2141. Preclinical Evaluation of PA-001: A Novel, Potential Macrocyclic Peptide-Based Treatment for COVID-19 Which Binds to the S2 Subunit of SARS-CoV-2 Spike Protein

• Published in: Open Forum Infectious Diseases Vol. 10; no. Supplement_2
• Main Authors: Kawamura, Tatsuro, Ohuchi, Masaki, Nagasawa, Takayuki, Ohashi, Hirofumi, Iwata-Yoshikawa, Naoko, Shiwa-Sudo, Nozomi, Sakai, Yusuke, Matsui, Katsuma, Matsumoto, Masatoshi, Kurasaki, Haruaki, Nagatomo, Kazutaka, Ito, Shoko, Kawamura, Naoki, Masuya, Keiichi, Nagata, Noriyo, Watashi, Koichi, Suzuki, Tadaki, Kitamura, Hidetomo, Murakami, Masato
• Format: Journal Article
• Language: English; Japanese
• Published: US Oxford University Press (OUP) 27.11.2023; Oxford University Press
• Subjects: Abstract
• DOI: 10.1093/ofid/ofad500.1764
• ISSN: 2328-8957

Abstract Background Despite the approval of a few COVID-19 drugs, various mutations of SARS-CoV-2 continue to emerge and pose as a threat to the efficacy of COVID-19 treatments. To address the unmet clinical need for broad-spectrum treatments, we identified and performed preclinical evaluation of PA-001, a macrocyclic peptide that targets the highly conserved S2 subunit (S2) of the spike protein of SARS-CoV-2, as a potential therapeutic agent with a new mechanism of action. Methods A diverse macrocyclic peptide library was constructed and screened for S2 binders employing PeptiDream’s proprietary technology, Peptide Discovery Platform System (PDPS). In vitro antiviral activity was evaluated in VeroE6/TMPRSS2 cells infected with SARS-CoV-2 using RT-qPCR. In vivo efficacy was evaluated in a lethal BALB/c mouse model infected with a mouse-adapted SARS-CoV-2 strain, QHmusX, where PA-001, the remdesivir metabolite GS-441524, alone or in combination, or molnupiravir were therapeutically administered for 3 consecutive days started at 1-day post-inoculation (Fig. 1).Figure 1.Schematic design of the in vivo efficacy study Results PA-001 was identified as a S2 binding peptide through PDPS. PA-001 showed in vitro antiviral activity against wild-type and variant strains of SARS-CoV-2 including Omicron (IC50: 1.7 – 9.6 nM). Therapeutic administration of PA-001 completely rescued mice from SARS-CoV-2-caused death at the anticipated clinical dose, while 80% of molnupiravir-administered mice died (Fig. 2A). In addition, treatment with PA-001 alone significantly suppressed body weight loss (Fig. 2B), decreased lung weight-to-body weight ratio (an indicator of lung inflammation), and reduced inflammatory cytokines secretion including IL-6 in lungs, and these effects were enhanced when combined with GS-441524.Figure 2.Survival rate and body weight change of SARS-CoV-2-infected mice Conclusion The S2-targeting peptide PA-001 showed potent in vitro antiviral activity and in vivo preclinical therapeutic efficacy. These data support the possibility that PA-001 could become a novel drug with a unique mechanism of action for the treatment of COVID-19. Currently, IND submission for PA-001 is in preparation to initiate clinical trials. Disclosures All Authors: No reported disclosures