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abew4me

01/21/25 12:09 PM

#481193 RE: boi568 #481192

Well, assuming the FDA and EMA both accept just one primary endpoint, it shouldn't take that long to develop. Recruiting and screening is another headache...but once again, I was just looking at this from a worst-case scenario.
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sab63090

01/21/25 1:12 PM

#481212 RE: boi568 #481192

boi568

👍️.........I guess I defer to you!
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Doc328

01/21/25 1:39 PM

#481218 RE: boi568 #481192

2029 would be best case if trial started this quarter. 2030 would be more realistic since Missling did not start the trial in 2023