Immunome Expects IMM-BCP-01 Antibody Cocktail To Neutralize the SARS-CoV-2 Omicron Variant
Immunome expects its antibody cocktail, IMM-BCP-01, to be effective against the Omicron variant of SARS-CoV-2. The company is performing laboratory testing to confirm this, with results anticipated in January 2022. IMM-BCP-01 targets three distinct epitopes, enhancing its potential resilience against mutations. The cocktail approach aims to improve viral neutralization, as demonstrated in preclinical tests against other variants. Immunome is advancing IMM-BCP-01 towards clinical trials, pending regulatory approval.
- Expecting IMM-BCP-01 to neutralize Omicron based on structural analysis.
- Antibody cocktail targets three distinct epitopes, enhancing therapeutic resilience.
- Plans to advance IMM-BCP-01 into clinical trials upon IND acceptance.
- None.
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Based on structural mapping of Omicron’s mutations and insights from direct preclinical testing of Alpha, Beta, Gamma and Delta variants,
Immunome expects its cocktail to be active against the Omicron variant - The Omicron variant has a number of mutations across the ACE2 receptor binding site, which may reduce the neutralization potency of some other antibodies under development and Emergency Use Authorization (EUA)
- Two of IMM-BCP-01’s antibodies target epitopes outside of the ACE2 receptor binding site
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Immunome is aggressively working to confirm IMM-BCP-01’s activity against Omicron in laboratory testing; expects availability of initial results inJanuary 2022
IMM-BCP-01 is an antibody cocktail designed to target three distinct, non-overlapping epitopes.
“Immunome designed its cocktail with multiple points of attack to be resilient in the face of a rapidly evolving virus,” stated
The Omicron Variant
The Omicron variant has a more extensive mutational burden than current and former
The Omicron variant includes a combination of mutations seen in previous variants of concern along with novel mutations. The spectrum of changes include escape variants and binding residues within the epitopes of some of the antibody therapeutics and cocktails that are currently in clinical trials or available under an EUA.1, 2, 3, 4
IMM-BCP-01
As previously described, IMM-BCP-01 includes three antibodies:
- IMM20190, targets an epitope within the ACE2 binding site and operates via an ACE2 dependent mechanism of action
- IMM20184, targets an epitope outside the ACE2 binding site but still operates via an ACE2 dependent mechanism of action
- IMM20253, targets an epitope outside the ACE2 binding site and operates via an ACE2 independent mechanism of action
Our testing of the cocktail’s activity against these variants demonstrates that not all antibodies within the cocktail need to be active against the variants for the cocktail to be effective. Specifically in the case of Beta, the activity of two antibodies in the cocktail was sufficient to neutralize the virus in vitro and significantly reduce the viral lung load in infected hamsters. With Omicron, we expect a similar result in preclinical testing and the cocktail to continue to perform as designed.
“The emergence of the Omicron variant has the potential to shift the therapeutic antibody landscape, and highlights the critical need for novel approaches,“ said
About IMM-BCP-01
IMM-BCP-01 is a three-antibody cocktail targeting non-overlapping regions of the Spike protein, including highly conserved, subdominant epitopes, which elicits both ACE2 and non-ACE2 dependent neutralization, and induce natural viral clearance mechanisms, such as antibody dependent cellular cytotoxicity, complement activation and phagocytosis. When tested in vivo, these mechanisms combine to significantly reduces viral load in lungs of the hamsters infected with SARS-CoV-2.
About
Forward-Looking Statements
This press release includes “forward-looking statements” as defined in the Private Securities Litigation Reform Act of 1995, as amended. These forward looking statements may include, but not be limited to, statements about the execution of Immunome’s regulatory, clinical and strategic plans and achievement of future milestones for IMM-BCP-01 as and when planned; expectations regarding the design, attributes and therapeutic potential and benefits of IMM-BCP-01, including its anticipated neutralizing and clearance activity against Omicron and other emerging variants; our ability to obtain and maintain regulatory approvals for IMM-BCP-01; and our ability to continue development of IMM-BCP-01 as and when planned.
Forward-looking statements may be identified by the words “anticipate,” believe,” “estimate,” “expect,” “intend,” “plan,” “project,” “may,” “will,” “could,” “should,” “seek,” “potential” and similar expressions. The forward-looking statements in this press release are based on Immunome’s current expectations, are neither promises nor guarantees, and you should not place undue reliance on them because they involve known and unknown risks, uncertainties and other factors, many of which are beyond Immunome’s control, that could cause actual results to differ materially from those expressed or implied by these forward-looking statements.
Factors that could cause actual results to differ include, but are not limited to, those risks and uncertainties associated with the following: the impact of the COVID-19 pandemic on Immunome’s business, operations, strategy, goals and anticipated milestones; Immunome’s ability to execute on its R&D strategy; the effectiveness of IMM-BCP-01, including the possibility that further preclinical data and any clinical trial data may be inconsistent with the data used for its advancement; Immunome’s ability to fund operations; Immunome’s reliance on vendors; the competitive landscape; and the additional risks and uncertainties set forth more fully under the caption “Risk Factors” in Immunome’s Annual Report on Form 10-K filed with the
References
- REGN EUA document (https://www.fda.gov/media/145611/download)
- LLY EUA document (https://www.fda.gov/media/145802/download)
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Pinto et
al Cross neutralization of SARS-CoV-2 by human monoclonal SASR-CoV antibody. Nature 583:290-295; 2020 -
Rappazzo et
al Broad and potent activity against SARS-like viruses by an engineered human monoclonal antibody. Science 371:823-829; 2021
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FAQ
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