[424B5] Cognition Therapeutics, Inc. Prospectus Supplement (Debt Securities)
Cognition Therapeutics (CGTX) is offering 14,700,000 shares of common stock in a registered direct offering and registering Placement Agent Warrants to purchase 514,500 shares exercisable at $2.78 beginning six months after closing and expiring after five years. The prospectus supplement states estimated net proceeds of approximately $27.9 million to fund Phase 3 preparation for zervimesine (CT1812), general corporate purposes and working capital. Recent clinical progress includes positive Phase 2 SHINE (Alzheimer's) results with safety/tolerability met and biomarker signals (plasma p-tau217 subgroup) and an FDA end-of-Phase 2 meeting that confirmed a Phase 3 design may support an NDA. SHIMMER (DLB) and MAGNIFY (GA) Phase 2 toplines reported favorable signals. Safety observations include 23 incidents (9.6%) of transient LFT increases >3xULN and higher discontinuations in treated participants. The company regained Nasdaq minimum bid compliance on August 26, 2025.
Cognition Therapeutics (CGTX) offre 14.700.000 azioni ordinarie in un'offerta diretta registrata e sta registrando warrant per l'Agente di Collocamento per l'acquisto di 514.500 azioni, esercitabili a $2,78 a partire da sei mesi dopo la chiusura e con scadenza a cinque anni. Il supplemento al prospetto indica proventi netti stimati di circa $27.9 million per finanziare la preparazione della Fase 3 per zervimesine (CT1812), scopi societari generali e capitale circolante. I progressi clinici recenti includono risultati positivi nella Fase 2 SHINE (Alzheimer) con criteri di sicurezza/tollerabilità soddisfatti e segnali da biomarcatori (sottogruppo plasma p-tau217); un incontro con la FDA di fine Fase 2 ha confermato che il disegno della Fase 3 potrebbe supportare una NDA. I topline della Fase 2 SHIMMER (DLB) e MAGNIFY (GA) hanno riportato segnali favorevoli. Tra le osservazioni sulla sicurezza: 23 casi (9,6%) di aumenti transitori degli LFT >3xULN e un tasso maggiore di interruzioni nei partecipanti trattati. La società ha riacquistato la conformità al prezzo minimo di Nasdaq il 26 agosto 2025.
Cognition Therapeutics (CGTX) ofrece 14.700.000 acciones ordinarias en una colocación directa registrada y está registrando Warrants del Agente Colocador para comprar 514.500 acciones, ejercitables a $2,78 a partir de seis meses tras el cierre y con vencimiento a los cinco años. El suplemento del prospecto indica ingresos netos estimados de aproximadamente $27.9 million para financiar la preparación de la Fase 3 de zervimesine (CT1812), fines corporativos generales y capital de trabajo. Los avances clínicos recientes incluyen resultados positivos en la Fase 2 SHINE (Alzheimer) con seguridad/tolerabilidad cumplidas y señales en biomarcadores (subgrupo de plasma p-tau217); una reunión de fin de Fase 2 con la FDA confirmó que el diseño de la Fase 3 podría respaldar una NDA. Los toplines de la Fase 2 SHIMMER (DLB) y MAGNIFY (GA) reportaron señales favorables. Observaciones de seguridad: 23 incidentes (9,6%) de incrementos transitorios de LFT >3xULN y más discontinuaciones en participantes tratados. La compañía recuperó el cumplimiento del precio mínimo de Nasdaq el 26 de agosto de 2025.
