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Inovio Pharmaceuticals (INO)
NASDAQ:INO

Inovio Pharmaceuticals (INO) AI Stock Analysis

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INO

Inovio Pharmaceuticals

(NASDAQ:INO)

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Neutral 47 (OpenAI - 5.2)
Rating:47Neutral
Price Target:
$1.50
▼(-11.24% Downside)
The score is held down primarily by very weak financial performance (persistent large losses, deeply negative cash flow, and negative TTM equity) and bearish technicals (below major moving averages with negative MACD). Offsetting factors include positive regulatory/pipeline milestones and cost reductions discussed on the earnings call, plus the FDA’s BLA acceptance, but near-term cash runway and funding needs remain key risks.
Positive Factors
Regulatory Milestone
Acceptance of the BLA formally advances INO-3107 toward potential approval and commercialization. This is a durable structural positive because regulatory acceptance validates clinical proof and creates a clear pathway to recurring product revenue and partner interest if approval follows.
Proprietary Platform Validation
Peer-reviewed proof-of-concept for DNA-encoded monoclonal antibodies strengthens Inovio's core technology moat. Durable platform validation supports broader pipeline applications, licensing opportunities, and partnership leverage across multiple indications over the medium term.
Cost Management
A sustained reduction in operating expenses indicates management discipline and structural cost control. Lower fixed burn improves runway and optionality for funding clinical and commercialization activities, reducing near-term dilution pressure if maintained.
Negative Factors
Persistent Negative Cash Flow
Chronic negative operating and free cash flow mean the business is not self-funding and must repeatedly access external capital. Over months this constrains R&D, commercialization spending and strategic flexibility, raising dilution and execution risk for pipeline advancement.
Balance Sheet Deterioration
Negative stockholders' equity is a material structural weakness: it limits borrowing capacity, complicates partner and vendor negotiations, and signals higher insolvency or dilution risk, making sustained investment to scale commercial operations more difficult.
Ongoing Financing Dependence
Repeated reliance on warrant extensions and public offerings evidences structural dependence on equity markets to fund operations. This increases long-term dilution risk and ties execution to capital-market access rather than operational cash generation, weakening financial resilience.

Inovio Pharmaceuticals (INO) vs. SPDR S&P 500 ETF (SPY)

Inovio Pharmaceuticals Business Overview & Revenue Model

Company DescriptionInovio Pharmaceuticals, Inc., a biotechnology company, focuses on the discovery, development, and commercialization of DNA medicines to treat and protect people from diseases associated with human papillomavirus (HPV), cancer, and infectious diseases. Its DNA medicines platform uses precisely designed SynCon that identify and optimize the DNA sequence of the target antigen, as well as CELLECTRA smart devices technology that facilitates delivery of the DNA plasmids. The company engages in conducting and planning clinical studies of its DNA medicines for HPV-associated precancers, including cervical, vulvar, and anal dysplasia; HPV-associated cancers, such as head and neck, cervical, anal, penile, vulvar, and vaginal; other HPV-associated disorders, including recurrent respiratory papillomatosis; glioblastoma multiforme; prostate cancer; HIV; Ebola; Middle East Respiratory Syndrome (MERS); and Lassa fever. Its partners and collaborators include ApolloBio Corp., AstraZeneca, Beijing Advaccine Biotechnology Co., Ltd., The Bill & Melinda Gates Foundation, Coalition for Epidemic Preparedness Innovations (CEPI), Defense Advanced Research Projects Agency (DARPA), Department of Defense (DoD), HIV Vaccines Trial Network, International Vaccine Institute, Kaneka Eurogentec, Medical CBRN Defense Consortium (MCDC), National Cancer Institute, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Ology Bioservices, the Parker Institute for Cancer Immunotherapy, Plumbline Life Sciences, Regeneron Pharmaceuticals, Thermo Fisher Scientific, University of Pennsylvania, Walter Reed Army Institute of Research, and The Wistar Institute. The company has an agreement with Richter-Helm BioLogics GmbH & Co. KG to support investigational DNA vaccine INO-4800 for COVID-19; and a partnership with International Vaccine Institute and Seoul National University Hospital. The company was founded in 1979 and is headquartered in Plymouth Meeting, Pennsylvania.
How the Company Makes MoneyInovio Pharmaceuticals generates revenue primarily through a combination of government grants, research collaborations, and funding from partnerships with larger pharmaceutical companies. The company also seeks to monetize its proprietary technology through licensing agreements, allowing other entities to utilize its DNA delivery platform for their own drug development. Revenue may also come from the advancement of its clinical trial programs, which can attract further investment as they progress. Additionally, Inovio may receive milestone payments and royalties from partners based on the success of products developed under collaborative agreements, contributing to its financial sustainability.

