[S-3ASR] Roivant Sciences Ltd. SEC Filing
Roivant Sciences Ltd. filed a Form S-3ASR prospectus dated October 3, 2025 establishing a base shelf and a Sales Agreement to offer common shares and other securities on a continuous or delayed basis. The prospectus expressly permits the issuance of Common Shares up to an aggregate offering price of $400.0 million pursuant to a Sales Agreement dated September 19, 2022 with TD Securities (USA) LLC (successor to Cowen and Company, LLC); as of filing $0 of that $400.0 million had been sold. The company states it has an active share repurchase program and may or may not use this registration statement.
The document discloses capital structure data as of June 30, 2025: 682,229,832 Common Shares issued and outstanding, 138,728,031 shares issuable upon exercise of options (weighted average exercise price $8.70), and 72,009,936 shares issuable upon settlement of RSUs/PRSU/CVARs. Audited financial statements for year ended March 31, 2025 and internal control effectiveness are reported by Ernst & Young LLP. The prospectus highlights extensive risk factors related to biopharmaceutical development, capital needs, regulatory approval, intellectual property, controlling shareholders, dilution and litigation risk, and states Common Shares trade on Nasdaq under ROIV.
Roivant Sciences Ltd. ha presentato un prospetto Form S-3ASR datato 3 ottobre 2025 che stabilisce una base di collocamento (base shelf) e un Accordo di Vendita per offrire azioni ordinarie e altri titoli in modo continuo o differito. Il prospetto consente espressamente l’emissione di Azioni Ordinarie fino a un prezzo aggregato di offerta di $400,0 milioni ai sensi di un Accordo di Vendita datato 19 settembre 2022 con TD Securities (USA) LLC (successore di Cowen and Company, LLC); al momento della presentazione sono stati venduti $0 di quell’importo. L’azienda afferma di avere un programma attivo di riacquisto azionario e potrebbe o meno utilizzare questa dichiarazione di registrazione.
Il documento rivela dati sulla struttura del capitale al 30 giugno 2025: 682.229.832 Azioni Ordinarie emesse e in circolazione, 138.728.031 azioni proponibili all’esercizio di opzioni (prezzo medio di esercizio $8,70), e 72.009.936 azioni proponibili al regolamento di RSU/PRSU/CVAR. I bilanci certificati per l’anno chiuso al 31 marzo 2025 e l’efficacia del controllo interno sono riportati da Ernst & Young LLP. Il prospetto evidenzia ampi fattori di rischio legati allo sviluppo biofarmaceutico, alle esigenze di capitale, all’approvazione regolamentare, alla proprietà intellettuale, agli azionisti di controllo, alla diluizione e al rischio di contenziosi, e afferma che le Azioni Ordinarie sono negoziate sul Nasdaq con simbolo ROIV.
Roivant Sciences Ltd. presentó un prospecto Form S-3ASR con fecha 3 de octubre de 2025 que establece una base de colocación y un Acuerdo de Venta para ofrecer acciones comunes y otros valores de forma continua o diferida. El prospecto permite expresamente la emisión de Acciones Comunes por un precio de oferta agregado de $400,0 millones conforme a un Acuerdo de Venta fechado el 19 de septiembre de 2022 con TD Securities (USA) LLC (sucesor de Cowen and Company, LLC); al momento de la presentación, se había vendido $0 de ese monto. La empresa indica que tiene un programa activo de recompra de acciones y podría o no utilizar este formulario de registro.
El documento divulga datos de la estructura de capital al 30 de junio de 2025: 682,229,832 Acciones Comunes emitidas y en circulación, 138,728,031 acciones susceptibles de ser ejercidas mediante opciones (precio medio de ejercicio $8,70), y 72,009,936 acciones susceptibles de liquidación de RSU/PRSU/CVARs. Los estados financieros auditados para el año terminado el 31 de marzo de 2025 y la eficacia del control interno son reportados por Ernst & Young LLP. El prospecto destaca amplios factores de riesgo relacionados con el desarrollo biofarmacéutico, las necesidades de capital, la aprobación regulatoria, la propiedad intelectual, los accionistas controladores, la dilución y el riesgo de litigios, y señala que las Acciones Comunes cotizan en Nasdaq bajo el símbolo ROIV.
Roivant Sciences Ltd.가 2025년 10월 3일자로 날짜가 기재된 Form S-3ASR 전문을 제출했고, 기본 Shelf(일반 인가 한도) 및 매출 계약(Sales Agreement)을 설정하여 보통주 및 기타 증권을 지속적 또는 지연 방식으로 제공하기로 했습니다. 전문은 2022년 9월 19일자 TD Securities (USA) LLC(Cowen and Company, LLC의 계승자)와의 매출 계약에 따라 총액 $400.0백만의 가격으로 일반주를 발행할 수 있음을 명시적으로 허용합니다. 제출 시점에 해당 금액의 $0가 매각되었습니다. 회사는 활성적인 자사주 매입 프로그램을 보유하고 있으며 이 등록서를 사용할지 여부는 확정되지 않았습니다.
문서는 2025년 6월 30일 기준 자본 구조 데이터를 공개합니다: 682,229,832주가 발행 및 유통 중인 보통주, 138,728,031주가 옵션 행사를 통해 취득 가능(가중평균 행사 가격 $8.70), 그리고 72,009,936주가 RSU/PRSU/CVARs의settlement에 의해 발행 가능합니다. 2025년 3월 31일로 종료되는 회계연도에 대한 감사 재무제표와 내부통제의 효과성은 Ernst & Young LLP에 의해 보고됩니다. 전문은 생물의약품 개발, 자본 필요, 규제 승인, 지적 재산권, 지배주주, 희석 및 소송 위험과 관련된 광범위한 위험 요소를 강조하며, 보통주는 ROIV로 나스닥에서 거래됩니다.
Roivant Sciences Ltd. a déposé un prospectus Form S-3ASR daté du 3 octobre 2025 établissant une ligne de base de mise en vente et un Accord de Vente pour offrir des actions ordinaires et d’autres valeurs sur une base continue ou différée. Le prospectus autorise expressément l’émission d’Actions Ordinaires pour un prix d’offre agrégé de $400,0 millions en vertu d’un Accord de Vente daté du 19 septembre 2022 avec TD Securities (USA) LLC (successeur de Cowen and Company, LLC); à la date de dépôt, $0 de ce montant avait été vendu. La société indique qu’elle dispose d’un programme actif de rachat d’actions et peut ou non utiliser cet enregistrement.
