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Arvinas Holding Company (ARVN)
NASDAQ:ARVN
US Market

Arvinas Holding Company (ARVN) AI Stock Analysis

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ARVN

Arvinas Holding Company

(NASDAQ:ARVN)

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Neutral 48 (OpenAI - 5.2)
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Neutral 48 (OpenAI - 5.2)
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Neutral 48 (OpenAI - 5.2)
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Neutral 48 (OpenAI - 5.2)
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Neutral 48 (OpenAI - 5.2)
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Neutral 48 (OpenAI - 5.2)
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Neutral 48 (OpenAI - 5.2)
Rating:48Neutral
Price Target:
$11.00
▼(-1.52% Downside)
Action:ReiteratedDate:03/19/26
The score is held down primarily by weak financial performance (ongoing losses, significant cash burn, and 2025 gross profit anomaly) and bearish technical signals (below key moving averages with negative MACD). Pipeline and catalyst messaging (earnings call and ARV-102 Phase 1 update) provide support but are tempered by the sharply reduced cash position and execution/partnering risk.
Positive Factors
PROTAC platform and diversified clinical pipeline
Arvinas’ core PROTAC platform and multiple clinical-stage programs materially reduce binary program risk versus a single-asset profile. Sustained pipeline breadth (LRRK2, KRAS, BCL6, polyQ) supports long-term upside from multiple potential clinical readouts, partnership paths, and eventual commercialization options if trials succeed.
Low leverage and capitalization flexibility
Very low debt relative to equity provides durable financial flexibility, lowering insolvency risk and enabling the company to prioritize R&D and partner negotiations without heavy interest burdens. This structural balance-sheet strength supports long-term program funding options and strategic deal-making.
Cost discipline and maintained runway into 2028
Meaningful year-over-year expense reductions and management's guidance for runway into 2028 signal sustained cost discipline. That structural spending control increases the probability the firm can fund critical Phase 1 readouts and advance multiple programs without immediate dilutive financing, supporting execution over the next 2–3 years.
Negative Factors
Sharp cash depletion and financing sensitivity
A ~91% year-over-year decline in cash creates structural sensitivity to upcoming milestones and partner deals. Even with cost cuts, the much smaller cash buffer increases the likelihood of equity raises, partnerships or contract-reliant funding, which can affect long-term program continuity and strategic optionality.
Persistent negative operating cash flow and cash burn
Sustained, large negative operating cash flows indicate the company requires recurrent external funding to sustain development. Over time this cash-burn profile pressures strategic choices, may force program reprioritization or dilution, and raises execution risk for advancing multiple clinical programs concurrently.
High clinical and partnering execution risk
Operating in crowded, competitive therapeutic areas requires clear differentiation and successful trials to secure regulatory and commercial value. Reliance on partnerships or milestone recognition (e.g., vepdegestrant commercialization) amplifies execution risk: failure to outperform benchmarks or secure partners could materially reduce long-term returns.

Arvinas Holding Company (ARVN) vs. SPDR S&P 500 ETF (SPY)

