ADC Therapeutics Releases its Annual Report on Form 20-F for the Fiscal Year Ended December 31, 2021
ADC Therapeutics, a biotechnology company focused on cancer treatment, announced the filing of its Annual Report on Form 20-F for the fiscal year ending December 31, 2021, with the SEC. The report, detailing comprehensive financial data and performance metrics, is accessible via the SEC website and the company's investor section. ADC's targeted antibody drug conjugates, like ZYNLONTA, which is FDA-approved for treating specific types of lymphoma, signify its commitment to innovative cancer therapies, alongside ongoing clinical developments for other ADCs.
- ADC's CD19-directed ADC ZYNLONTA is FDA-approved for treatment after multiple therapies.
- Multiple ADCs are currently in ongoing clinical and preclinical development.
- None.
ADC Therapeutics’ Annual Report on Form 20-F can be accessed by visiting either the SEC’s website at www.sec.gov or the Investor section of the Company’s website at ir.adctherapeutics.com. In addition, shareholders may request a hard copy of the Company’s audited financial statements, or its complete Annual Report on Form 20-F which include the audited financial statements, free of charge, by contacting IR@adctherapeutics.com.
About
ADC Therapeutics’ CD19-directed ADC ZYNLONTA® (loncastuximab tesirine-lpyl) is approved by the FDA 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. Cami (camidanlumab tesirine) is being evaluated in a pivotal Phase 2 trial for relapsed or refractory Hodgkin lymphoma and in a Phase 1b clinical trial for various advanced solid tumors. In addition to ZYNLONTA and Cami,
ZYNLONTA® is a registered trademark of
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Investors
Eugenia.Litz@adctherapeutics.com
+44 7879 627205
amanda.hamilton@adctherapeutics.com
+1 917-288-7023
EU Media
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+41 (0) 43 268 3231
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+1 914-552-4625
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