US14817C1071 - Common Stock
The company tested simufilam in patients with mild-to-moderate Alzheimer's disease.
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Simufilam did not show a significant reduction in cognitive or functional decline versus placebo in patients with mild-to-moderate Alzheimer’s disease in...
Webcast planned for Monday, November 25th at 8:00 AM ET
Webcast planned for Monday, November 25th at 8:00 AM ET...
Ms. Nassif brings an extensive track record of successfully developing commercial strategies for multiple FDA-approved drugs Appointment initiates...
Top-line Data for RETHINK-ALZ 52-week Phase 3 trial Expected Before the End of 2024 $149.0 Million in Cash and Cash Equivalents at September 30, 2024....
Conference call and webcast to begin at 8:30 AM ET
Conference call and webcast to begin at 8:30 AM ET...
Without admitting wrongdoing, the company put a regulatory controversy to rest, but this was expensive.
Drugmaker Cassava Sciences Inc. and two former executives agreed to pay more than $40 million to resolve US Securities and Exchange Commission claims they misled the public about the success of an Alzheimer’s drug trial.
AUSTIN, Texas, Sept. 26, 2024 (GLOBE NEWSWIRE) -- Cassava Sciences, Inc. (“Cassava” or the “Company”) (Nasdaq: SAVA), a biotechnology company focused on...