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[8-K] Welltower Inc. Reports Material Event

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Rhea-AI Filing Summary

Alvotech’s July 2025 Form 6-K details governance, commercial, regulatory and financing actions since its Q1 report.

  • Governance: Six directors re-elected; veteran executive Linda Jónsdóttir appointed CFO; COO Faysal Kalmoua exits board and management.
  • Commercial: Advanz Pharma partnership broadened to three new biosimilars (milestones up to €160 m) and separate AVT10 (Cimzia) deal; global Keytruda biosimilar co-development with Dr. Reddy’s.
  • M&A: Acquired Swiss packager Ivers-Lee and Xbrane’s Swedish R&D team plus Cimzia candidate for c.SEK 275 m.
  • Pipeline: CHMP positive opinion for AVT06 (Eylea); AVT23 (Xolair) study shows therapeutic equivalence.
  • Manufacturing risk: FDA pre-approval inspection (26 Jun–4 Jul) issued Form 483 citing operational, documentation and quality control deficiencies; detailed response submitted 25 Jul.
  • Financing: Oversubscribed SDR IPO (SEK 39 m) and institutional placement (SEK 750 m) add >3,000 new holders; term-loan amendment folds second tranche, trims margin to SOFR+6.0%, facility now $1.081 bn, cash $152 m.

New capital and partnerships enhance growth prospects, but regulatory remediation is critical for near-term BLA approvals.

Il Form 6-K di Alvotech di luglio 2025 riporta le azioni di governance, commerciali, regolatorie e finanziarie intraprese dalla società dopo il rapporto del primo trimestre.

  • Governance: Sei amministratori rieletti; la veterana dirigente Linda Jónsdóttir nominata CFO; il COO Faysal Kalmoua lascia il consiglio e la direzione.
  • Commerciale: Ampliata la partnership con Advanz Pharma a tre nuovi biosimilari (milestone fino a 160 milioni di euro) e accordo separato per AVT10 (Cimzia); co-sviluppo globale del biosimilare di Keytruda con Dr. Reddy’s.
  • M&A: Acquisiti il confezionatore svizzero Ivers-Lee e il team R&D svedese di Xbrane, oltre al candidato Cimzia per 275 milioni di corone svedesi.
  • Pipeline: Opinione positiva del CHMP per AVT06 (Eylea); studio su AVT23 (Xolair) dimostra equivalenza terapeutica.
  • Rischio produttivo: Ispezione FDA pre-approvazione (26 giu–4 lug) ha emesso un Form 483 evidenziando carenze operative, documentali e di controllo qualità; risposta dettagliata inviata il 25 luglio.
  • Finanziamenti: IPO SDR sovrasottoscritta (39 milioni SEK) e collocamento istituzionale (750 milioni SEK) hanno aggiunto oltre 3.000 nuovi azionisti; modifica del prestito a termine che elimina la seconda tranche, riduce il margine a SOFR+6,0%, struttura ora a 1,081 miliardi di dollari, liquidità di 152 milioni.

Il nuovo capitale e le partnership rafforzano le prospettive di crescita, ma la risoluzione delle questioni regolatorie è fondamentale per le approvazioni BLA a breve termine.

El Formulario 6-K de Alvotech de julio de 2025 detalla las acciones de gobernanza, comerciales, regulatorias y financieras desde su informe del primer trimestre.

  • Gobernanza: Seis directores reelegidos; la veterana ejecutiva Linda Jónsdóttir nombrada CFO; el COO Faysal Kalmoua sale del consejo y la gestión.
  • Comercial: Ampliada la asociación con Advanz Pharma a tres nuevos biosimilares (hitos hasta 160 millones de euros) y un acuerdo separado para AVT10 (Cimzia); co-desarrollo global del biosimilar de Keytruda con Dr. Reddy’s.
  • Fusiones y Adquisiciones: Adquirido el empaquetador suizo Ivers-Lee y el equipo sueco de I+D de Xbrane, además del candidato Cimzia por 275 millones de coronas suecas.
  • Pipeline: Opinión positiva del CHMP para AVT06 (Eylea); estudio de AVT23 (Xolair) muestra equivalencia terapéutica.
  • Riesgo de fabricación: Inspección FDA previa a la aprobación (26 jun–4 jul) emitió un Form 483 señalando deficiencias operativas, documentales y de control de calidad; respuesta detallada enviada el 25 de julio.
  • Financiación: IPO SDR sobresuscrita (39 millones SEK) y colocación institucional (750 millones SEK) que suman más de 3,000 nuevos accionistas; enmienda del préstamo a plazo que elimina la segunda tranche, reduce el margen a SOFR+6.0%, con una facilidad ahora de 1,081 mil millones de dólares y efectivo de 152 millones.

