STOCK TITAN

[SC TO-T/A] Blueprint Medicines Corporation Amended Third-Party Tender Offer

Filing Impact
(Low)
Filing Sentiment
(Neutral)
Form Type
SC TO-T/A
Rhea-AI Filing Summary

Sanofi’s wholly owned subsidiary Rothko Merger Sub, Inc. has advanced its $129.00-per-share cash tender offer for Blueprint Medicines (BPMC) by clearing several key regulatory hurdles. The amendment to Schedule TO confirms that the 30-day Hart-Scott-Rodino (HSR) waiting period expired on 9 July 2025, satisfying the principal U.S. antitrust closing condition. In Europe, Phase I review in Austria lapsed on 8 July 2025, the German Federal Cartel Office granted clearance on 30 June 2025, and Italy’s Presidency of the Council of Ministers ruled on 25 June 2025 that the merger does not fall within the scope of its foreign-investment regime. These approvals materially de-risk deal execution.

The consideration remains $129.00 in cash plus a non-transferable contingent value right (CVR) of up to $6.00 per share, payable upon achievement of specified milestones. All other terms contained in the original Offer to Purchase dated 17 June 2025 are unchanged and incorporated by reference.

Litigation update: Two stockholder suits—Williams v. Blueprint Medicines Corp. and Phillips v. Blueprint Medicines Corp.—were filed in New York State Supreme Court between 24–25 June 2025, alleging disclosure deficiencies in the Schedule 14D-9 and seeking, among other remedies, to enjoin the transaction. In addition, 12 stockholders issued demand letters requesting supplemental disclosure. Sanofi notes that similar filings may not be publicly announced in the absence of new material allegations.

Implications for investors: With U.S. and major EU antitrust reviews completed, regulatory risk is substantially reduced, increasing the likelihood of successful close and realization of the $129 cash consideration (plus potential CVR). Ongoing shareholder litigation represents a standard M&A hurdle and is not uncommon; however, it could introduce incremental timing or cost risk.

La controllata interamente posseduta da Sanofi, Rothko Merger Sub, Inc., ha fatto avanzare la sua offerta pubblica di acquisto in contanti a $129,00 per azione per Blueprint Medicines (BPMC), superando diversi ostacoli regolatori chiave. L'emendamento al Schedule TO conferma che il periodo di attesa di 30 giorni previsto dal Hart-Scott-Rodino (HSR) è scaduto il 9 luglio 2025, soddisfacendo la principale condizione antitrust statunitense per la chiusura. In Europa, la revisione di Fase I in Austria è scaduta l’8 luglio 2025, l'Ufficio federale tedesco per la concorrenza ha concesso l'autorizzazione il 30 giugno 2025 e la Presidenza del Consiglio dei Ministri italiana ha stabilito il 25 giugno 2025 che la fusione non rientra nel regime degli investimenti esteri. Queste approvazioni riducono significativamente i rischi legati all’esecuzione dell’operazione.

La controprestazione rimane $129,00 in contanti più un diritto di valore contingente non trasferibile (CVR) fino a $6,00 per azione, pagabile al raggiungimento di specifici obiettivi. Tutti gli altri termini contenuti nell’Offerta di Acquisto originale del 17 giugno 2025 restano invariati e sono incorporati per riferimento.

Aggiornamento sulle controversie legali: Due cause intentate da azionisti – Williams contro Blueprint Medicines Corp. e Phillips contro Blueprint Medicines Corp. – sono state depositate presso la Corte Suprema dello Stato di New York tra il 24 e il 25 giugno 2025, contestando carenze informative nel Schedule 14D-9 e chiedendo, tra le altre misure, di bloccare la transazione. Inoltre, 12 azionisti hanno inviato lettere di richiesta per ulteriori informazioni. Sanofi osserva che simili azioni legali potrebbero non essere rese pubbliche in assenza di nuove accuse rilevanti.

Implicazioni per gli investitori: Con il completamento delle revisioni antitrust negli Stati Uniti e nelle principali giurisdizioni europee, il rischio regolatorio è sostanzialmente ridotto, aumentando la probabilità di chiusura positiva e di realizzazione del corrispettivo in contanti di $129 (più il potenziale CVR). Le controversie in corso rappresentano un ostacolo tipico nelle operazioni di M&A e non sono insolite; tuttavia, potrebbero comportare rischi aggiuntivi in termini di tempistiche o costi.

