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Arvinas Reports Third Quarter 2024 Financial Results and Provides Corporate Update

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Arvinas (ARVN) reported Q3 2024 financial results with revenue of $102.4 million, up from $34.6 million in Q3 2023. The company maintains $1.1 billion in cash and equivalents, expected to fund operations into 2027. Key developments include ongoing enrollment in multiple clinical studies for vepdegestrant in breast cancer, with topline data from VERITAC-2 Phase 3 trial expected in Q4 2024 or Q1 2025. Research and development expenses were $86.9 million, while general and administrative expenses increased to $75.8 million, including a $43.4 million lease termination loss.

Arvinas (ARVN) ha riportato i risultati finanziari del terzo trimestre 2024 con ricavi di 102,4 milioni di dollari, in aumento rispetto ai 34,6 milioni di dollari del terzo trimestre 2023. L'azienda mantiene 1,1 miliardi di dollari in contante e equivalenti, previsti per finanziare le operazioni fino al 2027. Sviluppi chiave includono l'iscrizione in corso in diversi studi clinici per vepdegestrant nel cancro al seno, con i dati principali dello studio VERITAC-2 di Fase 3 attesi nel quarto trimestre 2024 o nel primo trimestre 2025. Le spese per ricerca e sviluppo sono state di 86,9 milioni di dollari, mentre le spese generali e amministrative sono aumentate a 75,8 milioni di dollari, inclusa una perdita di 43,4 milioni di dollari per cessazione di contratto di locazione.

Arvinas (ARVN) reportó los resultados financieros del tercer trimestre de 2024 con ingresos de 102,4 millones de dólares, un aumento desde los 34,6 millones de dólares en el tercer trimestre de 2023. La compañía mantiene 1,1 mil millones de dólares en efectivo y equivalentes, que se espera financien las operaciones hasta 2027. Los desarrollos clave incluyen la inscripción en curso en múltiples estudios clínicos para vepdegestrant en cáncer de mama, con datos preliminares del ensayo VERITAC-2 de Fase 3 esperados en el cuarto trimestre de 2024 o el primer trimestre de 2025. Los gastos en investigación y desarrollo fueron de 86,9 millones de dólares, mientras que los gastos generales y administrativos aumentaron a 75,8 millones de dólares, incluyendo una pérdida de arrendamiento por 43,4 millones de dólares.

Arvinas (ARVN)는 2024년 3분기 재무 결과를 보고하며 1억 240만 달러의 수익을 기록했으며, 이는 2023년 3분기의 3천460만 달러에서 증가한 수치입니다. 이 회사는 11억 달러의 현금 및 현금성 자산을 보유하고 있으며, 이는 2027년까지 운영 자금으로 사용될 것으로 예상됩니다. 주요 진행 사항으로는 유방암 치료를 위한 vepdegestrant에 대한 여러 임상 연구에 대한 지속적인 등록이 있으며, VERITAC-2 3상 시험의 주요 데이터는 2024년 4분기 또는 2025년 1분기에 예상됩니다. 연구 및 개발 비용은 8천690만 달러였으며, 일반 및 관리 비용은 7천580만 달러로 증가하였고, 여기에는 4천340만 달러의 임대 종료 손실이 포함됩니다.

Arvinas (ARVN) a annoncé ses résultats financiers du troisième trimestre 2024 avec des revenus de 102,4 millions de dollars, en hausse par rapport à 34,6 millions de dollars au troisième trimestre 2023. La société maintient 1,1 milliard de dollars en liquidités et équivalents, censés financer ses opérations jusqu'en 2027. Parmi les développements clés figurent l'inscription en cours à plusieurs études cliniques pour le vepdegestrant dans le cancer du sein, avec des données préliminaires de l'essai VERITAC-2 de phase 3 attendues au quatrième trimestre 2024 ou au premier trimestre 2025. Les dépenses de recherche et développement se sont élevées à 86,9 millions de dollars, tandis que les dépenses générales et administratives ont augmenté pour atteindre 75,8 millions de dollars, y compris une perte de résiliation de bail de 43,4 millions de dollars.

