Alpine Immune Sciences to Host Virtual Investor Event at 2022 AACR Annual Meeting
Alpine Immune Sciences (Nasdaq: ALPN) will host a virtual investor event on April 12, 2022, at 6:00pm ET, coinciding with the AACR Annual Meeting. The event will provide a corporate update and discuss the development strategy for davoceticept (ALPN-202), including insights from its oral presentation at the meeting. Participants can join via phone or webcast, with a replay available for 90 days. Davoceticept is a first-in-class immunotherapy for cancer treatment, showing superior efficacy in preclinical studies.
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- Alpine to hold Investor Event on
During the investor event, Alpine will provide a corporate update on the development strategy for davoceticept (ALPN-202) and review the company’s oral presentation at the AACR Annual Meeting (“Monotherapy dose escalation of davoceticept (ALPN-202), a conditional CD28 costimulator and dual checkpoint inhibitor, in advanced malignancies (NEON-1)”). Following the presentation, Alpine will hold a question-and-answer discussion.
Currently, abstract titles are now live on the AACR meeting website and a copy of Alpine’s presentation will be available on
Investor Event - Conference Call and Webcast Details:
To access the investor event by phone, dial (800) 816-3005 (domestic) or (857) 770-0069 (international) and reference conference ID: 4238059.
A live webcast of the investor event will be available online in the investor relations section of the company’s website at https://ir.alpineimmunesciences.com/events. A replay will be available on the company website for 90 days following the webcast.
About Davoceticept (ALPN-202)
Davoceticept (ALPN-202) is a first-in-class, conditional CD28 costimulator and dual checkpoint inhibitor intended for the treatment of cancer. Preclinical studies of davoceticept have successfully demonstrated superior efficacy in tumor models compared to checkpoint inhibition alone. Completion of dose escalation and initiation of expansion cohorts of NEON-1 (NCT04186637), a Phase 1 monotherapy dose escalation and expansion trial in patients with advanced malignancies, is anticipated in the first half of 2022. NEON-2 (NCT04920383), a combination study of davoceticept (ALPN-202) and pembrolizumab was initiated in
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Forward-Looking Statements
This release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, Section 21E of the Securities Exchange Act of 1934 and the Private Securities Litigation Reform Act of 1995. These forward-looking statements are not based on historical fact and include statements regarding our platform technology and potential therapies; the timing of and results from clinical trials; and the potential efficacy, safety profile, future development plans and regulatory success of our product candidates. 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,” “plan,” “intend,” and other similar expressions, among others. These forward-looking statements are based on current assumptions that involve risks, uncertainties, and other factors that may cause actual results, events, or developments to be materially different from those expressed or implied by such forward-looking statements. These risks and uncertainties, many of which are beyond our control, include, but are not limited to: the impact of the COVID-19 pandemic on our business, research and clinical development plans and timelines and results of operations, including the impact on our clinical trial sites, collaborators, and contractors who act for or on our behalf, may be more severe and prolonged than currently anticipated; clinical trials may not demonstrate safety and efficacy of any of our product candidates; the partial clinical hold on our NEON-2 study may not be lifted in a timely manner or at all; our ongoing discovery and preclinical efforts may not yield additional product candidates; our discovery-stage and preclinical programs may not advance into the clinic or result in approved products; any of our product candidates may fail in development, may not receive required regulatory approvals, or may be delayed to a point where they are not commercially viable; we may not achieve additional milestones in our proprietary or partnered programs; the impact of competition; adverse conditions in the general domestic and global economic markets; as well as the other risks identified in our filings with the
View source version on businesswire.com: https://www.businesswire.com/news/home/20220330005363/en/
Investor Relations
Director, Investor Relations and Corporate Development
206-788-4545
ir@alpineimmunesciences.com
Media Relations
Red House
kelli@redhousecomms.com
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