[424B5] Aquestive Therapeutics, Inc. Prospectus Supplement (Debt Securities)
Aquestive Therapeutics is offering 21,250,000 shares of common stock, listed on Nasdaq as "AQST," with delivery expected on or about August 15, 2025. The supplement states the last reported Nasdaq sale price was $4.01 on August 13, 2025 and that there were 99,353,270 shares outstanding as of June 30, 2025, before this offering. The filing discloses a range of dilution sources including options, RSUs, PSUs, warrants and reserved shares, and assumes no exercises for purposes of the offering. The company maintains an ATM facility with capacity up to $100.0 million, having sold ~27.3 million shares for net proceeds of ~$81.8 million to date. Underwriting terms note dealer concessions up to $0.144 per share, estimated offering expenses of ~$0.4 million, and reimbursement of up to $15,000 for FINRA counsel fees. The prospectus lists extensive risks including clinical and regulatory delays for Anaphylm, Libervant and AQST-108, manufacturing and commercialization risks, potential further dilution from future capital raises, reliance on revenue from a sunsetting licensed product (Suboxone®), debt default risk, intellectual property and litigation risks, and general market, geopolitical and macroeconomic risks. The underwriters may stabilize or engage in short covering in the market; lock-up restrictions and customary underwriting indemnities are described.
Aquestive Therapeutics offre 21.250.000 azioni ordinarie, quotate al Nasdaq con il simbolo "AQST", con consegna prevista approssimativamente per il 15 agosto 2025. Il supplemento indica che l'ultimo prezzo di vendita riportato al Nasdaq è stato $4,01 il 13 agosto 2025 e che, prima di questa offerta, erano in circolazione 99.353.270 azioni al 30 giugno 2025. La documentazione rivela varie potenziali fonti di diluizione — tra cui opzioni, RSU, PSU, warrant e azioni riservate — e, per i fini dell'offerta, presume l'assenza di esercizi. La società mantiene una linea ATM con capacità fino a $100,0 milioni, avendo venduto finora circa 27,3 milioni di azioni per proventi netti di circa $81,8 milioni. I termini di collocamento prevedono conguagli per i dealer fino a $0,144 per azione, spese stimate dell'offerta di circa $0,4 milioni e il rimborso fino a $15.000 per le parcelle del consulente FINRA. Il prospetto elenca numerosi rischi: ritardi clinici e regolatori per Anaphylm, Libervant e AQST-108, rischi legati alla produzione e alla commercializzazione, possibile ulteriore diluizione da future raccolte di capitale, dipendenza dai ricavi di un prodotto con licenza in fase di cessazione (Suboxone®), rischio di inadempienza sul debito, rischi di proprietà intellettuale e contenziosi, oltre a rischi di mercato, geopolitici e macroeconomici. Gli underwriter possono stabilizzare il mercato o coprire posizioni corte; sono descritte inoltre clausole di lock-up e le consuete indennità previste dall'accordo di collocamento.
Aquestive Therapeutics ofrece 21.250.000 acciones ordinarias, cotizadas en Nasdaq bajo el símbolo "AQST", con entrega prevista alrededor del 15 de agosto de 2025. El suplemento indica que el último precio de venta reportado en Nasdaq fue $4,01 el 13 de agosto de 2025 y que, antes de esta oferta, había 99.353.270 acciones en circulación al 30 de junio de 2025. El expediente revela diversas fuentes de dilución potencial, incluyendo opciones, RSU, PSU, warrants y acciones reservadas, y, a los efectos de la oferta, supone que no habrá ejercicios. La compañía mantiene una línea ATM con capacidad de hasta $100,0 millones, habiendo vendido hasta la fecha aproximadamente 27,3 millones de acciones por ingresos netos de alrededor de $81,8 millones. Los términos de colocación señalan concesiones a los distribuidores de hasta $0,144 por acción, gastos estimados de la oferta de aproximadamente $0,4 millones y el reembolso de hasta $15.000 por honorarios del asesor FINRA. El prospecto enumera numerosos riesgos: retrasos clínicos y regulatorios para Anaphylm, Libervant y AQST-108, riesgos de fabricación y comercialización, posible dilución adicional por futuras captaciones de capital, dependencia de los ingresos de un producto licenciado en fase de retirada (Suboxone®), riesgo de incumplimiento de deuda, riesgos de propiedad intelectual y litigios, y riesgos generales de mercado, geopolíticos y macroeconómicos. Los colocadores pueden estabilizar o cubrir posiciones cortas en el mercado; también se describen las restricciones de bloqueo y las indemnizaciones habituales de la suscripción.
Aquestive Therapeutics는 보통주 21,250,000주를 제안하며, 나스닥 티커는 "AQST"이고 인도 예정일은 2025년 8월 15일경입니다. 보충 서류는 마지막 보고된 나스닥 거래 가격이 2025년 8월 13일 $4.01였고, 본 공모 이전인 2025년 6월 30일 기준 발행주식 수는 99,353,270주였다고 명시합니다. 서류는 옵션, RSU, PSU, 워런트 및 예약주식 등 희석 요인을 여러 가지로 밝히며, 본 공모 목적상에는 권리행사가 없을 것으로 가정합니다. 회사는 최대 $1억 규모의 ATM(추가주식매출인출) 시설을 유지하고 있으며, 현재까지 약 2,730만 주를 매각해 순수입 약 $8,180만을 확보했습니다. 인수조건에는 주당 최대 $0.144의 딜러 보수, 약 $0.4백만의 예상 공모비용, FINRA 자문 수임료 최대 $15,000 환급이 포함됩니다. 설명서에는 Anaphylm, Libervant 및 AQST-108의 임상·규제 지연, 제조 및 상업화 리스크, 향후 자본조달로 인한 추가 희석 가능성, 라이선스 종료 예정 제품(Suboxone®)에 대한 매출 의존, 부채 디폴트 위험, 지적재산권 및 소송 리스크, 시장·지정학적·거시경제 리스크 등 광범위한 위험 요소가 열거되어 있습니다. 인수단은 시장 안정화 또는 숏커버를 시행할 수 있으며, 락업 제한 및 일반적인 인수인 보상 조항도 기술되어 있습니다.