Arvinas (ARVN) hat die Finanzzahlen für das 3. Quartal 2024 veröffentlicht, mit einem Umsatz von 102,4 Millionen Dollar, was einem Anstieg von 34,6 Millionen Dollar im 3. Quartal 2023 entspricht. Das Unternehmen hält 1,1 Milliarden Dollar an Bargeld und Äquivalenten, die voraussichtlich bis 2027 zur Finanzierung der Betriebe ausreichen. Zu den wichtigen Entwicklungen gehört die laufende Rekrutierung in mehreren klinischen Studien für Vepdegestrant bei Brustkrebs, wobei die Ergebnisse der VERITAC-2-Phase-3-Studie im vierten Quartal 2024 oder im ersten Quartal 2025 erwartet werden. Die Forschungs- und Entwicklungskosten betrugen 86,9 Millionen Dollar, während die allgemeinen und administrativen Kosten auf 75,8 Millionen Dollar gestiegen sind, einschließlich eines Mietaufhebungsverlustes von 43,4 Millionen Dollar.

Positive
  • Revenue increased significantly to $102.4M from $34.6M YoY
  • Strong cash position of $1.1B, providing runway into 2027
  • Multiple clinical trials progressing on schedule
  • Secured $76.7M revenue from Novartis license agreement
Negative
  • General and administrative expenses increased substantially to $75.8M from $22.6M YoY
  • $43.4M loss from laboratory and office space lease termination
  • Cash position decreased by $144.9M from December 2023
  • Research and development expenses increased to $86.9M

Insights

The Q3 2024 results showcase Arvinas's strong financial position with $1.12 billion in cash and equivalents, providing runway into 2027. Revenue significantly increased to $102.4 million, up from $34.6 million year-over-year, primarily driven by the Novartis license agreement contributing $76.7 million. However, operating expenses rose substantially, with R&D at $86.9 million and G&A expenses jumping to $75.8 million, including a $43.4 million lease termination loss. The substantial cash position and revenue growth are positive indicators, but increased expenses and the one-time lease termination impact warrant attention.

The clinical pipeline shows promising momentum, particularly with vepdegestrant's Phase 3 VERITAC-2 trial nearing completion. The upcoming topline data in Q4 2024/Q1 2025 represents a important milestone for ER+/HER2- breast cancer treatment. The expansion of combination studies with various CDK4/6 inhibitors demonstrates a comprehensive development strategy. Additionally, the preclinical data for ARV-102 in neurodegenerative diseases, showing LRRK2 degradation in CSF and 50% pathologic tau reduction, indicates potential therapeutic value beyond oncology. The advancement of ARV-393 for B-cell lymphomas further diversifies the pipeline.

– On track to report topline data from Phase 3 VERITAC-2 trial in 4Q24 or 1Q25 –

– Initial clinical data from Phase 1/2 TACTIVE-U sub-study of abemaciclib in combination with vepdegestrant to be presented at San Antonio Breast Cancer Symposium in December 2024 –

– Recently presented new preclinical data for the PROTAC LRRK2 degrader ARV-102 demonstrating that LRRK2 degradation affects biomarkers in the CSF –

- $1.1 billion in cash, cash equivalents and marketable securities as of Sept. 30, 2024 -

– Company to host conference call today at 8:00 a.m. ET –

NEW HAVEN, Conn., Oct. 30, 2024 (GLOBE NEWSWIRE) -- Arvinas, Inc. (Nasdaq: ARVN), a clinical-stage biotechnology company creating a new class of drugs based on targeted protein degradation, today reported financial results for the third quarter ended September 30, 2024, and provided a corporate update.

“We maintained strong momentum across our portfolio in the third quarter and remain on track to report topline data from VERITAC-2, our Phase 3 clinical trial in metastatic breast cancer, in the fourth quarter of 2024 or the first quarter of 2025,” said John Houston, Ph.D., Chairperson, Chief Executive Officer and President at Arvinas. “In partnership with our colleagues at Pfizer, we are excited by the possibility of changing the treatment paradigm for ER+/HER2- breast cancer and look forward to sharing results from VERITAC-2 in the coming months.”