La filial de propiedad total de Sanofi, Rothko Merger Sub, Inc., ha avanzado su oferta pública de adquisición en efectivo de $129.00 por acción para Blueprint Medicines (BPMC), superando varios obstáculos regulatorios clave. La enmienda al Schedule TO confirma que el período de espera de 30 días bajo la ley Hart-Scott-Rodino (HSR) expiró el 9 de julio de 2025, cumpliendo con la principal condición antimonopolio en EE.UU. En Europa, la revisión de Fase I en Austria terminó el 8 de julio de 2025, la Oficina Federal de Cárteles de Alemania otorgó la aprobación el 30 de junio de 2025 y la Presidencia del Consejo de Ministros de Italia dictaminó el 25 de junio de 2025 que la fusión no está sujeta a su régimen de inversiones extranjeras. Estas aprobaciones reducen significativamente el riesgo regulatorio para la ejecución del acuerdo.

La contraprestación sigue siendo $129.00 en efectivo más un derecho contingente de valor no transferible (CVR) de hasta $6.00 por acción, pagadero al alcanzar ciertos hitos especificados. Todos los demás términos contenidos en la Oferta de Compra original del 17 de junio de 2025 permanecen sin cambios y se incorporan por referencia.

Actualización de litigios: Dos demandas de accionistas —Williams contra Blueprint Medicines Corp. y Phillips contra Blueprint Medicines Corp.— fueron presentadas en la Corte Suprema del Estado de Nueva York entre el 24 y 25 de junio de 2025, alegando deficiencias en la divulgación del Schedule 14D-9 y buscando, entre otros remedios, impedir la transacción. Además, 12 accionistas enviaron cartas de solicitud para información adicional. Sanofi señala que presentaciones similares podrían no anunciarse públicamente en ausencia de nuevas alegaciones materiales.

Implicaciones para los inversores: Con la revisión antimonopolio completada en EE.UU. y las principales jurisdicciones europeas, el riesgo regulatorio se reduce sustancialmente, aumentando la probabilidad de cierre exitoso y la realización del pago en efectivo de $129 (más el posible CVR). Los litigios en curso representan un obstáculo estándar en fusiones y adquisiciones y no son inusuales; sin embargo, podrían introducir riesgos adicionales en términos de tiempo o costos.

Sanofi의 완전 자회사인 Rothko Merger Sub, Inc.가 Blueprint Medicines(BPMC)에 대한 주당 $129.00 현금 공개 매수 제안을 여러 핵심 규제 장벽을 넘으며 진전시켰습니다. Schedule TO 수정안은 30일간의 Hart-Scott-Rodino(HSR) 대기 기간이 2025년 7월 9일에 만료되어 미국 주요 반독점 거래 종료 조건을 충족했음을 확인합니다. 유럽에서는 오스트리아에서 1단계 심사가 2025년 7월 8일에 종료되었고, 독일 연방 카르텔청이 2025년 6월 30일에 승인했으며, 이탈리아 국무총리실은 2025년 6월 25일에 이번 합병이 외국인 투자 규제 대상이 아님을 판결했습니다. 이러한 승인들은 거래 실행의 위험을 크게 낮춥니다.

대금 조건은 현금 $129.00 및 특정 이정표 달성 시 지급되는 주당 최대 $6.00의 양도 불가능한 조건부 가치 권리(CVR)로 유지됩니다. 2025년 6월 17일자 원래 매수 제안서에 포함된 기타 조건들은 변경 없이 참조로 포함됩니다.

소송 현황: 2025년 6월 24일부터 25일 사이 뉴욕주 대법원에 Williams 대 Blueprint Medicines Corp.와 Phillips 대 Blueprint Medicines Corp.라는 두 건의 주주 소송이 제기되었으며, Schedule 14D-9 공개 내용의 부족을 주장하고 거래 중지를 포함한 구제를 요청하고 있습니다. 또한 12명의 주주가 추가 공개를 요구하는 서한을 발송했습니다. Sanofi는 새로운 중대한 주장 없이는 유사한 소송 제기가 공개되지 않을 수 있음을 언급합니다.

투자자에 대한 시사점: 미국 및 주요 유럽연합 반독점 심사가 완료되어 규제 리스크가 크게 줄어들었으며, 성공적인 거래 종료 및 $129 현금 대금(및 잠재적 CVR) 실현 가능성이 높아졌습니다. 진행 중인 주주 소송은 일반적인 M&A 장애물이며 드문 일이 아니지만, 추가적인 시간 지연이나 비용 위험을 초래할 수 있습니다.

