
lambris.com/pdf/118-article.… and
lambris.com/pdf/608-article.…)
Delighted to see that this journey of science and discovery has advanced to actual clinical studies in living recipients with the pioneering work of Bob Montgomery and his team and the inclusion of the C3 therapeutic Empaveli as part of the immunosuppressive regimen to prevent organ rejection. Empaveli is based on the second-generation
#compstatin derivative Cp05 discovered by my team at Penn Medicine (see
lambris.com/pdf/37-article.p…).
That said, the future for C3 therapeutics in xenotransplantation looks bright indeed!
Surgeons at NYU Langone Health recently completed the first-ever combined heart pump and gene-edited pig kidney transplant in a living patient with heart failure and end-stage kidney disease, who otherwise had no options for a better quality of life:
bit.ly/3vVkymw