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PDS Biotech to Present Updated VERSATILE-002 Data at ESMO Congress 2024

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PDS Biotechnology (PDSB) will present updated data from the VERSATILE-002 trial at the ESMO Congress 2024 on September 14, 2024, in Barcelona, Spain. The trial evaluates Versamune® HPV (formerly PDS0101) combined with KEYTRUDA® (pembrolizumab) as a first-line treatment for HPV16-positive recurrent/metastatic head and neck squamous cell carcinoma (HNSCC).

The poster presentation, titled 'VERSATILE-002: Survival with First-Line Treatment with PDS0101 Therapeutic Vaccine and Pembrolizumab in HPV16-positive Recurrent/Metastatic HNSCC', will be presented by Dr. Jared Weiss, Principal Investigator of the trial. The poster will be available on the company's website after the presentation.

PDS Biotechnology (PDSB) presenterà dati aggiornati dallo studio VERSATILE-002 al Congresso ESMO 2024 il 14 settembre 2024, a Barcellona, Spagna. Lo studio valuta Versamune® HPV (precedentemente PDS0101) combinato con KEYTRUDA® (pembrolizumab) come trattamento di prima linea per il carcinoma a cellule squamose della testa e del collo (HNSCC) recidivante/metastatico positivo per HPV16.

La presentazione del poster, intitolata 'VERSATILE-002: Sopravvivenza con il Trattamento di Prima Linea con il Vaccino Terapeutico PDS0101 e Pembrolizumab in HNSCC Recidivante/Metastatico Positivo per HPV16', sarà presentata dal Dr. Jared Weiss, Investigatore Principale dello studio. Il poster sarà disponibile sul sito web dell'azienda dopo la presentazione.

PDS Biotechnology (PDSB) presentará datos actualizados del ensayo VERSATILE-002 en el Congreso ESMO 2024 el 14 de septiembre de 2024 en Barcelona, España. El ensayo evalúa Versamune® HPV (anteriormente PDS0101) combinado con KEYTRUDA® (pembrolizumab) como tratamiento de primera línea para cáncer de cabeza y cuello de células escamosas (HNSCC) recurrente/metastásico positivo para HPV16.

La presentación del póster, titulada 'VERSATILE-002: Supervivencia con el Tratamiento de Primera Línea con la Vacuna Terapéutica PDS0101 y Pembrolizumab en HNSCC Recurrente/Metastásico Positivo para HPV16', será presentada por el Dr. Jared Weiss, Investigador Principal del ensayo. El póster estará disponible en el sitio web de la empresa después de la presentación.

PDS 바이오테크놀로지 (PDSB)는 2024년 9월 14일 스페인 바르셀로나에서 열리는 ESMO 컨그레스 2024에서 VERSATILE-002 시험의 업데이트된 데이터를 발표할 예정입니다. 이 임상 시험은 Versamune® HPV (이전 명칭 PDS0101)와 KEYTRUDA® (펨브롤리주맙)를 병용하여 HPV16 양성 재발/전이성 두경부 편평세포암 (HNSCC)에 대한 1차 치료제로 평가하고 있습니다.

'VERSATILE-002: HPV16 양성 재발/전이성 HNSCC에서 PDS0101 치료 백신과 펨브롤리주맙을 이용한 1차 치료와 생존'이라는 제목의 포스터 발표는 Dr. Jared Weiss가 임상 시험의 주관 연구자 자격으로 진행할 것입니다. 포스터는 발표 후 회사 웹사이트에서 확인할 수 있습니다.

PDS Biotechnology (PDSB) présentera des données mises à jour de l'essai VERSATILE-002 lors du Congrès ESMO 2024 qui se tiendra le 14 septembre 2024 à Barcelone, en Espagne. L'essai évalue Versamune® HPV (anciennement PDS0101) associé à KEYTRUDA® (pembrolizumab) en tant que traitement de première intention pour le carcinome épidermoïde de la tête et du cou récurrent/métastatique positif pour HPV16 (HNSCC).

La présentation d'affiche, intitulée 'VERSATILE-002 : Survie avec un traitement de première ligne par le vaccin thérapeutique PDS0101 et le Pembrolizumab dans le HNSCC récurrent/métastatique positif pour HPV16', sera présentée par Dr. Jared Weiss, Investigateur Principal de l'essai. L'affiche sera disponible sur le site Web de l'entreprise après la présentation.

