Which biotechs have raised new VC financing this week?

Aug 13, 2026
A vial of engasertib on a table at a clinical trial siteAI-generated from publicly available materials.

This week’s venture capital landscape in biotech showcases significant funding rounds, with Vaderis Therapeutics leading the pack with $152 million aimed at advancing its rare vascular disorder treatment.

Vaderis Therapeutics, based in Switzerland, has secured a substantial $152 million in its second financing round, primarily to support the HEROIC phase 3 trial of engasertib, an AKT inhibitor targeting hereditary hemorrhagic telangiectasia (HHT). This rare condition currently lacks FDA-approved therapies, and engasertib has shown promise in reducing symptoms like nosebleeds in earlier trials. The financing was led by Goldman Sachs Alternatives and TCGX, with participation from several notable investors.

Aureka Biotechnologies has also made headlines by raising $100 million in a Series B funding round, bringing its total to over $200 million. This funding will bolster its development of an AI-driven platform for drug discovery, which integrates advanced digital biology techniques. The company aims to enhance biomolecular structure predictions and molecular design through its innovative lab-in-the-loop approach.

Epicrispr Biotechnologies, focusing on epigenetic therapies, raised $90 million to advance EPI-321, a treatment for facioscapulohumeral muscular dystrophy (FSHD). The funding will support pivotal clinical testing phases, with early results indicating potential disease modification. Meanwhile, Infinimmune has secured $75 million to develop antibodies for atopic dermatitis, and Boulevard Bio has emerged with $65 million for its bispecific antibody targeting IgA nephropathy. These developments highlight a robust investment climate in biotech, reflecting increasing interest in innovative therapies for rare diseases.

The surge in venture capital funding underscores a growing recognition of the potential in biotech, particularly for rare and complex conditions. As these companies move forward with clinical trials, the implications for patient care and treatment options could be transformative, potentially leading to breakthroughs in areas that have long been underserved.

Read the original article: Pharmaphorum