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Inovio Awaits Oct. 30 FDA Decision on INO-3107 Accelerated Approval Data

Inovio Pharmaceuticals logoInovio Pharmaceuticals
Sig2.90Sen+3.10Env0.00Soc+2.20Gov+1.60

Inovio’s president and CEO said the clinical-stage biotechnology company is in the late stages of the FDA’s Accelerated Approval process for INO-3107 under the RRP-001 study. Patients who required at least two surgeries in the prior year showed a 72% rate of 50% to 100% surgery reduction in the first year, with a target FDA action date of Oct. 30. Inovio also discussed updates from partnered programs including VGX-3100 in China and SARS-CoV-2 antibody trials.

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