Aquestive Therapeutics propose 21 250 000 actions ordinaires, cotées au Nasdaq sous le symbole "AQST", avec livraison prévue vers le 15 août 2025. Le supplément indique que le dernier cours de vente reporté au Nasdaq était de 4,01 $ le 13 août 2025 et qu'avant cette offre il y avait 99 353 270 actions en circulation au 30 juin 2025. Le dépôt dévoile diverses sources potentielles de dilution, notamment les options, RSU, PSU, warrants et actions réservées, et suppose, pour les besoins de l'offre, qu'aucune levée n'a lieu. La société dispose d'un mécanisme ATM d'une capacité maximale de 100,0 millions de dollars, ayant vendu à ce jour environ 27,3 millions d'actions pour des produits nets d'environ 81,8 millions de dollars. Les conditions du placement prévoient des concessions aux teneurs de marché pouvant atteindre 0,144 $ par action, des frais estimés de l'offre d'environ 0,4 million de dollars et le remboursement jusqu'à 15 000 $ des honoraires du conseil FINRA. Le prospectus énumère de nombreux risques : retards cliniques et réglementaires concernant Anaphylm, Libervant et AQST-108, risques de fabrication et de commercialisation, dilution supplémentaire possible en cas de futurs appels de capitaux, dépendance aux revenus d'un produit sous licence en fin de cycle (Suboxone®), risque de défaut sur la dette, risques de propriété intellectuelle et de litiges, ainsi que risques de marché, géopolitiques et macroéconomiques généraux. Les preneurs fermes peuvent stabiliser ou couvrir des positions courtes sur le marché ; des restrictions de lock-up et les habituelles indemnités d'émission sont également décrites.
Aquestive Therapeutics bietet 21.250.000 Stammaktien an, die an der Nasdaq unter dem Kürzel "AQST" gehandelt werden, mit geplanter Lieferung circa 15. August 2025. Der Nachtrag führt aus, dass der zuletzt gemeldete Nasdaq-Verkaufspreis am 13. August 2025 bei $4,01 lag und vor dieser Emission am 30. Juni 2025 insgesamt 99.353.270 Aktien ausstanden. Die Einreichung benennt verschiedene mögliche Verwässerungsquellen – darunter Optionen, RSU, PSU, Warrants und reservierte Aktien – und geht für Zwecken dieses Angebots von keiner Ausübung aus. Das Unternehmen unterhält eine ATM-Fazilität mit einer Kapazität von bis zu $100,0 Millionen und hat bislang rund 27,3 Millionen Aktien für Nettomittelzuflüsse von etwa $81,8 Millionen veräußert. Die Platzierungsbedingungen sehen Händlerkonzessionen von bis zu $0,144 je Aktie, geschätzte Emissionskosten von rund $0,4 Millionen sowie die Erstattung von bis zu $15.000 für FINRA-Anwaltsgebühren vor. Der Prospekt nennt umfangreiche Risiken: klinische und regulatorische Verzögerungen für Anaphylm, Libervant und AQST-108, Produktions- und Kommerzialisierungsrisiken, mögliche weitere Verwässerung durch künftige Kapitalbeschaffungen, Abhängigkeit vom Umsatz eines auslaufenden lizenzierten Produkts (Suboxone®), Ausfallrisiken bei Verbindlichkeiten, Risiken im Bereich geistiges Eigentum und Rechtsstreitigkeiten sowie allgemeine Markt-, geopolitische und makroökonomische Risiken. Die Underwriter können den Markt stabilisieren oder Short-Positionen decken; Sperrfristen und die üblichen Haftungsfreistellungen sind beschrieben.
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Insights
TL;DR: This is a typical equity offering to raise capital that increases share count and highlights material clinical and liquidity risks.
The prospectus supplement details an at-the-market and underwritten offering that will increase fully diluted share count and may further dilute existing holders if options, warrants or RSUs are exercised. The company explicitly discloses prior ATM activity that generated approximately $81.8 million from ~27.3 million shares, indicating prior reliance on equity markets for funding. Key investor considerations are the current outstanding share base (99.35 million pre-offering), the offering size (21.25 million shares), and underwriting economics including a dealer concession up to $0.144 per share and estimated expenses of ~$0.4 million plus a $15,000 FINRA fee reimbursement. From a financial perspective, the document signals ongoing capital needs and exposure to market financing conditions rather than operating profitability improvements.
TL;DR: Multiple regulatory and clinical-development risks are highlighted; potential FDA requirements and exclusivity challenges could materially affect product approvals and market access.
The filing enumerates specific regulatory risks for Anaphylm, Libervant and AQST-108 including possible FDA comments on the NDA, need for additional clinical studies, PK/PD comparability concerns, and the challenge of overcoming another product's seven-year orphan exclusivity for certain Libervant pediatric indications. These are material near-term development risks because they directly affect the timing and likelihood of approval and subsequent commercialization. For investors, these points increase binary outcomes around product approvals and underscore why additional equity financing is being pursued. Given these regulatory uncertainties, the offering could be considered dilutive precautionary capital to fund development and regulatory responses.
Aquestive Therapeutics offre 21.250.000 azioni ordinarie, quotate al Nasdaq con il simbolo "AQST", con consegna prevista approssimativamente per il 15 agosto 2025. Il supplemento indica che l'ultimo prezzo di vendita riportato al Nasdaq è stato $4,01 il 13 agosto 2025 e che, prima di questa offerta, erano in circolazione 99.353.270 azioni al 30 giugno 2025. La documentazione rivela varie potenziali fonti di diluizione — tra cui opzioni, RSU, PSU, warrant e azioni riservate — e, per i fini dell'offerta, presume l'assenza di esercizi. La società mantiene una linea ATM con capacità fino a $100,0 milioni, avendo venduto finora circa 27,3 milioni di azioni per proventi netti di circa $81,8 milioni. I termini di collocamento prevedono conguagli per i dealer fino a $0,144 per azione, spese stimate dell'offerta di circa $0,4 milioni e il rimborso fino a $15.000 per le parcelle del consulente FINRA. Il prospetto elenca numerosi rischi: ritardi clinici e regolatori per Anaphylm, Libervant e AQST-108, rischi legati alla produzione e alla commercializzazione, possibile ulteriore diluizione da future raccolte di capitale, dipendenza dai ricavi di un prodotto con licenza in fase di cessazione (Suboxone®), rischio di inadempienza sul debito, rischi di proprietà intellettuale e contenziosi, oltre a rischi di mercato, geopolitici e macroeconomici. Gli underwriter possono stabilizzare il mercato o coprire posizioni corte; sono descritte inoltre clausole di lock-up e le consuete indennità previste dall'accordo di collocamento.