El nuevo capital y las asociaciones mejoran las perspectivas de crecimiento, pero la remediación regulatoria es crítica para las aprobaciones BLA a corto plazo.

Alvotech의 2025년 7월 Form 6-K는 1분기 보고서 이후의 거버넌스, 상업, 규제 및 금융 조치를 상세히 기술합니다.

  • 거버넌스: 6명의 이사 재선임; 베테랑 임원 Linda Jónsdóttir CFO로 임명; COO Faysal Kalmoua는 이사회 및 경영진에서 퇴임.
  • 상업: Advanz Pharma와의 파트너십이 세 가지 신규 바이오시밀러로 확대(마일스톤 최대 1억 6천만 유로) 및 별도의 AVT10 (Cimzia) 계약; Dr. Reddy’s와 글로벌 Keytruda 바이오시밀러 공동 개발.
  • M&A: 스위스 포장업체 Ivers-Lee와 Xbrane의 스웨덴 연구개발팀, 그리고 Cimzia 후보 물질을 약 2억 7,500만 SEK에 인수.
  • 파이프라인: AVT06 (Eylea)에 대한 CHMP 긍정적 의견; AVT23 (Xolair) 연구에서 치료적 동등성 확인.
  • 제조 리스크: FDA 사전 승인 검사(6월 26일~7월 4일)에서 운영, 문서 및 품질 관리 결함을 지적하는 Form 483 발행; 7월 25일 상세 답변 제출.
  • 금융: 초과 청약된 SDR IPO (3,900만 SEK) 및 기관 배정 (7억 5천만 SEK)으로 3,000명 이상의 신규 주주 확보; 조건부 대출 수정으로 두 번째 분할금 폐지, 마진은 SOFR+6.0%로 축소, 현재 시설 규모 10억 8,100만 달러, 현금 1억 5,200만 달러.

신규 자본과 파트너십은 성장 전망을 강화하지만, 단기 BLA 승인에는 규제 문제 해결이 필수적입니다.

Le Formulaire 6-K d'Alvotech de juillet 2025 détaille les actions de gouvernance, commerciales, réglementaires et financières depuis son rapport du premier trimestre.

  • Gouvernance : Six administrateurs réélus ; la cadre expérimentée Linda Jónsdóttir nommée CFO ; le COO Faysal Kalmoua quitte le conseil d'administration et la direction.
  • Commercial : Partenariat avec Advanz Pharma étendu à trois nouveaux biosimilaires (jalons jusqu'à 160 M€) et accord distinct pour AVT10 (Cimzia) ; co-développement mondial du biosimilaire de Keytruda avec Dr. Reddy’s.
  • Fusions & Acquisitions : Acquisition de l’emballeur suisse Ivers-Lee et de l’équipe R&D suédoise de Xbrane, ainsi que du candidat Cimzia pour 275 MSEK.
  • Pipeline : Avis positif du CHMP pour AVT06 (Eylea) ; étude AVT23 (Xolair) démontrant une équivalence thérapeutique.
  • Risque de fabrication : Inspection pré-approbation FDA (26 juin–4 juillet) ayant émis un Form 483 signalant des déficiences opérationnelles, documentaires et de contrôle qualité ; réponse détaillée soumise le 25 juillet.
  • Financement : IPO SDR sursouscrite (39 MSEK) et placement institutionnel (750 MSEK) ajoutant plus de 3 000 nouveaux actionnaires ; amendement du prêt à terme supprimant la deuxième tranche, réduisant la marge à SOFR+6,0 %, facilité portée à 1,081 Md$ et trésorerie à 152 M$.