“Our path to reaching our goal of becoming a multi-product, commercial-stage organization with a robust pipeline across several indications is clearly defined, and our novel PROTAC platform technology has the potential to enable opportunities across multiple therapeutic areas,” continued Dr. Houston. “We look forward to completing the multiple ascending dose portion of our Phase 1 clinical trial with ARV-102, our first PROTAC degrader with the potential to treat neurodegenerative diseases, and sharing data in 2025. We are also encouraged by the preclinical profile of ARV-393, our BCL6 PROTAC degrader currently being evaluated in a first-in-human Phase 1 clinical trial in patients with B-cell lymphomas. We look forward to sharing more about these programs in the coming months.”

3Q 2024 Business Highlights and Recent Developments

Vepdegestrant

  • Continued enrollment globally in multiple clinical studies of vepdegestrant in ER+/HER2- metastatic breast cancer.
    • VERITAC-2: Phase 3 monotherapy clinical trial in patients with metastatic breast cancer (ClinicalTrials.gov Identifier: NCT05654623)
    • TACTIVE-U: Phase 1b/2 combination umbrella trial evaluating combinations of vepdegestrant with abemaciclib, ribociclib, or samuraciclib (ClinicalTrials.gov Identifiers: NCT05548127, NCT05573555, and NCT06125522).
    • TACTIVE-K: Phase 1/2 clinical trial with vepdegestrant plus Pfizer’s novel CDK4 inhibitor atirmociclib (ClinicalTrials.gov Identifier: NCT06206837)

ARV-102: Oral PROTAC LRRK2 degrader

  • In October, presented preclinical data at the 2024 Michael J. Fox Foundation Parkinson’s Disease Conference further supporting the potential of PROTAC-induced leucine-rich repeat kinase 2 (LRRK2) degradation as a potential treatment for patients with neurodegenerative diseases. New findings presented included data demonstrating:
    • Orally delivered ARV-102 crosses the blood-brain barriers and degrades LRRK2 in the cerebrospinal fluid (CSF) of non-human primates (NHPs).
    • Degradation of LRRK2 by ARV-102 induces changes in pathway (lysosomal and inflammation) biomarkers in the CSF of NHPs, which has not previously been demonstrated by kinase inhibitors of LRRK2.
    • In murine tauopathy models, oral PROTAC LRRK2 degrader treatment led to ~50% pathologic tau reduction.
  • Initiated the multiple ascending dose portion of the ongoing Phase 1 clinical trial in healthy volunteers.

ARV-393: Oral PROTAC BCL6 degrader

  • Continued recruiting patients in the first-in-human Phase 1 clinical trial in patients with B-cell lymphomas.

Anticipated Upcoming Milestones and Expectations

Vepdegestrant

As part of Arvinas global collaboration with Pfizer, the companies plan to:

  • Complete enrollment (4Q24) and announce topline data (4Q24/1Q25) for the VERITAC-2 Phase 3 monotherapy clinical trial in patients with metastatic breast cancer.
  • Present initial safety and pharmacokinetic data from the TACTIVE-U sub-study (NCT05548127) of abemaciclib in combination with vepdegestrant at the San Antonio Breast Cancer Symposium (SABCS) in December 2024.
  • Present data from the Phase 1 healthy volunteer pharmacokinetic trial of vepdegestrant in combination with midazolam to assess potential for drug-drug interaction at SABCS in December 2024 (NCT06256510).
  • Continue enrollment of the ongoing Phase 1b/2 combination umbrella trial evaluating combinations of vepdegestrant with abemaciclib, ribociclib, or samuraciclib (TACTIVE-U; ClinicalTrials.gov Identifiers: NCT05548127, NCT05573555, and NCT06125522).
  • Evaluate data from the study lead-in of the VERITAC-3 Phase 3 trial (NCT05909397) in patients with ER+/HER2- locally advanced or metastatic breast cancer (2H24).
  • Continue enrollment and evaluate preliminary data from the ongoing clinical trial with vepdegestrant plus Pfizer’s novel CDK4 inhibitor atirmociclib (TACTIVE-K).
  • Start Phase 3 combination trials in the first- and second-line settings (anticipated in 2025; pending emerging data and regulatory feedback).
    • First-line setting with vepdegestrant plus atirmociclib or palbociclib.
    • Second-line setting with vepdegestrant plus palbociclib and/or another CDK4/6 inhibitor.

ARV-102: Oral PROTAC LRRK2 degrader

  • Complete enrollment in the ongoing multiple ascending dose portion of a Phase 1 trial evaluating ARV-102 in healthy volunteers
  • Present data from the Phase 1 trial in 2025.

