“But as Albert said, we're enthusiastic to look forward to the efficacy data later this year.”

In context

“ael Dolsten: On the PCV fourth generation, I hope you looked at today's data. And what you could see is that we are really the first company that have been able to put in place a whole set of new technology that can bring immune responses to a higher level than have been seen and that allow us to go with even more comprehensive coverage than the current 20. I'm not going to give your curiosity an answer how many serotype. I can just tell you it's considerable more than the 20. On danu, we look upon danuglipron as the once-a-day QD molecule because of the reformulation technologies that were put in place and already generated some clinical data on and are now concluding. So that's really how we look upon danuglipron and we'll have final data on the best formulation option early next year. But as Albert said, we're enthusiastic to look forward to the efficacy data later this year. So very exciting time. Operator: Next, we have David Risinger with Leerink Partners. David Risinger: I have another question on danuglipron since it appears to be the company's number one pipeline candidate based upon your forecasts. So regarding the Phase 2b results that are expected soon, how should we expect Pfizer to share those results? And then, with regard to the once daily formulation that you just mentioned, Mikael, will that be ready for the Phase 3 start assuming that the company moves to start Phase 3 shortly after the Phase 2b results are generated? Albert Bourla: The first question, given the importance [indiscernible]. But with a press release, we've made them publicly available. Now, Mikael, you want to take the second part of the question of David? Mikael Dolsten: Yeah,”