Inovio Pharmaceuticals

Inovio Pharmaceuticals

INO
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INO · Stock Price

USD 1.37-0.43 (-23.89%)
Market Cap: $113.8M

Historical price data

Overview

Inovio Pharmaceuticals is a U.S.-based clinical-stage biotech focused on developing DNA-based immunotherapies and vaccines. Its core strategy leverages a proprietary two-part platform—SynCon® for plasmid design and CELLECTRA® for delivery—to advance a pipeline targeting HPV-related diseases, cancer, and infectious diseases. The company's most significant near-term catalyst is the FDA review of its Biologics License Application (BLA) for INO-3107 in recurrent respiratory papillomatosis (RRP), which represents a potential first-in-class DNA medicine approval. With a seasoned leadership team and a history of strategic partnerships, Inovio is positioning itself at the forefront of nucleic acid therapeutics.

Infectious DiseaseOncologyHPV-Related Diseases

Technology Platform

Proprietary DNA medicine platform combining SynCon® for computer-designed plasmid optimization and CELLECTRA® for electroporation-based intracellular delivery, enabling in vivo production of therapeutic proteins.

Pipeline

47
47 drugs in pipeline3 in Phase 3
DrugIndicationStageWatch
VGX-3100 + PlaceboCervical DysplasiaPhase 3
VGX-3100 + Matched PlaceboCervical DysplasiaPhase 3
INO-4800 + PlaceboCoronavirus InfectionPhase 2/3
INO-3112 vaccine + Cisplatin chemotherapyUterine Cervical NeoplasmsPhase 2
INO-4700 + Placebo + INO-4700Middle East Respiratory Syndrome Coronavirus (MERS-CoV)Phase 2

Funding History

3
Total raised:$192M
PIPE$150M
IPO$30M
Series A$12M

Opportunities

Near-term opportunity lies in the potential first-ever U.S.
approval of a DNA medicine for the rare disease RRP, establishing a commercial beachhead.
Long-term, the versatile platform could be applied to larger markets in HPV-related oncology and rapid-response infectious disease vaccines, with next-gen DMAbs offering a novel in vivo antibody production modality.

Risk Factors

Extreme regulatory risk on the pending INO-3107 BLA review; failure would be catastrophic.
Commercialization risk exists due to the novel delivery device requiring training.
Financial risk is high, with future dilution likely, and clinical validation of the broader platform beyond the lead candidate remains unproven.

Competitive Landscape

Faces competition in HPV space from surgery, checkpoint inhibitors, and other therapeutic vaccines. Platform competes with dominant mRNA/LNP technologies (Moderna, BioNTech) and viral gene therapies, differentiating via electroporation delivery and a focus on potent T-cell responses without viral vectors or LNPs.