Le document divulgue des données sur la structure du capital au 30 juin 2025: 682 229 832 Actions Ordinaires émises et en circulation, 138 728 031 actions susceptibles d’être exercées par des options (prix d’exercice moyen $8,70), et 72 009 936 actions susceptibles de règlement des RSU/PRSU/CVARs. Les états financiers audités pour l’année terminée le 31 mars 2025 et l’efficacité du contrôle interne sont signalés par Ernst & Young LLP. Le prospectus met en évidence d’importants facteurs de risque liés au développement biopharmaceutique, aux besoins en capital, à l’approbation réglementaire, à la propriété intellectuelle, aux actionnaires contrôlants, à la dilutions et au risque de litige, et indique que les Actions Ordinaires se négocient sur Nasdaq sous le symbole ROIV.
Roivant Sciences Ltd. hat ein Form S-3ASR Prospekt datiert auf den 3. Oktober 2025 eingereicht, der eine Basis- shelf und eine Verkaufsvereinbarung zur kontinuierlichen oder verzögerten Angebotserstellung von Stammaktien und anderen Wertpapieren festlegt. Der Prospekt erlaubt ausdrücklich die Ausgabe von Stammaktien bis zu einem Gesamtangebotswert von $400,0 Millionen gemäß einer Verkaufsvereinbarung vom 19. September 2022 mit TD Securities (USA) LLC (Nachfolger von Cowen and Company, LLC); zum Zeitpunkt der Einreichung waren $0 von diesem Betrag verkauft worden. Das Unternehmen gibt an, ein aktives Aktienrückkaufprogramm zu haben und diese Registrierungsunterlage möglicherweise zu verwenden oder nicht.
Das Dokument macht Kapitalstruktur-Daten zum 30. Juni 2025 öffentlich: 682.229.832 ausgegebene und umlaufende Stammaktien, 138.728.031 Aktien, die durch Ausübung von Optionen erworben werden können (gewichteter durchschnittlicher Ausübungspreis $8,70), und 72.009.936 Aktien, die durch settlements von RSU/PRSU/CVARs ausgegeben werden können. Geprüfte Jahresabschlüsse für das am 31. März 2025 endende Geschäftsjahr und die Wirksamkeit der internen Kontrolle werden von Ernst & Young LLP berichtet. Der Prospekt hebt umfangreiche Risikofaktoren im Zusammenhang mit der biopharmazeutischen Entwicklung, Kapitalbedarf, regulatorischer Genehmigung, geistigem Eigentum, beherrschenden Aktionären, Verwässerung und Rechtsrisiken hervor und gibt an, dass Stammaktien an der Nasdaq unter dem Symbol ROIV gehandelt werden.
Roivant Sciences Ltd. قدمت نشرة من Form S-3ASR بتاريخ 3 أكتوبر 2025 تتيح قاعدة رف Shelf واتفاق بيع لعرض الأسهم العادية وأوراق مالية أخرى بشكل مستمر أو متأخر. تسمح النشرة صراحةً بإصدار الأسهم العادية حتى سعر عروض مجمع قدره $400.0 مليون19 سبتمبر 2022 مع TD Securities (USA) LLC (خلف Cowen and Company, LLC); حتى وقت الملَف، لم يتم بيع $0 من هذا المبلغ. تشير الشركة إلى وجود برنامج شراء أسهم نشط وقد تستخدم هذه البيان التنظيمي أو لا تستخدمه.
يكشف الوثيقة بيانات هيكل رأس المال حتى 30 يونيو 2025: 682,229,832 سهم عادي issued and outstanding، و 138,728,031 أسهم يمكن إصدارهـا عند ممارسة الخيارات (متوسط سعر ممارسة $8.70)، و 72,009,936 أسهم قابلة للتسوية لـ RSUs/PRSU/CVARs. تُورد البيانات المالية المدققة للسنة المنتهية في 31 مارس 2025 وكفاءة الرقابة الداخلية من قبل Ernst & Young LLP. تبرز النشرة مخاطر واسعة مرتبطة بتطوير الأدوية الحيوية، واحتياجات رأس المال، والموافقة التنظيمية، والملكية الفكرية، والمساهمين المسيطرين، والتخفيف وخطر الدعاوى، وتذكر أن الأسهم العادية يتم تداولها في Nasdaq تحت الرمز ROIV.
Roivant Sciences Ltd. 已提交日期为 2025年10月3日 的 Form S-3ASR 招股说明书,设定了基础备货架(base shelf)和销售协议,以持续或延迟方式发行普通股及其他证券。该招股说明书明确允许按与 TD Securities (USA) LLC(Cowen and Company, LLC 的继任者)于 2022年9月19日 签订的销售协议,发行普通股,总发行价不超过 $4.00亿;截至提交时,该金额的 $0 已售出。公司表示其有正在进行的股票回购计划,是否使用本注册声明尚未确定。
文件披露的资本结构数据截止至 2025年6月30日:已发行并在外流通的普通股 682,229,832 股;可通过行使期权取得的股份 138,728,031 股(加权平均行使价 $8.70);通过结算 RSU/PRSU/CVARs 可发行的股份 72,009,936 股。经审计的截至 2025年3月31日 的年度财政报表及内部控制有效性由 Ernst & Young LLP 报告。招股说明书强调与生物制药开发、资金需求、监管批准、知识产权、控股股东、摊薄和诉讼风险相关的广泛风险因素,并指出普通股在纳斯达克交易,代码为 ROIV。
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Insights
TL;DR: Shelf provides flexibility to raise up to $400M; no proceeds sold yet.
The prospectus establishes a shelf and a Sales Agreement allowing issuance of securities, including Common Shares up to $400.0M, giving the company optionality to access capital markets on a continuous basis. The filing explicitly notes $0 of the Sales Agreement amount has been sold as of the date of the prospectus, which means no immediate dilution from this shelf is recorded.
The capital table disclosed as of June 30, 2025—682,229,832 shares outstanding plus 138,728,031 options and 72,009,936 RSU/PRSU/CVAR settlements—identifies potential dilution if those instruments convert or are exercised.
TL;DR: Standard indemnities, Bermuda corporate provisions, and disclosure-by-reference approach are used.
