Vivesto receives approval to initiate a dose-finding study of Paccal Vet in cats

Solna, Sweden, January 16, 2025 – Vivesto AB, an oncology-focused development company, today announced that ethical approval has been obtained from the US Veterinary Review Board Clinical Studies Committee for a planned Paccal Vet dose-finding clinical trial in cats with cancer. The approval authorizes the participating clinical sites to enroll patients in the study.

The dose-finding study will initially be conducted at two clinical sites in Washington and Oregon, with the possibility to include more sites as the study progresses. The study will be managed by CASTR Alliance, the contract research organization (CRO) currently running Paccal Vet’s pilot clinical trial in dogs with splenic hemangiosarcoma in the US. FDA's Center for Veterinary Medicine, CVM, has previously confirmed that the cat study can be conducted under the existing INAD (Investigational New Animal Drug).

”As we approach the first interim read out in the pilot study in dogs, we are now advancing the Paccal Vet program and broadening the indication areas to include cancer in cats. This is an important move from both a medical and a commercial perspective, as millions of cats are diagnosed with cancer every year and there are still no approved drugs available to treat them. With this approval and the upcoming trial, the first crucial steps have been taken toward providing a new potential treatment option for cats with cancer while building shareholder value in the program,” said Erik Kinnman, CEO of Vivesto.

The dose-finding study will follow the 3+3 design, a widely used approach to determine the maximum tolerated dose (MTD). A maximum of 12 cats will be included, receiving Paccal Vet treatment in groups of three, with doses escalating for each group until the MTD is identified. This study design ensures patient safety while effectively identifying the appropriate dosage for Paccal Vet administration in cats.

Datum 2025-01-16, kl 14:00
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