COMPANY
Inovio Pharmaceuticals
Timeline
- Raise Follow-on offering: $20M (total, as published), announced Jul 29, 2026. Source: SEC filing. source ↗
- Raise Follow-on offering: $17.5M (total, as published), announced Apr 2, 2026. Source: SEC filing. source ↗
- Raise Follow-on offering: $25M (total, as published), announced Nov 11, 2025. Source: SEC filing. source ↗
- Raise Follow-on offering: $25M (total, as published), announced Jul 2, 2025. Source: SEC filing. source ↗
- Raise Follow-on offering: $30M (total, as published), announced Dec 13, 2024. Source: SEC filing. source ↗
- Trial start Phase 1: Safety, Tolerability and Immunogenicity of INO-4800 for COVID19 in Healthy Volunteers source ↗
- Trial start Phase 2: Safety, Tolerability and Immunogenicity of INO-4700 for MERS-CoV in Healthy Volunteers source ↗
- Trial start Phase 1: Dose-ranging Study: Safety, Tolerability and Immunogenicity of INO-4500 in Healthy Volunteers in Ghana source ↗
- Trial start Phase 2/Phase 3: Safety, Immunogenicity, and Efficacy of INO-4800 for COVID-19 in Adults at High Risk of SARS-CoV-2 Exposure source ↗
- Trial start Phase 1/Phase 2: INO-3107 With Electroporation (EP) in Participants With HPV-6- and/or HPV-11-Associated Recurrent Respiratory Papillomatosis (RRP) source ↗
- Trial start Phase 1: Safety, Tolerability and Immunogenicity of INO-4800 for COVID-19 in Healthy Volunteers source ↗
- Trial start Phase 1: Safety, Tolerability and Immunogenicity of INO-4500 in Healthy Volunteers source ↗
- Trial start Phase 3: REVEAL 2 Trial (Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL) source ↗
- Trial start Phase 1/Phase 2: INO-5401 + INO-9012 in Combination With Atezolizumab in Locally Advanced Unresectable or Metastatic/Recurrent Urothelial Carcinoma source ↗
- Trial start Phase 1/Phase 2: INO-5401 and INO-9012 Delivered by Electroporation (EP) in Combination With Cemiplimab (REGN2810) in Newly-Diagnosed Glioblastoma (GBM) source ↗
- Trial start Phase 2: VGX-3100 Delivered Intramuscularly (IM) Followed by Electroporation (EP) for the Treatment of HPV-16 and/or HPV-18 Related Anal or Anal/Peri-Anal, High Grade Squamous Intraepithelial Lesion ( source ↗
- Trial start Phase 2: Evaluation of VGX-3100 and Electroporation Alone or in Combination With Imiquimod for the Treatment of HPV-16 and/or HPV-18 Related Vulvar HSIL (Also Referred as: VIN 2 or VIN 3) source ↗
- Trial start Phase 3: REVEAL 1 (Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL) source ↗
- Trial start Phase 1: Trial to Evaluate Safety and Immunogenicity of INO-5150 Alone or With INO-9012 in Men With Prostate Cancer source ↗
- Trial start Phase 1: Open-Label Study of INO-4212 With or Without INO-9012, Administered IM or ID Followed by Electroporation in Healthy Volunteers source ↗
- Trial start I: Phase I Study of INO-1800 With or Without INO-9112 + EP in Chronic Hepatitis B Subjects source ↗
- Trial start Phase 1: hTERT Immunotherapy Alone or in Combination With IL-12 DNA Followed by Electroporation in Adults With Solid Tumors at High Risk of Relapse source ↗
- Trial start Phase 1/Phase 2: Study of HPV Specific Immunotherapy in Participants With HPV Associated Head and Neck Squamous Cell Carcinoma source ↗
- Trial start Phase 1/Phase 2: A Study of INO-3112 DNA Vaccine With Electroporation in Participants With Cervical Cancer source ↗