Inovio Pharmaceuticals Earnings Call Summary

Earnings Call Date:Nov 10, 2025
(Q3-2025)
|
% Change Since: |
Next Earnings Date:Mar 03, 2026
Earnings Call Sentiment Neutral
The earnings call highlighted significant milestones such as the BLA submission for INO-3107 and cost management achievements. However, challenges persist with increased net loss and reduced cash reserves. Progress in clinical trials and pipeline advancements are promising, but financial constraints pose concerns.
Q3-2025 Updates
Positive Updates
BLA Submission for INO-3107
Inovio achieved a primary objective by completing the rolling submission of the Biologics License Application (BLA) for INO-3107, marking a significant milestone in their DNA medicine platform.
Significant Reduction in Operating Expenses
Operating expenses decreased by 22% from $27.3 million in Q3 2024 to $21.2 million in Q3 2025, demonstrating effective cost management.
Promising Clinical Data for INO-3107
INO-3107 demonstrated a 50% to 100% reduction in surgeries for most patients in clinical trials, with continued benefits observed in the second year post-treatment.
Publication of DMAb Technology in Nature Medicine
Landmark proof-of-concept data on Inovio's DNA-encoded Monoclonal Antibody technology was published, showing sustained protein production without antidrug antibodies.
Advancements in DNA Medicine Pipeline
Progress in DNA encoded protein technology with upcoming presentations and promising preclinical data, highlighting potential in treating multiple diseases.
Negative Updates
Increased Net Loss
Net loss for Q3 2025 increased to $45.5 million from a loss of $27.3 million in Q3 2024, driven by a $22.5 million noncash loss on fair value adjustments related to warrant liabilities.
Reduction in Cash Reserves
Cash, cash equivalents, and short-term investments decreased to $50.8 million as of September 30, 2025, from $94.1 million at the end of 2024.
Company Guidance
During the Inovio Third Quarter 2025 Financial Results Conference Call, key guidance focused on the progress of its DNA medicine, INO-3107, for recurrent respiratory papillomatosis (RRP). Inovio completed its Biologics License Application (BLA) submission and anticipates FDA file acceptance by year-end, with a potential PDUFA date in mid-2026 if priority review is granted. The company reported a 22% decrease in operating expenses to $21.2 million compared to the previous year and a net loss of $45.5 million, primarily due to a $22.5 million noncash loss related to warrant liabilities. Inovio has $50.8 million in cash, projecting its cash runway into Q2 2026. Strategic focus remains on launching INO-3107 by mid-2026, with ongoing commercialization preparations and further development of its DNA-encoded monoclonal antibody (DMAb) and DNA-encoded protein (DPROT) technologies.

Inovio Pharmaceuticals Financial Statement Overview

Summary
Financial profile is very weak: revenue is minimal/declining, losses remain large with no clear path to breakeven, and operating/free cash flow are consistently deeply negative. Balance-sheet risk increased with the latest TTM showing stockholders’ equity turning negative alongside ongoing cash burn.
Income Statement
6
Very Negative
Results remain highly unprofitable, with large losses relative to revenue across the historical periods provided. Revenue has been volatile and has generally trended down from 2022 to 2024, and TTM (Trailing-Twelve-Months) revenue is extremely small, which amplifies the already very weak profitability profile. While annual net losses narrowed versus 2022, the company still shows no clear path to breakeven based on the reported operating results.
Balance Sheet
18
Very Negative
Leverage looks modest in the annual periods (debt appears low relative to equity), which is a positive for financial flexibility. However, the most recent TTM (Trailing-Twelve-Months) snapshot shows stockholders’ equity turning negative, a meaningful deterioration that raises balance-sheet risk and can limit funding options. Overall asset levels have also declined materially over time, consistent with ongoing cash burn.
Cash Flow
3
Very Negative
Cash generation is a major weakness: operating and free cash flow are consistently deeply negative in every period shown, indicating the business is not self-funding. Free cash flow has occasionally improved year over year, but it remains substantially negative, and TTM (Trailing-Twelve-Months) operating/free cash flow is exceptionally large in magnitude versus prior years, signaling heightened near-term cash pressure (based strictly on the provided figures).
BreakdownTTMDec 2024Dec 2023Dec 2022Dec 2021Dec 2020
Income Statement
Total Revenue182.34K217.76K832.01K10.26M1.77M7.41M
Gross Profit-1.34M217.76K832.01K10.26M1.77M7.41M
EBITDA-105.08M-103.95M-130.39M-270.90M-296.56M-149.56M
Net Income-108.09M-107.25M-135.12M-279.82M-303.66M-166.41M
Balance Sheet
Total Assets69.39M113.20M170.95M348.53M495.94M539.77M
Cash, Cash Equivalents and Short-Term Investments50.80M94.11M145.29M253.00M401.31M411.64M
Total Debt10.02M11.87M30.21M32.07M33.02M39.05M
Total Liabilities77.11M44.69M53.60M126.17M96.27M78.63M
Stockholders Equity-7.72M68.50M117.35M222.36M399.67M461.14M
Cash Flow
Free Cash Flow-20.88B-104.56M-124.69M-217.18M-216.94M-179.50M
Operating Cash Flow-20.88B-104.08M-124.37M-216.22M-215.71M-177.98M
Investing Cash Flow5.33B104.07M87.36M109.59M-175.34M-58.80M
Financing Cash Flow20.32M51.48M5.00M81.84M211.50M465.28M

