Well that is disappointing
“The study did not meet its primary efficacy endpoint of MACE reduction at 90 days. As a result, there are no plans for a near-term regulatory filing. There were no major safety or tolerability concerns with CSL112.”
the leading health company stumbles again.
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- Ann: Top-line Results from the Phase 3 AEGIS-II Trial
Ann: Top-line Results from the Phase 3 AEGIS-II Trial, page-25
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