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Immunovant, Inc. (IMVT)
:IMVT

Immunovant (IMVT) AI Stock Analysis

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Immunovant

(NASDAQ:IMVT)

37Underperform
Immunovant's overall stock score reflects significant financial challenges and a bearish technical outlook, offset by positive corporate developments. The company's strong equity position and successful fundraising efforts are promising, but persistent losses and negative cash flows are major concerns.
Positive Factors
Clinical improvement
Greater IgG reduction with batoclimab leads to greater clinical improvement, supporting the value proposition for the next-gen FcRn IMVT-1402.
Clinical profile
Batoclimab shows a competitive clinical profile compared to other FcRn therapies.
Efficacy
Batoclimab demonstrates impressive efficacy in MG and CIDP, with advanced development in IMVT-1402.
Negative Factors
Data comparison
Some pushback has been received regarding the lack of time course data, making comparisons with other trials challenging.
Placebo response
The stock has been bouncing up and down based on some confusion/debate on how to think about the high placebo response on the primary efficacy endpoint of MG-ADL in the MG study.
Sales expectations
The price objective for Immunovant, Inc. was lowered due to reduced peak sales expectations for the company's FcRn program in the MG indication.

Immunovant (IMVT) vs. S&P 500 (SPY)

Immunovant Business Overview & Revenue Model

Company DescriptionImmunovant, Inc., a clinical-stage biopharmaceutical company, develops monoclonal antibodies for the treatment of autoimmune diseases. It develops batoclimab, a novel fully human monoclonal antibody that selectively binds to and inhibits the neonatal fragment crystallizable receptor, which is in Phase IIa clinical trials for the treatment of myasthenia gravis and thyroid eye disease, as well as completed initiation of Phase II clinical trials for the treatment of warm autoimmune hemolytic anemia. The company was incorporated in 2018 is headquartered in New York, New York. Immunovant, Inc. is a subsidiary of Roivant Sciences Ltd.
How the Company Makes MoneyImmunovant generates potential revenue primarily through the development and commercialization of its drug candidates. The company's revenue model hinges on the successful clinical development, regulatory approval, and eventual marketing of its lead product candidate, batoclimab. Immunovant may earn revenue through partnerships, collaborations, or licensing agreements with other pharmaceutical companies, which can provide upfront payments, milestone payments, and royalties based on product sales. Additionally, funding from investors and strategic partnerships plays a crucial role in supporting its research and development activities until the drugs reach the market.

Immunovant Financial Statement Overview

Summary
Immunovant is facing substantial financial challenges, characterized by persistent losses and negative cash flows. While the company maintains a solid equity position and low leverage, the lack of revenue and profitability raises questions about its long-term viability. Investors should be cautious and consider the company's strategy for achieving sustainable growth and profitability.
Income Statement
15
Very Negative
Immunovant shows significant financial challenges, with negative EBIT, EBITDA, and net income margins in the TTM period. The gross profit margin is positive, but revenue growth is non-existent due to the lack of revenue in previous periods. This indicates an ongoing reliance on funding rather than operational success.
Balance Sheet
50
Neutral
The balance sheet reflects a strong equity position with a low debt-to-equity ratio, indicating minimal leverage risk. However, the return on equity is negative due to substantial net losses, which is a concern for investors looking for profitability.
Cash Flow
20
Very Negative
Cash flow from operations is negative, which raises concerns about the company's ability to sustain operations without external financing. Despite this, the company has managed to maintain a positive cash balance, likely due to financing activities. The free cash flow to net income ratio is not favorable, reflecting cash burn issues.
Breakdown
TTMMar 2024Mar 2023Mar 2022Mar 2021Mar 2020
Income StatementTotal Revenue
1.50M0.000.000.000.000.00
Gross Profit
1.36M-231.00K-1.32M-1.23M-998.00K-21.00K
EBIT
-405.20M-282.71M-198.47M-156.16M-107.79M-65.67M
EBITDA
-404.87M-269.98M-209.63M-155.58M-106.79M-65.64M
Net Income Common Stockholders
-382.71M-259.34M-210.96M-156.73M-107.43M-66.39M
Balance SheetCash, Cash Equivalents and Short-Term Investments
374.69M635.37M376.53M493.82M400.15M100.57M
Total Assets
420.93M666.37M405.84M515.56M412.49M109.39M
Total Debt
23.00K138.00K1.22M2.36M3.42M3.19M
Net Debt
-374.66M-635.23M-375.31M-491.45M-396.73M-97.38M
Total Liabilities
68.31M48.61M43.34M45.74M21.01M15.32M
Stockholders Equity
352.62M617.76M362.49M469.82M391.48M94.07M
Cash FlowFree Cash Flow
-325.64M-214.59M-188.39M-106.37M-83.54M-53.39M
Operating Cash Flow
-324.94M-214.23M-188.19M-106.11M-83.33M-53.36M
Investing Cash Flow
-708.00K-360.00K-197.00K-254.00K-210.00K-31.00K
Financing Cash Flow
5.42M472.43M70.89M200.13M383.11M146.97M

