Mettler-Toledo Exceeds Q3 Earnings Expectations Despite Year-over-Year Sales Drop
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Nov 07 2025
0mins
Should l Buy ADCT?
Source: NASDAQ.COM
Earnings and Sales Performance: Mettler-Toledo International reported third-quarter 2025 adjusted earnings of $11.15 per share, exceeding estimates by 4.99%, while net sales of $1.03 billion also surpassed expectations but declined 8% year-over-year.
Segment and Regional Sales: The company’s sales were driven by its Laboratory, Industrial, and Food Retail segments, with respective contributions of $565 million, $406 million, and $59 million, while regional sales showed growth in the Americas and Asia, but remained flat in Europe.
Financial Metrics: The gross margin contracted to 59.2%, with R&D and SG&A expenses rising year-over-year, leading to a decline in adjusted operating margin to 30.1%. Cash from operating activities was $299.4 million, with a free cash flow of $280.7 million.
Future Outlook: Mettler-Toledo anticipates a 3% increase in sales for Q4 2025 and expects adjusted earnings growth of 2-4% year-over-year, with projections for 2026 indicating a 4% sales increase and adjusted earnings growth of 8-9% over 2025.
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Analyst Views on ADCT
Wall Street analysts forecast ADCT stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for ADCT is 7.33 USD with a low forecast of 5.00 USD and a high forecast of 10.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
3 Analyst Rating
3 Buy
0 Hold
0 Sell
Strong Buy
Current: 3.910
Low
5.00
Averages
7.33
High
10.00
Current: 3.910
Low
5.00
Averages
7.33
High
10.00
About ADCT
ADC Therapeutics SA is a Switzerland-based clinical-stage oncology drug discovery and development company. It develops antibody drug conjugates (ADCs) for the treatment of both solid and hematological cancers. It employs monoclonal antibodies specific to particular tumor antigens conjugated to a class of pyrrolobenzodiazepine (PBD)-based warheads to selectively target and kill cancer cells. The Company has multiple PBD-based ADCs in ongoing clinical trials, ranging from first in human to pivotal Phase II clinical trials, and numerous preclinical ADCs in development. Its main drug candidates are ADCT-301 for the treatment of lymphoma and leukemia and ADCT-402 for the treatment of non-Hodgkin’s lymphoma and B-cell leukemia. It serves customers in the United States, Switzerland, and the United Kingdom.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- Compliance Assurance: The grants were made in reliance on the employment inducement exemption under NYSE's Listed Company Manual Rule 303A.08, ensuring that the company meets regulatory requirements while incentivizing its workforce.
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- Grant Details: The stock options will vest 25% on the first anniversary of the grant date, with 1/48th vesting monthly thereafter, ensuring full vesting by the fourth anniversary, which encourages employee retention.
- Compliance Assurance: The grants were made in reliance on the employment inducement exemption under NYSE's Listed Company Manual Rule 303A.08, ensuring that the company meets regulatory requirements while incentivizing its workforce.
- Company Background: ADC Therapeutics focuses on the development of antibody-drug conjugates (ADCs), with its product ZYNLONTA receiving accelerated approval from the FDA, highlighting the company's leadership in innovative drug development.
See More
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- Leadership Enhancement: Oncolytics Biotech appointed John McAdory as Executive Vice President of Strategy and Operations and Yujun Wu as Vice President of Biostatistics, both bringing extensive late-stage clinical trial experience to drive complex multi-country registration trials.
- Impressive Clinical Data: In colorectal cancer patients, the combination of pelareorep and chemotherapy achieved a 33% response rate, significantly surpassing the traditional 6-11% response rate, showcasing its competitive edge and potential commercial value in the market.
- Phase 3 Trial Design Approved: Oncolytics Biotech has secured FDA approval for its Phase 3 trial design for pancreatic cancer, marking the imminent launch of its registration trial in this notoriously difficult-to-treat area, further solidifying its market position.
See More
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- Leadership Enhancement: Oncolytics Biotech announced the hiring of two key executives, John McAdory as EVP of Strategy and Operations and Yujun Wu as VP of Biostatistics, whose extensive experience will enhance the company's execution in complex multi-country registration trials.
- Impressive Clinical Data: In colorectal cancer, pelareorep combined with chemotherapy achieved a 33% response rate, three times higher than traditional treatments, showcasing its competitive edge and likely attracting more investor interest.
- Regulatory Approval Secured: Oncolytics Biotech has received FDA approval for its Phase 3 trial design for pancreatic cancer, making it the only immunotherapy registration trial planned for this challenging disease, further solidifying its market position.
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- Investigation Launched: Pomerantz LLP is investigating whether ADC Therapeutics has engaged in securities fraud or other unlawful business practices, which could undermine investor confidence and lead to stock volatility.
- Clinical Trial Data: On December 3, 2025, ADC released data from the LOTIS-7 trial indicating that 36.7% of patients experienced cytokine release syndrome; despite positive framing, the occurrence of adverse events could tarnish the company's reputation.
- Stock Price Reaction: Following the clinical data release, ADC's stock price fell by $0.65, a 14.13% drop, closing at $3.95 per share, reflecting market concerns about the company's future prospects.
- Legal Context: Pomerantz LLP, a prominent securities class action firm with over 85 years of experience, is dedicated to protecting investor rights, and adverse findings from the investigation could result in significant financial liabilities for the company.
See More
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- Investigation Launched: Pomerantz LLP is investigating ADC Therapeutics for potential securities fraud, which could undermine investor confidence and lead to further stock price volatility.
- Clinical Trial Data Update: On December 3, 2025, ADC released data from the LOTIS-7 trial indicating that 36.7% of patients experienced cytokine release syndrome, and while the data was presented positively, the associated risks may affect market acceptance of its products.
- Stock Price Reaction: Following the release of adverse clinical data, ADC's stock price fell by $0.65, or 14.13%, closing at $3.95 per share on December 3, 2025, reflecting market concerns about the company's future prospects.
- Legal Implications: Pomerantz LLP, a prominent securities class action firm, may initiate legal proceedings against ADC, potentially impacting shareholder interests and the company's reputation.
See More
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- Clinical Progress: The company expects to complete enrollment for LOTIS-7 in the first half of 2026 and release topline data for LOTIS-5 in Q2 2026, laying the groundwork for future regulatory submissions and market introduction.
- Market Opportunities: With potential compendia inclusion in 2027 and regulatory approvals for LOTIS-5, ADC Therapeutics is poised for accelerated revenue growth, further solidifying its leadership position in the antibody-drug conjugate market.
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