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Friday, March 29th, 2024

Inovio’s COVID-19 vaccine candidate shows promise in trials

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Inovio, a biotechnology company, revealed that its COVID-19 vaccine candidate, INO-4800, was effective in protecting non-human primates, specifically rhesus macaques, from the virus 13 weeks after the last vaccination.

These results demonstrate that vaccine candidates reduced viral load in both the lower lungs and nasal passages in macaques that received two doses, four weeks apart, and then were challenged with live virus 13 weeks after the second dose.

The reduced viral loads at this timeframe demonstrate an important durable impact mediated by INO-4800. Previously reported monkey vaccine challenge studies were conducted at the time near their peak immune responses — 1-4 weeks from their last vaccination. INO-4800-treated animals demonstrated seroconversion after a single vaccination, with protective neutralizing antibodies and T cells lasting in their blood more than four months after the initial dose. Officials said the antibody levels were similar to or greater than those seen in patients who have recovered from COVID-19, and the T cell responses were significantly higher than those from convalescent patients.

“All other previously reported NHP vaccine protection studies actually challenged the animals at the peak of their immune response. Our study demonstrates that INO-4800 could provide protection in a more real-world setting, where vaccine-generated memory immune responses protected NHPs for more than three months (13 weeks) from the last vaccination,” Dr. J. Joseph Kim, president and CEO of Inovio, said. “Given the importance of protective antibody and T cell responses, this study gives us more confidence as we continue to advance INO-4800 in the clinic. We believe INO-4800 holds significant potential to help address this global public health crisis.”

The published data support that immunization with INO-4800 limits active viral replication and has the potential to reduce the severity of disease.

“As we eagerly anticipate initiating a Phase 2/3 efficacy trials this summer, an animal challenge is currently the closest thing we have to testing a vaccine’s efficacy when confronting a live virus. We are very encouraged with the duration of protection that INO-4800 demonstrated in this NHP study and look forward to reassessing its impact on durability of response at 12 months out from our other ongoing non-human primate and animal challenge studies,” Dr. Kate Broderick, Inovio’s senior vice president, research & development, said. “In addition to safety and efficacy, it is essential that any vaccine targeting SARS-CoV-2 generates a relevant durability of response,” Broderick added. “A vaccine that only provides protection for a very short period of time is not going to realistically solve the problem of this pandemic.”

A separate study evaluating the durability of INO-4800 at 12 months after vaccination is currently underway. INO-4800 is part of the federal government’s Operation Warp Speed.