PDS Biotechnology Corporation Announces Key Opinion Leader Event on HPV16-Positive Head and Neck Cancer and Phase 3 Clinical Trial for Versamune HPV
PDS Biotechnology Corporation Announces Key Opinion Leader Event on HPV16-Positive Head and Neck Cancer and Phase 3 Clinical Trial for Versamune HPV
PDS Biotech announces KOL event to discuss HPV16-positive HNSCC and upcoming clinical trial for Versamune HPV therapy.
pds biotechnology宣佈KOL活動,討論HPV16陽性頭頸部鱗狀細胞癌及即將進行的Versamune HPV治療臨床試驗。
Quiver AI Summary
Quiver AI 概要
PDS Biotechnology Corporation announced a Key Opinion Leader (KOL) event on December 17, 2024, to discuss the increasing prevalence of HPV16-positive head and neck squamous cell carcinoma (HNSCC) and the upcoming VERSATILE-003 Phase 3 clinical trial of their investigational treatment, Versamune HPV combined with pembrolizumab. The event will feature expert speakers, including Dr. Francis Worden from the University of Michigan and Dr. Kevin Harrington from The Institute of Cancer Research, and will be moderated by PDS Biotech's Chief Medical Officer, Dr. Kirk Shepard. The company aims to advance its targeted immunotherapy approach for treating this type of cancer and highlights its commitment to developing innovative treatments for both cancer and infectious diseases.
pds biotechnology公司於2024年12月17日宣佈了一場關鍵意見領袖(KOL)活動,討論HPV16陽性頭頸部鱗狀細胞癌(HNSCC)的日益普遍現象,以及他們研究性治療Versamune HPV聯合pembrolizumab的即將進行的VERSATILE-003第三階段臨床試驗。活動將邀請專家發言,包括來自密歇根大學的Francis Worden博士和來自癌症研究所的Kevin Harrington博士,由pds biotechnology的首席醫療官Kirk Shepard博士主持。該公司旨在推進其針對這種癌症的靶向免疫治療方案,並強調其在開發針對癌症和傳染病創新治療方面的承諾。
Potential Positives
潛在的積極因素
- The announcement of a Key Opinion Leader (KOL) event demonstrates PDS Biotech's commitment to engaging with the medical community and highlights the company's focus on HPV16-positive head and neck squamous cell carcinoma (HNSCC).
- Details about the upcoming VERSATILE-003 Phase 3 clinical trial for Versamune HPV + pembrolizumab signify potential advancements in treatment options for cancer patients, which could enhance the company's product visibility and credibility.
- The participation of renowned experts like Dr. Francis Worden and Dr. Kevin Harrington in the KOL event adds significant scientific authority and may attract increased interest from investors and the medical community.
- 關鍵意見領袖(KOL)活動的公告表明pds biotechnology致力於與醫療界互動,並突出了該公司對HPV16陽性頭頸部鱗狀細胞癌(HNSCC)的關注。
- 有關即將進行的VERSATILE-003第三階段臨床試驗的詳細信息,顯示了Versamune HPV + pembrolizumab在癌症患者治療選擇中的潛在進展,這可能增強公司的產品知名度和可信性。
- Francis Worden博士和Kevin Harrington博士等知名專家參與KOL活動,爲事件增添了重要的科學權威性,並可能吸引投資者和醫療界的更多關注。
Potential Negatives
潛在負面影響
- The press release emphasizes the company's reliance on upcoming clinical trials, indicating potential uncertainty in their product pipeline and future revenue generation.
- There is a significant risk associated with the company's ability to secure necessary financing, which may hinder their operations and product development.
- The mention of "forward-looking statements" highlights the inherent uncertainties and risks in their anticipated outcomes, which may raise concerns among investors about the company's stability and future prospects.
- 新聞稿強調了公司對即將進行的臨床試驗的依賴,表明其產品管道和未來營業收入可能存在不確定性。
- 公司獲取必要融資的能力存在重大風險,這可能阻礙他們的運營和產品開發。
- "前瞻性聲明"的提及突顯了他們預期結果中固有的不確定性和風險,這可能會引起投資者對公司穩定性和未來前景的擔憂。
FAQ
常見問題
What is the VERSATILE-003 clinical trial about?
VERSATILE-003 臨床試驗是關於什麼的?
The VERSATILE-003 trial examines Versamune HPV combined with pembrolizumab for treating recurrent HPV16-positive head and neck cancers.
