The Norwegian pharmaceutical company Lytix Biopharma AS provided an update at the recent BIO conference in Chicago on Phase I clinical trials of OncoporeTM (LTX-315) for the treatment of cancer.
During a session hosted by the European Cancer Cluster (Norwegian Oslo Cancer Cluster and French Cancer-Bio-Santé Cluster) at the recent BIO conference in Chicago, Head of Lytix Biopharma Business Development Anders Fugelli, PhD provided an update on the Phase I study of OncoporeTM (LTX-315) for the treatment of solid tumours. The study is set up to include patients at two main centres, The Norwegian Radium Hospital - National Hospital in Oslo, and the Karolinska University Hospital in Stockholm, Sweden, and will initially establish a safe and tolerated dose of LTX-315 when given to solid tumours amenable to injection. The study received regulatory and ethical approvals at the end of last year and is currently actively including patients. Up to 40 patients with transdermally accessible solid tumours will be included. The study will investigate the primary tumour necrotic event after local injection as well as the subsequent triggering of an anti-tumour immune response such as observed in animal models. The treatment of tumours by injection of OncoporeTM as an 'in situ vaccination' holds the potential to become a valuable new therapy for a variety of solid tumours.
Lytix Biopharma AS intends to develop OncoporeTM to a clinical Proof-of-Concept stage whilst seeking pharma/biotech partners to support later-stage clinical development and commercialisation.