Cognition Therapeutics CEO Participating in Longwood and Sachs Conferences

Rhea-AI Summary

Cognition Therapeutics (NASDAQ: CGTX) announced CEO Lisa Ricciardi's participation in upcoming conferences during JP Morgan Healthcare Conference 2025 week. The company reported significant developments in 2024, including positive topline results from their Phase 2 SHIMMER study in dementia with Lewy body (DLB) patients, which will be presented at the International Lewy Body Dementia Conference in Amsterdam.

The company is preparing for an end-of-Phase 2 meeting with the FDA to review results from their SHINE study in mild-to-moderate Alzheimer's disease. Additionally, they received clearance for the generic name 'zervimesine' for their candidate CT1812.

Ricciardi will participate in the Longwood Healthcare Leaders Stanford Summit on January 11, 2025, and the Sachs 8th Annual Neuroscience Innovation Forum on January 12, 2025, both in San Francisco.

Positive

• Positive topline results achieved in Phase 2 SHIMMER study for DLB
• FDA end-of-Phase 2 meeting scheduled for SHINE study in Alzheimer's disease
• Generic name 'zervimesine' approved for drug candidate CT1812

Negative

• None.

PURCHASE, N.Y., Jan. 08, 2025 (GLOBE NEWSWIRE) -- Cognition Therapeutics, Inc., (the “Company” or “Cognition”) (NASDAQ: CGTX), a clinical-stage company developing drugs that treat neurodegenerative disorders, announced that CEO Lisa Ricciardi will be participating at upcoming conferences taking place during the week of the JP Morgan Healthcare Conference 2025.

“I am looking forward to these opportunities to discuss the incredible progress we have made in 2024 with our Alzheimer’s and dementia with Lewy body (DLB) programs,” stated Ms. Ricciardi. “We capped off 2024 with positive topline results from our Phase 2 SHIMMER study in patients with DLB and are looking forward to presenting these findings at the International Lewy Body Dementia Conference at the end of January in Amsterdam. We are preparing now for our end-of-Phase 2 meeting with the FDA to review results from our SHINE study in mild-to-moderate Alzheimer’s disease, an important regulatory milestone. In addition, we received clearance for the generic name for our candidate, CT1812, which will be called zervimesine.”

Presentation Details:

Longwood Healthcare Leaders Stanford Summit

Dates: January 11, 2025
Panel (moderator): Accelerating Drug Development
Location: The Four Seasons, San Francisco, CA

Sachs 8th Annual Neuroscience Innovation Forum

Date: January 12, 2025
Panel: Innovation in AD/PD & Other Cognitive Disorders Panel
Corporate Presentation: 1:40 PM Track C Heritage Room
Location: Marines’ Memorial Club, San Francisco, CA

About Cognition Therapeutics, Inc.
Cognition Therapeutics, Inc., is a clinical-stage biopharmaceutical company discovering and developing innovative, small molecule therapeutics targeting age-related degenerative disorders of the central nervous system and retina. We currently are investigating our lead candidate, zervimesine (formerly CT1812) in clinical programs in Alzheimer’s disease, dementia with Lewy bodies (DLB) and dry age-related macular degeneration (dry AMD). We believe zervimesine and our pipeline of σ-2 receptor modulators can regulate pathways that are impaired in these diseases that are functionally distinct from other approaches for the treatment of degenerative diseases. More about Cognition Therapeutics and our pipeline can be found at https://cogrx.com. 

Forward-Looking Statements 
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. All statements contained in this press release, other than statements of historical facts or statements that relate to present facts or current conditions, including but not limited to, statements regarding our product candidates, including zervimesine (formerly CT1812), and any expected or implied benefits or results, including that initial clinical results observed with respect to zervimesine will be replicated in later trials and our clinical development plans, are forward-looking statements. These statements, including statements relating to the timing and expected results of our clinical trials involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance, or achievements to be materially different from any future results, performance, or achievements expressed or implied by the forward-looking statements. In some cases, you can identify forward-looking statements by terms such as “may,” “might,” “will,” “should,” “expect,” “plan,” “aim,” “seek,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “forecast,” “potential” or “continue” or the negative of these terms or other similar expressions. We have based these forward-looking statements largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition, and results of operations. These forward-looking statements speak only as of the date of this press release and are subject to a number of risks, uncertainties and assumptions, some of which cannot be predicted or quantified and some of which are beyond our control. Factors that may cause actual results to differ materially from current expectations include, but are not limited to: competition; our ability to secure new (and retain existing) grant funding; our ability to grow and manage growth, maintain relationships with suppliers and retain our management and key employees; our ability to successfully advance our current and future product candidates through development activities, preclinical studies and clinical trials and costs related thereto; uncertainties inherent in the results of preliminary data, pre-clinical studies and earlier-stage clinical trials being predictive of the results of early or later-stage clinical trials; the timing, scope and likelihood of regulatory filings and approvals, including regulatory approval of our product candidates; changes in applicable laws or regulations; the possibility that the we may be adversely affected by other economic, business or competitive factors, including ongoing economic uncertainty; our estimates of expenses and profitability; the evolution of the markets in which we compete; our ability to implement our strategic initiatives and continue to innovate our existing products; our ability to defend our intellectual property; impacts of ongoing global and regional conflicts on our business, supply chain and labor force; our ability to maintain the listing of our common stock on the Nasdaq Global Market and the risks and uncertainties described more fully in the “Risk Factors” section of our annual and quarterly reports filed with the Securities & Exchange Commission and are available at www.sec.gov. These risks are not exhaustive and we face both known and unknown risks. You should not rely on these forward-looking statements as predictions of future events. The events and circumstances reflected in our forward-looking statements may not be achieved or occur, and actual results could differ materially from those projected in the forward-looking statements. Moreover, we operate in a dynamic industry and economy. New risk factors and uncertainties may emerge from time to time, and it is not possible for management to predict all risk factors and uncertainties that we may face. Except as required by applicable law, we do not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise. 

Contact Information:    Cognition Therapeutics, Inc. info@cogrx.com

Casey McDonald (media)  Tiberend Strategic Advisors, Inc. cmcdonald@tiberend.com

Mike Moyer (investors) LifeSci Advisors  mmoyer@lifesciadvisors.com

This press release was published by a CLEAR® Verified individual.

FAQ

What were the results of Cognition Therapeutics' (CGTX) Phase 2 SHIMMER study in 2024?

Cognition Therapeutics reported positive topline results from their Phase 2 SHIMMER study in patients with dementia with Lewy body (DLB) in 2024.

When will CGTX present the SHIMMER study results for DLB treatment?

The SHIMMER study results will be presented at the International Lewy Body Dementia Conference in Amsterdam at the end of January 2025.

What is the generic name approved for Cognition Therapeutics' (CGTX) drug candidate CT1812?

CT1812 has received clearance for the generic name 'zervimesine'.

What upcoming regulatory milestone does CGTX have for their Alzheimer's treatment?

CGTX is preparing for an end-of-Phase 2 meeting with the FDA to review results from their SHINE study in mild-to-moderate Alzheimer's disease.