Nanjing Leads Biolabs Co, Ltd (9887.HK) announced on Thursday that it has completed patient enrollment in its pivotal single-arm registrational trial (CTR20213023) evaluating Opamtistomig (LBL-024) monotherapy for extrapulmonary neuroendocrine carcinoma (EP-NEC). This is the first global registrational study of an immunotherapy monotherapy for EP-NEC, led by Professor Shen Lin of Peking University Cancer Hospital across multiple centres in China.
The study targets patients with advanced EP-NEC who have failed at least two lines of chemotherapy. EP-NEC is a rare, aggressive, immunologically 'cold' tumour with no established second-line standard of care, underscoring significant unmet need.
Opamtistomig, developed using the company's X-Body bispecific platform, is a first-in-class PD-L1/4-1BB bispecific antibody. Its dual mechanism both reverses PD-L1-mediated immune suppression and selectively activates T cells, aiming to deliver synergistic anti-tumour effects. Phase I/II trials in China have shown encouraging efficacy and safety in EP-NEC, supporting the pursuit of accelerated approval.
Regulatory milestones include Breakthrough Therapy Designation from China's National Medical Products Administration in October 2024 and Orphan Drug Designation from the U.S. Food and Drug Administration in November 2024. Beyond EP-NEC, the therapy is in clinical trials for multiple high-need cancers including small cell lung cancer, biliary tract cancer, ovarian cancer and gastric cancer, with early signs of broad-spectrum oncology potential.
Basilea Pharmaceutica enters exclusive license agreement with Venatorx Pharmaceuticals
Nanoscope Therapeutics announces positive results from STARLIGHT clinical trial
Leads Biolabs completes patient enrollment in pivotal Opamtistomig trial for EP-NEC
Remegen's Telitacicept meets Sjogren's syndrome Phase III trial's primary endpoint
CuraCell secures German regulatory clearance for clinical trial of CC-38 TIL therapy
Insmed's BRINSUPRI (brensocatib) non-cystic fibrosis bronchiectasis treatment approved by US FDA
Ocular Therapeutix secures FDA special protocol assessment for AXPAXLI NPDR trial
Novartis reports positive Phase III trial results for ianalumab in immune thrombocytopenia
Merck reports positive Phase 3 results for Keytruda and Padcev in muscle-invasive bladder cancer
Fosun Pharma agrees XH-S004 overseas licensing deal
IO Biotech reports Phase 3 trial results for Cylembio plus pembrolizumab in advanced melanoma
Novartis reports positive Phase III results for ianalumab in Sjögren's disease
FDA grants priority review for GSK's gepotidacin gonorrhoea indication
Akeso doses first patient in Phase III Ivonescimab small cell lung cancer trial