PDS Biotechnology (PDSB) wird aktualisierte Daten aus der VERSATILE-002-Studie auf dem ESMO-Kongress 2024 am 14. September 2024 in Barcelona, Spanien, präsentieren. Die Studie bewertet Versamune® HPV (ehemals PDS0101) in Kombination mit KEYTRUDA® (Pembrolizumab) als Erstlinientherapie für HPV16-positive rezidivierende/metastatische Plattenepithelkarzinome der Kopf-Hals-Region (HNSCC).

Die Posterpräsentation mit dem Titel 'VERSATILE-002: Überleben mit der Erstlinientherapie mit dem therapeutischen Impfstoff PDS0101 und Pembrolizumab bei HPV16-positivem rezidivierenden/metastatischen HNSCC' wird von Dr. Jared Weiss, dem leitenden Prüfer der Studie, vorgestellt. Das Poster wird nach der Präsentation auf der Unternehmenswebsite verfügbar sein.

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Presentation of data will take place on Saturday, September 14, 2024

PRINCETON, N.J., Sept. 09, 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, will present updated data from the VERSATILE-002 trial evaluating first-line treatment with Versamune® HPV (formerly PDS0101) in combination with KEYTRUDA® (pembrolizumab) in patients with HPV16-positive recurrent/metastatic head and neck squamous cell carcinoma (HNSCC) during a poster presentation at the upcoming European Society for Medical Oncology (ESMO) Congress 2024 on September 14, 2024, in Barcelona, Spain.

Details of the presentation are as follows:

Poster number: 879P
Poster title: VERSATILE-002: Survival with First-Line Treatment with PDS0101 Therapeutic Vaccine and Pembrolizumab in HPV16-positive Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC)
Presenting author: Jared Weiss, M.D., Section Chief of Thoracic and Head/Neck Oncology, Professor of Medicine at University of North Carolina, and Principal Investigator of the VERSATILE-002 clinical trial

Following the presentation, the poster will be available in the Investor Relations section of the Company’s website at www.pdsbiotech.com.

About PDS Biotechnology
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 in 2024 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.

For more information, please visit www.pdsbiotech.com.

Forward Looking Statements
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 PDS01ADC, Versamune® HPV (formerly PDS0101), PDS0203 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 PDS01ADC, Versamune® HPV, PDS0203 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.  

Versamune® and Infectimune® are registered trademarks of PDS Biotechnology Corporation.

Keytruda® is a registered trademark of Merck Sharp and Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, N.J., USA.

Investor Contact:
Mike Moyer
LifeSci Advisors
Phone +1 (617) 308-4306
Email: mmoyer@lifesciadvisors.com

Media Contact:
Gina Mangiaracina
6 Degrees
Phone +1 (917) 797-7904
Email: gmangiaracina@6degreespr.com


FAQ

What is PDS Biotech presenting at ESMO Congress 2024?

PDS Biotech (PDSB) is presenting updated data from the VERSATILE-002 trial, which evaluates Versamune® HPV combined with KEYTRUDA® as a first-line treatment for HPV16-positive recurrent/metastatic head and neck squamous cell carcinoma (HNSCC).

When and where is PDS Biotech's presentation at ESMO Congress 2024?

PDS Biotech's presentation will take place on Saturday, September 14, 2024, in Barcelona, Spain, during the European Society for Medical Oncology (ESMO) Congress 2024.

Who is presenting the VERSATILE-002 trial data for PDS Biotech (PDSB)?

Dr. Jared Weiss, Section Chief of Thoracic and Head/Neck Oncology and Professor of Medicine at the University of North Carolina, who is also the Principal Investigator of the VERSATILE-002 clinical trial, will present the data.

What is the poster number and title for PDS Biotech's presentation at ESMO 2024?

The poster number is 879P, and the title is 'VERSATILE-002: Survival with First-Line Treatment with PDS0101 Therapeutic Vaccine and Pembrolizumab in HPV16-positive Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC)'.

Where can investors find PDS Biotech's (PDSB) ESMO 2024 presentation after the event?

Following the presentation, the poster will be available in the Investor Relations section of PDS Biotech's website at www.pdsbiotech.com.

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