Aquestive Therapeutics ofrece 21.250.000 acciones ordinarias, cotizadas en Nasdaq bajo el símbolo "AQST", con entrega prevista alrededor del 15 de agosto de 2025. El suplemento indica que el último precio de venta reportado en Nasdaq fue $4,01 el 13 de agosto de 2025 y que, antes de esta oferta, había 99.353.270 acciones en circulación al 30 de junio de 2025. El expediente revela diversas fuentes de dilución potencial, incluyendo opciones, RSU, PSU, warrants y acciones reservadas, y, a los efectos de la oferta, supone que no habrá ejercicios. La compañía mantiene una línea ATM con capacidad de hasta $100,0 millones, habiendo vendido hasta la fecha aproximadamente 27,3 millones de acciones por ingresos netos de alrededor de $81,8 millones. Los términos de colocación señalan concesiones a los distribuidores de hasta $0,144 por acción, gastos estimados de la oferta de aproximadamente $0,4 millones y el reembolso de hasta $15.000 por honorarios del asesor FINRA. El prospecto enumera numerosos riesgos: retrasos clínicos y regulatorios para Anaphylm, Libervant y AQST-108, riesgos de fabricación y comercialización, posible dilución adicional por futuras captaciones de capital, dependencia de los ingresos de un producto licenciado en fase de retirada (Suboxone®), riesgo de incumplimiento de deuda, riesgos de propiedad intelectual y litigios, y riesgos generales de mercado, geopolíticos y macroeconómicos. Los colocadores pueden estabilizar o cubrir posiciones cortas en el mercado; también se describen las restricciones de bloqueo y las indemnizaciones habituales de la suscripción.
Aquestive Therapeutics는 보통주 21,250,000주를 제안하며, 나스닥 티커는 "AQST"이고 인도 예정일은 2025년 8월 15일경입니다. 보충 서류는 마지막 보고된 나스닥 거래 가격이 2025년 8월 13일 $4.01였고, 본 공모 이전인 2025년 6월 30일 기준 발행주식 수는 99,353,270주였다고 명시합니다. 서류는 옵션, RSU, PSU, 워런트 및 예약주식 등 희석 요인을 여러 가지로 밝히며, 본 공모 목적상에는 권리행사가 없을 것으로 가정합니다. 회사는 최대 $1억 규모의 ATM(추가주식매출인출) 시설을 유지하고 있으며, 현재까지 약 2,730만 주를 매각해 순수입 약 $8,180만을 확보했습니다. 인수조건에는 주당 최대 $0.144의 딜러 보수, 약 $0.4백만의 예상 공모비용, FINRA 자문 수임료 최대 $15,000 환급이 포함됩니다. 설명서에는 Anaphylm, Libervant 및 AQST-108의 임상·규제 지연, 제조 및 상업화 리스크, 향후 자본조달로 인한 추가 희석 가능성, 라이선스 종료 예정 제품(Suboxone®)에 대한 매출 의존, 부채 디폴트 위험, 지적재산권 및 소송 리스크, 시장·지정학적·거시경제 리스크 등 광범위한 위험 요소가 열거되어 있습니다. 인수단은 시장 안정화 또는 숏커버를 시행할 수 있으며, 락업 제한 및 일반적인 인수인 보상 조항도 기술되어 있습니다.
Aquestive Therapeutics propose 21 250 000 actions ordinaires, cotées au Nasdaq sous le symbole "AQST", avec livraison prévue vers le 15 août 2025. Le supplément indique que le dernier cours de vente reporté au Nasdaq était de 4,01 $ le 13 août 2025 et qu'avant cette offre il y avait 99 353 270 actions en circulation au 30 juin 2025. Le dépôt dévoile diverses sources potentielles de dilution, notamment les options, RSU, PSU, warrants et actions réservées, et suppose, pour les besoins de l'offre, qu'aucune levée n'a lieu. La société dispose d'un mécanisme ATM d'une capacité maximale de 100,0 millions de dollars, ayant vendu à ce jour environ 27,3 millions d'actions pour des produits nets d'environ 81,8 millions de dollars. Les conditions du placement prévoient des concessions aux teneurs de marché pouvant atteindre 0,144 $ par action, des frais estimés de l'offre d'environ 0,4 million de dollars et le remboursement jusqu'à 15 000 $ des honoraires du conseil FINRA. Le prospectus énumère de nombreux risques : retards cliniques et réglementaires concernant Anaphylm, Libervant et AQST-108, risques de fabrication et de commercialisation, dilution supplémentaire possible en cas de futurs appels de capitaux, dépendance aux revenus d'un produit sous licence en fin de cycle (Suboxone®), risque de défaut sur la dette, risques de propriété intellectuelle et de litiges, ainsi que risques de marché, géopolitiques et macroéconomiques généraux. Les preneurs fermes peuvent stabiliser ou couvrir des positions courtes sur le marché ; des restrictions de lock-up et les habituelles indemnités d'émission sont également décrites.
Aquestive Therapeutics bietet 21.250.000 Stammaktien an, die an der Nasdaq unter dem Kürzel "AQST" gehandelt werden, mit geplanter Lieferung circa 15. August 2025. Der Nachtrag führt aus, dass der zuletzt gemeldete Nasdaq-Verkaufspreis am 13. August 2025 bei $4,01 lag und vor dieser Emission am 30. Juni 2025 insgesamt 99.353.270 Aktien ausstanden. Die Einreichung benennt verschiedene mögliche Verwässerungsquellen – darunter Optionen, RSU, PSU, Warrants und reservierte Aktien – und geht für Zwecken dieses Angebots von keiner Ausübung aus. Das Unternehmen unterhält eine ATM-Fazilität mit einer Kapazität von bis zu $100,0 Millionen und hat bislang rund 27,3 Millionen Aktien für Nettomittelzuflüsse von etwa $81,8 Millionen veräußert. Die Platzierungsbedingungen sehen Händlerkonzessionen von bis zu $0,144 je Aktie, geschätzte Emissionskosten von rund $0,4 Millionen sowie die Erstattung von bis zu $15.000 für FINRA-Anwaltsgebühren vor. Der Prospekt nennt umfangreiche Risiken: klinische und regulatorische Verzögerungen für Anaphylm, Libervant und AQST-108, Produktions- und Kommerzialisierungsrisiken, mögliche weitere Verwässerung durch künftige Kapitalbeschaffungen, Abhängigkeit vom Umsatz eines auslaufenden lizenzierten Produkts (Suboxone®), Ausfallrisiken bei Verbindlichkeiten, Risiken im Bereich geistiges Eigentum und Rechtsstreitigkeiten sowie allgemeine Markt-, geopolitische und makroökonomische Risiken. Die Underwriter können den Markt stabilisieren oder Short-Positionen decken; Sperrfristen und die üblichen Haftungsfreistellungen sind beschrieben.