Arvinas Holding Company Business Overview & Revenue Model

Company DescriptionArvinas, Inc., a clinical-stage biopharmaceutical company, engages in the discovery, development, and commercialization of therapies to degrade disease-causing proteins. Its lead product candidates include Bavdegalutamide, a proteolysis targeting chimera (PROTAC) protein degrader that is in phase I clinical trial targeting the androgen receptor (AR) protein for the treatment of men with metastatic castration-resistant prostate cancer (mCRPC); ARV-471, a PROTAC protein degrader targeting the estrogen receptor protein for the treatment of patients with metastatic ER positive/HER2 negative breast cancer; and ARV-766 an investigational orally bioavailable PROTAC protein degrader for the treatment of men with mCRPC. The company has collaborations with Pfizer Inc., Genentech, Inc., F. Hoffman-La Roche Ltd., and Bayer AG. Arvinas, Inc. was founded in 2013 and is based in New Haven, Connecticut.
How the Company Makes MoneyArvinas primarily makes money through biopharmaceutical collaboration economics rather than product sales, because it is a clinical-stage company and, to the extent publicly available, does not rely on commercialized-product revenue. Its key revenue streams typically include: (1) Collaboration and license revenue: upfront payments and ongoing revenue recognized from strategic partnerships in which Arvinas grants counterparties rights (e.g., licenses) to develop and commercialize certain PROTAC-based programs/targets. Depending on contract structure, this may also include reimbursement for research activities performed by Arvinas and recognition of collaboration revenue over time as obligations are satisfied. (2) Milestone payments: development, regulatory, and commercial milestones earned when partnered programs achieve predefined events (such as successful clinical trial progress, regulatory submissions/approvals, or sales-based triggers). These payments can be significant but are inherently intermittent and dependent on program success. (3) Royalties on net sales (if and when partnered products reach the market): for programs licensed to partners, Arvinas may be entitled to royalties based on future commercial sales; however, if specific royalty-bearing products are not yet commercialized, the associated royalty revenue would be limited or null. (4) Other income sources: interest income on cash and investments can contribute to total income, particularly for development-stage biotech companies that hold substantial cash balances from financings and partnership proceeds. Overall, Arvinas’ earnings potential is driven by the success of its internal pipeline (which could eventually generate product revenue if a candidate is approved and commercialized) and by the breadth and progress of its partnerships, which can deliver upfront consideration, cost-sharing or reimbursements, milestones, and potential future royalties.