La filiale en propriété exclusive de Sanofi, Rothko Merger Sub, Inc., a fait progresser son offre publique d'achat en espèces à 129,00 $ par action pour Blueprint Medicines (BPMC) en franchissant plusieurs étapes réglementaires clés. L’amendement au Schedule TO confirme que la période d’attente de 30 jours selon la loi Hart-Scott-Rodino (HSR) a expiré le 9 juillet 2025, satisfaisant la principale condition de clôture antitrust américaine. En Europe, l’examen de Phase I en Autriche a pris fin le 8 juillet 2025, l’Office fédéral allemand des cartels a donné son feu vert le 30 juin 2025, et la Présidence du Conseil des ministres italien a statué le 25 juin 2025 que la fusion n’entre pas dans le cadre de son régime des investissements étrangers. Ces approbations réduisent significativement les risques liés à l’exécution de la transaction.

La contrepartie reste de 129,00 $ en espèces plus un droit de valeur conditionnel non transférable (CVR) pouvant atteindre 6,00 $ par action, payable à la réalisation de jalons spécifiques. Toutes les autres conditions contenues dans l’offre d’achat initiale datée du 17 juin 2025 restent inchangées et sont incorporées par référence.

Mise à jour sur les litiges : Deux actions en justice de porteurs d’actions – Williams contre Blueprint Medicines Corp. et Phillips contre Blueprint Medicines Corp. – ont été déposées devant la Cour suprême de l’État de New York entre le 24 et le 25 juin 2025, alléguant des insuffisances dans les divulgations du Schedule 14D-9 et demandant, entre autres, à faire interdire la transaction. De plus, 12 actionnaires ont envoyé des lettres de demande de divulgations complémentaires. Sanofi note que des dépôts similaires peuvent ne pas être rendus publics en l’absence de nouvelles allégations importantes.

Implications pour les investisseurs : Avec la finalisation des examens antitrust aux États-Unis et dans les principales juridictions européennes, le risque réglementaire est substantiellement réduit, augmentant la probabilité d’une clôture réussie et la réalisation de la contrepartie en espèces de 129 $ (plus le CVR potentiel). Les litiges en cours représentent un obstacle standard dans les opérations de fusion-acquisition et ne sont pas inhabituels ; toutefois, ils pourraient entraîner des risques supplémentaires en termes de délais ou de coûts.

Die vollständig im Besitz von Sanofi befindliche Tochtergesellschaft Rothko Merger Sub, Inc. hat ihr Barangebot von 129,00 $ pro Aktie für Blueprint Medicines (BPMC) durch das Überwinden mehrerer wichtiger regulatorischer Hürden vorangetrieben. Die Änderung des Schedule TO bestätigt, dass die 30-tägige Hart-Scott-Rodino (HSR)-Wartefrist am 9. Juli 2025 abgelaufen ist und somit die wesentliche US-amerikanische kartellrechtliche Abschlussbedingung erfüllt wurde. In Europa lief die Phase-I-Prüfung in Österreich am 8. Juli 2025 ab, das deutsche Bundeskartellamt erteilte am 30. Juni 2025 die Freigabe, und die italienische Präsidentschaft des Ministerrats entschied am 25. Juni 2025, dass die Fusion nicht unter das ausländische Investitionsregime fällt. Diese Genehmigungen verringern das Risiko der Transaktionsdurchführung erheblich.

Die Gegenleistung bleibt 129,00 $ in bar plus ein nicht übertragbares bedingtes Wertrecht (CVR) von bis zu 6,00 $ pro Aktie, zahlbar bei Erreichen bestimmter Meilensteine. Alle weiteren Bedingungen des ursprünglichen Kaufangebots vom 17. Juni 2025 bleiben unverändert und werden durch Verweis einbezogen.

Aktualisierung zu Rechtsstreitigkeiten: Zwei Aktionärsklagen – Williams gegen Blueprint Medicines Corp. und Phillips gegen Blueprint Medicines Corp. – wurden zwischen dem 24. und 25. Juni 2025 beim New Yorker Obersten Gerichtshof eingereicht. Sie werfen Mängel bei der Offenlegung im Schedule 14D-9 vor und beantragen unter anderem die Unterbindung der Transaktion. Darüber hinaus haben 12 Aktionäre Aufforderungsschreiben mit der Bitte um ergänzende Offenlegung versandt. Sanofi weist darauf hin, dass ähnliche Klagen ohne neue wesentliche Vorwürfe möglicherweise nicht öffentlich bekannt gemacht werden.

Auswirkungen für Investoren: Mit Abschluss der US-amerikanischen und der wichtigsten EU-Kartellprüfungen ist das regulatorische Risiko erheblich reduziert, was die Wahrscheinlichkeit eines erfolgreichen Abschlusses und die Realisierung der Barzahlung von 129 $ (plus potenziellen CVR) erhöht. Laufende Aktionärsklagen stellen eine übliche Hürde bei M&A-Transaktionen dar und sind nicht ungewöhnlich; sie könnten jedoch zusätzliche zeitliche oder kostenseitige Risiken mit sich bringen.