Le nouveau capital et les partenariats renforcent les perspectives de croissance, mais la correction réglementaire est cruciale pour les approbations BLA à court terme.

Der Form 6-K von Alvotech im Juli 2025 beschreibt Governance-, kommerzielle, regulatorische und finanzielle Maßnahmen seit dem Q1-Bericht.

  • Governance: Sechs Direktoren wiedergewählt; die erfahrene Managerin Linda Jónsdóttir zur CFO ernannt; COO Faysal Kalmoua verlässt Vorstand und Management.
  • Kommerziell: Partnerschaft mit Advanz Pharma auf drei neue Biosimilars ausgeweitet (Meilensteine bis zu 160 Mio. €) sowie separates AVT10 (Cimzia)-Abkommen; globale Co-Entwicklung des Keytruda-Biosimilars mit Dr. Reddy’s.
  • M&A: Übernahme des Schweizer Verpackers Ivers-Lee und des schwedischen F&E-Teams von Xbrane sowie des Cimzia-Kandidaten für 275 Mio. SEK.
  • Pipeline: Positive CHMP-Stellungnahme für AVT06 (Eylea); AVT23 (Xolair)-Studie zeigt therapeutische Äquivalenz.
  • Fertigungsrisiko: FDA-Vorabgenehmigungsinspektion (26. Juni–4. Juli) erteilte Form 483 mit Hinweisen auf operative, dokumentarische und Qualitätskontrollmängel; detaillierte Antwort am 25. Juli eingereicht.
  • Finanzierung: Überzeichnetes SDR-IPO (39 Mio. SEK) und institutionelle Platzierung (750 Mio. SEK) bringen über 3.000 neue Anteilseigner; Änderung des Terminkredits, zweite Tranche entfällt, Marge auf SOFR+6,0% gesenkt, Kreditlinie nun 1,081 Mrd. USD, Barbestand 152 Mio.

Neues Kapital und Partnerschaften stärken die Wachstumsaussichten, aber regulatorische Nachbesserungen sind für kurzfristige BLA-Zulassungen entscheidend.

Positive
  • €160 m milestone expansion of Advanz Pharma partnership covering three new biosimilars
  • Global Keytruda biosimilar collaboration with Dr. Reddy’s broadens high-value oncology pipeline
  • CHMP positive opinion for AVT06 and successful AVT23 efficacy study de-risk European approvals
  • SEK 789 m equity raises were oversubscribed, adding >3,000 shareholders and improving liquidity
  • Term-loan amendment lowers interest by 50 bp and simplifies capital structure, reducing financing costs
Negative
  • FDA Form 483 cites multiple manufacturing and documentation deficiencies that could delay four pending BLAs
  • Executive turnover with COO departure may disrupt operational continuity during critical remediation phase

Insights

TL;DR – Strong deals and financing offset by FDA Form 483 risk; net impact neutral.

Commercial wins with Advanz (€160 m milestones) and Dr. Reddy’s expand the oncology & autoimmune pipeline while Ivers-Lee adds downstream capacity. SEK 789 m of fresh equity plus a 50 bp interest cut strengthen liquidity and reduce cash burn. However, the Form 483 covers multiple quality-system gaps tied to four BLAs; approval timing for AVT02/03/05/06 now depends on FDA classification, creating binary regulatory risk. Overall, strategic momentum is positive but valuation upside is capped until inspection issues are fully resolved.

TL;DR – Form 483 elevates approval risk; remediation plan is submitted but outcome uncertain.

The inspection observations span manufacturing controls, documentation and lab practices—areas often requiring re-inspection. While management claims some issues are historical, FDA follow-up could delay launch-ready assets and trigger additional costs. Positive CHMP feedback on AVT06 underscores EU progress, yet U.S. revenue inflection depends on clearing the Form 483. Investors should monitor FDA’s classification letter (OAI, VAI or NAI) and potential impact on 2025–26 launch schedules.