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Per Share | Total | |||||
Offering price | $4.00 | $85,000,000 | ||||
Underwriting discounts and commissions(1) | $0.24 | $5,100,000 | ||||
Proceeds to us, before expenses | $3.76 | $79,900,000 | ||||
(1) | See “Underwriting” for a description of compensation payable to the underwriters. |
Leerink Partners | Cantor | Oppenheimer & Co. | ||||
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Page | |||
ABOUT THIS PROSPECTUS SUPPLEMENT | S-1 | ||
PROSPECTUS SUPPLEMENT SUMMARY | S-2 | ||
THE OFFERING | S-4 | ||
RISK FACTORS | S-5 | ||
SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS | S-8 | ||
USE OF PROCEEDS | S-11 | ||
DIVIDEND POLICY | S-12 | ||
DILUTION | S-13 | ||
UNDERWRITING | S-14 | ||
LEGAL MATTERS | S-22 | ||
EXPERTS | S-22 | ||
WHERE YOU CAN FIND MORE INFORMATION | S-22 | ||
INCORPORATION BY REFERENCE | S-23 | ||
Page | |||
ABOUT THIS PROSPECTUS | 1 | ||
SUMMARY | 2 | ||
RISK FACTORS | 6 | ||
SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS | 7 | ||
USE OF PROCEEDS | 10 | ||
DESCRIPTION OF CAPITAL STOCK | 11 | ||
DESCRIPTION OF DEBT SECURITIES | 15 | ||
DESCRIPTION OF WARRANTS | 22 | ||
DESCRIPTION OF RIGHTS | 24 | ||
DESCRIPTION OF UNITS | 26 | ||
PLAN OF DISTRIBUTION | 27 | ||
LEGAL MATTERS | 30 | ||
EXPERTS | 30 | ||
WHERE YOU CAN FIND MORE INFORMATION | 30 | ||
INCORPORATION OF CERTAIN INFORMATION BY REFERENCE | 31 | ||
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• | 7,186,867 shares of common stock issuable upon exercise of outstanding options pursuant to our stock incentive plans at a weighted average option exercise price of $5.30 per share as of June 30, 2025; |
• | 3,290,351 shares of common stock issuable upon vesting of restricted stock units outstanding under our stock incentive plans as of June 30, 2025; |
• | Up to 2,799,525 shares of common stock issuable under performance stock units outstanding under our 2018 Equity Incentive Plan as of June 30, 2025 upon the satisfaction of performance criteria; |
• | 2,910,548 shares of common stock issuable upon exercise of outstanding warrants as of June 30, 2025: 2,750,000 shares of which are exercisable at an exercise price of $2.60 per share, and 160,548 shares of which are exercisable at an exercise price of $0.96 per share; |
• | 1,792,023 shares of common stock reserved for future issuance under the 2018 Equity Incentive Plan as of June 30, 2025; |
• | 1,000,000 shares of common stock reserved for future issuance under the 2022 Inducement Equity Incentive Plan as of June 30, 2025; and |
• | 328,166 shares of common stock available for future purchases under our Employee Stock Purchase Plan as of June 30, 2025. |
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• | risks associated with our development work, including any delays or changes to the timing, cost and success of our product development activities and clinical trials and plans, including those relating to Anaphylm, AQST-108, and our other product candidates; |
• | risk of delays in advancement of the regulatory approval process through the FDA of our product candidates, including for Anaphylm and AQST-108, or failure to receive FDA approval at all of any of these product candidates; |
• | risk of the Company’s ability to generate sufficient clinical data for approval of our product candidates, including with respect to our pharmacokinetic and pharmacodynamic (PK/PD) comparability submission for FDA approval of Anaphylm; |
• | risks associated with our ability to address the FDA’s comments on our NDA, including the risk that the FDA may require additional clinical studies for approval of Anaphylm; |
• | risks associated with the success of any competing products, including generics; |
• | risks and uncertainties inherent in commercializing a new product (including technology risks, financial risks, market risks and implementation risks and regulatory limitations); |
• | risk of development of a sales and marketing capability for commercialization of our product candidates, including Anaphylm, Libervant and AQST-108; |
• | risks associated with the potential impact on the value of the Company of the sale or outlicensing of our product and product candidates, including Libervant and Anaphylm and other product candidates, including the effects of potentially transforming our business model from direct commercialization to depending on royalty and milestone payments from a licensing partner; |
• | risk of insufficient capital and cash resources, including insufficient access to available debt and equity financing, including under our ATM Facility, and revenues from operations, to satisfy all of our |
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• | risk that our manufacturing capabilities will be insufficient to support demand of our product candidates in the U.S. and abroad, if approved by the FDA and other regulatory authorities, and our licensed products in the U.S. and abroad; |
• | risk of eroding market share for Suboxone® as a sunsetting product, which accounts for a substantial part of our current operating revenue; risk of default of our debt instruments; |
• | risks related to the outsourcing of certain sales, marketing and other operational and staff functions to third parties; |
• | risk of the rate and degree of market acceptance in the U.S. and abroad of Libervant, Anaphylm, AQST-108 and our other product candidates, should these product candidates be approved by the FDA and other regulatory authorities, and for our licensed products in the U.S. and abroad; |
• | risk associated with the size and growth of our product markets; |
• | risk associated with our compliance with all FDA and other governmental and customer requirements for our manufacturing facilities; |
• | risks associated with intellectual property rights and infringement claims relating to our products; |
• | risk that our patent applications for our product candidates, including for Anaphylm and AQST-108, will not be timely issued, or issued at all, by the U.S. Patent and Trademark Office; |
• | risk of unexpected patent developments; |
• | risk of legislation and regulatory actions and changes in laws or regulations affecting our business including relating to our products and product candidates and product pricing, reimbursement or access therefor; |
• | risk of loss of significant customers; |
• | risks related to claims and legal proceedings against us including patent infringement, securities, business torts, investigative, product safety or efficacy and antitrust litigation matters; |
• | risk of product recalls and withdrawals; |
• | risks related to any disruptions in our information technology networks and systems, including the impact of cybersecurity attacks; |
• | risk of increased cybersecurity attacks and data accessibility disruptions due to remote working arrangements; |
• | risk of adverse developments affecting the financial services industry; |
• | risks related to inflation and changing interest rates; |
• | risks related to the impact of other pandemic diseases on our business; |
• | risks and uncertainties related to general economic, political (including the Ukraine and Israel wars and other acts of war and terrorism), business, industry, regulatory, financial and market conditions and other unusual items; |
• | risks related to uncertainty about the current U.S. federal administration initiatives and their impact on our business, including imposition of tariffs and other trade restrictions; |
• | risks relating to the restrictions that the terms of the Purchase Agreement place on our operating and financial flexibility; |
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• | other uncertainties affecting us including those described in the “Risk Factors” section of this prospectus supplement, in our most recent Annual Report on Form 10-K and subsequent Quarterly Reports on 10-Q filed with the SEC; and |
• | use of our existing cash and cash equivalents and the anticipated use of net proceeds from this offering. |
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Offering price per share | $4.00 | |||||
Net tangible book value (deficit) per share as of June 30, 2025 | $(0.73) | |||||