ARV-393: Oral PROTAC BCL6 degrader

  • Continue recruiting patients in the first-in-human Phase 1 clinical trial evaluating ARV-393 in patients with B-cell lymphomas.

Novel PROTAC KRAS G12D degrader

  • File an Investigational New Drug (IND) application in 2025.

Financial Guidance
Based on its current operating plan, Arvinas believes its cash, cash equivalents, and marketable securities as of September 30, 2024, is sufficient to fund planned operating expenses and capital expenditure requirements into 2027.

Third Quarter Financial Results

Cash, Cash Equivalents, and Marketable Securities Position: As of September 30, 2024, cash, cash equivalents and marketable securities were $1,121.6 million as compared with cash, cash equivalents, restricted cash and marketable securities of $1,266.5 million as of December 31, 2023. The decrease in cash, cash equivalents and marketable securities of $144.9 million for the nine months ended September 30, 2024 was primarily related to cash used in operations of $158.1 million (net of $150.0 million received from the Novartis agreements), inclusive of a one-time cash termination fee in the amount of $41.5 million related to the termination of our laboratory and office space lease with 101 College Street LLC in August 2024 and the purchase of lab equipment and leasehold improvements of $1.5 million, partially offset by proceeds from the exercise of stock options of $7.7 million and unrealized gains on marketable securities of $7.2 million.

Research and Development Expenses:  Research and development expenses were $86.9 million for the quarter ended September 30, 2024, as compared with $85.9 million for the quarter ended September 30, 2023. The increase in research and development expenses of $1.0 million for the quarter was primarily due to an increase in compensation and related personnel expenses of $2.8 million, which are not allocated by program, partially offset by a decrease in external expenses of $2.2 million. External expenses include program-specific expenses, which decreased by $1.1 million, primarily driven by decreases in our ARV-766 and ARV-110 programs of $3.8 million and $1.6 million, respectively, partially offset by increases in our ARV-102 and ARV-393 programs of $2.5 million and $1.4 million, respectively, and our non-program specific expenses, which decreased by $1.1 million.

General and Administrative Expenses:  General and administrative expenses were $75.8 million for the quarter ended September 30, 2024, as compared with $22.6 million for the quarter ended September 30, 2023. The increase in general and administrative expenses of $53.2 million for the quarter was primarily due to a loss on the termination of our laboratory and office space lease with 101 College Street LLC of $43.4 million as well as increases in personnel and infrastructure related costs of $5.0 million, professional fees of $3.4 million and in developing our commercial operations of $1.2 million.

Revenue:  Revenue was $102.4 million for the quarter ended September 30, 2024 as compared with $34.6 million for the quarter ended September 30, 2023. Revenue for the quarter is related to the license agreement with Novartis, the Vepdegestrant (ARV-471) Collaboration Agreement with Pfizer, the collaboration and license agreement with Bayer and the collaboration and license agreement with Pfizer. The increase in revenue of $67.8 million was primarily due to revenue from the Novartis license agreement of $76.7 million, offset by a decrease in revenue from the Vepdegestrant (ARV-471) Collaboration Agreement with Pfizer of $7.6 million related to timing differences in clinical trials and program expenses and a decrease in revenue from Bayer of $1.1 million related to the termination of the Bayer Collaboration Agreement in August 2024.

Investor Call & Webcast Details

Arvinas will host a conference call and webcast today, October 30, 2024, at 8:00 a.m. ET to review its third quarter 2024 financial results and discuss recent corporate updates. Participants are invited to listen by going to the Events and Presentation section under the Investors page on the Arvinas website at www.arvinas.com. A replay of the webcast will be available on the Arvinas website following the completion of the event and will be archived for up to 30 days.

About Vepdegestrant
Vepdegestrant is an investigational, orally bioavailable PROTAC protein degrader designed to specifically target and degrade the estrogen receptor (ER) for the treatment of patients with ER positive (ER+)/human epidermal growth factor receptor 2 (HER2) negative (ER+/HER2-) breast cancer. Vepdegestrant is being developed as a potential monotherapy and as part of combination therapy across multiple treatment settings for ER+/HER2- metastatic breast cancer.