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Insights

TL;DR – Key antitrust clearances in U.S. & EU reduce deal risk; litigation appears routine.

The expiration of the HSR waiting period and receipt of Austrian, German and Italian approvals eliminate the majority of regulatory barriers for Sanofi’s acquisition of Blueprint Medicines. Absent unexpected second-request investigations in other jurisdictions, the transaction timetable should compress, bringing the $129 cash payment (41% premium to BPMC’s unaffected price) and potential $6 CVR closer to realization. Shareholder suits alleging disclosure inadequacies are typical in U.S. take-privates and rarely derail deals; settlement via supplemental disclosure and fee payment is common. Overall impact skews positive, supporting merger-arbitrage spreads tightening.

TL;DR – Regulatory milestones cleared; standard plaintiff challenges emerge.

The amendment signals tangible progress: the HSR clock is over, Austria’s Phase I expired, Germany issued clearance, and Italy confirmed non-applicability. These decisions satisfy critical closing conditions in Section 16 and remove hurdles that often extend deal timelines. Remaining approvals, if any, are not mentioned, implying a clear path subject to customary conditions. Plaintiff bar activity—two suits and 12 demands—reflects a routine “disclosure-only” strategy; historical precedent suggests low probability of blocking the deal. Therefore, the update is materially deal-positive and should bolster market confidence in completion probability.

La controllata interamente posseduta da Sanofi, Rothko Merger Sub, Inc., ha fatto avanzare la sua offerta pubblica di acquisto in contanti a $129,00 per azione per Blueprint Medicines (BPMC), superando diversi ostacoli regolatori chiave. L'emendamento al Schedule TO conferma che il periodo di attesa di 30 giorni previsto dal Hart-Scott-Rodino (HSR) è scaduto il 9 luglio 2025, soddisfacendo la principale condizione antitrust statunitense per la chiusura. In Europa, la revisione di Fase I in Austria è scaduta l’8 luglio 2025, l'Ufficio federale tedesco per la concorrenza ha concesso l'autorizzazione il 30 giugno 2025 e la Presidenza del Consiglio dei Ministri italiana ha stabilito il 25 giugno 2025 che la fusione non rientra nel regime degli investimenti esteri. Queste approvazioni riducono significativamente i rischi legati all’esecuzione dell’operazione.

La controprestazione rimane $129,00 in contanti più un diritto di valore contingente non trasferibile (CVR) fino a $6,00 per azione, pagabile al raggiungimento di specifici obiettivi. Tutti gli altri termini contenuti nell’Offerta di Acquisto originale del 17 giugno 2025 restano invariati e sono incorporati per riferimento.

Aggiornamento sulle controversie legali: Due cause intentate da azionisti – Williams contro Blueprint Medicines Corp. e Phillips contro Blueprint Medicines Corp. – sono state depositate presso la Corte Suprema dello Stato di New York tra il 24 e il 25 giugno 2025, contestando carenze informative nel Schedule 14D-9 e chiedendo, tra le altre misure, di bloccare la transazione. Inoltre, 12 azionisti hanno inviato lettere di richiesta per ulteriori informazioni. Sanofi osserva che simili azioni legali potrebbero non essere rese pubbliche in assenza di nuove accuse rilevanti.

Implicazioni per gli investitori: Con il completamento delle revisioni antitrust negli Stati Uniti e nelle principali giurisdizioni europee, il rischio regolatorio è sostanzialmente ridotto, aumentando la probabilità di chiusura positiva e di realizzazione del corrispettivo in contanti di $129 (più il potenziale CVR). Le controversie in corso rappresentano un ostacolo tipico nelle operazioni di M&A e non sono insolite; tuttavia, potrebbero comportare rischi aggiuntivi in termini di tempistiche o costi.

La filial de propiedad total de Sanofi, Rothko Merger Sub, Inc., ha avanzado su oferta pública de adquisición en efectivo de $129.00 por acción para Blueprint Medicines (BPMC), superando varios obstáculos regulatorios clave. La enmienda al Schedule TO confirma que el período de espera de 30 días bajo la ley Hart-Scott-Rodino (HSR) expiró el 9 de julio de 2025, cumpliendo con la principal condición antimonopolio en EE.UU. En Europa, la revisión de Fase I en Austria terminó el 8 de julio de 2025, la Oficina Federal de Cárteles de Alemania otorgó la aprobación el 30 de junio de 2025 y la Presidencia del Consejo de Ministros de Italia dictaminó el 25 de junio de 2025 que la fusión no está sujeta a su régimen de inversiones extranjeras. Estas aprobaciones reducen significativamente el riesgo regulatorio para la ejecución del acuerdo.

