Communications Biology (Sep 2024)

Nonclinical characterization of ICVB-1042 as a selective oncolytic adenovirus for solid tumor treatment

  • Yu Kato,
  • Nathaniel Rice,
  • Michael Pokrass,
  • Jinkil Jeong,
  • Ruben Rodriguez,
  • Jessica J. Field,
  • Heba Nowyhed

DOI
https://doi.org/10.1038/s42003-024-06839-6
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 14

Abstract

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Abstract ICVB-1042 is an oncolytic adenovirus containing modifications to enhance replication, lysis, and viral spreading in tumor cells. The anti-tumor activity, immune activation, tropism, selectivity, and mechanism of action were evaluated in preparation for a first-in-human study. ICVB-1042 was at least 100-fold more cytotoxic in A549 cells than in normal primary cells tested, demonstrating its high tumor selectivity and a low likelihood of targeting primary tissues. ICVB-1042 administered to mice intravenously or intratumorally was effective in reducing tumor burden. Its intravenous administration also inhibited tumor growth in orthotopic models. ICVB-1042 was well tolerated in mice compared to HAdV-C5 (Wt Ad5), with reduced liver sequestration, supporting safety of the drug for systemic delivery. These preclinical data demonstrating the safety and potency of ICVB-1042 for treatment of various solid tumors support the ongoing clinical investigation (NCT05904236).