VERSATILE-003 試驗考察了 Versamune HPV 與 pembrolizumab 聯合治療復發 HPV16 陽性頭頸癌。
Who are the key speakers at the KOL event?
KOL 事件的主要發言人是誰?
The event features Dr. Francis Worden from the University of Michigan and Dr. Kevin Harrington from The Institute of Cancer Research, UK.
此次活動的發言人包括來自密歇根大學的 Dr. Francis Worden 和來自英國癌症研究所的 Dr. Kevin Harrington。
When will the KOL event take place?
KOL活動將於何時舉行?
The KOL event is scheduled for December 17, 2024, from 12 p.m. to 1:30 p.m. ET.
KOL活動定於2024年12月17日舉行,時間爲東部時間中午12點到下午1點30分。
How can I register for the KOL event?
我如何註冊KOL活動?
Registration details for the event can be found on the PDS Biotechnology website or directly via the provided link.
活動的註冊細節可以在pds biotechnology網站上找到或通過提供的鏈接直接註冊。
What is PDS Biotechnology focused on?
pds biotechnology專注於什麼?
PDS Biotechnology specializes in immunotherapy aimed at treating cancers and developing vaccines for infectious diseases.
pds biotechnology專注於免疫療法,旨在治療癌症和開發傳染病疫苗。
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
免責聲明:這是由GlobeNewswire分發的新聞稿的人工智能生成摘要。用於總結這份稿件的模型可能會出錯。請在這裏查看完整發布。
$PDSB Hedge Fund Activity
$PDSb對沖基金活動
We have seen 16 institutional investors add shares of $PDSB stock to their portfolio, and 63 decrease their positions in their most recent quarter.
我們看到有16家機構投資者將$PDSb股票加入他們的投資組合,63家在最近的一個季度減少了持倉。
Here are some of the largest recent moves:
以下是一些最近最大的交易動態:
- GOLDMAN SACHS GROUP INC removed 317,460 shares (-100.0%) from their portfolio in Q3 2024
- NORTHERN TRUST CORP removed 147,331 shares (-61.4%) from their portfolio in Q3 2024
- MILLENNIUM MANAGEMENT LLC removed 147,202 shares (-38.6%) from their portfolio in Q3 2024
- SOFINNOVA INVESTMENTS, INC. removed 142,635 shares (-100.0%) from their portfolio in Q3 2024
- JANE STREET GROUP, LLC removed 114,032 shares (-100.0%) from their portfolio in Q3 2024
- VANGUARD GROUP INC added 112,704 shares (+8.0%) to their portfolio in Q3 2024
- NUVEEN ASSET MANAGEMENT, LLC removed 110,296 shares (-100.0%) from their portfolio in Q2 2024
- 高盛集團在2024年第三季度從他們的投資組合中移除了317,460股(-100.0%)。
- northern trust corp在2024年第三季度從他們的投資組合中移除了147,331股(-61.4%)。
- 千禧管理有限責任公司在2024年第三季度從他們的投資組合中移除了147,202股(-38.6%)。
- 索菲諾瓦投資公司在2024年第三季度從他們的投資組合中移除了142,635股(-100.0%)。
- 簡街集團在2024年第三季度從他們的投資組合中移除了114,032股(-100.0%)。
- 先鋒集團在2024年第三季度向他們的投資組合中增加了112,704股(+8.0%)。
- NUVEEN 資產管理有限公司在2024年第二季度從其投資組合中移除了110,296股(-100.0%)
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
要追蹤對沖基金的股票組合,請查看Quiver Quantitative的機構持股儀表板。
Full Release
全面發佈
PRINCETON, N.J., Dec. 03, 2024 (GLOBE NEWSWIRE) -- PDS Biotechnology Corporation (Nasdaq: PDSB) ("PDS Biotech" or the "Company"), a late-stage immunotherapy company focused on transforming how the immune system targets and kills cancers and the development of infectious disease vaccines, today announced a Key Opinion Leader ("KOL") event to discuss the pathology and growing prevalence of HPV16-positive head and neck squamous cell carcinoma ("HNSCC") as well as the Company's upcoming VERSATILE-003 Phase 3 clinical trial of Versamune
HPV + pembrolizumab for first-line treatment of recurrent and/or metastatic HPV16-positive HNSCC.