Arvinas Holding Company Earnings Call Summary

Earnings Call Date:Feb 24, 2026
(Q4-2025)
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% Change Since: |
Next Earnings Date:Apr 30, 2026
Earnings Call Sentiment Neutral
The call conveyed strong scientific and clinical momentum—multiple programs advancing, encouraging early biomarker and preclinical signals, and disciplined cost reductions—while simultaneously revealing material financial pressure from a steep decline in cash and a large quarter-over-quarter revenue drop. The company maintained guidance for cash runway into 2028 and emphasized partner discussions, but the balance sheet tightening and competitive landscape create meaningful execution and financing risk alongside the positive clinical developments.
Q4-2025 Updates
Positive Updates
Pipeline Advancement and Clinical Momentum
Four clinical-stage programs (ARV-102, ARV-806, ARV-393, ARV-027) ongoing with multiple readouts planned in 2026; first‑in‑human dosing initiated for ARV-027 (polyQ AR degrader) and ARV-6723 (HPK1) expected to enter clinic later in 2026.
LRRK2 Program (ARV-102) — Biomarker and Presentation Win
ARV-102 showed >50% reduction in LRRK2 in CSF in healthy volunteers and demonstrated pathway biomarker engagement (GPNMB and CD68); Phase 1 patient data accepted for oral presentation at AD/PD and a Phase 1b in PSP planned in H1 2026 with potential registrational trial late 2026 pending regulatory feedback.
KRAS G12D Program (ARV-806) — Fast Enrollment and Preclinical Potency
ARV-806 enrollment advanced faster-than-expected; company expects first clinical data disclosures in 2026. Preclinical data cited >25-fold greater potency versus clinical KRAS G12D inhibitors and the degrader eliminates both on/off forms of KRAS.
BCL6 Program (ARV-393) — Early Clinical Responses and Strong Preclinical Combo Data
ARV-393 Phase 1 dose escalation progressing with observed responses in both B- and T-cell lymphomas at early cohorts despite exposures below predicted efficacious levels; robust BCL6 degradation and tolerability support continued escalation. Preclinical combination with glofitamab produced 91% tumor growth inhibition vs 36% for glofitamab alone.
Immuno-Oncology and Pan-KRAS Preclinical Strength
ARV-6723 (HPK1 degrader) showed robust single-agent and combination activity in preclinical models, outperforming HPK1 inhibitors and anti–PD-1 in several settings. Pan-KRAS degrader program shows selective KRAS degradation (vs HRAS/NRAS), activity across mutants and KRAS-amplified models, and planned AACR data comparing to inhibitors.
Cost Reduction and Expense Control
Company reduced spend in 2025: Q4 G&A down to $23.0M from $34.1M (≈-32.6% QoQ year-ago quarter), Q4 R&D down to $61.1M from $83.3M (≈-26.7%), FY G&A $95.9M vs $165.4M (≈-42.0% YoY), and FY R&D $285.2M vs $348.2M (≈-18.1%), reflecting deliberate cost-cutting and operational efficiencies.
Cash Runway Guidance Maintained
Management maintained cash runway guidance into 2028 to support upcoming data readouts and program advancement despite recent balance sheet changes.
Negative Updates
Sharp Decline in Cash Balance
Cash, cash equivalents and marketable securities fell to just over $85M at 12/31/2025 from just over $1.0B at the end of 2024 — an approximate decline of ~91% year-over-year, creating a heightened sensitivity to upcoming milestones, partner deals, or financing.
Q4 Revenue Collapse vs Prior Year Quarter
Quarterly revenue dropped to $9.5M in Q4 2025 from $59.2M in Q4 2024, an ≈-83.9% decline, primarily driven by a $40.3M decrease in revenue from the Novartis license agreement; though FY revenue remained roughly flat ($262.6M vs $263.4M, ≈-0.3%).
Share Repurchase Program Suspended After Large Buyback
Board-authorized repurchase program ended with ~10M shares repurchased at an average $9.09/share for a total of $91.9M; program now suspended, signaling a pause in buybacks amid tightened cash position.
Competitive and Clinical Risk Across Programs
Several programs (notably KRAS G12D and pan‑KRAS) operate in highly competitive fields with other drugs already ahead in clinic; company must demonstrate clear differentiation (e.g., ARV-806 needs to exceed benchmark response rates cited ~35%) to secure clinical/regulatory and commercial advantage.
Target-Specific Safety Monitoring and Uncertainties
LRRK2-targeting approach carries on‑target lung biology risks requiring pulmonary function monitoring (PFTs/HRCT) and careful safety assessment; early data windows are short and longer-duration safety/readthrough remains to be demonstrated.
Dependence on Partnering and Milestones (vepdegestrant)
Vepdegestrant NDA filed with a June 5 PDUFA date and an active search for a commercialization/partnering third party; success depends on partner selection by PDUFA or alternative commercialization plans, posing execution risk if not finalized.
Company Guidance
Arvinas guided that 2026 will be a catalyst year with multiple Phase 1 data readouts and clinical advances — expecting data from ARV‑102, ARV‑806 and ARV‑393, with ARV‑027 newly in the clinic and ARV‑6723 planned to enter first‑in‑human later in the year — and reiterated cash runway into 2028 after ending Q4 with just over $85M in cash and marketable securities (vs. just over $1.0B at 12/31/2024); Q4 revenue was $9.5M (vs. $59.2M), FY revenue was $262.6M (vs. $263.4M), Q4 G&A was $23.0M (non‑GAAP G&A $15.3M) and FY G&A $95.9M, Q4 R&D was $61.1M (non‑GAAP R&D $56.5M) and FY R&D $285.2M, with total non‑GAAP expenses of $71.8M in Q4 and $323.4M for the year; the board had authorized up to $100M for buybacks and repurchased ~10M shares at an average $9.09 per share for ~$91.9M (program now suspended); clinically the company highlighted specific metrics/targets including >50% CSF LRRK2 reduction for ARV‑102 (AD/PD presentation), >25‑fold preclinical potency for ARV‑806 versus clinical inhibitors and a need to exceed ~35% response benchmarks in the G12D space, ARV‑393 responses in early cohorts at exposures below predicted efficacious levels plus preclinical combo tumor growth inhibition of 91% vs 36% for glofitamab alone, and plans to select a commercialization partner for vepdegestrant ahead of the June 5 PDUFA date.

