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ADC Therapeutics to Participate in the 24th Annual Needham Virtual Healthcare Conference ADC Therapeutics SA (NYSE: ADCT) announced today that Ameet Mallik, Chief Executive Officer, will present a company overview at the 24th Annual...

Key Takeaway: ADC Therapeutics announced that CEO Ameet Mallik will present an overview at the 24th Annual Needham Virtual Healthcare Conference on April 8, 2025. The conference will be accessible via a live webcast, with a replay available for 30 days. ADC Therapeutics is noted for its advancements in antibody drug conjugates, particularly with its FDA-approved treatment ZYNLONTA for certain lymphomas. The company continues to work on expanding its ADC technology across various cancers.

Market Sentiment Analysis

POSITIVE FACTORS

  • ADC Therapeutics will present at the 24th Annual Needham Virtual Healthcare Conference, showcasing their leadership in antibody drug conjugates.
  • The CEO's participation reflects the company's commitment to transparency and engagement with investors.
  • The company has received FDA accelerated approval for its ADC ZYNLONTA, demonstrating progress in the treatment of aggressive lymphomas.

Full Press Release Details

LAUSANNE , Switzerland , April 1, 2025 /PRNewswire/ -- ADC Therapeutics SA (NYSE: ADCT ) announced today that Ameet Mallik , Chief Executive Officer, will present a company overview at the 24th Annual Needham Virtual Healthcare Conference on Tuesday, April 8, 2025 , at 8:00 a.m. ET .
A live webcast of the presentation will be available via the Events & Presentations page in the Investors section of ADC Therapeutics' website, ir.adctherapeutics.com . A replay of the webcast will be available for approximately 30 days.
About ADC Therapeutics
ADC Therapeutics (NYSE: ADCT ) is a commercial-stage global leader and pioneer in the field of antibody drug conjugates (ADCs). The Company is advancing its proprietary ADC technology to transform the treatment paradigm for patients with hematologic malignancies and solid tumors.
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 has multiple ADCs in ongoing clinical and preclinical development.
ADC Therapeutics is based in Lausanne (Biopôle), Switzerland and has operations in London , the San Francisco Bay Area and New Jersey . For more information, please visit https://adctherapeutics.com/ and follow the Company on LinkedIn .
ZYNLONTA ® is a registered trademark of ADC Therapeutics SA.
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 timing and future results of the Company's early research in exatecan-based Claudin-6, PSMA and ASCT2-targeting antibody-drug conjugates; the expected cash runway into mid-2026 the Company's ability to grow ZYNLONTA ® revenue in the United States ; 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 and ADCT 602; 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.
Investors Marcy Graham ADC Therapeutics [email protected] +1 650-667-6450
Media Nicole Riley ADC Therapeutics [email protected] +1 862-926-9040
SOURCE ADC Therapeutics SA

21 %

Frequently Asked Questions

When will ADC Therapeutics present at the Needham Conference?

ADC Therapeutics will present on April 8, 2025, at 8:00 a.m. ET.

How can I access the ADC Therapeutics presentation?

The presentation will be available live on their Investors Events page.

What is ZYNLONTA used for?

ZYNLONTA is approved for relapsed or refractory diffuse large B-cell lymphoma.

Where is ADC Therapeutics located?

ADC Therapeutics is based in Lausanne, Switzerland.

What are the current developments at ADC Therapeutics?

They are advancing multiple ADCs in clinical and preclinical development.

Last updated: Apr 1, 2025