La contraprestación sigue siendo $129.00 en efectivo más un derecho contingente de valor no transferible (CVR) de hasta $6.00 por acción, pagadero al alcanzar ciertos hitos especificados. Todos los demás términos contenidos en la Oferta de Compra original del 17 de junio de 2025 permanecen sin cambios y se incorporan por referencia.

Actualización de litigios: Dos demandas de accionistas —Williams contra Blueprint Medicines Corp. y Phillips contra Blueprint Medicines Corp.— fueron presentadas en la Corte Suprema del Estado de Nueva York entre el 24 y 25 de junio de 2025, alegando deficiencias en la divulgación del Schedule 14D-9 y buscando, entre otros remedios, impedir la transacción. Además, 12 accionistas enviaron cartas de solicitud para información adicional. Sanofi señala que presentaciones similares podrían no anunciarse públicamente en ausencia de nuevas alegaciones materiales.

Implicaciones para los inversores: Con la revisión antimonopolio completada en EE.UU. y las principales jurisdicciones europeas, el riesgo regulatorio se reduce sustancialmente, aumentando la probabilidad de cierre exitoso y la realización del pago en efectivo de $129 (más el posible CVR). Los litigios en curso representan un obstáculo estándar en fusiones y adquisiciones y no son inusuales; sin embargo, podrían introducir riesgos adicionales en términos de tiempo o costos.

Sanofi의 완전 자회사인 Rothko Merger Sub, Inc.가 Blueprint Medicines(BPMC)에 대한 주당 $129.00 현금 공개 매수 제안을 여러 핵심 규제 장벽을 넘으며 진전시켰습니다. Schedule TO 수정안은 30일간의 Hart-Scott-Rodino(HSR) 대기 기간이 2025년 7월 9일에 만료되어 미국 주요 반독점 거래 종료 조건을 충족했음을 확인합니다. 유럽에서는 오스트리아에서 1단계 심사가 2025년 7월 8일에 종료되었고, 독일 연방 카르텔청이 2025년 6월 30일에 승인했으며, 이탈리아 국무총리실은 2025년 6월 25일에 이번 합병이 외국인 투자 규제 대상이 아님을 판결했습니다. 이러한 승인들은 거래 실행의 위험을 크게 낮춥니다.

대금 조건은 현금 $129.00 및 특정 이정표 달성 시 지급되는 주당 최대 $6.00의 양도 불가능한 조건부 가치 권리(CVR)로 유지됩니다. 2025년 6월 17일자 원래 매수 제안서에 포함된 기타 조건들은 변경 없이 참조로 포함됩니다.

소송 현황: 2025년 6월 24일부터 25일 사이 뉴욕주 대법원에 Williams 대 Blueprint Medicines Corp.와 Phillips 대 Blueprint Medicines Corp.라는 두 건의 주주 소송이 제기되었으며, Schedule 14D-9 공개 내용의 부족을 주장하고 거래 중지를 포함한 구제를 요청하고 있습니다. 또한 12명의 주주가 추가 공개를 요구하는 서한을 발송했습니다. Sanofi는 새로운 중대한 주장 없이는 유사한 소송 제기가 공개되지 않을 수 있음을 언급합니다.

투자자에 대한 시사점: 미국 및 주요 유럽연합 반독점 심사가 완료되어 규제 리스크가 크게 줄어들었으며, 성공적인 거래 종료 및 $129 현금 대금(및 잠재적 CVR) 실현 가능성이 높아졌습니다. 진행 중인 주주 소송은 일반적인 M&A 장애물이며 드문 일이 아니지만, 추가적인 시간 지연이나 비용 위험을 초래할 수 있습니다.

La filiale en propriété exclusive de Sanofi, Rothko Merger Sub, Inc., a fait progresser son offre publique d'achat en espèces à 129,00 $ par action pour Blueprint Medicines (BPMC) en franchissant plusieurs étapes réglementaires clés. L’amendement au Schedule TO confirme que la période d’attente de 30 jours selon la loi Hart-Scott-Rodino (HSR) a expiré le 9 juillet 2025, satisfaisant la principale condition de clôture antitrust américaine. En Europe, l’examen de Phase I en Autriche a pris fin le 8 juillet 2025, l’Office fédéral allemand des cartels a donné son feu vert le 30 juin 2025, et la Présidence du Conseil des ministres italien a statué le 25 juin 2025 que la fusion n’entre pas dans le cadre de son régime des investissements étrangers. Ces approbations réduisent significativement les risques liés à l’exécution de la transaction.

