Handok CI (Photo by Handok)

Handok CI (Photo by Handok)

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[Asia Economy Reporter Chunhee Lee] Handok announced on the 20th that it will present the key results of the Phase 2 clinical trial of 'HD-B001A (CTX-009, ABL001)' for cholangiocarcinoma patients, currently under development, as a poster at the Gastrointestinal Cancers Symposium (ASCO GI 2023) of the American Society of Clinical Oncology (ASCO) to be held next month.


HD-B001A is a next-generation anticancer drug developed using bispecific antibody platform technology. Handok holds the rights in Korea through a licensing agreement with ABL Bio. Since last year, Handok has been focusing on cholangiocarcinoma and conducting a domestic Phase 2 clinical trial of HD-B001A. Based on the domestic trial, they are laying the groundwork for expanding HD-B001A into global clinical trials and are also collaborating with Compass Therapeutics on clinical trials in the United States.


This Phase 2 clinical trial was conducted at four domestic institutions, including Seoul National University Hospital, targeting patients with unresectable advanced, metastatic, or recurrent cholangiocarcinoma who had previously received first- or second-line systemic chemotherapy. The treatment regimen combined paclitaxel with HD-B001A.



At ASCO GI 2023, Handok plans to share plans for Phase 2 and 3 clinical trials of HD-B001A in cholangiocarcinoma patients as well as a Phase 2 clinical trial in colorectal cancer patients. The Phase 2 and 3 trials for cholangiocarcinoma patients will be randomized, open-label clinical trials comparing combination therapy of paclitaxel and HD-B001A versus paclitaxel monotherapy in patients with unresectable advanced cholangiocarcinoma who have received one prior systemic chemotherapy and experienced metastasis or recurrence. The Phase 2 trial for colorectal cancer patients will target patients with colorectal cancer metastasized to 2 to 3 sites.


This content was produced with the assistance of AI translation services.

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