Alpine Immune Sciences Announces Oral Presentation at the 2022 AACR Annual Meeting
Alpine Immune Sciences (NASDAQ: ALPN) has announced that an abstract for the NEON-1 clinical trial results of davoceticept (ALPN-202) will be presented at the AACR Annual Meeting in New Orleans from April 8-13, 2022. This Phase 1 clinical trial focuses on the monotherapy dose escalation of davoceticept in patients with advanced malignancies. The presentation is scheduled for April 12 from 2:30 pm to 4:30 pm CDT, showcasing promising outcomes as Alpine progresses in its immunotherapy development.
- Abstract accepted for presentation at AACR Annual Meeting, enhancing visibility.
- Davoceticept (ALPN-202) shows superior efficacy in preclinical studies compared to traditional checkpoint inhibitors.
- Phase 1 trial NEON-1 is progressing towards completion of dose escalation and initiation of expansion cohorts.
- NEON-2 trial is currently on partial clinical hold, which could delay further development.
- NEON-1 Data Selected for Minisymposium Oral Presentation -
Results from the dose escalation portion of NEON-1, a Phase 1 clinical trial of davoceticept (ALPN-202) as monotherapy will be presented in a Minisymposium as follows:
Presentation Title: Monotherapy dose escalation of davoceticept (ALPN-202), a conditional CD28 costimulator and dual checkpoint inhibitor, in advanced malignancies (NEON-1)
Session Title: Immunotherapy Combination Strategies in Clinical Trials
Session Date, Time:
Presentation Number: CT041
The abstract for the oral presentation will be live on the AACR website on
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 trial of davoceticept (ALPN-202) and pembrolizumab was initiated in
About
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 trial 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
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Director, Investor Relations and Corporate Development
206-788-4545
ir@alpineimmunesciences.com
Media Relations
kelli@redhousecomms.com
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FAQ
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