Sotio’s cell platform, called DCVAC, starts with a patient’s peripheral blood mononuclear cells, which are grown into dendritic cells (DCs). In parallel, the company uses a proprietary device to pressurize tumor cells from cell lines, and the right amount of HHP makes the cells more immunogenic. The company picks “cell lines with expression profiles that show the most overlap with a patient’s tumor profile,” says Sotio’s CTO, Luděk Sojka, PhD. Then, adding the HHP-killed tumor cells to a patient’s DCs makes them express a variety of tumor antigens on their surface.

As the superbug crisis heats up around the world, Scynexis says it has new data from two interim analyses that prove its antifungal has the potential to treat a broad range of infections.

X4 Pharmaceuticals is developing a class of small molecule therapeutics that work as antagonists of chemokine receptor, CXCR4, the disruption of which is implicated in a number of primary immunodeficiencies (PIs) and cancers.

That’s the question a new biotech is aiming to answer, as SalioGen Therapeutics emerges from stealth Monday morning with a $20 million Series A. And they believe they’ve found a new delivery system that can more precisely deliver genes in vivo than the relatively large adeno-associated virus or CRISPR system: mammalian-derived enzymes.

Cidara Therapeutics is exploring echinocandin derivatives. The company’s clinical candidate rezafungin is a derivative of anidulafungin, a compound originally discovered at Eli Lilly and Company and currently marketed by Pfizer. Chemists placed a choline group at a critical point on the molecule, a feature that stabilizes the echinocandin ring and prevents metabolic breakdown of the molecule, explains Cidara’s president and CEO, Jeff Stein.