Cognition Therapeutics (CGTX)는 등록 직접공모 방식으로 보통주 14,700,000주를 제공하며, 배치먼트 에이전트 워런트로 514,500주를 매수할 수 있는 권리를 등록하고 있습니다. 워런트 행사가격은 $2.78이며 종결 후 6개월부터 행사가 가능하고 만기는 5년입니다. 증권설명서 보충서에는 zervimesine(CT1812) 3상 준비, 일반 기업 목적 및 운전 자금 조달을 위해 약 $27.9 million의 순수익 예상이 명시되어 있습니다. 최근 임상 진전으로는 안전성/내약성이 충족된 긍정적인 2상 SHINE(알츠하이머) 결과와 바이오마커 신호(혈장 p-tau217 서브그룹)가 있으며, FDA와의 End-of-Phase 2 미팅에서 3상 설계가 NDA를 뒷받침할 수 있음을 확인받았습니다. 2상 SHIMMER(DLB)와 MAGNIFY(GA) 톱라인도 유리한 신호를 보고했습니다. 안전성 관찰로는 LFT가 >3xULN으로 일시적 상승한 사례 23건(9.6%)과 치료군에서 중단율 증가가 있었습니다. 회사는 2025년 8월 26일 나스닥 최소 호가 기준을 다시 충족했습니다.
Cognition Therapeutics (CGTX) propose 14 700 000 actions ordinaires dans une offre directe enregistrée et enregistre des Warrants d'Agent de Placement permettant d'acheter 514 500 actions, exerçables à 2,78 $ à partir de six mois après la clôture et arrivant à échéance après cinq ans. Le supplément de prospectus indique des produits nets estimés à environ $27.9 million pour financer la préparation de la Phase 3 pour zervimesine (CT1812), des fins générales d'entreprise et le fonds de roulement. Les progrès cliniques récents incluent des résultats positifs de la Phase 2 SHINE (Alzheimer) avec sécurité/tolérabilité respectées et signaux de biomarqueurs (sous-groupe plasma p-tau217); une réunion FDA de fin de Phase 2 a confirmé qu'un plan de Phase 3 pourrait soutenir une NDA. Les résultats topline de Phase 2 SHIMMER (DLB) et MAGNIFY (GA) ont signalé des signes favorables. Observations de sécurité : 23 incidents (9,6 %) d'élévations transitoires des LFT >3xULN et plus d'interruptions chez les participants traités. La société a retrouvé la conformité au prix minimum Nasdaq le 26 août 2025.
Cognition Therapeutics (CGTX) bietet 14.700.000 Stammaktien in einem registrierten Direktangebot an und registriert Placement-Agent-Warrants zum Erwerb von 514.500 Aktien, ausübbar zu $2,78 ab sechs Monaten nach Closing und mit einer Laufzeit von fünf Jahren. Der Prospektergänzung zufolge werden geschätzte Nettoerlöse von ca. $27.9 million zur Finanzierung der Phase-3-Vorbereitung für zervimesine (CT1812), für allgemeine Unternehmenszwecke und Betriebskapital erwartet. Kürzliche klinische Fortschritte umfassen positive Phase-2-SHINE-(Alzheimer)-Ergebnisse mit erfüllten Sicherheits-/Verträglichkeitskriterien und Biomarker-Signalen (Plasma p-tau217-Subgruppe), und ein FDA-End-of-Phase-2-Meeting bestätigte, dass ein Phase-3-Design eine NDA stützen könnte. Die Phase-2-Toplines von SHIMMER (DLB) und MAGNIFY (GA) zeigten ebenfalls günstige Signale. Zu den Sicherheitsbefunden zählen 23 Vorfälle (9,6%) mit vorübergehend erhöhten Leberwerten (LFT >3xULN) und höhere Abbruchraten bei behandelten Teilnehmern. Das Unternehmen erfüllte die Nasdaq-Mindestnotierung wieder am 26. August 2025.