Il Form 6-K di Alvotech di luglio 2025 riporta le azioni di governance, commerciali, regolatorie e finanziarie intraprese dalla società dopo il rapporto del primo trimestre.

  • Governance: Sei amministratori rieletti; la veterana dirigente Linda Jónsdóttir nominata CFO; il COO Faysal Kalmoua lascia il consiglio e la direzione.
  • Commerciale: Ampliata la partnership con Advanz Pharma a tre nuovi biosimilari (milestone fino a 160 milioni di euro) e accordo separato per AVT10 (Cimzia); co-sviluppo globale del biosimilare di Keytruda con Dr. Reddy’s.
  • M&A: Acquisiti il confezionatore svizzero Ivers-Lee e il team R&D svedese di Xbrane, oltre al candidato Cimzia per 275 milioni di corone svedesi.
  • Pipeline: Opinione positiva del CHMP per AVT06 (Eylea); studio su AVT23 (Xolair) dimostra equivalenza terapeutica.
  • Rischio produttivo: Ispezione FDA pre-approvazione (26 giu–4 lug) ha emesso un Form 483 evidenziando carenze operative, documentali e di controllo qualità; risposta dettagliata inviata il 25 luglio.
  • Finanziamenti: IPO SDR sovrasottoscritta (39 milioni SEK) e collocamento istituzionale (750 milioni SEK) hanno aggiunto oltre 3.000 nuovi azionisti; modifica del prestito a termine che elimina la seconda tranche, riduce il margine a SOFR+6,0%, struttura ora a 1,081 miliardi di dollari, liquidità di 152 milioni.

Il nuovo capitale e le partnership rafforzano le prospettive di crescita, ma la risoluzione delle questioni regolatorie è fondamentale per le approvazioni BLA a breve termine.

El Formulario 6-K de Alvotech de julio de 2025 detalla las acciones de gobernanza, comerciales, regulatorias y financieras desde su informe del primer trimestre.

  • Gobernanza: Seis directores reelegidos; la veterana ejecutiva Linda Jónsdóttir nombrada CFO; el COO Faysal Kalmoua sale del consejo y la gestión.
  • Comercial: Ampliada la asociación con Advanz Pharma a tres nuevos biosimilares (hitos hasta 160 millones de euros) y un acuerdo separado para AVT10 (Cimzia); co-desarrollo global del biosimilar de Keytruda con Dr. Reddy’s.
  • Fusiones y Adquisiciones: Adquirido el empaquetador suizo Ivers-Lee y el equipo sueco de I+D de Xbrane, además del candidato Cimzia por 275 millones de coronas suecas.
  • Pipeline: Opinión positiva del CHMP para AVT06 (Eylea); estudio de AVT23 (Xolair) muestra equivalencia terapéutica.
  • Riesgo de fabricación: Inspección FDA previa a la aprobación (26 jun–4 jul) emitió un Form 483 señalando deficiencias operativas, documentales y de control de calidad; respuesta detallada enviada el 25 de julio.
  • Financiación: IPO SDR sobresuscrita (39 millones SEK) y colocación institucional (750 millones SEK) que suman más de 3,000 nuevos accionistas; enmienda del préstamo a plazo que elimina la segunda tranche, reduce el margen a SOFR+6.0%, con una facilidad ahora de 1,081 mil millones de dólares y efectivo de 152 millones.

El nuevo capital y las asociaciones mejoran las perspectivas de crecimiento, pero la remediación regulatoria es crítica para las aprobaciones BLA a corto plazo.

Alvotech의 2025년 7월 Form 6-K는 1분기 보고서 이후의 거버넌스, 상업, 규제 및 금융 조치를 상세히 기술합니다.

