In order for a T-cell based cancer vaccine to work, it must be able to induce T cell recognition and elimination of cells expressing one or several target proteins (antigens). These are typically presented by the cells either via receptors called MHC-I or MHC-II. RhoVac's cancer vaccine candidate, onilcamotide, is predominantly driven by T cells of the CD4+ sub-type, and these cells require the antigen to be presented by MHC-II receptors. The pre-clinical study collaboration with Dr Sweta Srivastava, a faculty within St. Johns National Academy of Health Sciences (St. John's Research Institute), CBCI, has now shown that these types of receptors (MHC-II) are found in many different forms of cancer cells, and that RhoC appears to be co-located with these receptors on the cell surface. The data suggests that onilcamotide is tissue agnostic, i.e., that it could be used across cancer types. The data has even documented the presence of MHC-II receptors in more types of cancer than previously known. Fore reference, please find a first article on the findings here: https://www.biorxiv.org/content/10.1101/2022.05.15.492002v1.full.pdf.

RhoVac CEO, Anders Månsson, comments: "We are very excited about these findings that coincide with previous pre-clinical findings suggesting a potential broad use of onilcamotide in cancer, provided we also get a first clinical proof of concept for its use in prostate cancer. If this also comes true - and we will find out soon - our drug candidate has a huge possibility of being used in many different cancers going forward."    

This disclosure contains information that RhoVac is obliged to make public pursuant to the EU Market Abuse Regulation (EU nr 596/2014). The information was submitted for publication, through the agency of the contact person, on 18-05-2022 18:11 CET.