Increase in as adjusted net tangible book value per share attributable to new investors in this offering | $0.79 | |||||
As adjusted net tangible book value per share as of June 30, 2025, after giving effect to this offering | $0.06 | |||||
Dilution per share to new investors purchasing shares in this offering | $3.94 | |||||
• | 7,186,867 shares of common stock issuable upon exercise of outstanding options pursuant to our stock incentive plans at a weighted average option exercise price of $5.30 per share as of June 30, 2025; |
• | 3,290,351 shares of common stock issuable upon vesting of restricted stock units outstanding under our stock incentive plans as of June 30, 2025; |
• | Up to 2,799,525 shares of common stock issuable under performance stock units outstanding under our 2018 Equity Incentive Plan as of June 30, 2025 upon the satisfaction of performance criteria; |
• | 2,910,548 shares of common stock issuable upon exercise of outstanding warrants as of June 30, 2025: 2,750,000 shares of which are exercisable at an exercise price of $2.60 per share, and 160,548 shares of which are exercisable at an exercise price of $0.96 per share; |
• | 1,792,023 shares of common stock reserved for future issuance under the 2018 Equity Incentive Plan as of June 30, 2025; |
• | 1,000,000 shares of common stock reserved for future issuance under the 2022 Inducement Equity Incentive Plan as of June 30, 2025; and |
• | 328,166 shares of common stock available for future purchases under our Employee Stock Purchase Plan as of June 30, 2025. |
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Underwriter | Number of Shares | ||
Leerink Partners LLC | 9,350,000 | ||
Cantor Fitzgerald & Co. | 6,375,000 | ||
Oppenheimer & Co. Inc. | 3,187,500 | ||
H.C. Wainwright & Co., LLC | 2,125,000 | ||
Brookline Capital Markets, a division of Arcadia Securities, LLC | 212,500 | ||
Total | 21,250,000 | ||
Per Share | |||
Offering price | $4.00 | ||
Underwriting discounts and commissions | $0.24 | ||
Proceeds, before expenses, to us | $3.76 | ||
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• | offer, pledge, sell or contract to sell any common stock; |
• | sell any option or contract to purchase any common stock; |
• | purchase any option or contract to sell any common stock; |
• | grant any option, right or warrant for the sale of any common stock; |
• | otherwise dispose of or transfer any common stock; |
• | submit or file a registration statement related to the common stock or request or demand that we file a registration statement related to the common stock; or |
• | enter into any hedging, swap or other agreement or any transaction that transfers, in whole or in part, the economic consequence of ownership of any common stock, whether any such swap, agreement or transaction is to be settled by delivery of shares or other securities, in cash or otherwise. |
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A. | to any legal entity which is a qualified investor as defined under Article 2 of the Prospectus Regulation; |
B. | to fewer than 150 natural or legal persons (other than qualified investors as defined under Article 2 of the Prospectus Regulation), subject to obtaining the prior consent of the underwriters; or |
C. | in any other circumstances falling within Article 1(4) of the Prospectus Regulation, |
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A. | to any legal entity which is a qualified investor as defined under Article 2 of the UK Prospectus Regulation; |
B. | to fewer than 150 natural or legal persons (other than qualified investors as defined under Article 2 of the UK Prospectus Regulation), subject to obtaining the prior consent of the underwriters for any such offer; or |
C. | in any other circumstances falling within Section 86 of the Financial Services and Markets Act 2000, |
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a) | a corporation (which is not an accredited investor (as defined in Section 4A of the SFA)) the sole business of which is to hold investments and the entire share capital of which is owned by one or more individuals, each of whom is an accredited investor; or |
b) | a trust (where the trustee is not an accredited investor) whose sole purpose is to hold investments and each beneficiary of the trust is an individual who is an accredited investor, |
a) | to an institutional investor or to a relevant person, or to any person arising from an offer referred to in Section 275(1A) or Section 276(4)(i)(B) of the SFA; |
b) | where no consideration is or will be given for the transfer; |
c) | where the transfer is by operation of law; |
d) | as specified in Section 276(7) of the SFA; or |
e) | as specified in Regulation 32 of the Securities and Futures (Offers of Investments) (Shares and Debentures) Regulations of 2005 of Singapore (Regulation 32). |
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• | released, issued, distributed or caused to be released, issued or distributed to the public in France; or |
• | used in connection with any offer for subscription or sale of the shares to the public in France. |
• | Such offers, sales and distributions will be made in France only: |
• | to qualified investors (investisseurs qualifiés) and/or to a restricted circle of investors (cercle restreint d’investisseurs), in each case investing for their own account, all as defined in, and in accordance with articles L.411-2, D.411-1, D.411-2, D.734-1, D.744-1, D.754-1 and D.764-1 of the French Code monétaire et financier; |
• | to investment services providers authorized to engage in portfolio management on behalf of third parties; or |
• | in a transaction that, in accordance with article L.411-2-II-1"-or-2"-or 3" of the French Code monétaire et financier and article 211-2 of the General Regulations (Règlement Général) of the Autorité des Marchés Financiers, does not constitute a public offer (appel public à l’épargne). |
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• | our Annual Report on Form 10-K for the year ended December 31, 2024, filed with the SEC on March 5, 2025; |
• | our Definitive Proxy Statement on Schedule 14A, filed with the SEC on April 25, 2025 (to the extent incorporated by reference into Part III of our Annual Report on Form 10-K for the fiscal year ended December 31, 2022); |
• | our Quarterly Report on Form 10-Q for the quarter ended March 31, 2025 filed with the SEC on May 12, 2025; |
• | our Quarterly Report on Form 10-Q for the quarter ended June 30, 2025 filed with the SEC on August 11, 2025; |
• | our Current Reports on Form 8-K filed with the SEC on February 12, 2025, June 11, 2025, July 15, 2025 and August 14, 2025 (to the extent the information in such reports is filed and not furnished); and |
• | the description of our common stock contained in our Registration Statement on Form 8-A, filed with the SEC on July 20, 2018, as the description therein has been updated and superseded by the description of our securities contained in Exhibit 4.12 to our Annual Report on Form 10-K for the fiscal year ended December 31, 2024, as filed with the SEC on March 5, 2025. |
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Page | |||
ABOUT THIS PROSPECTUS | 1 | ||
SUMMARY | 2 | ||
RISK FACTORS | 6 | ||
SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS | 7 | ||
USE OF PROCEEDS | 10 | ||
DESCRIPTION OF CAPITAL STOCK | 11 | ||
DESCRIPTION OF DEBT SECURITIES | 15 | ||
DESCRIPTION OF WARRANTS | 22 | ||
DESCRIPTION OF RIGHTS | 24 | ||
DESCRIPTION OF UNITS | 26 | ||
PLAN OF DISTRIBUTION | 27 | ||
LEGAL MATTERS | 30 | ||
EXPERTS | 30 | ||
WHERE YOU CAN FIND MORE INFORMATION | 30 | ||
INCORPORATION OF CERTAIN INFORMATION BY REFERENCE | 31 | ||
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• | designation or classification; |
• | aggregate principal amount or aggregate offering price; |
• | maturity; |
• | original issue discount, if any; |
• | rates and times of payment of interest or dividends, if any; |
• | redemption, conversion, exchange or sinking fund terms, if any; |
• | conversion or exchange prices or rates, if any, and, if applicable, any provisions for changes to or adjustments in the conversion or exchange prices or rates and in the securities or other property receivable upon conversion or exchange; |
