Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
APAVAC is a personalized, autologous cancer immunotherapy used primarily in veterinary medicine. The vaccine is formulated individually from a biopsy of the patient’s tumor, combining tumor-derived heat shock proteins (HSPPCs) and hydroxyapatite ceramic powder. The mechanism involves hydroxyapatite serving as an adjuvant and antigen-presenting matrix, adsorbing heat shock proteins that capture a broad repertoire of tumor antigens. This approach aims to activate cytotoxic T lymphocytes to target and destroy the animal's own tumor cells, thereby redirecting the immune response specifically against cancer. APAVAC is administered via subcutaneous or intradermal injection and is well tolerated, with no reported serious toxicity or autoimmune reactions. It is considered a standard therapy for diffuse large cell B lymphoma in dogs and has also shown benefit in treating other tumors, including osteosarcoma, mammary carcinoma, oral melanoma, squamous cell carcinoma, and sarcoid tumors in dogs, cats, horses, and small mammals. Clinical studies have documented improved time to progression and survival when combined with chemotherapy compared to chemotherapy alone[2][3][5][6][7][8].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on APAVAC.