- Trial start Phase 1: Immunotherapy in Subjects With HPV-6 Associated Aerodigestive Precancerous Lesions and Malignancies source ↗
Upcoming milestones
- Dec 31, 2026 (ESTIMATED) · Phase 1/Phase 2 · INO-5401 and INO-9012 Delivered by Electroporation (EP) in Combination With Cemiplimab (REGN2810) in Newly-Diagnosed Glioblastoma (GBM) · NCT03491683
Funding
- Follow-on offering: $20M (total, as published), announced Jul 29, 2026. Source: SEC filing. source ↗
- Follow-on offering: $17.5M (total, as published), announced Apr 2, 2026. Source: SEC filing. source ↗
- Follow-on offering: $25M (total, as published), announced Nov 11, 2025. Source: SEC filing. source ↗
- Follow-on offering: $25M (total, as published), announced Jul 2, 2025. Source: SEC filing. source ↗
- Follow-on offering: $30M (total, as published), announced Dec 13, 2024. Source: SEC filing. source ↗
Clinical trials (lead sponsor) 31
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT03502785 | INO-5401 + INO-9012 in Combination With Atezolizumab in Locally Advanced Unresectable or Metastatic/Recurrent Urothelial Carcinoma | Phase 1/Phase 2 | Completed | Jul 24, 2018 | May 9, 2025 (actual) |
| NCT03491683 | INO-5401 and INO-9012 Delivered by Electroporation (EP) in Combination With Cemiplimab (REGN2810) in Newly-Diagnosed Glioblastoma (GBM) | Phase 1/Phase 2 | Active, not recruiting | May 31, 2018 | Dec 31, 2026 (estimated) |
| NCT04398433 | INO-3107 With Electroporation (EP) in Participants With HPV-6- and/or HPV-11-Associated Recurrent Respiratory Papillomatosis (RRP) | Phase 1/Phase 2 | Completed | Oct 7, 2020 | Dec 15, 2022 (actual) |
| NCT04588428 | Safety, Tolerability and Immunogenicity of INO-4700 for MERS-CoV in Healthy Volunteers | Phase 2 | Completed | Jun 21, 2021 | Jan 19, 2023 (actual) |
| NCT03721978 | REVEAL 2 Trial (Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL) | Phase 3 | Completed | Feb 28, 2019 | Aug 23, 2022 (actual) |
| NCT04642638 | Safety, Immunogenicity, and Efficacy of INO-4800 for COVID-19 in Adults at High Risk of SARS-CoV-2 Exposure | Phase 2/Phase 3 | Terminated | Nov 30, 2020 | Sep 13, 2022 (actual) |
| NCT03180684 | Evaluation of VGX-3100 and Electroporation Alone or in Combination With Imiquimod for the Treatment of HPV-16 and/or HPV-18 Related Vulvar HSIL (Also Referred as: VIN 2 or VIN 3) | Phase 2 | Completed | Aug 31, 2017 | Jul 23, 2020 (actual) |
| NCT03185013 | REVEAL 1 (Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL) | Phase 3 | Completed | Jun 28, 2017 | Jul 8, 2020 (actual) |
| NCT03499795 | VGX-3100 Delivered Intramuscularly (IM) Followed by Electroporation (EP) for the Treatment of HPV-16 and/or HPV-18 Related Anal or Anal/Peri-Anal, High Grade Squamous Intraepithelial Lesion (HSIL) in Individuals Seronegative for Human Immunodeficiency Virus (HIV)-1/2 | Phase 2 | Completed | May 15, 2018 | Jun 16, 2020 (actual) |
| NCT04093076 | Dose-ranging Study: Safety, Tolerability and Immunogenicity of INO-4500 in Healthy Volunteers in Ghana | Phase 1 | Completed | Jan 27, 2021 | Oct 14, 2022 (actual) |
| NCT05430958 | Safety, Tolerability and Immunogenicity of INO-4800 for COVID19 in Healthy Volunteers | Phase 1 | Withdrawn | 2022-10 | 2024-03 (estimated) |
| NCT04336410 | Safety, Tolerability and Immunogenicity of INO-4800 for COVID-19 in Healthy Volunteers | Phase 1 | Completed | Apr 3, 2020 | Feb 10, 2022 (actual) |