Immunovant Technical Analysis

Technical Analysis Sentiment
Negative
Last Price14.79
Price Trends
50DMA
19.02
Negative
100DMA
22.37
Negative
200DMA
25.92
Negative
Market Momentum
MACD
-0.89
Positive
RSI
28.92
Positive
STOCH
17.78
Positive
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For IMVT, the sentiment is Negative. The current price of 14.79 is below the 20-day moving average (MA) of 17.28, below the 50-day MA of 19.02, and below the 200-day MA of 25.92, indicating a bearish trend. The MACD of -0.89 indicates Positive momentum. The RSI at 28.92 is Positive, neither overbought nor oversold. The STOCH value of 17.78 is Positive, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for IMVT.

Immunovant Risk Analysis

Immunovant disclosed 83 risk factors in its most recent earnings report. Immunovant 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

Immunovant Peers Comparison

Overall Rating
UnderperformOutperform
Sector (48)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
61
Neutral
$2.61B10.1254.39%624.05%
50
Neutral
$2.46B-93.55%97.02%64.32%
48
Neutral
$6.36B1.28-45.04%2.64%19.24%1.69%
46
Neutral
$3.01B-19.20%-89.95%-123.71%
45
Neutral
$2.56B-82.95%-22.34%
45
Neutral
$2.57B-32.02%-0.12%
37
Underperform
$2.53B-74.17%-43.10%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
IMVT
Immunovant
14.68
-14.67
-49.98%
PTGX
Protagonist Therapeutics
40.89
13.85
51.22%
CRSP
Crispr Therapeutics AG
34.26
-26.41
-43.53%
APLS
Apellis Pharmaceuticals
19.42
-32.37
-62.50%
SRRK
Scholar Rock Holding
26.31
12.86
95.61%
CRNX
Crinetics Pharmaceuticals
26.85
-17.74
-39.78%