The prospectus uses incorporation by reference of prior SEC filings including the Form 10-K (year ended March 31, 2025) and subsequent reports, and relies on Ernst & Young LLP reports for audited financials. It includes Bermuda law provisions on indemnification and shareholder waivers, and discloses the company’s bye-laws waive shareholder claims against directors/officers except for fraud or dishonesty.
The document also cautions that many risk factors apply (regulatory, IP, trials, controlling shareholders) and notes the Nasdaq symbol ROIV.
Roivant Sciences Ltd. ha presentato un prospetto Form S-3ASR datato 3 ottobre 2025 che stabilisce una base di collocamento (base shelf) e un Accordo di Vendita per offrire azioni ordinarie e altri titoli in modo continuo o differito. Il prospetto consente espressamente l’emissione di Azioni Ordinarie fino a un prezzo aggregato di offerta di $400,0 milioni ai sensi di un Accordo di Vendita datato 19 settembre 2022 con TD Securities (USA) LLC (successore di Cowen and Company, LLC); al momento della presentazione sono stati venduti $0 di quell’importo. L’azienda afferma di avere un programma attivo di riacquisto azionario e potrebbe o meno utilizzare questa dichiarazione di registrazione.
Il documento rivela dati sulla struttura del capitale al 30 giugno 2025: 682.229.832 Azioni Ordinarie emesse e in circolazione, 138.728.031 azioni proponibili all’esercizio di opzioni (prezzo medio di esercizio $8,70), e 72.009.936 azioni proponibili al regolamento di RSU/PRSU/CVAR. I bilanci certificati per l’anno chiuso al 31 marzo 2025 e l’efficacia del controllo interno sono riportati da Ernst & Young LLP. Il prospetto evidenzia ampi fattori di rischio legati allo sviluppo biofarmaceutico, alle esigenze di capitale, all’approvazione regolamentare, alla proprietà intellettuale, agli azionisti di controllo, alla diluizione e al rischio di contenziosi, e afferma che le Azioni Ordinarie sono negoziate sul Nasdaq con simbolo ROIV.
Roivant Sciences Ltd. presentó un prospecto Form S-3ASR con fecha 3 de octubre de 2025 que establece una base de colocación y un Acuerdo de Venta para ofrecer acciones comunes y otros valores de forma continua o diferida. El prospecto permite expresamente la emisión de Acciones Comunes por un precio de oferta agregado de $400,0 millones conforme a un Acuerdo de Venta fechado el 19 de septiembre de 2022 con TD Securities (USA) LLC (sucesor de Cowen and Company, LLC); al momento de la presentación, se había vendido $0 de ese monto. La empresa indica que tiene un programa activo de recompra de acciones y podría o no utilizar este formulario de registro.
El documento divulga datos de la estructura de capital al 30 de junio de 2025: 682,229,832 Acciones Comunes emitidas y en circulación, 138,728,031 acciones susceptibles de ser ejercidas mediante opciones (precio medio de ejercicio $8,70), y 72,009,936 acciones susceptibles de liquidación de RSU/PRSU/CVARs. Los estados financieros auditados para el año terminado el 31 de marzo de 2025 y la eficacia del control interno son reportados por Ernst & Young LLP. El prospecto destaca amplios factores de riesgo relacionados con el desarrollo biofarmacéutico, las necesidades de capital, la aprobación regulatoria, la propiedad intelectual, los accionistas controladores, la dilución y el riesgo de litigios, y señala que las Acciones Comunes cotizan en Nasdaq bajo el símbolo ROIV.
Roivant Sciences Ltd.가 2025년 10월 3일자로 날짜가 기재된 Form S-3ASR 전문을 제출했고, 기본 Shelf(일반 인가 한도) 및 매출 계약(Sales Agreement)을 설정하여 보통주 및 기타 증권을 지속적 또는 지연 방식으로 제공하기로 했습니다. 전문은 2022년 9월 19일자 TD Securities (USA) LLC(Cowen and Company, LLC의 계승자)와의 매출 계약에 따라 총액 $400.0백만의 가격으로 일반주를 발행할 수 있음을 명시적으로 허용합니다. 제출 시점에 해당 금액의 $0가 매각되었습니다. 회사는 활성적인 자사주 매입 프로그램을 보유하고 있으며 이 등록서를 사용할지 여부는 확정되지 않았습니다.
문서는 2025년 6월 30일 기준 자본 구조 데이터를 공개합니다: 682,229,832주가 발행 및 유통 중인 보통주, 138,728,031주가 옵션 행사를 통해 취득 가능(가중평균 행사 가격 $8.70), 그리고 72,009,936주가 RSU/PRSU/CVARs의settlement에 의해 발행 가능합니다. 2025년 3월 31일로 종료되는 회계연도에 대한 감사 재무제표와 내부통제의 효과성은 Ernst & Young LLP에 의해 보고됩니다. 전문은 생물의약품 개발, 자본 필요, 규제 승인, 지적 재산권, 지배주주, 희석 및 소송 위험과 관련된 광범위한 위험 요소를 강조하며, 보통주는 ROIV로 나스닥에서 거래됩니다.
Roivant Sciences Ltd. a déposé un prospectus Form S-3ASR daté du 3 octobre 2025 établissant une ligne de base de mise en vente et un Accord de Vente pour offrir des actions ordinaires et d’autres valeurs sur une base continue ou différée. Le prospectus autorise expressément l’émission d’Actions Ordinaires pour un prix d’offre agrégé de $400,0 millions en vertu d’un Accord de Vente daté du 19 septembre 2022 avec TD Securities (USA) LLC (successeur de Cowen and Company, LLC); à la date de dépôt, $0 de ce montant avait été vendu. La société indique qu’elle dispose d’un programme actif de rachat d’actions et peut ou non utiliser cet enregistrement.
Le document divulgue des données sur la structure du capital au 30 juin 2025: 682 229 832 Actions Ordinaires émises et en circulation, 138 728 031 actions susceptibles d’être exercées par des options (prix d’exercice moyen $8,70), et 72 009 936 actions susceptibles de règlement des RSU/PRSU/CVARs. Les états financiers audités pour l’année terminée le 31 mars 2025 et l’efficacité du contrôle interne sont signalés par Ernst & Young LLP. Le prospectus met en évidence d’importants facteurs de risque liés au développement biopharmaceutique, aux besoins en capital, à l’approbation réglementaire, à la propriété intellectuelle, aux actionnaires contrôlants, à la dilutions et au risque de litige, et indique que les Actions Ordinaires se négocient sur Nasdaq sous le symbole ROIV.
