Cognition Therapeutics Inc（CGTX）资讯与事件CGTXCognition Therapeutics Inc

Cognition Therapeutics Cash Reserves Sufficient Until Q4 2027

As of June 30, 2026, the company reported having approximately $34.8M in cash, cash equivalents, and restricted cash equivalents, alongside $21.6M in total obligated grant funds remaining from the National Institute of Aging. Cognition Therapeutics estimates its current cash reserves will be sufficient to fund operations and capital expenditures into Q4 2027. "The second quarter marked important progress across both our clinical and corporate priorities," said CEO Lisa Ricciardi.

Cognition Therapeutics Aligns with FDA, Plans Key Trial to Start in 2027

Cognition Therapeutics announced that it received written feedback from the FDA following its recent meeting. The FDA agreed that psychosis associated with dementia with Lewy bodies could be an approvable outcome and reached alignment with the company on key aspects of a pivotal trial to support a new drug application, or NDA. The registrational program is expected to begin in mid-2027. As discussed with the FDA, Cognition expects the Phase 3 study will enroll people with DLB who experience psychosis symptoms of hallucinations and delusions. Patients receiving stable background treatment with off-label antipsychotic medications will be eligible. Following screening, participants will be randomized to receive either 100 mg of once-daily oral zervimesine or placebo for nine months. The company will work with the FDA on the analytical and statistical details for the use of the neuropsychiatric inventory as a novel primary endpoint for a pivotal trial in DLB psychosis.

Cognition Therapeutics Receives Patent Allowance Valid Until 2050

Cognition Therapeutics announced that a notice of allowance has been received from the United States Patent and Trademark Office, or USPTO, for patent application 19/563,468. The allowed patent covers a polymorphic crystalline form of zervimesine. Once issued, the patent will provide protection for this key formulation through 2045 and, if granted a standard five-year extension, could offer protection through 2050.