In July 2021, Arvinas announced a global collaboration with Pfizer for the co-development and co-commercialization of vepdegestrant; Arvinas and Pfizer will share worldwide development costs, commercialization expenses, and profits.

The U.S. Food and Drug Administration (FDA) has granted vepdegestrant Fast Track designation as a monotherapy in the treatment of adults with ER+/HER2- locally advanced or metastatic breast cancer previously treated with endocrine-based therapy.

About Arvinas
Arvinas (Nasdaq: ARVN) is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases. Through its PROTAC® (PROteolysis Targeting Chimera) protein degrader platform, the Company is pioneering the development of protein degradation therapies designed to harness the body’s natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins. Arvinas is currently progressing multiple investigational drugs through clinical development programs, including vepdegestrant, targeting the estrogen receptor for patients with locally advanced or metastatic ER+/HER2- breast cancer; ARV-393, targeting BCL6 for relapsed/refractory non-Hodgkin Lymphoma; and ARV-102, targeting LRRK2 for neurodegenerative disorders. Arvinas is headquartered in New Haven, Connecticut. For more information about Arvinas, visit www.arvinas.com and connect on LinkedIn and X

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995 that involve substantial risks and uncertainties, including statements regarding the expected timing in connection with the completion of enrollment and reporting of topline data from the VERITAC-2 clinical trial; the potential to change the treatment paradigm for ER+/HER2- breast cancer; the goal of becoming a multi-product, commercial-stage organization with a robust pipeline across several indications; novel PROTAC platform technology having the potential to enable opportunities across multiple therapeutic areas; plans to present initial safety and pharmacokinetic data from the TACTIVE-U sub-study of abemaciclib in combination with vepdegestrant at SABCS; plans to present data from the Phase 1 healthy volunteer pharmacokinetic trial of vepdegestrant in combination with midazolam at SABCS; plans to continue enrollment in the TACTIVE-U study and evaluate data from the study lead-in of the VERITAC-3 Phase 3 clinical trial; plans to continue enrollment and evaluate preliminary data from the TACTIVE-K clinical trial; the expected timing of initiation of Phase 3 vepdegestrant combination trials in the first- and second-line settings, pending emerging data and regulatory feedback; expected timing of filing an investigational new drug application for a KRAS G12D degrader; plans to compete enrollment in the multiple ascending dose portion of the ARV-102 Phase 1 clinical trial, the timing of the presentation of data from such clinical trial, and the timing of sharing additional information about the program; plans to continue recruiting patients in the Phase 1 ARV-393 clinical trial and timing of sharing additional information about the program; and statements regarding Arvinas’ cash, cash equivalents and marketable securities. All statements, other than statements of historical fact, contained in this press release, including statements regarding Arvinas’ strategy, future operations, future financial position, future revenues, projected costs, prospects, plans and objectives of management, are forward-looking statements. The words “anticipate,” “believe,” “estimate,” “expect,” “intend,” “may,” “might,” “plan,” “predict,” “project,” “target,” “goal,” “potential,” “will,” “would,” “could,” “should,” “continue,” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.

Arvinas may not actually achieve the plans, intentions or expectations disclosed in these forward-looking statements, and you should not place undue reliance on such forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements Arvinas makes as a result of various risks and uncertainties, including but not limited to: Arvinas’ and Pfizer’s performance of the respective obligations with respect to Arvinas’ collaboration with Pfizer; whether Arvinas and Pfizer will be able to successfully conduct and complete clinical development for vepdegestrant; whether Arvinas will be able to successfully conduct and complete development for its other product candidates, including whether Arvinas initiates and completes clinical trials for its product candidates and receives results from its clinical trials and preclinical studies on its expected timelines or at all; whether Arvinas and Pfizer, as appropriate, will be able to obtain marketing approval for and commercialize vepdegestrant and other product candidates on current timelines or at all; Arvinas’ ability to protect its intellectual property portfolio; whether Arvinas’ cash and cash equivalent resources will be sufficient to fund its foreseeable and unforeseeable operating expenses and capital expenditure requirements, and other important factors discussed in the “Risk Factors” section of Arvinas’ Annual Report on Form 10-K for the year ended December 31, 2023 and subsequent other reports on file with the U.S. Securities and Exchange Commission. The forward-looking statements contained in this press release reflect Arvinas’ current views with respect to future events, and Arvinas assumes no obligation to update any forward-looking statements, except as required by applicable law. These forward-looking statements should not be relied upon as representing Arvinas’ views as of any date subsequent to the date of this release.

