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VBL Therapeutics presents vascular disruptive agent preclinical data

VBL Therapeutics has presented the preclinical data of VB-111, a dual-action, anti-angiogenic and vascular disruptive agent (VDA) that utilizes VBL’s proprietary platform technology Vascular Targeting System (VTS) for cancer therapy.

The first trail results showed that VB-111 was safe and specific and may offer additive effect to chemotherapy.

In the trial, the researchers investigated the safety and efficacy of VB-111 as monotherapy, in combination with bevacizumab and in combination with carboplatin and pemetrexed in a Lewis Lung metastasis model and found that VB-111 induced a dose-dependent tumor reduction of up to 90%.

However, in the second study, VB-111 stands as a promising candidate as a treatment for glioblastoma.

The second trial examined the impact of VB-111 on tumor growth in rats with established intracranial xenografts.

The results demonstrated decreased tumor size in animals treated with VB-111, with those rats showing a median survival of 48 days, versus 38 days for untreated rats.