  • 거버넌스: 6명의 이사 재선임; 베테랑 임원 Linda Jónsdóttir CFO로 임명; COO Faysal Kalmoua는 이사회 및 경영진에서 퇴임.
  • 상업: Advanz Pharma와의 파트너십이 세 가지 신규 바이오시밀러로 확대(마일스톤 최대 1억 6천만 유로) 및 별도의 AVT10 (Cimzia) 계약; Dr. Reddy’s와 글로벌 Keytruda 바이오시밀러 공동 개발.
  • M&A: 스위스 포장업체 Ivers-Lee와 Xbrane의 스웨덴 연구개발팀, 그리고 Cimzia 후보 물질을 약 2억 7,500만 SEK에 인수.
  • 파이프라인: AVT06 (Eylea)에 대한 CHMP 긍정적 의견; AVT23 (Xolair) 연구에서 치료적 동등성 확인.
  • 제조 리스크: FDA 사전 승인 검사(6월 26일~7월 4일)에서 운영, 문서 및 품질 관리 결함을 지적하는 Form 483 발행; 7월 25일 상세 답변 제출.
  • 금융: 초과 청약된 SDR IPO (3,900만 SEK) 및 기관 배정 (7억 5천만 SEK)으로 3,000명 이상의 신규 주주 확보; 조건부 대출 수정으로 두 번째 분할금 폐지, 마진은 SOFR+6.0%로 축소, 현재 시설 규모 10억 8,100만 달러, 현금 1억 5,200만 달러.

신규 자본과 파트너십은 성장 전망을 강화하지만, 단기 BLA 승인에는 규제 문제 해결이 필수적입니다.

Le Formulaire 6-K d'Alvotech de juillet 2025 détaille les actions de gouvernance, commerciales, réglementaires et financières depuis son rapport du premier trimestre.

  • Gouvernance : Six administrateurs réélus ; la cadre expérimentée Linda Jónsdóttir nommée CFO ; le COO Faysal Kalmoua quitte le conseil d'administration et la direction.
  • Commercial : Partenariat avec Advanz Pharma étendu à trois nouveaux biosimilaires (jalons jusqu'à 160 M€) et accord distinct pour AVT10 (Cimzia) ; co-développement mondial du biosimilaire de Keytruda avec Dr. Reddy’s.
  • Fusions & Acquisitions : Acquisition de l’emballeur suisse Ivers-Lee et de l’équipe R&D suédoise de Xbrane, ainsi que du candidat Cimzia pour 275 MSEK.
  • Pipeline : Avis positif du CHMP pour AVT06 (Eylea) ; étude AVT23 (Xolair) démontrant une équivalence thérapeutique.
  • Risque de fabrication : Inspection pré-approbation FDA (26 juin–4 juillet) ayant émis un Form 483 signalant des déficiences opérationnelles, documentaires et de contrôle qualité ; réponse détaillée soumise le 25 juillet.
  • Financement : IPO SDR sursouscrite (39 MSEK) et placement institutionnel (750 MSEK) ajoutant plus de 3 000 nouveaux actionnaires ; amendement du prêt à terme supprimant la deuxième tranche, réduisant la marge à SOFR+6,0 %, facilité portée à 1,081 Md$ et trésorerie à 152 M$.

Le nouveau capital et les partenariats renforcent les perspectives de croissance, mais la correction réglementaire est cruciale pour les approbations BLA à court terme.

Der Form 6-K von Alvotech im Juli 2025 beschreibt Governance-, kommerzielle, regulatorische und finanzielle Maßnahmen seit dem Q1-Bericht.

  • Governance: Sechs Direktoren wiedergewählt; die erfahrene Managerin Linda Jónsdóttir zur CFO ernannt; COO Faysal Kalmoua verlässt Vorstand und Management.
  • Kommerziell: Partnerschaft mit Advanz Pharma auf drei neue Biosimilars ausgeweitet (Meilensteine bis zu 160 Mio. €) sowie separates AVT10 (Cimzia)-Abkommen; globale Co-Entwicklung des Keytruda-Biosimilars mit Dr. Reddy’s.
  • M&A: Übernahme des Schweizer Verpackers Ivers-Lee und des schwedischen F&E-Teams von Xbrane sowie des Cimzia-Kandidaten für 275 Mio. SEK.
  • Pipeline: Positive CHMP-Stellungnahme für AVT06 (Eylea); AVT23 (Xolair)-Studie zeigt therapeutische Äquivalenz.
  • Fertigungsrisiko: FDA-Vorabgenehmigungsinspektion (26. Juni–4. Juli) erteilte Form 483 mit Hinweisen auf operative, dokumentarische und Qualitätskontrollmängel; detaillierte Antwort am 25. Juli eingereicht.
  • Finanzierung: Überzeichnetes SDR-IPO (39 Mio. SEK) und institutionelle Platzierung (750 Mio. SEK) bringen über 3.000 neue Anteilseigner; Änderung des Terminkredits, zweite Tranche entfällt, Marge auf SOFR+6,0% gesenkt, Kreditlinie nun 1,081 Mrd. USD, Barbestand 152 Mio.