Roivant Sciences Ltd. hat ein Form S-3ASR Prospekt datiert auf den 3. Oktober 2025 eingereicht, der eine Basis- shelf und eine Verkaufsvereinbarung zur kontinuierlichen oder verzögerten Angebotserstellung von Stammaktien und anderen Wertpapieren festlegt. Der Prospekt erlaubt ausdrücklich die Ausgabe von Stammaktien bis zu einem Gesamtangebotswert von $400,0 Millionen gemäß einer Verkaufsvereinbarung vom 19. September 2022 mit TD Securities (USA) LLC (Nachfolger von Cowen and Company, LLC); zum Zeitpunkt der Einreichung waren $0 von diesem Betrag verkauft worden. Das Unternehmen gibt an, ein aktives Aktienrückkaufprogramm zu haben und diese Registrierungsunterlage möglicherweise zu verwenden oder nicht.
Das Dokument macht Kapitalstruktur-Daten zum 30. Juni 2025 öffentlich: 682.229.832 ausgegebene und umlaufende Stammaktien, 138.728.031 Aktien, die durch Ausübung von Optionen erworben werden können (gewichteter durchschnittlicher Ausübungspreis $8,70), und 72.009.936 Aktien, die durch settlements von RSU/PRSU/CVARs ausgegeben werden können. Geprüfte Jahresabschlüsse für das am 31. März 2025 endende Geschäftsjahr und die Wirksamkeit der internen Kontrolle werden von Ernst & Young LLP berichtet. Der Prospekt hebt umfangreiche Risikofaktoren im Zusammenhang mit der biopharmazeutischen Entwicklung, Kapitalbedarf, regulatorischer Genehmigung, geistigem Eigentum, beherrschenden Aktionären, Verwässerung und Rechtsrisiken hervor und gibt an, dass Stammaktien an der Nasdaq unter dem Symbol ROIV gehandelt werden.
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Bermuda (State or Other Jurisdiction of Incorporation or Organization) | 98-1173944 (I.R.S. Employer Identification Number) | ||
Large accelerated filer ☒ | Accelerated filer ☐ | ||
Non-accelerated filer ☐ | Smaller reporting company ☐ | ||
Emerging growth company ☐ | |||
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• | a base prospectus which covers the offering, issuance and sale from time to time of common shares, $0.0000000341740141 par value per share (the “Common Shares”), preference shares, debt securities, warrants to purchase Common Shares, preference shares or debt securities, and units consisting of two or more types of the foregoing securities; and |
• | a prospectus covering the offering, issuance and sale by us of Common Shares up to a maximum aggregate offering price of $400.0 million pursuant to a Sales Agreement, dated September 19, 2022 with TD Securities (USA) LLC, successor to Cowen and Company, LLC (the “Sales Agreement”). |
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Page | |||
About This Prospectus | ii | ||
Prospectus Summary | 1 | ||
Risk Factors | 2 | ||
Forward-Looking Statements | 3 | ||
Use of Proceeds | 5 | ||
Description of Share Capital | 6 | ||
Description of Debt Securities | 13 | ||
Description of Warrants | 19 | ||
Description of Units | 20 | ||
Forms of Securities | 21 | ||
Plan of Distribution | 23 | ||
Legal Matters | 25 | ||
Experts | 25 | ||
Where You Can Find Additional Information | 25 | ||
Incorporation of Certain Information by Reference | 26 | ||
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• | our relatively limited operating history and the inherent uncertainties and risks involved in biopharmaceutical product development and commercialization; |
• | our ability to acquire, in-license or discover new product candidates; |
• | the allocation of capital and personnel across our businesses; |
• | our Vant structure; |
• | potential future payments we may owe in connection with our product candidates; |
• | acquisitions, divestitures and other strategic transactions; |
• | the use of our cash, cash equivalents and marketable securities; |
• | the potential future need for additional capital to fund our operations; |
• | clinical trials and preclinical studies, which are very expensive, time-consuming, difficult to design and implement and involve uncertain outcomes; |
• | unfavorable, uncertain and rapidly changing global and regional economic, political and public health conditions; |
• | the fact that designing and implement clinical trials and preclinical studies is very expensive, time-consuming and difficult; |
• | difficulties we may encounter enrolling and retaining patients in clinical trials, which could adversely affect or otherwise delay clinical development activities; |
• | the results of our preclinical studies and clinical trials not supporting our proposed claims for a product candidate or regulatory approval; |
• | interim, preliminary or top-line data from our clinical trials changing as more data become available or data being delayed due to audit or verification procedures; |
• | changes in product candidate manufacturing or formulation that could result in additional costs or delays; |
• | the fact that obtaining approval of a new drug is an extensive, lengthy, expensive and inherently uncertain process and the FDA or another regulatory authority may delay, limit or deny approval; |
• | the failure of our clinical trials to demonstrate substantial evidence of the safety and efficacy of our product candidates; |
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• | undesirable side effects caused by our product candidates that halt their clinical development, delay or prevent their regulatory approval, limit the scope of any approved label or market acceptance or result in negative consequences; |
• | our inability to obtain regulatory approval for a product candidate in certain jurisdictions, even if we are able to obtain approval in certain other jurisdictions; |
• | the failure of any third-party we rely upon to conduct, supervise and monitor our clinical trials to perform in a satisfactory manner or to comply with applicable legal, regulatory or other requirements; |
• | our reliance on third parties to produce clinical and commercial supplies of our product candidates; |
• | our dependence on key personnel and our ability to attract, motivate and retain highly qualified personnel; |
• | the potential that our use of AI could expose us to liability; |
• | our ability to obtain and maintain patent and other intellectual property protection for our technology and product candidates; |
• | the failure to issue (or the threatening of their validity, patentability, enforceability, breadth or strength of protection) or provide meaningful exclusivity for our product candidates of our patent applications that we own or have in-licensed; |
• | the inadequacy of patent terms and their scope to protect our competitive position; |
• | the fact that our largest shareholders own a significant percentage of our stock and will be able to exert significant control over matters subject to shareholder approval; |
• | dilution of ownership caused by future sales and issuances of our or the Vants’ equity securities or rights to purchase equity securities; |
• | future sales, or the perception of future sales, of our common shares by us or our existing shareholders, and the impact thereof on the price of our common shares; |
• | the outcome of any pending or potential litigation, including but not limited to our expectations regarding the outcome of any such litigation and costs and expenses associated with such litigation; |
• | changes in applicable laws or regulations; |
• | the possibility that we may be adversely affected by other economic, business or competitive factors; and |
• | any other risks and uncertainties indicated from time to time in filings made with the SEC. |
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• | prior to the date of the transaction that resulted in the shareholder becoming an interested shareholder, our board of directors approved either the business combination or the transaction that resulted in the shareholder becoming an interested shareholder; |
