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ADC Therapeutics to Host Third Quarter 2024 Financial Results Conference Call on November 7, 2024

ADC Therapeutics to Host Third Quarter 2024 Financial Results Conference Call on November 7, 2024

adc therapeutics將於2024年11月7日舉行第三季度財務業績電話會議
PR Newswire ·  10/31 19:15

LAUSANNE, Switzerland, Oct. 31, 2024 /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 Thursday, November 7, 2024, at 8:30 a.m. EST to report financial results for the third quarter 2024 and provide operational updates.

瑞士洛桑,2024年10月31日/ PRNewswire/ - adc therapeutics(紐交所:ADCT), 一家商業階段的全球領導者和抗體藥物連接物(ADCs)領域的先驅,今天宣佈將於2024年11月7日星期四上午8:30舉行電話會議和實時網絡直播,報告2024年第三季度的財務業績並提供運營更新。

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.

要參加電話會議,請在此註冊。北美和加拿大的參與者免費撥打電話號碼爲1-800-836-8184。建議您在活動開始前10分鐘加入,儘管您可以隨時進行預先註冊。電話會議的實時網絡直播將在 adc therapeutics 網站的投資者部分「事件和演示文稿」下提供,網址爲ir.adctherapeutics.com。電話會議後,網絡直播將保留30天。

About ADC Therapeutics

關於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(紐交所:ADCT)是一家商業化階段的全球領先者和先鋒,致力於抗體藥物結合物(ADCs)領域。公司正在推進其專有ADC技術,改變對患有血液惡性腫瘤和實體瘤患者的治療範式。

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的CD19-定向ADC ZYNLONTA (loncastuximab tesirine-lpyl) 已獲得FDA的加速批准和歐洲委員會的有條件批准,用於治療兩條或以上全身療法經治療失敗或複發性瀰漫大B細胞淋巴瘤。ZYNLONTA還在與其他藥物聯用及早期治療方案的開發中。除了ZYNLONTA外,ADC Therapeutics還有多個ADC正在進行臨床和臨床前開發。

ADC Therapeutics is based in Lausanne (Biopôle), Switzerland, and has operations in London and New Jersey. For more information, please visit and follow the Company on LinkedIn.

adc therapeutics 總部位於瑞士洛桑(Biopôle),在倫敦和新澤西設有運營。欲了解更多信息,請訪問 並在社交媒體上關注公司。LinkedIn.

ZYNLONTA is a registered trademark of ADC Therapeutics SA.

ZYNLONTA是adc therapeutics SA的註冊商標。

Forward-Looking Statements

前瞻性聲明

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 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, ADCT 601 and 602 as well as early research in certain solid tumors with different targets, linkers and payloads; 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.

本新聞稿包含根據1995年《私人證券訴訟改革法》中安全港條款的前瞻性陳述。在某些情況下,您可以通過「可能」,「將」,「應該」,「將」,「期望」,「打算」,「計劃」,「預計」,「相信」,「估計」,「預測」,「潛力」,「看起來」,「尋找」,「未來」,「繼續」或「出現」或這些術語的否定形式或類似表達方式來識別前瞻性陳述,儘管並非所有前瞻性陳述都包含這些識別詞。前瞻性陳述受到某些風險和不確定性的影響,這些風險和不確定性可能導致實際結果與描述不符。可能導致此類差異的因素包括但不限於:預期的現金儲備將持續到2026年中期公司在美國增加ZYNLONTA的收入能力;我們的合作伙伴在國外市場商業化ZYNLONTA的能力;從此類合作伙伴獲得我們的未來收入和付款的時間和金額以及他們在國外司法管轄區獲得ZYNLONTA的監管批准的能力;公司或其合作伙伴的研發項目或臨床試驗(包括LOTIS 5和7、ADCt 601和602以及針對不同靶點、連接劑和有效荷的某些實體腫瘤的早期研究)的時間和結果;由調查者發起的試驗(包括研究FL和MZL的試驗)的時間和結果,以及未來的監管和/或彙編策略和機會;公司產品或產品候選人的監管提交時間和結果;FDA或外國監管機構的行動;預測的收入和支出;公司的負債情況,包括醫療保健版稅管理、Blue Owl和Oaktree機構以及這些負債對公司活動的限制,履行各種協議和償還該負債所需的大量現金;以及公司獲得其研究、開發、臨床和商業活動的財務和其他資源的能力。關於這些因素和其他可能導致實際結果與前瞻性陳述中預期結果不符的因素的更多信息,詳見公司的10-k年度報告中的《風險因素》部分以及公司的其他定期和現行報告以及向美國證券交易委員會的備案文件。本聲明涉及已知和未知的風險、不確定因素和其他因素,這些因素可能導致實際結果、績效、成就或前景與所包含的前瞻性陳述中表述的任何未來結果、績效、成就或前景有實質差異。本公司提醒投資者不要對本文件中包含的前瞻性陳述過分依賴。

CONTACTS:
Investors
Marcy Graham
ADC Therapeutics
[email protected]
+1 650-667-6450
Media
Nicole Riley
ADC Therapeutics
[email protected]
+1 862-926-9040

聯繫方式:
投資者
馬西·格雷厄姆
adc therapeutics
[email protected]
+1 650-667-6450
媒體
Nicole Riley
adc therapeutics
[email protected]
+1 862-926-9040

SOURCE ADC Therapeutics SA

adc therapeutics SA來源

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譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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