PRINCETON, N.J., Dec. 03, 2024 (GLOBE NEWSWIRE) -- PDS Biotechnology Corporation (Nasdaq: PDSB) ("PDS Biotech" or the "Company"), a late-stage immunotherapy company focused on transforming how the immune system targets and kills cancers and the development of infectious disease vaccines, today announced a Key Opinion Leader ("KOL") event to discuss the pathology and growing prevalence of HPV16-positive head and neck squamous cell carcinoma ("HNSCC") as well as the Company's upcoming VERSATILE-003 Phase 3 clinical trial of Versamune
HPV + pembrolizumab for first-line treatment of recurrent and/or metastatic HPV16-positive HNSCC.
The KOL event will take place on Tuesday, December 17, 2024, at 12 p.m. ET and panel participants include:
KOL活動將於2024年12月17日星期二下午12點在東部時間舉行,參與討論的專家包括:
-
Francis "Frank" Worden, M.D., Rogel Cancer Center, University of Michigan
-
Kevin Harrington, MBBS, Ph.D., The Institute of Cancer Research, United Kingdom
-
Francis「弗蘭克」沃登.D.,羅格爾癌症中心,密歇根大學
-
Kevin Harrington,MBBS,博士,英國癌症研究所
The event will be moderated by Kirk Shepard, M.D., PDS Biotech's Chief Medical Officer.
本次活動由pds生物技術公司首席醫學官Kirk Shepard博士主持。
Webcast and Registration Details
網絡直播和註冊詳情
Date: Tuesday, December 17, 2024
Time: 12 p.m. - 1:30 p.m. ET
Registration:
Click here
日期:2024年12月17日星期二
時間:下午12點至1:30點ET
註冊:
點擊這裏
About Our Speakers
關於我們的演講者
Francis Worden, M.D., is a clinical professor awarded the Nancy Wigginton Oncology Research Professor of Thyroid Cancer endowed chair at the Rogel Cancer Center at the University of Michigan. He is a clinical investigator with the multidisciplinary head and neck cancer and lung cancer teams. Dr. Worden is a leading expert in the treatment of HPV-positive oropharyngeal cancer. He has co-authored over 190 peer-reviewed articles and participated in approximately 20 clinical trials with three ongoing trials in HNSCC, including the VERSATILE-002 trial. Dr. Worden received his medical degree from the Indiana University School of Medicine. He completed a combined internal medicine and pediatrics residency at the Detroit Medical Center and finished a medical oncology/hematology fellowship at the University of Michigan. In 2000, Dr. Worden joined the University of Michigan Rogel Cancer Center faculty.
Francis Worden萬.D.,是密歇根大學Rogel癌症中心研究教授,被授予南希·維金頓甲狀腺癌研究教授的名譽主席。他是一個在多學科頭頸癌和肺癌團隊中擔任臨床研究員。Worden醫生是HPV陽性口咽癌治療的領先專家。他共同撰寫了190多篇同行評審文章,並參與約20個臨床試驗,其中包括頭頸癌的三個正在進行的試驗,包括VERSATILE-002試驗。Worden博士從印第安納大學醫學院獲得醫學學位。他在底特律醫學中心完成了內科和兒科聯合住院醫師培訓,並在密歇根大學完成了醫學腫瘤/血液學的研究生課程。2000年,Worden博士加入了密歇根大學Rogel癌症中心的教職。
Kevin Harrington, MBBS, Ph.D., is Head of the Division of Radiotherapy and Imaging at The Institute of Cancer Research in the United Kingdom. Dr. Harrington is a Professor of Biological Cancer Therapies at The Institute of Cancer Research. He was the principal investigator for KEYNOTE-048, the pivotal clinical trial that supported the U.S. Food and Drug Administration approval for the use of pembrolizumab and pembrolizumab + chemotherapy in the first-line treatment of recurrent and/or metastatic HNSCC. Earlier this year, Dr. Harrington presented the results of the VERSATILE-002 clinical trial during the European Society of Medical Oncology Congress. He studied medicine at St. Bartholomew's Hospital in London and began focusing on head and neck cancer as a Ph.D. student at Hammersmith Hospital. Dr. Harrington completed post-doctoral research in molecular medicine at the Mayo Clinic, before being appointed as a Consultant Oncologist at The Royal Marsden National Health Service Foundation in 2001. He has published more than 600 articles on cancer treatment.