• | ranking; |
• | restrictive covenants, if any; |
• | voting or other rights, if any; and |
• | important U.S. federal income tax considerations. |
• | the names of those underwriters or agents; |
• | applicable fees, discounts and commissions to be paid to them; |
• | details regarding over-allotment options, if any; and |
• | the estimated net proceeds to us. |
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• | risks associated with our development work, including any delays or changes to the timing, cost and success of our product development activities and clinical trials and plans, including those relating to Anaphylm™ (epinephrine) Sublingual Film and Libervant™ (diazepam) Buccal Film; |
• | risk of delays in regulatory advancement through the FDA of Anaphylm, Libervant and our other drug candidates or failure to receive FDA approval at all; |
• | the risk that we may not overcome the seven-year orphan drug exclusivity granted by the FDA for the approved nasal spray product of another company in the U.S. in order for Libervant to be granted U.S. market access for any age group of patients; |
• | risk of litigation brought by third parties relating to overcoming their orphan drug exclusivity of an FDA approved product should the FDA approve Libervant for U.S. market access for any age group of this epilepsy patient population; |
• | risk that a competing pediatric epilepsy product of Libervant will receive FDA approval prior to the Company’s receipt of FDA approval of the Libervant NDA for these epilepsy patients between two and five years of age; |
• | risk in obtaining market access for Libervant for other reasons; |
• | risk in obtaining market access from the FDA for our other product candidates; |
• | risk inherent in commercializing a new product (including technology risks, financial risks, market risks and implementation risks and regulatory limitations); |
• | risks and uncertainties concerning the revenue stream from the monetization of our royalty rights for the product KYNMOBI®, as well as the achievement of royalty targets worldwide or in any jurisdiction and certain other commercial targets required for contingent payments under the KYNMOBI® monetization transaction, and the Company may not receive any of the additional aggregate contingent payments under the monetization agreement; |
• | risk of development of a sales and marketing capability for future commercialization of our product candidates; |
• | risk of sufficient capital and cash resources, including access to available debt and equity financing, including under our at-the-market facility and the Common Stock Purchase Agreement entered into with Lincoln Park Capital Fund, LLC on April 12, 2022, and from revenues from operations, to satisfy all of our short-term and longer-term cash requirements and other cash needs, at the times and in the amounts needed, including near-term debt amortization schedules; |
• | risk of failure to satisfy all financial and other debt covenants and of any default under our debt facility; |
• | short-term and long-term liquidity and cash requirements, cash funding and cash burn; |
• | risk related to government and other claims against Indivior Inc. for which we license, manufacture and sell Suboxone® and which accounts for the substantial part of our current operating revenues, including the risk related to the recent product liability multi-district litigation related to Suboxone®; |
• | risks related to the outsourcing of certain operational and staff functions to third parties; |
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• | risk of the rate and degree of market acceptance of our product and product candidates; |
• | the success of any competing products including generics; |
• | risk of the size and growth of our product markets; |
• | risk of compliance with all FDA and other governmental and customer requirements for our manufacturing facilities; |
• | risks associated with intellectual property rights and infringement claims relating to our products; |
• | risk of unexpected patent developments; |
• | risk of legislation and regulatory actions and changes in laws or regulations affecting our business including relating to our products and product candidates and product pricing, reimbursement or access therefor; |
• | risk of loss of significant customers; |
• | risks related to claims and legal proceedings including patent infringement, securities, business torts, investigative, product safety or efficacy and antitrust litigation matters; |
• | risk of product recalls and withdrawals; |
• | risks related to any disruptions in our information technology networks and systems, including the impact of cyberattacks; |
• | risk of increased cybersecurity attacks and data accessibility disruptions due to remote working arrangements; |
• | risks related to adverse developments affecting the financial services industry; |
• | risks related to inflation and rising interest rates; |
• | risks related to the impact of a health pandemic on our business, including with respect to our clinical trials and the site initiation, patient enrollment and timing and adequacy of those clinical trials, regulatory submissions and regulatory reviews and approvals of our product candidates, availability of pharmaceutical ingredients and other raw materials used in our products and product candidates, supply chain, manufacture and distribution of our products and product candidates; and |
• | risks and uncertainties related to general economic, political (including the wars in Ukraine and Israel and other acts of war and terrorism), business, industry, regulatory and market conditions and other unusual items. |
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• | the title of the series of debt securities; |
• | any limit upon the aggregate principal amount that may be issued; |
• | the maturity date or dates; |
• | the form of the debt securities of the series; |
• | the applicability of any guarantees; |
• | whether or not the debt securities will be secured or unsecured, and the terms of any secured debt; |
• | whether the debt securities rank as senior debt, senior subordinated debt, subordinated debt or any combination thereof, and the terms of any subordination; |
• | if the price (expressed as a percentage of the aggregate principal amount thereof) at which such debt securities will be issued is a price other than the principal amount thereof, the portion of the principal amount thereof payable upon declaration of acceleration of the maturity thereof, or if applicable, the portion of the principal amount of such debt securities that is convertible into another security or the method by which any such portion shall be determined; |
• | the interest rate or rates, which may be fixed or variable, or the method for determining the rate and the date interest will begin to accrue, the dates interest will be payable and the regular record dates for interest payment dates or the method for determining such dates; |
• | our right, if any, to defer payment of interest and the maximum length of any such deferral period; |
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• | if applicable, the date or dates after which, or the period or periods during which, and the price or prices at which, we may, at our option, redeem the series of debt securities pursuant to any optional or provisional redemption provisions and the terms of those redemption provisions; |
• | the date or dates, if any, on which, and the price or prices at which we are obligated, pursuant to any mandatory sinking fund or analogous fund provisions or otherwise, to redeem, or at the holder’s option to purchase, the series of debt securities and the currency or currency unit in which the debt securities are payable; |
• | the denominations in which we will issue the series of debt securities, if other than denominations of $1,000 and any integral multiple thereof; |
• | any and all terms, if applicable, relating to any auction or remarketing of the debt securities of that series and any security for our obligations with respect to such debt securities and any other terms which may be advisable in connection with the marketing of debt securities of that series; |
