Company News

2026-10-19
ImmuneOnco Doses First Patient in Phase Ib Trial of Subcutaneous Amulirafusp Alfa (IMM0306S) in Systemic Lupus Erythematosus
This milestone marks a key progress in the clinical development of IMM0306S in autoimmune diseases and demonstrates the potential to improve long-term treatment experience and adherence for patients.
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2026-10-15
ImmuneOnco Subsidiary ImmuneCare's IND Application for IMC-003 in Pulmonary Hypertension Associated with Left Heart Disease Accepted by China's CDE
The application covers the treatment of combined post- and pre-capillary pulmonary hypertension associated with heart failure with preserved ejection fraction ("CpcPH-HFpEF"), a high-risk phenotype within pulmonary hypertension associated with left heart disease ("PH-LHD").
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2026-10-10
ImmuneOnco to Present Latest Phase Ib/II Clinical Results of IMM0306 in Systemic Lupus Erythematosus at ACR 2026
IMC-002 (IMM0306), a bispecific CD20×CD47 fusion protein, demonstrates improvements in active Systemic Lupus Erythematosus patients in a phase Ib/II study
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2026-09-23
ImmuneOnco Reports Breakthrough Phase II Data for IMM0306 in Combination with Lenalidomide: ORR of 92.3% in R/R MZL and 88.6% in R/R FL, Demonstrating a Compelling Efficacy and Safety Profile
The latest data demonstrate that the combination regimen delivers high response rates, durable progression-free survival benefits, and a favorable safety profile in patients with R/R marginal zone lymphoma (MZL) and R/R follicular lymphoma (FL), offering a highly promising new therapeutic option for patients with R/R indolent B-cell lymphomas. The Phase II clinical study is ongoing.
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2026-08-27
ImmuneOnco Doses First Patient in Phase II Trial of Palverafusp Alfa (IMM2510) in Combination with Tazlestobart (IMM27M) for First-Line Advanced Hepatocellular Carcinoma
The study is designed to assess the preliminary anti-tumor efficacy and safety of the combination in this patient population.
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2026-08-25
ImmuneCare Achieves Dual Milestones for IMC-003 in Clinical Progress: First PAH Patient Dosed, All SAD/MAD Cohorts Completed
These achievements mark significant progress in the program's advancement toward patient validation.
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