CORRECTION – FDA Submission to Change the Primary Endpoint into an Industry First and Robust Clinical Measure for Superiority of CIN Phase 3 Study
BeyondSpring, Inc. - Ordinary Shares (BYSI)
Last beyondspring, inc. - ordinary shares earnings: 4/30 07:00 am
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ir.beyondspringpharma.com
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Source: GlobeNewswire
NEW YORK, April 29, 2020 (GLOBE NEWSWIRE) -- In a release issued under the same headline earlier today by BeyondSpring Inc. (NASDAQ: BYSI) please note that in the fifth paragraph of the release, the correct percentage in the second sentence is 40.9, not 37.5 as previously stated. Additionally, in the third sentence, the correct percentage increase is 53, not 67 as previously stated. The corrected release follows: BeyondSpring Inc. (the “Company” or “BeyondSpring”) (NASDAQ: BYSI), a New York-based global biopharmaceutical company focused on the development of innovative immuno-oncology cancer therapies, today announced that, following discussions with the U.S. Food and Drug Administration (FDA), the Company has formally changed the primary endpoint for its Study 106 Phase 3 superiority clinical trial with first-in-class lead asset, Plinabulin, for chemotherapy-induced neutropenia (CIN) prevention. For more than 20 years, the standard primary endpoint for CIN trials has been the dura
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News
- BeyondSpring GAAP EPS of -$0.05 [Seeking Alpha]Seeking Alpha
- BeyondSpring Reports Third-Quarter 2025 Financial Results and Provides Corporate UpdateGlobeNewswire
- BeyondSpring (NASDAQ:BYSI) had its "sell (d)" rating reaffirmed by analysts at <a style="font-weight:bold" href="https://weissratings.com/">Weiss Ratings</a>.MarketBeat
BYSI
Sec Filings
- 11/21/25 - Form 8-K
- 11/17/25 - Form 424B5
- 11/12/25 - Form 10-Q
- BYSI's page on the SEC website