La contrepartie reste de 129,00 $ en espèces plus un droit de valeur conditionnel non transférable (CVR) pouvant atteindre 6,00 $ par action, payable à la réalisation de jalons spécifiques. Toutes les autres conditions contenues dans l’offre d’achat initiale datée du 17 juin 2025 restent inchangées et sont incorporées par référence.

Mise à jour sur les litiges : Deux actions en justice de porteurs d’actions – Williams contre Blueprint Medicines Corp. et Phillips contre Blueprint Medicines Corp. – ont été déposées devant la Cour suprême de l’État de New York entre le 24 et le 25 juin 2025, alléguant des insuffisances dans les divulgations du Schedule 14D-9 et demandant, entre autres, à faire interdire la transaction. De plus, 12 actionnaires ont envoyé des lettres de demande de divulgations complémentaires. Sanofi note que des dépôts similaires peuvent ne pas être rendus publics en l’absence de nouvelles allégations importantes.

Implications pour les investisseurs : Avec la finalisation des examens antitrust aux États-Unis et dans les principales juridictions européennes, le risque réglementaire est substantiellement réduit, augmentant la probabilité d’une clôture réussie et la réalisation de la contrepartie en espèces de 129 $ (plus le CVR potentiel). Les litiges en cours représentent un obstacle standard dans les opérations de fusion-acquisition et ne sont pas inhabituels ; toutefois, ils pourraient entraîner des risques supplémentaires en termes de délais ou de coûts.

Die vollständig im Besitz von Sanofi befindliche Tochtergesellschaft Rothko Merger Sub, Inc. hat ihr Barangebot von 129,00 $ pro Aktie für Blueprint Medicines (BPMC) durch das Überwinden mehrerer wichtiger regulatorischer Hürden vorangetrieben. Die Änderung des Schedule TO bestätigt, dass die 30-tägige Hart-Scott-Rodino (HSR)-Wartefrist am 9. Juli 2025 abgelaufen ist und somit die wesentliche US-amerikanische kartellrechtliche Abschlussbedingung erfüllt wurde. In Europa lief die Phase-I-Prüfung in Österreich am 8. Juli 2025 ab, das deutsche Bundeskartellamt erteilte am 30. Juni 2025 die Freigabe, und die italienische Präsidentschaft des Ministerrats entschied am 25. Juni 2025, dass die Fusion nicht unter das ausländische Investitionsregime fällt. Diese Genehmigungen verringern das Risiko der Transaktionsdurchführung erheblich.

Die Gegenleistung bleibt 129,00 $ in bar plus ein nicht übertragbares bedingtes Wertrecht (CVR) von bis zu 6,00 $ pro Aktie, zahlbar bei Erreichen bestimmter Meilensteine. Alle weiteren Bedingungen des ursprünglichen Kaufangebots vom 17. Juni 2025 bleiben unverändert und werden durch Verweis einbezogen.

Aktualisierung zu Rechtsstreitigkeiten: Zwei Aktionärsklagen – Williams gegen Blueprint Medicines Corp. und Phillips gegen Blueprint Medicines Corp. – wurden zwischen dem 24. und 25. Juni 2025 beim New Yorker Obersten Gerichtshof eingereicht. Sie werfen Mängel bei der Offenlegung im Schedule 14D-9 vor und beantragen unter anderem die Unterbindung der Transaktion. Darüber hinaus haben 12 Aktionäre Aufforderungsschreiben mit der Bitte um ergänzende Offenlegung versandt. Sanofi weist darauf hin, dass ähnliche Klagen ohne neue wesentliche Vorwürfe möglicherweise nicht öffentlich bekannt gemacht werden.

Auswirkungen für Investoren: Mit Abschluss der US-amerikanischen und der wichtigsten EU-Kartellprüfungen ist das regulatorische Risiko erheblich reduziert, was die Wahrscheinlichkeit eines erfolgreichen Abschlusses und die Realisierung der Barzahlung von 129 $ (plus potenziellen CVR) erhöht. Laufende Aktionärsklagen stellen eine übliche Hürde bei M&A-Transaktionen dar und sind nicht ungewöhnlich; sie könnten jedoch zusätzliche zeitliche oder kostenseitige Risiken mit sich bringen.