凱文·哈林頓(Kevin Harrington),MBBS,博士,是英國癌症研究所放射治療與影像部主任。哈林頓博士是英國癌症研究所的生物癌症療法教授。他是KEYNOTE-048的主要研究員,該關鍵臨床試驗爲美國食品和藥物管理局批准了使用pembrolizumab和pembrolizumab + 化療作爲復發和/或轉移性頭頸癌一線治療的依據。今年早些時候,哈林頓博士在歐洲醫學腫瘤學會大會上報告了VERSATILE-002臨床試驗的結果。他在倫敦聖巴索醫院學習醫學,並作爲博士生在哈默史密斯醫院專注於頭頸癌研究。哈林頓博士在美國梅奧診所進行了分子醫學的博士後研究,然後於2001年被任命爲皇家馬斯登國民衛生服務基金會的顧問腫瘤學家。他在癌症治療方面發表了600多篇文章。
About PDS Biotechnology
關於pds生物技術公司
PDS Biotechnology is a late-stage immunotherapy company focused on transforming how the immune system targets and kills cancers and the development of infectious disease vaccines. The Company plans to initiate a pivotal clinical trial to advance its lead program in advanced HPV16-positive head and neck squamous cell cancers. PDS Biotech's lead investigational targeted immunotherapy Versamune
HPV is being developed in combination with a standard-of-care immune checkpoint inhibitor, and also in a triple combination including PDS01ADC, an IL-12 fused antibody drug conjugate (ADC), and a standard-of-care immune checkpoint inhibitor.
pds biotechnology是一家晚期免疫治療公司,專注於改變免疫系統針對癌症的攻擊和殺死癌細胞的方式,以及開發傳染病疫苗。公司計劃啓動一項關鍵臨床試驗,以推進其在晚期HPV16陽性頭頸部鱗狀細胞癌中的主要項目。pds biotech的首個研究性靶向免疫治療Versamune
HPV正在與標準護理的免疫檢查點抑制劑聯合開發,並且還在包括PDS01ADC(一種IL-12融合抗體藥物偶聯物)和標準護理免疫檢查點抑制劑的三聯組合中進行開發。
For more information, please visit
欲了解更多信息,請訪問
Forward Looking Statements
前瞻性聲明
This communication contains forward-looking statements (including within the meaning of Section 21E of the United States Securities Exchange Act of 1934, as amended, and Section 27A of the United States Securities Act of 1933, as amended) concerning PDS Biotechnology Corporation (the "Company") and other matters. These statements may discuss goals, intentions and expectations as to future plans, trends, events, results of operations or financial condition, or otherwise, based on current beliefs of the Company's management, as well as assumptions made by, and information currently available to, management. Forward-looking statements generally include statements that are predictive in nature and depend upon or refer to future events or conditions, and include words such as "may," "will," "should," "would," "expect," "anticipate," "plan," "likely," "believe," "estimate," "project," "intend," "forecast," "guidance", "outlook" and other similar expressions among others. Forward-looking statements are based on current beliefs and assumptions that are subject to risks and uncertainties and are not guarantees of future performance. Actual results could differ materially from those contained in any forward-looking statement as a result of various factors, including, without limitation: the Company's ability to protect its intellectual property rights; the Company's anticipated capital requirements, including the Company's anticipated cash runway and the Company's current expectations regarding its plans for future equity financings; the Company's dependence on additional financing to fund its operations and complete the development and commercialization of its product candidates, and the risks that raising such additional capital may restrict the Company's operations or require the Company to relinquish rights to the Company's technologies or product candidates; the Company's limited operating history in the Company's current line of business, which makes it difficult to evaluate the Company's prospects, the Company's business plan or the likelihood of the Company's successful implementation of such business plan; the timing for the Company or its partners to initiate the planned clinical trials for Versamune
HPV, PDS01ADC and other Versamune
and Infectimune
based product candidates; the future success of such trials; the successful implementation of the Company's research and development programs and collaborations, including any collaboration studies concerning Versamune
HPV, PDS01ADC and other Versamune
and Infectimune
based product candidates and the Company's interpretation of the results and findings of such programs and collaborations and whether such results are sufficient to support the future success of the Company's product candidates; the success, timing and cost of the Company's ongoing clinical trials and anticipated clinical trials for the Company's current product candidates, including statements regarding the timing of initiation, pace of enrollment and completion of the trials (including the Company's ability to fully fund its disclosed clinical trials, which assumes no material changes to the Company's currently projected expenses), futility analyses, presentations at conferences and data reported in an abstract, and receipt of interim or preliminary results (including, without limitation, any preclinical results or data), which are not necessarily indicative of the final results of the Company's ongoing clinical trials; any Company statements about its understanding of product candidates mechanisms of action and interpretation of preclinical and early clinical results from its clinical development programs and any collaboration studies; the Company's ability to continue as a going concern; and other factors, including legislative, regulatory, political and economic developments not within the Company's control. The foregoing review of important factors that could cause actual events to differ from expectations should not be construed as exhaustive and should be read in conjunction with statements that are included herein and elsewhere, including the other risks, uncertainties, and other factors described under "Risk Factors," "Management's Discussion and Analysis of Financial Condition and Results of Operations" and elsewhere in the documents we file with the U.S. Securities and Exchange Commission. The forward-looking statements are made only as of the date of this press release and, except as required by applicable law, the Company undertakes no obligation to revise or update any forward-looking statement, or to make any other forward-looking statements, whether as a result of new information, future events or otherwise.
