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GeoVax Labs Inc

GeoVax Labs, Inc. is a clinical-stage biotechnology company that develops human vaccines and immunotherapies for infectious diseases and solid tumor cancers using proprietary platforms in the United States. Its pipeline includes GEO-CM04S1, a COVID-19 vaccine candidate in Phase 2 trials; Gedeptin, a patented product/technology for solid tumors in Phase 1/2 trials for advanced head and neck squamous cell carcinoma; and GEO-CM02, a pan-coronavirus vaccine. The company also has preclinical candidates: GEO-MVA-MUC1 for solid tumor cancers, GEO-ZM02 for Zika, GEO-EMO1-Z for Ebola Zaire, GEO-EMO1-S for Ebola Sudan, GEO-MM01 for Marburg, and GEO-MVA for Mpox and smallpox. It has collaboration and partnership agreements with the National Institute of Allergy and Infectious Diseases of the National Institutes of Health and the U.S. Department of Defense. GeoVax Labs, Inc. was incorporated in 1988 and is based in Smyrna, Georgia.

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United States
Biotech & Genomic Medicine▼

GeoVax Appeals Nasdaq Delisting, Hearing Set for October 13

GeoVax Labs has requested a hearing before the Nasdaq Hearings Panel to appeal the delisting determination it received on August 27, 2026, tied to the minimum bid price requirement under Nasdaq Listing Rule 5550(a)(2), with the hearing scheduled for October 13, 2026. The hearing request has stayed any suspension or delisting action pending the hearing and any extension period the Panel may grant, so GeoVax's common stock is expected to continue trading on The Nasdaq Capital Market under the symbol GOVX at least through that period. At the hearing, the company intends to present its plan to regain and maintain compliance with applicable Nasdaq listing standards. Chairman and Chief Executive Officer David Dodd said the Nasdaq process does not change GeoVax's strategic priorities, and that the company continues to advance GEO-MVA toward its planned pivotal Phase 3 clinical program, pursue manufacturing and global preparedness opportunities, and engage potential strategic, funding and development partners. GeoVax's priority program, GEO-MVA, is an investigational Modified Vaccinia Ankara-based vaccine targeting mpox and smallpox, and in oncology the company is developing Gedeptin, a gene-directed enzyme prodrug therapy that has completed a multicenter Phase 1/2 clinical trial in advanced head and neck cancer.
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Biotech & Genomic Medicine › Vaccines (Recombinant & Traditional) Capital
GOVX · Regulation · Negative GeoVax received a Nasdaq delisting determination tied to the minimum bid price rule and is appealing to the Hearings Panel.
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United States
Biotech & Genomic Medicine▲

GeoVax Highlights Moderna-Merck Phase 3 Data Supporting Gedeptin Strategy

GeoVax Labs highlighted positive Phase 3 results from Moderna and Merck's intismeran autogene plus KEYTRUDA combination in resected high-risk melanoma, calling it clinical validation for its planned Gedeptin plus KEYTRUDA study. The INTerpath-001 trial met its primary endpoint of recurrence-free survival and a key secondary endpoint of distant metastasis-free survival, showing statistically significant and clinically meaningful improvements over KEYTRUDA alone. GeoVax believes the success reinforces the broader paradigm of combining checkpoint inhibition with therapies that generate or enhance anti-tumor immune responses, directly supporting its Gedeptin development strategy. Gedeptin uses a gene-directed enzyme prodrug therapy to destroy tumors locally and prime the tumor microenvironment, and published preclinical research showed enhanced anti-tumor immune responses when combined with anti-PD-1 therapy. GeoVax is preparing the next phase of Gedeptin clinical development in combination with KEYTRUDA for head and neck squamous cell carcinoma.
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Biotech & Genomic Medicine › Immuno-Oncology / Checkpoint ▲Competition
GOVX · Technology · Positive Positive Phase 3 data from Moderna-Merck validates Gedeptin's strategy, supporting its planned combination study.
MRK · Technology · Positive Merck's KEYTRUDA combination showed significant efficacy in melanoma, reinforcing its immunotherapy franchise.
MRNA · Technology · Positive Moderna's intismeran autogene plus KEYTRUDA met endpoints, validating its personalized cancer vaccine approach.
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