• | whether the debt securities of the series shall be issued in whole or in part in the form of a global security or securities; the terms and conditions, if any, upon which such global security or securities may be exchanged in whole or in part for other individual securities; and the depositary for such global security or securities; |
• | if applicable, the provisions relating to conversion or exchange of any debt securities of the series and the terms and conditions upon which such debt securities will be so convertible or exchangeable, including the conversion or exchange price, as applicable, or how it will be calculated and may be adjusted, any mandatory or optional (at our option or the holders’ option) conversion or exchange features, the applicable conversion or exchange period and the manner of settlement for any conversion or exchange; |
• | if other than the full principal amount thereof, the portion of the principal amount of debt securities of the series which shall be payable upon declaration of acceleration of the maturity thereof; |
• | additions to or changes in the covenants applicable to the particular debt securities being issued, including, among others, the consolidation, merger or sale covenant; |
• | additions to or changes in the events of default with respect to the securities and any change in the right of the trustee or the holders to declare the principal, premium, if any, and interest, if any, with respect to such securities to be due and payable; |
• | additions to or changes in or deletions of the provisions relating to covenant defeasance and legal defeasance; |
• | additions to or changes in the provisions relating to satisfaction and discharge of the indenture; |
• | additions to or changes in the provisions relating to the modification of the indenture both with and without the consent of holders of debt securities issued under the indenture; |
• | the currency of payment of debt securities if other than U.S. dollars and the manner of determining the equivalent amount in U.S. dollars; |
• | whether interest will be payable in cash or additional debt securities at our or the holders’ option and the terms and conditions upon which the election may be made; |
• | the terms and conditions, if any, upon which we will pay amounts in addition to the stated interest, premium, if any and principal amounts of the debt securities of the series to any holder that is not a “United States person” for federal tax purposes; |
• | any restrictions on transfer, sale or assignment of the debt securities of the series; and |
• | any other specific terms, preferences, rights or limitations of, or restrictions on, the debt securities, any other additions or changes in the provisions of the indenture, and any terms that may be required by us or advisable under applicable laws or regulations. |
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• | if we fail to pay interest when due and payable and our failure continues for 90 days and the time for payment has not been extended; |
• | if we fail to pay the principal, premium or sinking fund payment, if any, when due and payable at maturity, upon redemption or repurchase or otherwise, and the time for payment has not been extended; |
• | if we fail to observe or perform any other covenant contained in the debt securities or the indenture, other than a covenant specifically relating to another series of debt securities, and our failure continues for 90 days after we receive notice from the trustee or we and the trustee receive notice from the holders of at least 25% in aggregate principal amount of the outstanding debt securities of the applicable series; and |
• | if specified events of bankruptcy, insolvency or reorganization occur. |
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• | the direction so given by the holder is not in conflict with any law or the applicable indenture; and |
• | subject to its duties under the Trust Indenture Act, the trustee need not take any action that might involve it in personal liability or might be unduly prejudicial to the holders not involved in the proceeding. |
• | the holder has given written notice to the trustee of a continuing event of default with respect to that series; |
• | the holders of at least 25% in aggregate principal amount of the outstanding debt securities of that series have made a written request and such holders have offered reasonable indemnity to the trustee or security satisfactory to it against any loss, liability or expense or to be incurred in compliance with instituting the proceeding as trustee; and |
• | the trustee does not institute the proceeding and does not receive from the holders of a majority in aggregate principal amount of the outstanding debt securities of that series other conflicting directions within 90 days after the notice, request and offer. |
• | to cure any ambiguity, defect or inconsistency in the indenture; |
• | to comply with the provisions described above under “Description of Debt Securities—Consolidation, Merger or Sale;” |
• | to comply with any requirements of the SEC in connection with the qualification of any indenture under the Trust Indenture Act; |
• | to add to, delete from or revise the conditions, limitations, and restrictions on the authorized amount, terms, or purposes of issue, authentication and delivery of debt securities, as set forth in the indenture; |
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• | to provide for the issuance of and establish the form and terms and conditions of the debt securities of any series as provided above under “Description of Debt Securities—General” to establish the form of any certifications required to be furnished pursuant to the terms of the indenture or any series of debt securities, or to add to the rights of the holders of any series of debt securities; |
• | to evidence and provide for the acceptance of appointment under any indenture by a successor trustee; |
• | to provide for uncertificated debt securities and to make all appropriate changes for such purpose; |
• | to add such new covenants, restrictions, conditions or provisions for the benefit of the holders, to make the occurrence, or the occurrence and the continuance, of a default in any such additional covenants, restrictions, conditions or provisions an event of default or to surrender any right or power conferred to us in the indenture; or |
• | to make any change that does not adversely affect the interests of any holder of debt securities of any series in any material respect. |
• | extending the fixed maturity of any debt securities of any series; |
• | reducing the principal amount, reducing the rate of or extending the time of payment of interest, or reducing any premium payable upon the redemption of any series of any debt securities; or |
• | reducing the percentage of debt securities, the holders of which are required to consent to any amendment, supplement, modification or waiver. |
• | register the transfer or exchange of debt securities of the series; |
• | replace stolen, lost or mutilated debt securities of the series; |
• | maintain paying agencies; |
• | hold monies for payment in trust; |
• | recover excess money held by the trustee; |
• | compensate and indemnify the trustee; and |
• | appoint any successor trustee. |
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• | issue, register the transfer of, or exchange any debt securities of that series during a period beginning at the opening of business 15 days before the day of mailing a notice of redemption of any debt securities that may be selected for redemption and ending at the close of business on the day of the mailing; or |
• | register the transfer of or exchange any debt securities so selected for redemption, in whole or in part, except the unredeemed portion of any debt securities we are redeeming in part. |
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• | the title of such securities; |
• | the offering and exercise price or prices and aggregate number of warrants offered; |
• | the currency or currencies for which the warrants may be purchased; |