- Estimated $27.9 million net proceeds to fund Phase 3 preparation and general corporate purposes
- FDA end-of-Phase 2 minutes confirmed that the proposed Phase 3 design may support an NDA filing for zervimesine
- Positive Phase 2 topline results across SHINE (Alzheimer's), SHIMMER (DLB) and MAGNIFY (GA) with biomarker and clinical signals
- Nasdaq compliance regained on August 26, 2025, removing minimum bid noncompliance concern
- Expanded access program funded for DLB following a philanthropic donation
- Safety signal: 23 incidents (9.6%) of transient LFT increases >3xULN among zervimesine-treated participants across Phase 2 studies
- Immediate dilution: new investors face $1.58 per share dilution in net tangible book value (pro forma as adjusted)
- Higher discontinuation rate: 11.8% of zervimesine-treated participants discontinued due to treatment-emergent AEs versus 4.6% for placebo
- Concentration risk: company is highly dependent on a single lead candidate (zervimesine) for near-term value realization
- Placement Agent Warrants and ATM shares may create future overhang and additional dilution
Insights
TL;DR: This financing materially extends runway for Phase 3 planning while diluting new investors; clinical signals and FDA feedback increase program value.
The offering of 14.7 million shares with estimated net proceeds of $27.9 million meaningfully bolsters near-term funding to prepare zervimesine Phase 3 programs and supports operations without immediate additional equity raises. The registered Placement Agent Warrants add potential future overhang. Regaining Nasdaq compliance reduces listing risk. Immediate dilution to new investors is significant and management retains broad discretion over proceeds.
TL;DR: Phase 2 toplines across Alzheimer’s, DLB and GA show consistent biomarker and clinical signals, and FDA end-of-Phase 2 minutes support a Phase 3 path.
SHINE met safety and tolerability and identified plasma p-tau217 as a potential predictive biomarker with pronounced benefit in below-median subgroup; pooled AD cognitive slowing (38% at six months) was observed though not statistically significant in the overall population. SHIMMER showed strong functional and neuropsychiatric improvements in DLB. MAGNIFY showed ~28–29% GA lesion reduction and an improving effect over time. Safety signals include transient LFT elevations that resolved on cessation; these will require monitoring in Phase 3 protocols.
Cognition Therapeutics (CGTX) offre 14.700.000 azioni ordinarie in un'offerta diretta registrata e sta registrando warrant per l'Agente di Collocamento per l'acquisto di 514.500 azioni, esercitabili a $2,78 a partire da sei mesi dopo la chiusura e con scadenza a cinque anni. Il supplemento al prospetto indica proventi netti stimati di circa $27.9 million per finanziare la preparazione della Fase 3 per zervimesine (CT1812), scopi societari generali e capitale circolante. I progressi clinici recenti includono risultati positivi nella Fase 2 SHINE (Alzheimer) con criteri di sicurezza/tollerabilità soddisfatti e segnali da biomarcatori (sottogruppo plasma p-tau217); un incontro con la FDA di fine Fase 2 ha confermato che il disegno della Fase 3 potrebbe supportare una NDA. I topline della Fase 2 SHIMMER (DLB) e MAGNIFY (GA) hanno riportato segnali favorevoli. Tra le osservazioni sulla sicurezza: 23 casi (9,6%) di aumenti transitori degli LFT >3xULN e un tasso maggiore di interruzioni nei partecipanti trattati. La società ha riacquistato la conformità al prezzo minimo di Nasdaq il 26 agosto 2025.
Cognition Therapeutics (CGTX) ofrece 14.700.000 acciones ordinarias en una colocación directa registrada y está registrando Warrants del Agente Colocador para comprar 514.500 acciones, ejercitables a $2,78 a partir de seis meses tras el cierre y con vencimiento a los cinco años. El suplemento del prospecto indica ingresos netos estimados de aproximadamente $27.9 million para financiar la preparación de la Fase 3 de zervimesine (CT1812), fines corporativos generales y capital de trabajo. Los avances clínicos recientes incluyen resultados positivos en la Fase 2 SHINE (Alzheimer) con seguridad/tolerabilidad cumplidas y señales en biomarcadores (subgrupo de plasma p-tau217); una reunión de fin de Fase 2 con la FDA confirmó que el diseño de la Fase 3 podría respaldar una NDA. Los toplines de la Fase 2 SHIMMER (DLB) y MAGNIFY (GA) reportaron señales favorables. Observaciones de seguridad: 23 incidentes (9,6%) de incrementos transitorios de LFT >3xULN y más discontinuaciones en participantes tratados. La compañía recuperó el cumplimiento del precio mínimo de Nasdaq el 26 de agosto de 2025.
