California-based precision medicine oncology company IDEAYA Biosciences Inc (Nasdaq: IDYA) and Hengrui Pharma, a China-based global pharmaceutical company focused on scientific and technological innovation, presented initial data from Hengrui's Phase 1 clinical trial of IDE849 (SHR-4849), a potential first-in-class delta-like ligand 3 (DLL3)-targeting Topoisomerase-1 (TOP1) antibody drug conjugate (ADC), in an oral presentation on Sunday at the IASLC 2025 World Conference on Lung Cancer (WCLC) in Barcelona, Spain.
The presentation included data from a total of 100 patients who received IDE849 at doses between 0.8 mg/kg to 4.2 mg/kg with a once every 3-week dosing interval.
Data in the presentation were as of a cut-off date of 20 June 2025, and included 87 patients with small-cell lung cancer (SCLC) and 13 patients with other neuroendocrine carcinomas (NEC). All patients had progressed after front-line therapy, with 33 percent having progressed after two prior lines and 15 percent after three or more prior lines of therapy.
IDEAYA will review the data that was presented by Hengrui at its 10-Year Anniversary R&D Day on 8 September 2025 in New York.
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