Harbour BioMed’s IND for HBM7004 Cleared by FDA

The U.S. Food and Drug Administration (FDA) has cleared Harbour BioMed’s Investigational New Drug (IND) application for HBM7004, enabling the initiation of a first-in-human (FIH) Phase I clinical trial. The study will evaluate the safety, tolerability, pharmacokinetics, and anti-tumor activity of HBM7004 in subjects with advanced solid tumors.

HBM7004 is a novel B7H4xCD3 bispecific antibody developed using the Company’s HBICE platform. This bispecific antibody is designed to provide a differentiated approach to cancer immunotherapy with the potential to enhance both efficacy and safety. The development of HBM7004 further demonstrated the HBICE platform’s versatility and plug-and-play advantages. In preclinical studies, HBM7004 demonstrated an intratumor B7H4-dependent T cell activation manner. In multiple animal models, HBM7004 showed strong anti-tumor efficacy, remarkable in vivo stability, and reduced systemic toxicity. Additionally, in preclinical models, HBM7004 exhibited a strong synergistic effect when combined with a B7H4x4-1BB bispecific antibody at a low effector-to-target cell ratio, indicating an encouraging therapeutic window.

“The FDA’s IND clearance for our B7H4xCD3 bispecific antibody HBM7004 marks an important step in advancing our innovative pipeline for patients with advanced solid tumors,” said Dr. Jingsong Wang, Founder, Chairman and CEO of Harbour BioMed. “This program reflects our continued focus on developing differentiated biotherapeutics leveraging our industry-leading proprietary platforms to address significant unmet needs in oncology. We are confident in the potential of HBM7004 and look forward to evaluating its clinical benefit in patients with advanced solid tumors.”

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