本通信包含前瞻性陳述(包括根據修訂後的1934年美國證券交易法第21E節和修訂後的1933年美國證券法第27A節的含義)關於pds biotechnology corporation("公司")和其他事項。這些陳述可能討論目標、意圖以及對未來計劃、趨勢、事件、運營結果或財務狀況的期望,或者其他基於公司管理層當前信念、管理層作出的假設以及目前可用的信息。前瞻性陳述通常包括預測性質的陳述,依賴或提及未來事件或條件,包括諸如「可能」、「將」、「應該」、「會」、「期望」、「預期」、「計劃」、「可能」、「相信」、「估計」、「項目」、「打算」、「預測」、「指導」、「展望」等類似表達。前瞻性陳述是基於當前的信念和假設,這些信念和假設面臨風險和不確定性,並不保證未來的表現。實際結果可能因多種因素而與任何前瞻性陳述中包含的信息大相徑庭,包括但不限於:公司的知識產權保護能力;公司預計的資本需求,包括公司預計的現金支出和公司對未來股權融資計劃的當前預期;公司依賴額外融資來資助其運營並完成其產品候選者的開發和商業化的風險,以及籌集這樣額外資本可能會限制公司的運營或要求公司放棄對其技術或產品候選者的權益;公司在當前業務領域有限的運營歷史,導致很難評估公司前景、商業計劃或公司成功實施該商業計劃的可能性;公司或其合作伙伴啓動Versamune計劃的臨床試驗的時間。
HPV,pds biotechnology和其他Versamune
和Infectimune
基於的產品候選;此類試驗未來成功的可能性;公司的研究和開發項目及合作的成功實施,包括任何關於Versamune的合作研究
HPV,pds biotechnology和其他Versamune
和Infectimune
基於的產品候選以及公司對這些項目和合作的結果和發現的解讀,以及這些結果是否足以支持公司產品候選的未來成功;公司的持續臨床試驗和預期臨床試驗的成功、時機和成本,包括關於試驗開始時間、招募進度和完成時間的聲明(包括公司完全資助其披露的臨床試驗的能力,假設公司目前預計的費用沒有重大變化)、無效分析、在會議上的演示和列入摘要的數據,以及中期或初步結果的接收(包括但不限於任何臨床前結果或數據),這些數據並不一定會反映公司持續臨床試驗的最終結果;公司對產品候選機制作用的理解及其臨床開發項目及任何合作研究的臨床前和早期臨床結果的解讀;公司能否繼續作爲一個持續經營體;以及其他因素,包括不在公司控制範圍內的立法、監管、政治和經濟發展。以上對可能導致實際事件與預期不同的重要因素的審查不應被視爲詳盡,應與此處以及其他地方包含的聲明一同閱讀,包括在我們向美國證券交易委員會提交的文件中描述的其他風險、不確定性和其他因素。前瞻性聲明僅在本新聞稿發佈之日作出,除非適用法律要求,公司沒有義務修訂或更新任何前瞻性聲明,或作出任何其他前瞻性聲明,無論是由於新信息、未來事件還是其他原因。
Versamune
and Infectimune
are registered trademarks of PDS Biotechnology Corporation.
Versamune
和Infectimune
是PDS Biotechnology公司的註冊商標。
Investor Contact:
Mike Moyer
LifeSci Advisors
Phone +1 (617) 308-4306
Email:
mmoyer@lifesciadvisors.com
投資者聯繫人:
邁克·莫迪爾
LifeSci顧問
電子郵件:mmoyer@lifesciadvisors.com
電子郵件:
mmoyer@lifesciadvisors.com
Media Contact:
Janine McCargo
6 Degrees
Phone +1 (646) 528-4034
Email:
jmccargo@6degreespr.com
媒體聯繫:
Janine McCargo
6 Degrees
電話 +1 (646) 528-4034
電子郵件:
jmccargo@6degreespr.com