 
 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

 

SCHEDULE TO

Tender Offer Statement under Section 14(d)(1) or 13(e)(1)

of the Securities Exchange Act of 1934

(Amendment No. 1)

 

 

Blueprint Medicines Corporation

(Name of Subject Company (Issuer))

ROTHKO MERGER SUB, INC.

AVENTIS INC.

SANOFI

(Names of Filing Persons — Offerors)

Common Stock, Par Value $0.001 Per Share

(Title of Class of Securities)

09627Y109

(Cusip Number of Class of Securities)

Roy Papatheodorou

Executive Vice President, General Counsel, Head of Legal Ethics & Business Integrity

Sanofi

46, avenue de la Grande Armée, 75017

Paris, France

Telephone: 011 + 33 1 53 77 40 00

(Name, Address and Telephone Number of Person Authorized to Receive Notices and Communications on Behalf of Filing Persons)

Copies to:

Michael J. Aiello, Esq.

Sachin Kohli, Esq.

Weil, Gotshal & Manges LLP

767 Fifth Avenue

New York, New York 10153

(212) 310-8000

 

 

 

Check the box if any part of the fee is offset as provided by Rule 0-11(a)(2) and identify the filing with which the offsetting fee was previously paid. Identify the previous filing by registration statement number, or the form or schedule and the date of its filing.

 

Amount Previously Paid: 1,465,193.42    Filing Party: Sanofi, Aventis Inc. and Rothko Merger Sub, Inc.
Form or Registration No.: Schedule TO-T (File No. 005-88827)    Date Filed: June 17, 2025

 

Check the box if the filing relates solely to preliminary communications made before the commencement of a tender offer.

Check the appropriate boxes below to designate any transactions to which the statement relates:

 

  ☒ 

Third-party tender offer subject to Rule 14d-1.

  ☐ 

Issuer tender offer subject to Rule 13e-4.

  ☐ 

Going-private transaction subject to Rule 13e-3.

  ☐ 

Amendment to Schedule 13D under Rule 13d-2.

Check the following box if the filing is a final amendment reporting the results of the tender offer: ☐

If applicable, check the appropriate box(es) below to designate the appropriate rule provision(s) relied upon:

 

  ☐ 

Rule 13e-4(i) (Cross-Border Issuer Tender Offer)

  ☐ 

Rule 14d-1(d) (Cross-Border Third-Party Tender Offer)

 

 
 


This Amendment No. 1 (this “Amendment”) amends and supplements the Tender Offer Statement on Schedule TO filed by (i) Rothko Merger Sub, Inc., a Delaware corporation (“Purchaser”) and an indirect wholly owned subsidiary of SANOFI, a French société anonyme (“Parent”), (ii) Parent, and (iii) Aventis Inc., a Pennsylvania corporation and wholly owned subsidiary of Parent and direct parent of Purchaser (“Aventis”) on June 17, 2025 (together with any amendments or supplements thereto, including this Amendment, the “Schedule TO”), relating to the offer by Purchaser to purchase all of the outstanding shares of common stock, par value, $0.001 per share (each a “Share” and collectively, “Shares”), of Blueprint Medicines Corporation, a Delaware corporation (the “Company”), for $129.00 per Share in cash, without interest (the “Cash Offer Price”) and subject to any withholding of taxes required by applicable legal requirements, plus one (1) non-transferable contractual contingent value right (each, a “CVR”) per Share, representing the right to receive contingent payments of up to an aggregate amount of $6.00 per Share in cash, without interest, upon the achievement of one or both of the milestones on or prior to the expiration of the applicable milestone period set forth in the CVR Agreement to be entered into with a Rights Agent mutually agreeable to Aventis and the Company (the CVR, together with the Cash Offer Price, or any other amount paid pursuant to the Offer to the extent permitted under the Merger Agreement, the “Offer Consideration”), on the terms and subject to the conditions set forth in the Offer to Purchase, dated June 17, 2025 (together with any amendments or supplements thereto, the “Offer to Purchase”) and in the accompanying Letter of Transmittal, which are annexed to and filed with the Schedule TO as Exhibits (a)(1)(A) and (a)(1)(B), respectively.

All information set forth in the Offer to Purchase, including Schedule I thereto, is incorporated by reference herein in response to Items 1 through 9 and Item 11 of this Schedule TO and is supplemented by the information specifically provided in this Amendment, except as otherwise set forth below. This Amendment should be read together with the Schedule TO. Capitalized terms used and not otherwise defined in this Amendment have the meanings given to such terms in the Offer to Purchase.

Items 1 through 9 and Item 11.

