Details of the company’s presentations are as follows:
- Keystone Symposia’s Cancer Immunotherapy: Beyond Immune Checkpoint Blockade and Overcoming Resistance
Title: VISTA checkpoint targeting by SNS-101, a pH-selective antibody with enhanced safety and pharmacokinetic profiles, alters the tumor microenvironment and overcomes immune checkpoint inhibitor resistance
Presenter:Edward van der Horst , Ph.D., Chief Scientific Officer
Session: Progress in Drugging the TIGIT and VISTA Pathways
Date and time:Tuesday, March 19, 2024 , 3 – 4:30 p.m. PT
Material from the presentation will also be presented in a poster at the conference, as detailed:
Poster Number: 3021
Session: Poster Session 3
Date and time:Wednesday, March 20, 2024 , at7:30 p.m. PT American Association for Cancer Research (AACR) Annual Meeting 2024
Title: Conditionally active CD28xVISTA bispecific antibodies induce myeloid-driven tumor-specific T-cell co-stimulation for improved cancer immunotherapy
Presentation Type: Poster Presentation
Session Category: Immunology
Session Title: Immune Modulation Employing Agonist or Co-Stimulatory Approaches
Date and Time:Tuesday, April 9, 2024 ,1:30 p.m. - 5:00 p.m. PT
Location: Poster Section 3
Abstract Number: 5294
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Cautionary Note Regarding Forward-Looking Statements
Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. These statements may be identified by words and phrases such as “believe”, “designed to,” “expect”, “may”, “plan”, “potential”, “will”, and similar expressions, and are based on Sensei’s current beliefs and expectations. These forward-looking statements include expectations regarding the development and potential therapeutic benefits and safety profile of Sensei’s product candidates. These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements. Risks and uncertainties that may cause actual results to differ materially include uncertainties inherent in the development of therapeutic product candidates, such as the risk that any one or more of Sensei’s product candidates will not be successfully developed or commercialized; the risk of delay or cessation of any planned clinical trials of Sensei’s product candidates; the risk that prior results, such as signals of safety, activity or durability of effect, observed from preclinical trials and early results from the clinical trial of SNS-101, will not be replicated or will not continue in ongoing or future studies or clinical trials involving Sensei’s product candidates, including SNS-101; the risk that Sensei’s product candidates or procedures in connection with the administration thereof will not have the safety or efficacy profile that Sensei anticipates; risks associated with Sensei’s dependence on third-party suppliers and manufacturers, including sole source suppliers, over which Sensei may not always have full control; risks regarding the accuracy of Sensei’s estimates of expenses, capital requirements and needs for additional financing; and other risks and uncertainties that are described in Sensei’s Annual Report on Form 10-K filed with the
Investor Contact:
Senior Director, Investor Relations
mbiega@senseibio.com
Media Contact:
Jallaire@lifesciadvisors.com
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