Arvinas Holding Company Financial Statement Overview

Summary
Balance sheet strength is a key positive (very low debt vs equity), but operating fundamentals remain weak: the company is still loss-making, 2025 revenue declined year over year, and cash burn is substantial with consistently negative operating/free cash flow. The unusual negative gross profit in 2025 is an additional quality/volatility concern.
Income Statement
28
Negative
Revenue scaled sharply versus earlier years (2025: $262.6M vs 2023: $78.5M), but momentum weakened with 2025 annual revenue down ~15.9% year over year. Profitability remains the core issue: the company is still loss-making (2025 net loss: ~$80.8M; 2024 net loss: ~$198.9M) with negative operating profitability, despite a material improvement in losses from 2023–2024. 2025 shows an unusual negative gross profit (gross profit margin ~-152%), which is a notable quality/volatility flag and weighs on the score.
Balance Sheet
72
Positive
Balance sheet leverage is very low, with minimal debt (2025 total debt: ~$8.5M) relative to equity (2025 equity: ~$433.9M), supporting financial flexibility. However, equity and assets have declined from prior years (equity down from ~$660.0M in 2023; assets down from ~$1.30B in 2023), and returns remain negative due to ongoing losses (2025 return on equity ~-18.6%). Overall: strong capitalization with limited balance-sheet risk, but weakening capital base and continued losses are the key offsets.
Cash Flow
24
Negative
Cash generation is pressured with consistently negative operating cash flow in recent years (2025: ~-$273.8M; 2024: ~-$259.3M; 2023: ~-$347.8M) and similarly negative free cash flow (2025: ~-$275.7M), indicating ongoing cash burn. Free cash flow also deteriorated in 2025 (down ~16.3% year over year). While free cash flow broadly tracks net income (free cash flow to net income ~1.0), the absolute level of burn and negative operating cash flow versus net income signal continued funding needs.
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue262.60M263.40M78.50M131.40M53.60M
Gross Profit257.40M263.40M78.50M131.40M53.60M
EBITDA-75.30M-243.60M-394.80M-255.00M-182.40M
Net Income-80.80M-198.90M-367.30M-282.50M-191.00M
Balance Sheet
Total Assets717.90M1.09B1.30B1.27B1.58B
Cash, Cash Equivalents and Short-Term Investments685.40M1.04B1.26B1.21B1.50B
Total Debt8.50M9.70M3.20M5.50M5.00M
Total Liabilities284.00M529.70M644.60M703.90M799.90M
Stockholders Equity433.90M561.70M660.00M564.90M781.70M
Cash Flow
Free Cash Flow-275.70M-261.10M-350.70M-280.30M554.70M
Operating Cash Flow-273.80M-259.30M-347.80M-273.50M559.40M
Investing Cash Flow407.60M34.70M203.50M242.80M-1.31B
Financing Cash Flow-91.40M7.90M374.70M4.70M278.60M

Arvinas Holding Company Technical Analysis

Technical Analysis Sentiment
Negative
Last Price11.17
Price Trends
50DMA
12.74
Negative
100DMA
12.08
Negative
200DMA
9.99
Positive
Market Momentum
MACD
-0.30
Positive
RSI
35.21
Neutral
STOCH
6.36
Positive
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For ARVN, the sentiment is Negative. The current price of 11.17 is below the 20-day moving average (MA) of 12.81, below the 50-day MA of 12.74, and above the 200-day MA of 9.99, indicating a neutral trend. The MACD of -0.30 indicates Positive momentum. The RSI at 35.21 is Neutral, neither overbought nor oversold. The STOCH value of 6.36 is Positive, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for ARVN.