The Offer to Purchase and Items 1 through 9 and Item 11 of the Schedule TO, to the extent such Items incorporate by reference the information contained in the Offer to Purchase, are hereby amended and supplemented as follows:

 

(1)

The second paragraph of the subsection entitled “Antitrust Compliance” in Section 16 – “Certain Legal Matters; Regulatory Approvals” is amended and supplemented by deleting the second paragraph and adding the following paragraph:

“Under the HSR Act, the purchase of Shares may not be completed until the expiration of a 30-calendar day waiting period following the filing of certain required information and documentary material concerning the Offer with the FTC and the Antitrust Division, unless the waiting period is earlier terminated by the FTC and the Antitrust Division. The waiting period under the HSR Act expired, effective July 9, 2025 at 11:59 p.m., Eastern Time. Accordingly, the condition to the Offer requiring that the waiting period (or any extension thereof) applicable to the Offer and the Merger under the HSR Act shall have expired or been terminated has been satisfied.”

 

(2)

The subsection entitled “Austria Merger Control Compliance” in Section 16 – “Certain Legal Matters; Regulatory Approvals” is amended and supplemented by deleting the last sentence of the paragraph and adding the following sentence at the end of the paragraph:

“The expiry of the statutory (Phase I) waiting period occurred on July 8, 2025 (24:00 Central European Time).”


(3)

The subsection entitled “Germany Merger Control Compliance” in Section 16 – “Certain Legal Matters; Regulatory Approvals” is deleted and is amended and supplemented by adding the following paragraph:

“Under part I chapter VII of the Act against Restraints of Competition (“ARC”), certain acquisitions, including the Purchaser’s purchase of Shares pursuant to the Offer, may not be consummated until certain information has been furnished for review by the Federal Cartel Office (“FCO”) and either the FCO has declared clearance of the transaction or certain waiting periods have expired. The parties submitted a notification to the FCO on June 10, 2025. German merger control clearance was received on June 30, 2025.”

 

(4)

The subsection entitled “Italy Foreign Direct Investment Compliance” in Section 16 – “Certain Legal Matters; Regulatory Approvals” is amended and supplemented by deleting the last two sentences of the paragraph and adding the following sentence at the end of the paragraph:

“The parties submitted a notification on June 9, 2025. On June 25, 2025, the Presidency of the Council of Ministers in Italy confirmed that the Merger does not fall within the scope of Law Decree No. 21/2012.”

 

(5)

Section 16 — “Certain Legal Matters; Regulatory Approvals” is hereby amended and supplemented by adding the following to the end of such Section after the subsection captioned “State Takeover Laws”:

Legal Proceedings Relating to the Tender Offer. Between June 24, 2025 and July 10, 2025, two complaints were filed in the Supreme Court of the State of New York, County of New York (“Sup. Ct. N.Y. Cnty.”) by purported stockholders of the Company: Williams v. Blueprint Medicines Corp., et al., No. 653805/2025 (Sup. Ct. N.Y. Cnty., filed June 24, 2025); and Phillips v. Blueprint Medicines Corp., et al., No. 653820/2025 (Sup. Ct. N.Y. Cnty., filed June 25, 2025) (collectively, the “Merger Actions”). The Merger Actions name the Company and the members of the board of directors of the Company as defendants. The Merger Actions generally allege that the Schedule 14D-9 is materially incomplete and misleading by allegedly failing to disclose purportedly material information, and assert claims for negligent misrepresentation and concealment, and negligence under New York law against the Company and the Company Board. The Merger Actions seek, among other things, an injunction enjoining the consummation of the Transactions, rescission of the Transactions if consummated, costs of the action, including attorneys’ fees and experts’ fees and expenses, an award of damages, and any other relief the court may deem just and proper. In addition, between June 18, 2025 and July 10, 2025, twelve purported stockholders of the Company sent demand letters requesting that the Company supplement the disclosures contained in the Schedule 14D-9. If additional similar demand letters are received or complaints are filed, absent new or different allegations that are material, Purchaser, Parent or the Company will not necessarily announce such additional filings.”


SIGNATURES

After due inquiry and to the best knowledge and belief of the undersigned, each of the undersigned certifies that the information set forth in this statement is true, complete and correct.

Date: July 10, 2025

 

  Rothko Merger Sub, Inc.
By:  

/s/ Michael J. Tolpa

  Name: Michael J. Tolpa
  Title: President
  SANOFI
By:  

/s/ Roy Papatheodorou

  Name: Roy Papatheodorou
  Title: Executive Vice President, General Counsel
  Aventis Inc.
By:  

/s/ Jamie Haney

  Name: Jamie Haney
  Title: Vice President, General Counsel, Secretary
Blueprint Medicines Corp

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