Inovio Pharmaceuticals Technical Analysis

Technical Analysis Sentiment
Neutral
Last Price1.69
Price Trends
50DMA
1.85
Negative
100DMA
2.08
Negative
200DMA
1.99
Negative
Market Momentum
MACD
-0.06
Negative
RSI
48.70
Neutral
STOCH
73.65
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For INO, the sentiment is Neutral. The current price of 1.69 is above the 20-day moving average (MA) of 1.58, below the 50-day MA of 1.85, and below the 200-day MA of 1.99, indicating a neutral trend. The MACD of -0.06 indicates Negative momentum. The RSI at 48.70 is Neutral, neither overbought nor oversold. The STOCH value of 73.65 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Neutral sentiment for INO.

Inovio Pharmaceuticals Risk Analysis

Inovio Pharmaceuticals disclosed 58 risk factors in its most recent earnings report. Inovio Pharmaceuticals reported the most risks in the "Legal & Regulatory" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Inovio Pharmaceuticals Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
52
Neutral
$104.20M-745.66%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
49
Neutral
$98.14M-9.03-62.16%11.78%
47
Neutral
$116.80M-0.65-328.45%-10.36%42.36%
45
Neutral
$97.26M-33.41%81.19%
44
Neutral
$48.90M-0.62-50.60%1.40%
43
Neutral
$48.14M-1.57-48.89%-9.42%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
INO
Inovio Pharmaceuticals
1.67
-0.37
-18.14%
AGEN
Agenus
2.89
-1.01
-25.90%
ONCY
Oncolytics Biotech
0.90
0.16
21.62%
ATOS
Atossa Therapeutics
5.29
-7.45
-58.49%
ANIX
Anixa Biosciences
2.92
-0.08
-2.67%
TIL
Instil Bio
7.42
-14.84
-66.67%

Inovio Pharmaceuticals Corporate Events

Business Operations and StrategyPrivate Placements and Financing
Inovio Extends Series A Warrants, Enhancing Capital Flexibility
Positive
Jan 27, 2026

On January 27, 2026, Inovio Pharmaceuticals amended the terms of its outstanding Series A warrants, originally issued in a July 2025 underwritten public offering, to extend their expiration from January 28, 2026 to 5:00 p.m. New York City time on March 31, 2026. The Series A warrants, which remain unchanged in all other respects, are exercisable for up to 13,564,268 shares of common stock or equivalent pre-funded warrants at an exercise price of $1.75 per share (or $1.749 per pre-funded warrant), a move that gives investors more time to exercise their warrants and potentially provides Inovio with additional access to equity capital tied to its progress on INO-3107 following the FDA’s acceptance of its Biologic License Application.

The most recent analyst rating on (INO) stock is a Hold with a $1.50 price target. To see the full list of analyst forecasts on Inovio Pharmaceuticals stock, see the INO Stock Forecast page.

Business Operations and StrategyProduct-Related AnnouncementsRegulatory Filings and Compliance
FDA Accepts Inovio’s BLA for INO-3107 Review
Positive
Dec 29, 2025

On December 29, 2025, INOVIO announced that the U.S. Food and Drug Administration accepted for review its Biologics License Application for INO-3107, an investigational DNA medicine intended to treat adults with recurrent respiratory papillomatosis, a rare HPV-driven disease currently managed primarily through repeated surgeries. The application, filed under the accelerated approval pathway and granted a standard review with an October 30, 2026 PDUFA target decision date and no planned advisory committee meeting, is supported by Phase 1/2 data showing substantial reductions in surgery frequency and durable clinical benefit, but the FDA has flagged whether INOVIO has provided sufficient justification for accelerated approval, prompting the company to seek further discussions with regulators as it pursues a non-surgical, first-of-its-kind therapeutic option in a niche but significantly underserved market.

The most recent analyst rating on (INO) stock is a Hold with a $2.00 price target. To see the full list of analyst forecasts on Inovio Pharmaceuticals stock, see the INO Stock Forecast page.

Private Placements and Financing
Inovio Pharmaceuticals Announces Public Offering Agreement
Neutral
Nov 12, 2025

On November 11, 2025, INOVIO Pharmaceuticals announced an underwriting agreement with Piper Sandler & Co. for a public offering of 13,158,000 shares of its common stock at $1.90 per share, with an option for underwriters to purchase an additional 1,973,700 shares, which was fully exercised. The offering is expected to generate approximately $26.5 million in net proceeds, with the closing anticipated around November 12, 2025, subject to customary conditions. This move aims to bolster INOVIO’s financial position and support its ongoing efforts in the biotechnology sector.

The most recent analyst rating on (INO) stock is a Buy with a $13.00 price target. To see the full list of analyst forecasts on Inovio Pharmaceuticals stock, see the INO 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: Jan 28, 2026