• | upon consummation of the transaction that resulted in the shareholder becoming an interested shareholder, the interested shareholder owned at least 85% of our issued and voting shares outstanding at the time the transaction commenced; or |
• | after the date of the transaction that resulted in the shareholder becoming an interested shareholder, the business combination is approved by our board of directors and authorized at an annual or special meeting of shareholders by the affirmative vote of at least 662/3% of our issued and outstanding voting shares that are not owned by the interested shareholder. |
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• | classification as senior or subordinated debt securities; |
• | ranking of the specific series of debt securities relative to other outstanding indebtedness, including subsidiaries’ debt; |
• | if the debt securities are subordinated, the aggregate amount of outstanding indebtedness, as of a recent date, that is senior to the subordinated securities, and any limitation on the issuance of additional senior indebtedness; |
• | the designation, aggregate principal amount and authorized denominations; |
• | the maturity date; |
• | the interest rate, if any, and the method for calculating the interest rate; |
• | the interest payment dates and the record dates for the interest payments; |
• | any mandatory or optional redemption terms or prepayment, conversion, sinking fund or exchangeability or convertibility provisions; |
• | the place where we will pay principal and interest; |
• | if other than denominations of $1,000 or multiples of $1,000, the denominations the debt securities will be issued in; |
• | whether the debt securities will be issued in the form of global securities or certificates; |
• | additional provisions, if any, relating to the defeasance of the debt securities; |
• | the currency or currencies, if other than the currency of the United States, in which principal and interest will be paid; |
• | any United States federal income tax consequences; |
• | the dates on which premium, if any, will be paid; |
• | our right, if any, to defer payment interest and the maximum length of this deferral period; |
• | any listing on a securities exchange; |
• | the initial public offering price; and |
• | other specific terms, including any additional events of default or covenants. |
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• | any insolvency or bankruptcy proceedings, or any receivership, liquidation, reorganization or other similar proceedings which concern us or a substantial part of our property; |
• | a default having occurred for the payment of principal, premium, if any, or interest on or other monetary amounts due and payable on any senior indebtedness or any other default having occurred concerning any senior indebtedness, which permits the holder or holders of any senior indebtedness to accelerate the maturity of any senior indebtedness with notice or lapse of time, or both. Such an event of default must have continued beyond the period of grace, if any, provided for such event of default, and such an event of default shall not have been cured or waived or shall not have ceased to exist; or |
• | the principal of, and accrued interest on, any series of the subordinated debt securities having been declared due and payable upon an event of default pursuant to the subordinated debt indenture. This declaration must not have been rescinded and annulled as provided in the subordinated debt indenture. |
(i) | we default in the payment of principal of such debt securities when it becomes due and payable at maturity, upon acceleration, redemption or mandatory repurchase, including as a sinking fund installment or otherwise; |
(ii) | we default in the payment of interest on such debt securities when it becomes due and payable and such default continues for a period of 30 days or more; |
(iii) | we default in the performance of, or breach, any other covenant or agreement in the indenture with respect to such debt securities or in such debt securities (other than defaults specified in clause (i) or (ii) above) and such default or breach continues for a period of 30 days or more after written notice to |
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(iv) | certain events of bankruptcy, insolvency, reorganization, administration or similar proceedings with respect to us or any material subsidiary has occurred; or |
(v) | any other Events of Default set forth in the prospectus supplement. |
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• | cure any ambiguity, defect or inconsistency; provided that such amendments or supplements do not materially and adversely affect the interests of the holders; |
• | provide for the assumption of our obligations in the case of a merger or consolidation; |
• | comply with any requirements of the SEC in connection with qualification of the indenture under the Trust Indenture Act; |
• | evidence and provide for the acceptance of appointment by a successor trustee and add to or change any of the provisions of the indenture; |
• | establish the form or forms or terms of debt securities of any series or of the coupons appertaining to such debt securities; |
• | provide for uncertificated or unregistered debt securities and make all appropriate changes for such purpose; and |
• | make any change that does not materially and adversely affect the rights of any holder. |
• | change the stated maturity of the principal of, or any sinking fund obligation or any installment of interest on, such holder’s debt security; |
• | reduce the principal amount of such holder’s debt security or the rate of interest thereon (including any amount in respect of original issue discount); |
• | reduce the percentage of outstanding debt securities the consent of whose holders is necessary to modify or amend the indenture with respect to the debt securities; and |
• | reduce the percentage in principal amount of outstanding debt securities the consent of whose holders is required for any supplemental indenture or for any waiver of compliance with certain provisions of the indenture or certain defaults and their consequences provided for in the indenture. |
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• | we have paid or caused to be paid the principal of and interest on such series of debt securities as and when such debt securities become due and payable; |
• | we have delivered to the trustee for cancellation all debt securities of such series that have been authenticated; or |
• | all debt securities of such series not delivered to the trustee for cancellation have become due and payable, or by their terms to become due and payable within one year or are to be called for redemption within one year under arrangements satisfactory to the trustee for the giving of notice of redemption, and we have irrevocably deposited or caused to be deposited with the trustee the entire amount in cash or |
• | rights of registration of transfer and exchange, and our right of optional redemption; |
• | substitution of apparently mutilated, defaced, destroyed, lost or stolen debt securities; |
• | rights of holders to receive payments of principal of the debt securities and interest thereon, upon the original stated due dates (but not upon acceleration); |
• | the rights, obligations and immunities of the trustee; and |
• | the rights of the holders of debt securities of such series as beneficiaries with respect to the property deposited with the trustee payable to all or any of them. |