Cognition Therapeutics (CGTX)는 등록 직접공모 방식으로 보통주 14,700,000주를 제공하며, 배치먼트 에이전트 워런트로 514,500주를 매수할 수 있는 권리를 등록하고 있습니다. 워런트 행사가격은 $2.78이며 종결 후 6개월부터 행사가 가능하고 만기는 5년입니다. 증권설명서 보충서에는 zervimesine(CT1812) 3상 준비, 일반 기업 목적 및 운전 자금 조달을 위해 약 $27.9 million의 순수익 예상이 명시되어 있습니다. 최근 임상 진전으로는 안전성/내약성이 충족된 긍정적인 2상 SHINE(알츠하이머) 결과와 바이오마커 신호(혈장 p-tau217 서브그룹)가 있으며, FDA와의 End-of-Phase 2 미팅에서 3상 설계가 NDA를 뒷받침할 수 있음을 확인받았습니다. 2상 SHIMMER(DLB)와 MAGNIFY(GA) 톱라인도 유리한 신호를 보고했습니다. 안전성 관찰로는 LFT가 >3xULN으로 일시적 상승한 사례 23건(9.6%)과 치료군에서 중단율 증가가 있었습니다. 회사는 2025년 8월 26일 나스닥 최소 호가 기준을 다시 충족했습니다.
Cognition Therapeutics (CGTX) propose 14 700 000 actions ordinaires dans une offre directe enregistrée et enregistre des Warrants d'Agent de Placement permettant d'acheter 514 500 actions, exerçables à 2,78 $ à partir de six mois après la clôture et arrivant à échéance après cinq ans. Le supplément de prospectus indique des produits nets estimés à environ $27.9 million pour financer la préparation de la Phase 3 pour zervimesine (CT1812), des fins générales d'entreprise et le fonds de roulement. Les progrès cliniques récents incluent des résultats positifs de la Phase 2 SHINE (Alzheimer) avec sécurité/tolérabilité respectées et signaux de biomarqueurs (sous-groupe plasma p-tau217); une réunion FDA de fin de Phase 2 a confirmé qu'un plan de Phase 3 pourrait soutenir une NDA. Les résultats topline de Phase 2 SHIMMER (DLB) et MAGNIFY (GA) ont signalé des signes favorables. Observations de sécurité : 23 incidents (9,6 %) d'élévations transitoires des LFT >3xULN et plus d'interruptions chez les participants traités. La société a retrouvé la conformité au prix minimum Nasdaq le 26 août 2025.
Cognition Therapeutics (CGTX) bietet 14.700.000 Stammaktien in einem registrierten Direktangebot an und registriert Placement-Agent-Warrants zum Erwerb von 514.500 Aktien, ausübbar zu $2,78 ab sechs Monaten nach Closing und mit einer Laufzeit von fünf Jahren. Der Prospektergänzung zufolge werden geschätzte Nettoerlöse von ca. $27.9 million zur Finanzierung der Phase-3-Vorbereitung für zervimesine (CT1812), für allgemeine Unternehmenszwecke und Betriebskapital erwartet. Kürzliche klinische Fortschritte umfassen positive Phase-2-SHINE-(Alzheimer)-Ergebnisse mit erfüllten Sicherheits-/Verträglichkeitskriterien und Biomarker-Signalen (Plasma p-tau217-Subgruppe), und ein FDA-End-of-Phase-2-Meeting bestätigte, dass ein Phase-3-Design eine NDA stützen könnte. Die Phase-2-Toplines von SHIMMER (DLB) und MAGNIFY (GA) zeigten ebenfalls günstige Signale. Zu den Sicherheitsbefunden zählen 23 Vorfälle (9,6%) mit vorübergehend erhöhten Leberwerten (LFT >3xULN) und höhere Abbruchraten bei behandelten Teilnehmern. Das Unternehmen erfüllte die Nasdaq-Mindestnotierung wieder am 26. August 2025.
