Agenus tries again with the FDA
A July meeting with the FDA could determine whether Agenus’s bot-bal combo has a shot at a 2024 filing.
A July meeting with the FDA could determine whether Agenus’s bot-bal combo has a shot at a 2024 filing.
Amid doubts about early data with FG-3246, the group is scathing about its rivals.
Fuelled with a $500m Summit windfall Akeso advances its lead bispecific.
Other projects new to the clinic include Haisco’s USP1 inhibitor and and Avistone’s type II c-MET blocker.
Checkmate-9DW scores a topline win on overall survival, when failure seemed more likely.
Data on the group’s lead project, the PD-1 x CTLA-4 bispecific vudalimab, are far from emphatic.
Opdivo plus Yervoy scores a remarkable survival benefit in Checkmate-8HW, whose control arm presents some comparability difficulties.
Akeso’s cadonilimab hits in its first-line study, but there’s no US data and no US partner.
But efficacy still needs to go up, as several groups try to combine PD-1 and CTLA-4 using differing approaches.