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ADC Therapeutics to Host Second Quarter 2025 Financial Results Conference Call on August 12, 2025 ADC Therapeutics SA (NYSE: ADCT), a commercial-stage global leader and pioneer in the field of antibody drug conjugates (ADCs), today announced that...

Key Takeaway: ADC Therapeutics SA (NYSE: ADCT) has announced a conference call scheduled for August 12, 2025, to discuss its financial results for the second quarter of 2025. The call reflects the company’s commitment to keeping shareholders informed and engaged. ADC Therapeutics continues to advance its portfolio, notably with the FDA-approved ZYNLONTA for treating lymphoma and ongoing developments in its PSMA-targeting ADC. However, the company has also acknowledged risks related to future clinical and regulatory processes that may affect their operational outcomes.

Market Sentiment Analysis

POSITIVE FACTORS

  • ADC Therapeutics is hosting a financial results conference call, indicating transparency and engagement with investors.
  • The company continues to innovate in the field of antibody drug conjugates, particularly with their developments around ZYNLONTA.
  • They have received FDA and European approval for ZYNLONTA, signifying successful regulatory progress.

CONCERNS & RISKS

  • The forward-looking statements warn of risks and uncertainties that may affect actual results, including regulatory actions.
  • The company mentions potential challenges with cash flow and debt obligations that could impact operations.

Full Press Release Details

LAUSANNE , Switzerland , Aug. 5, 2025 /PRNewswire/ -- ADC Therapeutics SA (NYSE: ADCT ), a commercial-stage global leader and pioneer in the field of antibody drug conjugates (ADCs), today announced that it will host a conference call and live webcast on Tuesday, August 12, 2025 , at 8:30 a.m. EDT to report financial results for the second quarter of 2025 and provide operational updates.
To access the conference call, please register here . The participant toll-free dial-in number is 1-800-836-8184 for North America and Canada . It is recommended that you join 10 minutes before the event, though you may pre-register at any time. A live webcast of the call will be available under "Events and Presentations" in the Investors section of the ADC Therapeutics website at ir.adctherapeutics.com . The archived webcast will be available for 30 days following the call.
About ADC Therapeutics
ADC Therapeutics (NYSE: ADCT ) is a commercial-stage global leader and pioneer in the field of antibody drug conjugates (ADCs), transforming treatment for patients through our focused portfolio with ZYNLONTA and a PSMA-targeting ADC.
ADC Therapeutics' CD19-directed ADC ZYNLONTA (loncastuximab tesirine-lpyl) received accelerated approval by the FDA and conditional approval from the European Commission for the treatment of relapsed or refractory diffuse large B-cell lymphoma after two or more lines of systemic therapy. ZYNLONTA is also in development in combination with other agents and in earlier lines of therapy. In addition to ZYNLONTA, ADC Therapeutics is leveraging its expertise to advance IND-enabling activities for a next-generation PSMA-targeting ADC which utilizes a differentiated exatecan-based payload with a novel hydrophilic linker.
Forward-Looking Statements This press release contains forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. In some cases you can identify forward-looking statements by terminology such as "may", "will", "should", "would", "expect", "intend", "plan", "anticipate", "believe", "estimate", "predict", "potential", "seem", "seek", "future", "continue", or "appear" or the negative of these terms or similar expressions, although not all forward-looking statements contain these identifying words. Forward-looking statements are subject to certain risks and uncertainties that can cause actual results to differ materially from those described. Factors that may cause such differences include, but are not limited to: the success of the Company's strategic restructuring plan; changes in estimated costs associated with the restructuring plan including the workforce reduction and planned closure of the UK facility; the expected cash runway into 2028 which assumes use of minimum liquidity amount required to be maintained under its loan agreement covenants; whether future LOTIS-7 clinical trial results will be consistent with or different from the LOTIS-7 data presented at EHA and ICML and future compendia and regulatory strategy and opportunity; the timing of the PFS events for LOTIS-5 and the results of the trial and full FDA approval; the Company's ability to grow ZYNLONTA ® revenue in the United States and potential peak revenue; the ability of our partners to commercialize ZYNLONTA ® in foreign markets, the timing and amount of future revenue and payments to us from such partnerships and their ability to obtain regulatory approval for ZYNLONTA ® in foreign jurisdictions; the timing and results of the Company's or its partners' research and development projects or clinical trials including LOTIS 5 and 7, as well as early pre-clinical research for our exatecan-based ADC targeting PSMA; the timing and results of investigator-initiated trials including those studying FL and MZL and the potential regulatory and/or compendia strategy and the future opportunity; the timing and outcome of regulatory submissions for the Company's products or product candidates; actions by the FDA or foreign regulatory authorities; projected revenue and expenses; the Company's indebtedness, including Healthcare Royalty Management and Blue Owl and Oaktree facilities, and the restrictions imposed on the Company's activities by such indebtedness, the ability to comply with the terms of the various agreements and repay such indebtedness and the significant cash required to service such indebtedness; and the Company's ability to obtain financial and other resources for its research, development, clinical, and commercial activities. Additional information concerning these and other factors that may cause actual results to differ materially from those anticipated in the forward-looking statements is contained in the "Risk Factors" section of the Company's Annual Report on Form 10-K and in the Company's other periodic and current reports and filings with the U.S. Securities and Exchange Commission. These statements involve known and unknown risks, uncertainties and other factors that may cause actual results, performance, achievements or prospects to be materially different from any future results, performance, achievements or prospects expressed in or implied by such forward-looking statements. The Company cautions investors not to place undue reliance on the forward-looking statements contained in this document.
CONTACTS: Investors and Media Nicole Riley ADC Therapeutics [email protected] +1 862-926-9040
SOURCE ADC Therapeutics SA

21 %

Frequently Asked Questions

When will ADC Therapeutics host its financial results call?

ADC Therapeutics will host its financial results call on August 12, 2025, at 8:30 a.m. EDT.

How can I access the ADC Therapeutics conference call?

You can register online and join the conference call at 1-800-836-8184, North America.

What product does ADC Therapeutics offer for lymphoma?

ADC Therapeutics offers ZYNLONTA, an FDA-approved ADC for treating relapsed large B-cell lymphoma.

What are ADC Therapeutics' future developments?

The company is developing a next-generation PSMA-targeting ADC utilizing an innovative payload.

Where can I find the webcast after the event?

The archived webcast will be available for 30 days on their Investors section.

Last updated: Aug 5, 2025