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.
Roivant to announce Q3 2026 financial results
Avacta secures FDA clearance for second pre|CISION oncology programme
OncoHost receives BIG Innovation Award in Health category
Summit Therapeutics and GSK form collaboration to study ivonescimab combination therapy
Summit Therapeutics submits FDA application for ivonescimab in EGFR-mutated lung cancer
Antin to acquire clinical trial equipment provider Emsere
Merck completes acquisition of Cidara Therapeutics for USD9.2bn
Bambusa Therapeutics reports first patient dosed in proof-of-concept COPD trial
Kelun-Biotech lung cancer drug granted Breakthrough Therapy Designation in China
INOVIO's INO-3107 Biologics License Application accepted by US FDA
Sanofi and Regeneron's Dupixent gains Japan approval for paediatric asthma patients aged 6 to 11
Aqualung Therapeutics' Phase 2a lung fibrosis study approved by US FDA