Chiome Bioscience Inc. ((JP:4583)) announced an update on their ongoing clinical study.
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Chiome Bioscience Inc. is conducting a Phase I clinical trial titled A Phase I, First in Human Study of CBA-1205, Anti-DLK1 Monoclonal Antibody in Patients With Advanced Solid Tumors. The primary aim is to assess the safety and tolerability of CBA-1205, a novel monoclonal antibody, in treating advanced solid tumors, including hepatocellular carcinoma (HCC), melanoma, and pediatric cancers. This study is significant as it explores a new therapeutic avenue for these challenging conditions.
The intervention being tested is CBA-1205, an experimental drug administered intravenously. It is designed to target and inhibit DLK1, a protein implicated in tumor growth, thereby potentially offering a new treatment option for patients with these cancers.
The study follows a non-randomized, sequential intervention model with single masking for outcome assessors. Its primary purpose is treatment, focusing on evaluating the drug’s safety profile through a standard 3+3 dose escalation method across five parts.
The study began on September 30, 2024, with primary completion anticipated in the near future. The latest update was submitted on September 15, 2025. These timelines are crucial as they indicate the study’s progress and potential for upcoming data releases.
This update could positively influence Chiome Bioscience Inc.’s stock performance by boosting investor confidence in the company’s innovative pipeline. The successful development of CBA-1205 may position Chiome as a competitive player in the oncology market, potentially impacting investor sentiment and market dynamics.
The study is ongoing, with further details available on the ClinicalTrials portal.