Information for Veterinary Professionals

In many canine cancers, treatment is limited by toxicity and quality-of-life considerations. CaniVax has a pipeline of tumour-specific cancer vaccines developed using its proprietary and robust platforms and tested through clinical trials.

Scientific rationale

A central challenge in veterinary oncology is achieving meaningful tumour control while maintaining tolerability over time. Many current therapies are constrained by cumulative toxicity, limiting treatment duration, intensity, or suitability for individual patients. Dog owners frequently decline the treatment because of the unpleasant side effects apparent in their pets upon treatment.

CaniVax's approach is based on identifying tumour-specific antigens and using these antigens to design vaccines that guide an antigen-specific immune response to the tumour, with the aim of improving the therapeutic outcome without the cytotoxic side effects.

Veterinarians examining dog in vet's surgery

Mechanism overview

CaniVax's vaccine platform is designed to link antigen discovery with clinical application through a scientifically driven process:

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Tumour Antigens

Tumour-specific antigens present on cancer cells are identified through state-of-the-art technologies and platform

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Ex vivo Immune Activation Testing

CaniVax's proprietary platform allows identification of immunogenic antigens that generate a robust T-cell response.

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Vaccine Design and Engineering

CaniVax designs and engineers its vaccines using AI tools and proprietary algorithms, enabling the development of optimised vaccines for the patient's immune system.

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Clinical Evaluation

CaniVax develops and evaluates its vaccines in patients suffering from the appropriate cancer.

Small dog sits in veterinary clinic waiting checkup. Cute puppy poses at vet. Animal health care. Ultrasound machine at background. Pet at examination by veterinarian. Dog at modern clinic.

Evidence and development

CaniVax vaccine programs progress through a tested and validated set of laboratory procedures that encompass translational studies in canine patients to characterise the immune response, feasibility, and safety. These results inform the design of veterinary clinical studies intended to generate evidence relevant to regulatory review and submission, and post-approval clinical practice.

Clinical trials are designed to complement existing standards-of-care and to reflect real-world treatment constraints, including tolerability and quality-of-life considerations.

Regulatory framework

CaniVax engages with relevant regulatory authorities at an early stage during development to ensure that scientific and clinical milestones align with veterinary regulatory requirements. Compassionate use of our cancer vaccines occurs under appropriate authorisation, and any future supply would require endorsement by regulatory authorities, veterinary prescription and clinical oversight.

Commercial availability is dependent on successful regulatory review and approval.

Veterinarian using a digital tablet during a dog check up in a modern veterinary clinic
Golden retriever receiving a vaccination from a veterinarian in a clinical setting. The dog appears calm on the examination table while the vet administers care. Image made using Generative AI.

Translational strategy

CaniVax follows a structured, stepwise translational development framework that links biological discovery with clinical evaluation. Early stages focus on antigen validation and immune characterisation, followed by progressive evaluation in veterinary clinical settings under appropriate regulatory guidance and authorisation.

Development decisions are data-driven at each stage, allowing programmes to advance and be refined, reflecting emerging evidence.

Clinical evaluation context

Veterinary clinical studies are designed to characterise safety, tolerability, immune activation, and feasibility in client-owned dogs with naturally occurring disease. Study designs are intended to reflect real-world veterinary oncology practice and to generate data relevant to both regulatory review and future clinical integration.

Investigational vaccines are supplied without commercial intent during development and are administered under veterinary oversight.

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Scope and current status

CaniVax programmes are investigational and under active development. Initial efforts focus on a limited number of high-incidence canine cancers where tumour biology, clinical need, and immune targeting potential align.

Scientific and clinical updates will be shared as programmes reach defined milestones.

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Photo credit © Adrian Baughan - Oxford Dog Photography.