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Inovio Pharmaceuticals

NASDAQ: INO ↗$1.45 USD~$82M MCAP

Inovio Pharmaceuticals is a clinical-stage biotechnology company developing DNA medicines for HPV-related diseases, cancer and infectious disease. Its platform pairs SynCon-designed plasmid DNA with the CELLECTRA delivery device, which uses electroporation to drive uptake of the DNA construct. The lead programme is INO-3107, now approved by the U.S. Food and Drug Administration as VOCERYQ in October 2026 to reduce the frequency of surgery in adults with recurrent respiratory papillomatosis, an HPV-driven orphan disease and the first plasmid DNA-based immunotherapy cleared in the United States; the pipeline also includes VGX-3100 for HPV-related cervical high-grade squamous intraepithelial lesions, INO-3112 in oropharyngeal cancer, INO-5401 in glioblastoma, INO-4201 for Ebola virus disease and INO-6160 for HIV. In October 2026 the company secured an $80.4 million judgment against VGXI and GeneOne Life Science over a breached 2020 supply and technology-transfer agreement, while cautioning that the defendants' financial condition may impair collection. Inovio was founded in 1979, incorporated in 1983, listed on Nasdaq in 1998, and is headquartered in Plymouth Meeting, Pennsylvania.

Company Info

Sector:Biotechnology / DNA Medicines
Headquarters:Plymouth Meeting, Pennsylvania, USA
Founded:1979

Clinical Development Pipeline

INO-3107

Target: DNA-encoded HPV 6/11 antigens delivered with CELLECTRA
HPV-related recurrent respiratory papillomatosis
Preclinical
Phase 1
Phase 2
Phase 3
Approved

VGX-3100

Target: DNA immunotherapy against HPV 16/18 E6 and E7
HPV-related cervical high-grade squamous intraepithelial lesions
Preclinical
Phase 1
Phase 2
Phase 3
Approved

INO-3112

Target: DNA immunotherapy against HPV 16/18 antigens
HPV-related oropharyngeal squamous cell carcinoma
Preclinical
Phase 1
Phase 2
Phase 3
Approved

INO-5401

Target: DNA immunotherapy against hTERT and WT1
Glioblastoma multiforme
Preclinical
Phase 1
Phase 2
Phase 3
Approved

INO-4201

Target: DNA vaccine against Ebola glycoprotein
Ebola virus disease
Preclinical
Phase 1
Phase 2
Phase 3
Approved

INO-6160

Target: DNA-encoded broadly neutralising antibody induction
HIV
Preclinical
Phase 1
Phase 2
Phase 3
Approved

Recent News

Leadership Team

Jacqueline Shea, Ph.D.

President and Chief Executive Officer

Careers & Job Openings

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