Arvinas Holding Company Risk Analysis

Arvinas Holding Company disclosed 69 risk factors in its most recent earnings report. Arvinas Holding Company reported the most risks in the "Tech & Innovation" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Arvinas Holding Company Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
57
Neutral
$1.86B-101.811813.84%196.42%53.92%
56
Neutral
$1.19B-5.93-27.17%-103.95%
52
Neutral
$970.67M-12.74-43.61%-100.00%-28.79%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
48
Neutral
$714.44M-9.53-14.25%
47
Neutral
$591.61M-3.30-1065.47%96.83%-61.92%
47
Neutral
$1.30B-13.39-42.90%17.23%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
ARVN
Arvinas Holding Company
11.17
2.42
27.66%
ANAB
AnaptysBio
64.72
47.64
278.92%
MGTX
Meiragtx Holdings
7.35
-0.21
-2.78%
CMPX
Compass Therapeutics
5.39
3.08
133.33%
OLMA
Olema Pharmaceuticals
14.96
10.73
253.66%
BCAX
Bicara Therapeutics Inc.
18.79
5.55
41.92%

Arvinas Holding Company Corporate Events

Business Operations and StrategyProduct-Related Announcements
Arvinas Reports Positive Phase 1 Data for ARV-102
Positive
Mar 18, 2026

Arvinas, Inc., a clinical-stage biotech focused on PROTAC-based targeted protein degradation, reported positive Phase 1 data on March 18, 2026, for ARV-102, an oral LRRK2 degrader designed to cross the blood-brain barrier in Parkinson’s disease patients. The trial showed dose-dependent brain penetration and sustained reductions of LRRK2 and related endolysosomal and neuroinflammatory biomarkers, with ARV-102 generally safe and well tolerated across all tested doses.

In the single-center, randomized, double-blind, placebo-controlled multiple-dose cohort, daily ARV-102 at 20 mg to 80 mg achieved approximately 50% or greater LRRK2 degradation in cerebrospinal fluid by day 14, maintained through day 28, alongside peripheral LRRK2 degradation and biomarker changes consistent with healthy-volunteer data. On the back of these results, which suggest a differentiated biomarker impact versus prior LRRK2 inhibitors, Arvinas plans to extend development of ARV-102 into additional LRRK2- and lysosomal dysfunction–associated neurodegenerative diseases, including a Phase 1b study in progressive supranuclear palsy expected to begin in the second quarter of 2026 while it assesses further paths in Parkinson’s disease.

The most recent analyst rating on (ARVN) stock is a Buy with a $20.00 price target. To see the full list of analyst forecasts on Arvinas Holding Company stock, see the ARVN Stock Forecast page.

Business Operations and StrategyExecutive/Board Changes
Arvinas Announces Leadership Transition and New CEO Appointment
Neutral
Feb 12, 2026

On February 10, 2026, Arvinas president, CEO and board chair John Houston, Ph.D., notified the company he would resign from those roles effective February 12, 2026, while remaining on the board and transitioning to a consulting position through March 1, 2027. On February 11, 2026, the board named lead independent director Briggs Morrison, M.D., as chair and appointed long‑time executive Randy Teel, Ph.D., as president, CEO, principal executive officer and director, under an amended employment agreement that sets his compensation, equity grants and detailed severance protections, including enhanced benefits and accelerated vesting in the event of a qualifying termination following a change in control.

The consulting agreement with Dr. Houston provides for a lump‑sum COBRA‑related payment, a cash amount equivalent to his 2025 bonus had he remained CEO, additional hourly fees beyond a baseline level of consulting hours and continued equity vesting. The leadership transition concentrates strategic and operational authority with Dr. Teel, who has held multiple senior roles at Arvinas since 2018, while preserving continuity and access to Dr. Houston’s expertise, a combination that may help stabilize governance and signal longer‑term planning to shareholders and employees.

The most recent analyst rating on (ARVN) stock is a Buy with a $14.50 price target. To see the full list of analyst forecasts on Arvinas Holding Company stock, see the ARVN Stock Forecast page.

Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Mar 19, 2026