We are thrilled to share that the FDA granted Fast Track designation to the lunresertib-camonsertib combination for the treatment of platinum-resistant ovarian cancer. Learn more here: https://lnkd.in/e5n8Acxn #precisiononcology #syntheticlethality #fasttrackdesignation #ovariancancer
Really a ground breaking discovery. And probably this is just a start. Besides ATR, I am sure lunresertib (RP-6306) first-in-class, oral PKMYT1 inhibitor will do equally well or even better in the ongoing Phase 1 in combination with Wee1 inhibitor from Debiopharm. Again credit goes to Repare! With efficacy granted, what remains to be seen is whether FDA would grant Fast Track designation to this PKMYT1/WEE1 combination, when both of RP-6306 and Debio-0123 are still in Phase 1 and Phase 1/2 clinical trials as standalone therapies with no prior drug approvals coming from either of the drug targets.
Wonderful news. Congratulations!
Great news, well deserved
Great news. Well done team Repare
Fantastic work, kudos to the Repare team.
This is a great achievement Steve Forte, Lloyd Mitchell Segal and Repare Therapeutics!
Amazing news!
Fantastic news, Lloyd! Wishing you continued success!
Sensational!
Chief Medical Officer at Repare Therapeutics
4moSo satisfying to work with a great team that delivers great medicines to offer promise to patients- the promise will soon become a reality …..that’s why we all are doing this work = pleasure