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BioVaxys Technology Corp. develops immunotherapy and vaccine programs based on its DPX antigen delivery and immune-educating technology platform. The clinical-stage biotechnology company reports developments across oncology, infectious disease, allergy, and other immune-disease applications, with recurring updates on DPX-formulated products such as maveropepimut-S, or MVP-S, and DPX-SurMAGE.
BioVaxys news commonly covers clinical-study results in cancer indications including ovarian, bladder, and breast cancer; licensing activity tied to DPX technology; SpayVac-related immunocontraceptive vaccine developments through a licensee; integration of former IMV assets; and capital-structure actions such as share consolidation, financing activity, warrants, and asset-purchase agreement amendments.
BioVaxys (OTCQB: BVAXF) reported positive preliminary Phase 1B/2 PESCO results for maveropepimut-S (MVP-S) combined with pembrolizumab and low-dose cyclophosphamide in recurrent epithelial ovarian cancer (EOC) on January 20, 2026. In 47 patients (16 phase 1, 31 phase 2) overall response rate (ORR) was 24% and disease control rate (DCR) 82% in patients described as high grade endometrial cancer. Platinum-sensitive patients had ORR 40% and DCR 90%; platinum-resistant patients showed ORR 16% and DCR 54% versus ~11.8% ORR for single-agent chemotherapy. Longest immune response lasted 195 weeks with a 3-year complete response; survivin-specific immune responses occurred in 62% of tested patients and correlated with disease control in 93%.
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BioVaxys (OTCQB: BVAXF) reported Phase 1 safety and immunogenicity results for two DPX-formulated cancer vaccines, maveropepimut-S (MVP-S) and DPX-SurMAGE, in 12 patients with recurrent non-muscle invasive bladder cancer (NMIBC) treated prior to transurethral resection.
Both products were well tolerated and induced systemic antigen-specific T cell responses measured by IFN-γ ELISPOT at Days 0, 28, 49 and 109; 55% of MVP-S recipients showed peak responses at Day 28 and 33% of DPX-SurMAGE recipients showed stronger responses at Day 49. The study confirmed multivalent antigen delivery with DPX and supports advancement to further clinical study.
BioVaxys (OTCQB: BVAXF) reported positive Phase 1 results for maveropepimut-S (MVP-S) combined with neoadjuvant letrozole in postmenopausal women with HR+/HER2- stage II-III breast cancer on December 17, 2025. In three patients (Ki-67 >10%) who received two doses of MVP-S and seven weeks of letrozole, median Ki-67 fell from 24% to 6% (ranges 12–43% to 5–8%). One patient showed an 8-fold increase in survivin-specific IFN-γ T cells. Company and investigators plan expanded profiling and a Phase 2 study to evaluate tumor immune modulation.
BioVaxys licensee SpayVac-for-Wildlife (BVAXD) reported peer-reviewed results from a one-year study in the Bavarian Forest showing a single dose of SpayVac reduced fertility to 11% vs 86% in controls in 47 free-ranging red deer monitored with camera traps, GPS collars and fecal progesterone. The liposome-delivered vaccine platform is licensed from BioVaxys and has now shown contraceptive efficacy across three deer species: fallow, white-tailed and red deer.
SpayVac-for-Wildlife has initiated the regulatory submission process for SpayVac targeting feral horses and free-ranging deer; the companies anticipate a potential royalty stream from sales.
BioVaxys Technology Corp. (OTCQB: BVAXF) has announced a 10:1 share consolidation of its common shares, expected to commence trading on September 11, 2025. Following the consolidation, the company's outstanding shares will reduce from 293,425,203 to approximately 29,342,496 shares.
The consolidation will adjust the exercise price and number of shares for outstanding convertible securities proportionally, except for Debenture Warrants. Registered shareholders with physical certificates must submit them along with a transmittal letter to Odyssey Trust Company, while shareholders without physical certificates need not take action.
BioVaxys is a clinical-stage biopharmaceutical company developing immunotherapies, including its DPX™ platform and HapTenix© tumor cell construct platform for treating cancers and other immunological diseases.
BioVaxys Technology Corp. (BVAXF) and SpayVac for Wildlife have expanded their License Agreement to include commercial aquaculture and farm-raised fish markets. The expansion targets a significant market opportunity in farm-raised Atlantic salmon and rainbow trout, with an annual harvest of approximately 3.28 million metric tons (800 million individual fish).
SpayVac's single-dose fertility-control vaccines offer an alternative to triploidy in aquaculture, with initial proof-of-concept trials progressing to the second phase. The technology uses a patented liposome-based delivery platform, demonstrating 4-10 years of contraceptive efficacy in various species.
The company is pursuing regulatory approval for feral horses and free-ranging deer populations, with the U.S. Bureau of Land Management (BLM) as a potential lead customer. The BLM currently manages 53,797 horses on the range, significantly above the Appropriate Management Level of 22,637, spending 66% of its $153 million budget on long-term holding costs.