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• | we have deposited or caused to be irrevocably deposited with the trustee as trust funds in trust, specifically pledged as security for, and dedicated solely to, the benefit of the holders of the debt securities of such series, (i) money in an amount, or (ii) U.S. government obligations which through the payment of interest and principal in respect thereof in accordance with their terms will provide not later than one day before the due date of any payment money in an amount, or (iii) a combination thereof, sufficient to pay and discharge without consideration of the reinvestment of such interest and after payment of all federal, state and local taxes or other charges and assessments in respect thereof payable by the trustee (x) the principal of, premium, if any, and each installment of interest on the outstanding debt securities of such series on the due dates thereof and (y) any mandatory sinking fund payments or analogous payments applicable to the debt securities of such series on the day on which such payments are due and payable in accordance with the terms of debt securities of such series and the indenture; |
• | we have delivered to the trustee (i) an opinion of counsel to the effect that holders of debt securities of such series will not recognize income, gain or loss for U.S. federal income tax purposes as a result of our exercise of legal defeasance or covenant defeasance and will be subject to U.S. federal income tax on the same amount and in the same manner and at the same times as would have been the case if such deposit, defeasance and discharge had not occurred, or a ruling directed to the trustee received from the U.S. Internal Revenue Service to the same effect as such opinion of counsel and (ii) an opinion of counsel to the effect that the creation of the defeasance trust does not violate the Investment Company Act of 1940 and after the passage of 123 days following the deposit, the trust fund will not be subject to the effect of Section 547 of the U.S. Bankruptcy Code or Section 15 of the New York Debtor and Creditor Law; |
• | immediately after giving effect to such deposit on a pro forma basis, no event of default, or event that after the giving of notice or lapse of time or both would become an event of default, shall have occurred and be continuing on the date of such deposit or during the period ending on the 123rd day after the date of such deposit, and such deposit shall not result in a breach or violation of, or constitute a default under, any other agreement or instrument to which we are a party or by which we are bound; |
• | if at such time the debt securities of such series are listed on a national securities exchange, we have delivered to the trustee an opinion of counsel to the effect that the debt securities of such series will not be delisted as a result of such deposit, defeasance and discharge; |
• | we have delivered to the trustee an officers’ certificate and an opinion of counsel, each stating that all conditions precedent to the defeasance and discharge have been complied with; and |
• | in the case of covenant defeasance, if the debt securities of such series are to be redeemed prior to the final maturity thereof (other than from mandatory sinking fund payments or analogous payments), notice of such redemption has been duly given pursuant to the indenture. |
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• | the title of such warrants; |
• | the aggregate number of such warrants; |
• | the price or prices at which such warrants will be issued; |
• | the currency or currencies in which the price of such warrants will be payable; |
• | the securities or other rights, including rights to receive payment in cash or securities based on the value, rate or price of one or more specified commodities, currencies, securities or indices, or any combination of the foregoing, purchasable upon exercise of such warrants; |
• | the price at which and the currency or currencies in which the securities or other rights purchasable upon exercise of such warrants may be purchased; |
• | the date on which the right to exercise such warrants shall commence and the date on which such right shall expire; |
• | if applicable, the minimum or maximum amount of such warrants which may be exercised at any one time; |
• | if applicable, the designation and terms of the securities with which such warrants are issued and the number of such warrants issued with each such security; |
• | if applicable, the date on and after which such warrants and the related securities will be separately transferable; |
• | information with respect to book-entry procedures, if any; |
• | if applicable, a discussion of any material United States Federal income tax considerations; and |
• | any other terms of such warrants, including terms, procedures and limitations relating to the exchange and exercise of such warrants. |
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• | the terms of the units and of the warrants, debt securities, preference shares and Common Shares comprising the units, including whether and under what circumstances the securities comprising the units may be traded separately; |
• | a description of the terms of any unit agreement governing the units; and |
• | a description of the provisions for the payment, settlement, transfer or exchange of the units. |
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• | 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 any underwriters, dealers, agents or other purchasers; |
• | the required information with respect to any selling shareholder, if any; |
• | the purchase price of the securities or other consideration therefor, and the proceeds, if any, we will receive from the sale; |
• | any options to purchase additional shares or other options under which underwriters, dealers, agents or other purchasers may purchase additional securities from us or any selling shareholder; |
• | any agency fees or underwriting discounts and other items constituting agents’ or underwriters’ compensation; |
• | any public offering price; |
• | any discounts or concessions allowed or reallowed or paid to dealers; 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 March 31, 2025, filed with the SEC on May 29, 2025; |
• | our Quarterly Report on Form 10-Q for the quarter ended June 30, 2025, filed with the SEC on August 11, 2025; |
• | the information specifically incorporated by reference in our Annual Report on Form 10-K for the year ended March 31, 2025 from our Definitive Proxy Statement on Schedule 14A relating to our 2025 annual meeting of shareholders, filed with the SEC on July 29, 2025; |
• | our Current Report on Form 8-K filed with the SEC on June 25, 2025, September 3, 2025 (only with respect to Item 8.01), September 11, 2025 and September 17, 2025 (only with respect to Item 8.01); and |
• | the description of our Common Shares contained in Exhibit 4.2 to our Annual Report on Form 10-K filed with the SEC on May 29, 2025, including any amendments thereto or reports filed for the purpose of updating such description. |
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Page | |||
About This Prospectus | ii | ||
Prospectus Summary | 1 | ||
The Offering | 2 | ||
Risk Factors | 3 | ||
Forward-Looking Statements | 4 | ||
Use of Proceeds | 6 | ||
Plan of Distribution | 7 | ||
Legal Matters | 8 | ||
Experts | 8 | ||
Where You Can Find Additional Information | 8 | ||
Incorporation of Certain Information by Reference | 9 | ||
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• | 138,728,031 Common Shares issuable upon the exercise of options outstanding as of June 30, 2025, having a weighted average exercise price of $8.70 per share; and |
• | 72,009,936 Common Shares issuable upon settlement of outstanding restricted stock units, performance restricted stock units and capped value appreciation rights as of June 30, 2025. |