(To Prospectus dated January 3, 2023)
![[MISSING IMAGE: lg_cognition-4c.jpg]](https://www.sec.gov/Archives/edgar/data/0001455365/000110465925084835/lg_cognition-4c.jpg)
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Per Share
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Total
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Offering Price
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| | | $ | 2.05 | | | | | $ | 30,135,000 | | |
Placement Agent fees(1)
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| | | $ | 0.1316 | | | | | $ | 1,934,450 | | |
Proceeds to Cognition, before expenses(2)
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| | | $ | 1.9184 | | | | | $ | 28,200,550 | | |
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ABOUT THIS PROSPECTUS SUPPLEMENT
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PROSPECTUS SUPPLEMENT SUMMARY
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| | | | S-1 | | |
THE OFFERING
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RISK FACTORS
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CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
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USE OF PROCEEDS
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DILUTION
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DESCRIPTION OF SECURITIES
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MATERIAL U.S. FEDERAL INCOME TAX CONSIDERATIONS
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PLAN OF DISTRIBUTION
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LEGAL MATTERS
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EXPERTS
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WHERE YOU CAN FIND MORE INFORMATION
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INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
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Page
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ABOUT THIS PROSPECTUS
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WHERE YOU CAN FIND MORE INFORMATION
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INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
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CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
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ABOUT THE COMPANY
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RISK FACTORS
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USE OF PROCEEDS
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DESCRIPTION OF CAPITAL STOCK
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DESCRIPTION OF DEBT SECURITIES
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DESCRIPTION OF WARRANTS
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DESCRIPTION OF UNITS
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DESCRIPTION OF OUR SUBSCRIPTION RIGHTS
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GLOBAL SECURITIES
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PLAN OF DISTRIBUTION
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LEGAL MATTERS
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EXPERTS
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offering
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Offering price per share
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| | | | | | | | | $ | 2.05 | | |
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Net tangible book value per share as of June 30, 2025
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| | | $ | 0.11 | | | | | | | | |
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Pro forma net tangible book value per share
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| | | $ | 0.18 | | | | | | | | |
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Increase in net tangible book value per share attributable to this offering
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| | | $ | 0.29 | | | | | | | | |
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Pro forma as adjusted net tangible book value per share as of June 30, 2025, after giving effect to this offering
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| | | | | | | | | $ | 0.47 | | |
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Dilution per share to new investors purchasing shares in this offering
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| | | | | | | | | $ | 1.58 | | |
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Per Share
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Total
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Offering Price
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| | | $ | 2.05 | | | | | $ | 30,135,000 | | |
Placement Agent fees
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| | | $ | 0.1316 | | | | | $ | 1,934,450 | | |
Proceeds to Cognition, before expenses(1)
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| | | $ | 1.9184 | | | | | $ | 28,200,550 | | |
![[MISSING IMAGE: lg_cognition-4c.jpg]](https://www.sec.gov/Archives/edgar/data/0001455365/000110465925084835/lg_cognition-4c.jpg)
Preferred Stock
Debt Securities
Warrants
Units
Subscription Rights
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ABOUT THIS PROSPECTUS
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WHERE YOU CAN FIND MORE INFORMATION
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INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
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CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
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ABOUT THE COMPANY
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RISK FACTORS
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USE OF PROCEEDS
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DESCRIPTION OF CAPITAL STOCK
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DESCRIPTION OF DEBT SECURITIES
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DESCRIPTION OF WARRANTS
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DESCRIPTION OF UNITS
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DESCRIPTION OF OUR SUBSCRIPTION RIGHTS
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GLOBAL SECURITIES
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PLAN OF DISTRIBUTION
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LEGAL MATTERS
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EXPERTS
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![[MISSING IMAGE: lg_cognition-4c.jpg]](https://www.sec.gov/Archives/edgar/data/0001455365/000110465925084835/lg_cognition-4c.jpg)