• | if applicable, the designation and terms of the securities with which the warrants are issued, and the number of warrants issued with each such security or each principal amount of such security; |
• | if applicable, the date on and after which the warrants and the related securities will be separately transferable; |
• | if applicable, the minimum or maximum amount of such warrants which may be exercised at any one time; |
• | in the case of warrants to purchase debt securities, the principal amount of debt securities purchasable upon exercise of one warrant and the price at which, and currency in which, this principal amount of debt securities may be purchased upon such exercise; |
• | in the case of warrants to purchase common stock or preferred stock, the number of shares of common stock or preferred stock, as the case may be, purchasable upon the exercise of one warrant and the price at which, and the currency in which, these shares may be purchased upon such exercise; |
• | the effect of any merger, consolidation, sale or other disposition of our business on the warrant agreements and the warrants; |
• | the terms of any rights to redeem or call the warrants; |
• | the terms of any rights to force the exercise of the warrants; |
• | any provisions for changes to or adjustments in the exercise price or number of securities issuable upon exercise of the warrants; |
• | the dates on which the right to exercise the warrants will commence and expire; |
• | the manner in which the warrant agreements and warrants may be modified; |
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• | a discussion of any material or special U.S. federal income tax consequences of holding or exercising the warrants; |
• | the terms of the securities issuable upon exercise of the warrants; and |
• | any other specific terms, preferences, rights or limitations of or restrictions on the warrants. |
• | in the case of warrants to purchase debt securities, the right to receive payments of principal of, or premium, if any, or interest on, the debt securities purchasable upon exercise or to enforce covenants in the applicable indenture; or |
• | in the case of warrants to purchase common stock or preferred stock, the right to receive dividends, if any, or, payments upon our liquidation, dissolution or winding up or to exercise voting rights, if any. |
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• | the title and aggregate number of the rights; |
• | the subscription price or a formula for the determination of the subscription price for the rights and the currency or currencies in which the subscription price may be payable; |
• | if applicable, the designation and terms of the securities with which the rights are issued and the number of rights issued with each such security or each principal amount of such security; |
• | the number or a formula for the determination of the number of the rights issued to each stockholder; |
• | the extent to which the rights are transferable; |
• | in the case of rights to purchase debt securities, the principal amount of debt securities purchasable upon exercise of one right; |
• | in the case of rights to purchase common stock or preferred stock, the type of stock and number of shares of stock purchasable upon exercise of one right; |
• | the date on which the right to exercise the rights will commence, and the date on which the rights will expire (subject to any extension); |
• | if applicable, the minimum or maximum amount of the rights that may be exercised at any one time; |
• | the extent to which such rights include an over-subscription privilege with respect to unsubscribed securities; |
• | if applicable, the procedures for adjusting the subscription price and number of shares of common stock or preferred stock purchasable upon the exercise of each right upon the occurrence of certain events, including stock splits, reverse stock splits, combinations, subdivisions or reclassifications of common stock or preferred stock; |
• | the effect on the rights of any merger, consolidation, sale or other disposition of our business; |
• | the terms of any rights to redeem or call the rights; |
• | information with respect to book-entry procedures, if any; |
• | the terms of the securities issuable upon exercise of the rights; |
• | if applicable, the material terms of any standby underwriting, backstop or other purchase arrangement that we may enter into in connection with the rights offering; |
• | if applicable, a discussion of certain U.S. Federal income tax considerations; and |
• | any other terms of the rights, including terms, procedures and limitations relating to the exchange and exercise of the rights. |
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• | the designation and terms of the units and of the securities comprising the units, including whether and under what circumstances those securities may be held or transferred separately; |
• | any provisions of the governing unit agreement that differ from those described below; and |
• | any provisions for the issuance, payment, settlement, transfer or exchange of the units or of the securities comprising the units. |
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• | underwritten public offerings; |
• | negotiated transactions; |
• | block trades; |
• | “At the Market Offerings,” within the meaning of Rule 415(a)(4) of the Securities Act, into an existing trading market, at prevailing market prices; or |
• | through a combination of these methods. |
• | at a fixed price or prices, which may be changed; |
• | at market prices prevailing at the time of sale; |
• | at prices related to such prevailing market prices; or |
• | at negotiated prices. |
• | the name or names of the underwriters, dealers or agents, if any; |
• | if the securities are to be offered through the selling efforts of brokers or dealers, the plan of distribution and the terms of any agreement, arrangement, or understanding entered into with broker(s) or dealer(s) prior to the effective date of the registration statement, and, if known, the identity of any broker(s) or dealer(s) who will participate in the offering and the amount to be offered through each; |
• | the purchase price of the securities or other consideration therefor, and the proceeds, if any, we will receive from the sale; |
• | if any of the securities being registered are to be offered otherwise than for cash, the general purposes of the distribution, the basis upon which the securities are to be offered, the amount of compensation and other expenses of distribution, and by whom they are to be borne; |
• | any delayed delivery arrangements; |
• | any over-allotment or other options under which underwriters may purchase additional securities from us; |
• | any agency fees or underwriting discounts and other items constituting agents’ or underwriters’ compensation; |
• | any public offering price; |
• | any discounts, commissions or concessions allowed or reallowed or paid to dealers; |
• | the identity and relationships of any finders, if applicable; and |
• | any securities exchange or market on which the securities may be listed. |
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• | our Annual Report on Form 10-K for the year ended December 31, 2023, filed with the SEC on March 5, 2024; |
• | our Definitive Proxy Statement on Schedule 14A, filed with the SEC on April 28, 2023 (to the extent incorporated by reference into Part III of our Annual Report on Form 10-K for the fiscal year ended December 31, 2022); |
• | our Current Reports on Form 8-K filed with the SEC on March 15, 2024, March 21, 2024, April 1, 2024 and April 22, 2024 (to the extent the information in such report is filed and not furnished); and |
• | the description of our common stock contained in our Registration Statement on Form 8-A, filed with the SEC on July 20, 2018, as the description therein has been updated and superseded by the description of our securities contained in Exhibit 4.7 to our Annual Report on Form 10-K for the fiscal year ended December 31, 2019, as filed with the SEC on March 11, 2020. |
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Leerink Partners | Cantor | Oppenheimer & Co. | ||||