Zelgen Biopharmaceuticals’ ZG006 Earns NMPA Approval for Clinical Trials in Solid Tumors

Suzhou Zelgen Biopharmaceuticals Co., Ltd (SHA: 688266), a China-based biopharmaceutical company, has announced that it has received clinical trial approval from the National Medical Products Administration (NMPA) for its pipeline candidate, ZG006. The molecule is set to enter trials targeting general advanced solid tumors.

ZG006: A Pioneering Tri-Specific Antibody
ZG006 is a tri-specific antibody developed through the company’s bispecific antibody (BsAb)/multi-specific antibody platform. It uniquely targets CD3 and two different DLL3 epitopes, making it the world’s first tri-specific antibody (CD3×DLL3×DLL3) designed to target DLL3-expressing tumors. Preclinical studies have demonstrated that ZG006 possesses significant tumor inhibitory effects and exhibits good safety characteristics, positioning it as a promising candidate for further development.

Implications for Advanced Solid Tumor Treatments
The approval of ZG006 for clinical trials marks a significant step forward in the development of novel treatments for advanced solid tumors. As a tri-specific antibody, ZG006 has the potential to offer a new therapeutic approach, targeting tumors with a unique mechanism of action that engages both CD3 and DLL3, which could lead to more effective cancer treatments.-Fineline Info & Tech

Insight, China's Pharmaceutical Industry