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• | our relatively limited operating history and the inherent uncertainties and risks involved in biopharmaceutical product development and commercialization; |
• | our ability to acquire, in-license or discover new product candidates; |
• | the allocation of capital and personnel across our businesses; |
• | our Vant structure; |
• | potential future payments we may owe in connection with our product candidates; |
• | acquisitions, divestitures and other strategic transactions; |
• | the use of our cash, cash equivalents and marketable securities; |
• | the potential future need for additional capital to fund our operations; |
• | clinical trials and preclinical studies, which are very expensive, time-consuming, difficult to design and implement and involve uncertain outcomes; |
• | unfavorable, uncertain and rapidly changing global and regional economic, political and public health conditions; |
• | the fact that designing and implement clinical trials and preclinical studies is very expensive, time-consuming and difficult; |
• | difficulties we may encounter enrolling and retaining patients in clinical trials, which could adversely affect or otherwise delay clinical development activities; |
• | the results of our preclinical studies and clinical trials not supporting our proposed claims for a product candidate or regulatory approval; |
• | interim, preliminary or top-line data from our clinical trials changing as more data become available or data being delayed due to audit or verification procedures; |
• | changes in product candidate manufacturing or formulation that could result in additional costs or delays; |
• | the fact that obtaining approval of a new drug is an extensive, lengthy, expensive and inherently uncertain process and the FDA or another regulatory authority may delay, limit or deny approval; |
• | the failure of our clinical trials to demonstrate substantial evidence of the safety and efficacy of our product candidates; |
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• | undesirable side effects caused by our product candidates that halt their clinical development, delay or prevent their regulatory approval, limit the scope of any approved label or market acceptance or result in negative consequences; |
• | our inability to obtain regulatory approval for a product candidate in certain jurisdictions, even if we are able to obtain approval in certain other jurisdictions; |
• | the failure of any third-party we rely upon to conduct, supervise and monitor our clinical trials to perform in a satisfactory manner or to comply with applicable legal, regulatory or other requirements; |
• | our reliance on third parties to produce clinical and commercial supplies of our product candidates; |
• | our dependence on key personnel and our ability to attract, motivate and retain highly qualified personnel; |
• | the potential that our use of AI could expose us to liability; |
• | our ability to obtain and maintain patent and other intellectual property protection for our technology and product candidates; |
• | the failure to issue (or the threatening of their validity, patentability, enforceability, breadth or strength of protection) or provide meaningful exclusivity for our product candidates of our patent applications that we own or have in-licensed; |
• | the inadequacy of patent terms and their scope to protect our competitive position; |
• | the fact that our largest shareholders own a significant percentage of our stock and will be able to exert significant control over matters subject to shareholder approval; |
• | dilution of ownership caused by future sales and issuances of our or the Vants’ equity securities or rights to purchase equity securities; |
• | future sales, or the perception of future sales, of our common shares by us or our existing shareholders, and the impact thereof on the price of our common shares; |
• | the outcome of any pending or potential litigation, including but not limited to our expectations regarding the outcome of any such litigation and costs and expenses associated with such litigation; |
• | changes in applicable laws or regulations; |
• | the possibility that we may be adversely affected by other economic, business or competitive factors; and |
• | any other risks and uncertainties indicated from time to time in filings made with the SEC. |
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• | our Annual Report on Form 10-K for the year ended March 31, 2025, filed with the SEC on May 29, 2025; |
• | our Quarterly Report on Form 10-Q for the quarter ended June 30, 2025, filed with the SEC on August 11, 2025; |
• | the information specifically incorporated by reference in our Annual Report on Form 10-K for the year ended March 31, 2025 from our Definitive Proxy Statement on Schedule 14A relating to our 2025 annual meeting of shareholders, filed with the SEC on July 29, 2025; |
• | our Current Report on Form 8-K filed with the SEC on June 25, 2025, September 3, 2025 (only with respect to Item 8.01), September 11, 2025 and September 17, 2025 (only with respect to Item 8.01); and |
• | the description of our Common Shares contained in Exhibit 4.2 to our Annual Report on Form 10-K filed with the SEC on May 29, 2025, including any amendments thereto or reports filed for the purpose of updating such description. |
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Item 14. | Other Expenses of Issuance and Distribution |
Amount | |||
SEC registration fee(1) | $92,712.29 | ||
Nasdaq Global Select Market fee | (2) | ||
FINRA filing fee | (2) | ||
Accounting fees and expenses | (2) | ||
Legal fees and expenses | (2) | ||
Transfer agent and registrar fees and expenses | (2) | ||
Printing and miscellaneous fees and expenses | (2) | ||
Total | (2) | ||
(1) | In accordance with Rules 456(b) and 457(r), the Registrant is deferring payment of all applicable registration fees for the securities offered under this registration statement, other than the $92,712.29 of fees due in connection with the $400,000,000 of our common stock that may be issued and sold from time to time under a sales agreement with TD Securities (USA) LLC, successor to Cowen and Company, LLC. The filing fee previously paid in connection with the securities registered in the registration statement on Form S-3 (File No. 333-267503), all of which remain unsold, will be carried forward and applied to the securities registered under this registration statement. Please see the registration fee table contained in Exhibit 107 to this registration statement for more information. |
(2) | The amount of securities and number of offerings are indeterminable and the expenses cannot be estimated at this time. An estimate of the aggregate expenses in connection with the sale and distribution of securities being offered will be included in the applicable prospectus supplement. |
Item 15. | Indemnification of Directors and Officers |
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Item 16. | Exhibits |
Incorporation By Reference | ||||||||||||||||||
Exhibit Number | Exhibit Description | Form | SEC File No. | Exhibit | Filing Date | Filed Herewith | ||||||||||||
1.1* | Form of Underwriting Agreement. | |||||||||||||||||
1.2 | Sales Agreement, by and between the Registrant and TD Securities (USA) LLC, successor to Cowen and Company, LLC, dated September 19, 2022. | S-3 | 333-267503 | 1.2 | 09/19/2022 | |||||||||||||
3.1 | Memorandum of Association of Roivant Sciences Ltd. | S-4/A | 333-256165 | 3.1 | 07/01/2021 | |||||||||||||
3.2 | Amended and Restated Bye-laws of Roivant Sciences Ltd. | 8-K | 001-40782 | 3.1 | 10/01/2021 | |||||||||||||