Neues Kapital und Partnerschaften stärken die Wachstumsaussichten, aber regulatorische Nachbesserungen sind für kurzfristige BLA-Zulassungen entscheidend.

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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 OR 15(d) of
The Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): July 28, 2025
Welltower Inc.
(Exact name of registrant as specified in its charter)
Delaware1-892334-1096634
(State or other jurisdiction
of Incorporation)
(Commission
File Number)
(IRS Employer
Identification No.)
4500 Dorr Street, Toledo, Ohio43615
(Address of principal executive offices)(Zip Code)

Registrant's telephone number, including area code: (419) 247-2800
Not Applicable
(Former name or former address, if changed since last report.)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
    Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
    Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
    Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
    Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Securities registered pursuant to Section 12(b) of the Act:
Title of each classTrading Symbol(s)Name of each exchange on which registered
Common stock, $1.00 par value per shareWELLNew York Stock Exchange
Guarantee of 4.800% Notes due 2028 issued by Welltower OP LLCWELL/28New York Stock Exchange
Guarantee of 4.500% Notes due 2034 issued by Welltower OP LLCWELL/34New York Stock Exchange
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company    
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.



Item 2.02  Results of Operations and Financial Condition.
On July 28, 2025, Welltower Inc. issued a press release that announced operating results for its second quarter ended June 30, 2025. The press release refers to a supplemental information package that is available on the Company's website (www.welltower.com), free of charge. Copies of the press release and supplemental information package have been furnished as Exhibits 99.1 and 99.2, respectively, to this Current Report, and are incorporated herein by reference.
The information included in this Item 2.02, including Exhibits 99.1 and 99.2, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), and shall not be incorporated by reference into any filing of the Company under the Securities Act of 1933, as amended, or the Exchange Act, regardless of any general incorporation language in such filing.
Item 9.01 Financial Statements and Exhibits.
(d)  Exhibits.
99.1    Press release of Welltower Inc. dated July 28, 2025, announcing earnings for the quarter ended June 30, 2025.
99.2    Welltower Inc. Supplemental Information Package for the quarter ended June 30, 2025.
104     Cover Page Interactive Data File - the cover page XBRL tags are embedded within the Inline XBRL document.




SIGNATURE
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
WELLTOWER INC.
By:/s/ Matthew McQueen
Name:Matthew McQueen
Title:Chief Legal Officer and General Counsel
 
Dated:  July 28, 2025

FAQ

What regulatory setback did Alvotech (ALVO) disclose in the July 2025 6-K?

The FDA issued a Form 483 after a 26 Jun–4 Jul pre-approval inspection of the Reykjavik plant, noting quality-system deficiencies.

How much capital did Alvotech raise through recent share offerings?

Alvotech raised SEK 39 m via an SDR IPO and SEK 750 m through a private placement in June 2025.

What are the financial terms of the amended term-loan facility?

Post-amendment, the entire $1.081 bn facility bears SOFR + 6.0% cash interest, 50 bp lower than before, maturing July 2029.

Which pipeline assets received positive European feedback?

AVT06 (biosimilar to Eylea) received a positive CHMP opinion, and AVT23 (Xolair) met its primary endpoint in a confirmatory study.

What is the potential value of the expanded Advanz Pharma partnership?

The agreement includes up to €160 m in development and commercial milestones plus revenue sharing.
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