| NCT00198315 | Medpulser Electroporation With Bleomycin Study to Treat Anterior Head and Neck Squamous Cell Carcinoma | Phase 3 | Terminated | 2004-06 | 2007-06 (actual) |
| NCT00198328 | Medpulser Electroporation With Bleomycin Study to Treat Posterior Head and Neck Squamous Cell Carcinoma | Phase 3 | Terminated | 2004-11 | 2007-06 (actual) |
| NCT02172911 | A Study of INO-3112 DNA Vaccine With Electroporation in Participants With Cervical Cancer | Phase 1/Phase 2 | Completed | Jun 6, 2014 | Sep 7, 2017 (actual) |
| NCT02163057 | Study of HPV Specific Immunotherapy in Participants With HPV Associated Head and Neck Squamous Cell Carcinoma | Phase 1/Phase 2 | Completed | Aug 13, 2014 | Jan 23, 2017 (actual) |
| NCT03805984 | Safety, Tolerability and Immunogenicity of INO-4500 in Healthy Volunteers | Phase 1 | Completed | May 9, 2019 | Oct 21, 2020 (actual) |
| NCT02431312 | Phase I Study of INO-1800 With or Without INO-9112 + EP in Chronic Hepatitis B Subjects | I | Completed | Jan 12, 2015 | May 22, 2018 (actual) |
| NCT02464670 | Open-Label Study of INO-4212 With or Without INO-9012, Administered IM or ID Followed by Electroporation in Healthy Volunteers | Phase 1 | Completed | 2015-05 | May 24, 2018 (actual) |
| NCT02960594 | hTERT Immunotherapy Alone or in Combination With IL-12 DNA Followed by Electroporation in Adults With Solid Tumors at High Risk of Relapse | Phase 1 | Completed | 2014-12 | Nov 9, 2018 (actual) |
| NCT02241369 | Immunotherapy in Subjects With HPV-6 Associated Aerodigestive Precancerous Lesions and Malignancies | Phase 1 | Completed | 2014-05 | 2018-09 (actual) |
| NCT01304524 | A Study of VGX-3100 DNA Vaccine With Electroporation in Patients With Cervical Intraepithelial Neoplasia Grade 2/3 or 3 | Phase 2 | Completed | 2011-04 | 2014-05 (actual) |
| NCT01188850 | Fourth Dose of Human Papillomavirus (HPV) DNA Plasmid (VGX-3100) + EP in Adult Females Previously Vaccinated With Three Doses of VGX-3100 | Phase 1 | Completed | 2010-07 | 2011-10 (actual) |
| NCT02514213 | Trial to Evaluate Safety and Immunogenicity of INO-5150 Alone or With INO-9012 in Men With Prostate Cancer | Phase 1 | Completed | 2015-07 | Dec 12, 2017 (actual) |
| NCT00198276 | Study Using the MedPulser Electroporation System With Bleomycin to Treat Cutaneous and Subcutaneous Cancer | Phase 4 | Completed | 2004-02 | 2008-09 (actual) |
| NCT00198263 | Study Using the Medpulser Electroporation System With Bleomycin to Treat Head and Neck Cancer | Phase 4 | Completed | 2004-01 | 2008-09 (actual) |
| NCT00685412 | Phase I of Human Papillomavirus (HPV) DNA Plasmid (VGX-3100) + Electroporation for CIN 2 or 3 | I | Completed | 2008-05 | 2011-01 (actual) |
| NCT01403155 | A Follow-On Study With an H5 Influenza Vaccine for Subjects Who Participated in Study FLU-001 | Phase 1 | Completed | 2011-05 | 2012-08 (actual) |
| NCT01142362 | Study of VGX-3400X, H5N1 Avian Influenza Virus DNA Plasmid + Electroporation in Healthy Adults | Phase 1 | Completed | 2010-06 | 2011-11 (actual) |
| NCT01405885 | A Study of DNA Vaccine With Electroporation for the Prevention of Disease Caused by H1 and H5 Influenza Virus | Phase 1 | Completed | 2011-05 | 2013-08 (actual) |
| NCT01082692 | Study of PENNVAX™-B (Gag, Pol, Env) + Electroporation in HIV-1 Infected Adult Participants | Phase 1 | Completed | 2011-01 | 2012-08 (actual) |