4.1* | Specimen Preference Shares Certificate and Form of Certificate of Designation of Preference Shares. | |||||||||||||||||
4.2 | Form of Senior Debt Indenture. | S-3 | 333-267503 | 4.2 | 09/19/2022 | |||||||||||||
4.3 | Form of Subordinated Debt Indenture. | S-3 | 333-267503 | 4.3 | 09/19/2022 | |||||||||||||
4.4* | Form of Senior Note. | |||||||||||||||||
4.4* | Form of Subordinated Note. | |||||||||||||||||
4.5* | Form of Warrant Agreement and Warrant Certificate. | |||||||||||||||||
4.6* | Form of Unit Agreement. | |||||||||||||||||
5.1 | Opinion of Conyers Dill & Pearman Limited, Bermuda law counsel to Roivant Sciences Ltd. | X | ||||||||||||||||
5.2 | Opinion of Davis Polk & Wardwell LLP, U.S. counsel of Roivant Sciences Ltd. | X | ||||||||||||||||
23.1 | Consent of Ernst & Young LLP, Independent Registered Public Accounting Firm of Roivant Sciences Ltd. | X | ||||||||||||||||
23.2 | Consent of Conyers Dill & Pearman Limited (included in Exhibit 5.1). | X | ||||||||||||||||
23.3 | Consent of Davis Polk & Wardwell LLP (included in Exhibit 5.2). | X | ||||||||||||||||
24.1 | Power of Attorney. Reference is made to the signature pages of this Form S-3. | |||||||||||||||||
25.1** | Statement of Eligibility of Trustee under the Indenture. | |||||||||||||||||
107 | Calculation of Filing Fee Tables | X | ||||||||||||||||
* | To be filed by amendment or as an exhibit to a Current Report on Form 8-K and incorporated herein by reference, if applicable. |
** | To be filed in accordance with the requirements of Section 305(b)(2) of the Trust Indenture Act of 1939, as amended, and the applicable rules thereunder. |
Item 17. | Undertakings |
(1) | To file, during any period in which offers or sales are being made, a post-effective amendment to this registration statement: |
(i) | to include any prospectus required by Section 10(a)(3) of the Securities Act of 1933; |
(ii) | to reflect in the prospectus any facts or events arising after the effective date of the registration statement (or the most recent post-effective amendment thereof) which, individually or in the aggregate, represent a fundamental change in the information set forth in the registration |
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(iii) | to include any material information with respect to the plan of distribution not previously disclosed in the registration statement or any material change to such information in the registration statement; |
(2) | That, for the purpose of determining any liability under the Securities Act of 1933, each such post-effective amendment shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof. |
(3) | To remove from registration by means of a post-effective amendment any of the securities being registered which remain unsold at the termination of the offering. |
(4) | That, for the purpose of determining liability under the Securities Act of 1933 to any purchaser: |
(i) | Each prospectus filed by the registrant pursuant to Rule 424(b)(3) shall be deemed to be part of the registration statement as of the date the filed prospectus was deemed part of and included in the registration statement; and |
(ii) | Each prospectus required to be filed pursuant to Rule 424(b)(2), (b)(5), or (b)(7) as part of a registration statement in reliance on Rule 430B relating to an offering made pursuant to Rule 415(a)(1)(i), (vii), or (x) for the purpose of providing the information required by Section 10(a) of the Securities Act of 1933 shall be deemed to be part of and included in the registration statement as of the earlier of the date such form of prospectus is first used after effectiveness or the date of the first contract of sale of securities in the offering described in the prospectus. As provided in Rule 430B, for liability purposes of the issuer and any person that is at that date an underwriter, such date shall be deemed to be a new effective date of the registration statement relating to the securities in the registration statement to which that prospectus relates, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof. Provided, however, that no statement made in a registration statement or prospectus that is part of the registration statement or made in a document incorporated or deemed incorporated by reference into the registration statement or prospectus that is part of the registration statement will, as to a purchaser with a time of contract of sale prior to such effective date, supersede or modify any statement that was made in the registration statement or prospectus that was part of the registration statement or made in any such document immediately prior to such effective date. |
(5) | That, for the purpose of determining liability of the registrant under the Securities Act of 1933 to any purchaser in the initial distribution of the securities, the undersigned registrant undertakes that in a primary offering of securities of the undersigned registrant pursuant to this registration statement, regardless of the underwriting method used to sell the securities to the purchaser, if the securities are offered or sold to such purchaser by means of any of the following communications, the undersigned registrant will be a seller to the purchaser and will be considered to offer or sell such securities to such purchaser: |
(i) | Any preliminary prospectus or prospectus of the undersigned registrant relating to the offering required to be filed pursuant to Rule 424; |
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(ii) | Any free writing prospectus relating to the offering prepared by or on behalf of the undersigned registrant or used or referred to by the undersigned registrant; |
(iii) | The portion of any other free writing prospectus relating to the offering containing material information about the undersigned registrant or its securities provided by or on behalf of the undersigned registrant; and |
(iv) | Any other communication that is an offer in the offering made by the undersigned registrant to the purchaser. |
(6) | That, for the purpose of determining liability of the registrant under the Securities Act of 1933, each filing of the registrant’s annual report pursuant to Section 13(a) or Section 15(d) of the Securities Exchange Act of 1934 (and, where applicable, each filing of an employee benefit plan’s annual report pursuant to section 15(d) of the Securities Exchange Act of 1934) that is incorporated by reference in the registration statement shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof. |
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ROIVANT SCIENCES LTD. | |||||||||
By: | /s/ Keyur Parekh | ||||||||
Name: | Keyur Parekh | ||||||||
Title: | Authorized Signatory | ||||||||
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Name | Title | Date | ||||
/s/ Matthew Gline | Chief Executive Officer and Director (principal executive officer) | October 3, 2025 | ||||
Matthew Gline | ||||||
/s/ Richard Pulik | Chief Financial Officer (principal financial officer) | October 3, 2025 | ||||
Richard Pulik | ||||||
/s/ Jennifer Humes | Chief Accounting Officer (principal accounting officer) | October 3, 2025 | ||||
Jennifer Humes | ||||||
/s/ Mayukh Sukhatme | President and Chief Investment Officer and Director | October 3, 2025 | ||||
Mayukh Sukhatme | ||||||
/s/ Keith Manchester | Director | October 3, 2025 | ||||
Keith Manchester | ||||||
/s/ Ilan Oren | Director | October 3, 2025 | ||||
Ilan Oren | ||||||
/s/ Daniel Gold | Director | October 3, 2025 | ||||
Daniel Gold | ||||||
/s/ Melissa Epperly | Director | October 3, 2025 | ||||
Melissa Epperly | ||||||
/s/ Meghan FitzGerald | Director | October 3, 2025 | ||||
Meghan FitzGerald | ||||||
/s/ James C. Momtazee | Director | October 3, 2025 | ||||
James C. Momtazee | ||||||