Immunovant Earnings Call Summary

Earnings Call Date: Feb 6, 2025 | % Change Since: -34.30% | Next Earnings Date: May 28, 2025
Earnings Call Sentiment Positive
The earnings call highlighted significant advancements in Immunovant's development programs, particularly for IMVT-1402, with promising data in Graves' disease and a strategic approach in rheumatoid arthritis. However, the company faces challenges in the thyroid eye disease program's enrollment and efficacy demonstration for FcRn inhibitors. Overall, the sentiment leans towards optimism due to strategic progress despite some hurdles.
Highlights
Significant Progress with IMVT-1402 Development
In 2024, Immunovant cleared 5 INDs across a range of therapeutic areas, ahead of their schedule, and is on track to launch 10 indications by March 2026.
Promising Data on Graves' Disease
Recent data shows a 60% ATD-free response rate in patients whose IgG was lowered by 70% or more, indicating strong potential for IMVT-1402 in treating Graves' disease.
Introduction of Rheumatoid Arthritis Program
The rheumatoid arthritis program targets difficult-to-treat patients with a biomarker-driven strategy, leveraging prior proof-of-principle data with FcRn inhibitors.
Open-Label Trial Design for Rheumatoid Arthritis
The innovative trial design offers an open-label lead-in period, enhancing patient enrollment and providing early data catalysts.
Lowlights
Challenges in Thyroid Eye Disease Program Enrollment
Increased competition for patients with acute and very active thyroid eye disease has led to a delay in the expected data readout to the second half of next year.
Potential Limitations of Current FcRn Inhibitor Data
The previous FcRn inhibitor study (nipocalimab) did not meet its primary endpoint, indicating challenges in demonstrating efficacy across all rheumatoid arthritis patients.
Company Guidance
During the Q2 2025 earnings call, Immunovant provided substantial guidance on their development progress, particularly highlighting their lead asset, IMVT-1402. The company has cleared five Investigational New Drug (IND) applications ahead of schedule, aiming to launch 10 indications by March 2026, with four to five potentially registrational trials starting by March 2025. They expect data readouts from their myasthenia gravis (MG) and chronic inflammatory demyelinating polyneuropathy (CIDP) programs, which are fully enrolled, in the upcoming months. Immunovant also shared promising data on Graves' disease, where IMVT-1402 demonstrated significant IgG suppression, correlating with improved clinical outcomes. The company is also exploring an innovative trial design for difficult-to-treat rheumatoid arthritis, targeting patients with high ACPA levels to validate the efficacy of deeper IgG reduction, aiming for a high impact in this high unmet need population.

Immunovant Corporate Events

Product-Related AnnouncementsBusiness Operations and Strategy
Immunovant Announces Positive Phase 3 Study Results
Positive
Mar 19, 2025

On March 19, 2025, Immunovant announced positive results from its Phase 3 study of batoclimab for myasthenia gravis (MG) and initial results from its Phase 2b study for chronic inflammatory demyelinating polyneuropathy (CIDP). The MG study met its primary endpoint with significant improvements in the MG-ADL score, while the CIDP study showed promising improvements in disability scores. These results suggest deeper IgG reductions correlate with better clinical outcomes, supporting the potential of Immunovant’s therapies to address unmet needs in autoimmune conditions. Immunovant plans to focus on its lead asset IMVT-1402 for future studies, rather than seeking immediate regulatory approval for batoclimab.

Product-Related AnnouncementsBusiness Operations and Strategy
Immunovant Progresses in Autoimmune Therapy Development
Positive
Jan 14, 2025

Immunovant, Inc. announced its participation in the 43rd Annual J.P. Morgan Healthcare Conference on January 14, 2025, where it will present a corporate overview. The company is making significant progress in its clinical trials, particularly with IMVT-1402, across multiple autoimmune conditions. With a strengthened financial position and a strategic focus on anti-FcRn therapies, Immunovant is poised to enhance its market position and offer potentially transformative treatments for autoimmune patients. Key trials and milestones are expected to yield significant data by March 2025, reflecting the company’s rapid advancement in drug development and commercialization efforts.

Private Placements and FinancingBusiness Operations and Strategy
Immunovant Raises $450 Million Through Share Purchase Agreement
Positive
Jan 13, 2025

Immunovant, Inc. has entered into a share purchase agreement with several institutional accredited investors to sell 22,500,000 shares at $20.00 each, raising approximately $450 million in a private placement expected to close by January 15, 2025. The funds will be used for advancing its development pipeline and other corporate purposes, with the shares to be registered for resale with the SEC.

Glossary
OutperformA stock rated as "Outperform" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests that the stock is likely to deliver higher returns compared to the average returns of other stocks in the same sector or market index. Investors might consider this stock a good buying opportunity.
NeutralA stock rated as "Neutral" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly attractive nor unattractive for investment. Investors may consider holding onto the stock, as it is not expected to either significantly outperform or underperform the market.
UnderperformA stock rated as "Underperform" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests that the stock may deliver lower returns compared to the average returns of other stocks in the same sector or market index. Investors might consider selling the stock or avoiding it as an investment.

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.