Contacts
Investors:
Jeff Boyle
+1 (347) 247-5089
Jeff.Boyle@arvinas.com

Media:
Kirsten Owens
+1 (203) 584-0307
Kirsten.Owens@arvinas.com


Arvinas, Inc.
Condensed Consolidated Balance Sheets (Unaudited)
   
(dollars and shares in millions, except per share amounts)September 30, 
2024
December 31,
2023
Assets  
Current assets:  
Cash and cash equivalents$85.2 $311.7 
Restricted cash   5.5 
Marketable securities 1,036.4  949.3 
Accounts receivable 7.3   
Other receivables 7.5  7.2 
Prepaid expenses and other current assets 13.1  6.5 
Total current assets 1,149.5  1,280.2 
Property, equipment and leasehold improvements, net 6.8  11.5 
Operating lease right of use assets 1.0  2.5 
Collaboration contract asset and other assets 9.8  10.4 
Total assets$1,167.1 $1,304.6 
Liabilities and stockholders' equity  
Current liabilities:  
Accounts payable and accrued liabilities$75.9 $92.2 
Deferred revenue 199.2  163.0 
Current portion of operating lease liabilities 0.8  1.9 
Total current liabilities 275.9  257.1 
Deferred revenue 304.5  386.2 
Long-term debt 0.6  0.8 
Operating lease liabilities 0.1  0.5 
Total liabilities 581.1  644.6 
Stockholders’ equity:  
Preferred stock, $0.001 par value, zero shares issued and outstanding as of September 30, 2024 and December 31, 2023, respectively    
Common stock, $0.001 par value; 68.7 and 68.0 shares issued and outstanding as of September 30, 2024 and December 31, 2023, respectively 0.1  0.1 
Accumulated deficit (1,486.5) (1,332.7)
Additional paid-in capital 2,068.3  1,995.7 
Accumulated other comprehensive income (loss) 4.1  (3.1)
Total stockholders’ equity 586.0  660.0 
Total liabilities and stockholders’ equity$1,167.1 $1,304.6 
   



Arvinas, Inc.
Condensed Consolidated Statements of Operations (Unaudited)
     
 Three Months Ended September 30,Nine Months Ended September 30,
(dollars and shares in millions, except per share amounts) 2024  2023  2024  2023 
Revenue$102.4 $34.6 $204.2 $121.6 
Operating expenses:    
Research and development 86.9  85.9  264.9  284.5 
General and administrative 75.8  22.6  131.3  73.3 
Total operating expenses 162.7  108.5  396.2  357.8 
Loss from operations (60.3) (73.9) (192.0) (236.2)
Interest and other income, net 11.7  10.0  39.2  25.5 
Net loss before income taxes and loss from equity method investment (48.6) (63.9) (152.8) (210.7)
Income tax (expense) benefit (0.6)   (1.0) 0.7 
Loss from equity method investment   (0.1)   (2.5)
Net loss$(49.2)$(64.0)$(153.8)$(212.5)
Net loss per common share, basic and diluted$(0.68)$(1.18)$(2.14)$(3.97)
Weighted average common shares outstanding, basic and diluted 72.1  54.1  71.9  53.6 
     

FAQ

What was Arvinas (ARVN) revenue in Q3 2024?

Arvinas reported revenue of $102.4 million in Q3 2024, compared to $34.6 million in Q3 2023.

When will Arvinas (ARVN) report VERITAC-2 Phase 3 trial results?

Arvinas expects to report topline data from the VERITAC-2 Phase 3 trial in Q4 2024 or Q1 2025.

How much cash does Arvinas (ARVN) have as of Q3 2024?

Arvinas had $1.1 billion in cash, cash equivalents, and marketable securities as of September 30, 2024.

What caused the increase in Arvinas (ARVN) Q3 2024 revenue?

The revenue increase was primarily due to $76.7 million from the Novartis license agreement.

Arvinas, Inc

NASDAQ:ARVN

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