HanAll Biopharma, Restructured to Seung-kook Park and Seung-..
Harbour BioMed, HanAll Biopharma’s Chinese
partner, announced the first dosing of Phase 3 trial of HL036 in dry eye
disease, a novel, topical anti-TNF alpha biologic, in China on the 12th.
The purpose of this Phase III clinical
trial is to evaluate the effectiveness and safety of Tanfanercept(HBM9036) eye
drops(0.25%) compared with placebo in the treatment of moderate-to-severe DED
patients in China. This clinical trial is led by Professor Zuguo Liu, Chairman
of Asia Dry Eye Society(ADES) and Director of Eye Institute of Xiamen
University.
Dry eye disease is a chronic eye disease
with various causes. It can cause visual impairment and damage on the surface
of the eye and is a disease that lowers the patient’s quality of life.
According to Harbour BioMed data, 21-30% of the Chinese population suffers from
dry eye disease, and the number of patients is expected to increase
considerably due to aging, excessive use of smartphones, changes in the
atmospheric environment, and other factors.
Dr. Jingsong Wang, Founder, Chairman, and
CEO of Harbour BioMed said: “Owing to the changing lifestyle and aging
population, the number of DED patients in China has been increasing
significantly in recent years crossing 300 million in 2020. Following the
initiation of Phase III clinical trial, we aim to further accelerate the
commercialization of this novel therapeutic solution for DED to Chinese
patients very soon.”
In 2017, Harbour BioMed obtained the rights
to the development and commercialization of HL036, a medicine for dry eye
disease, and HL161, a therapeutic antibody for autoimmune diseases, for the
China region including Taiwan, Hong Kong, and Macao through a licensing
agreement with HanAll Biopharma. Under the terms of the agreement, HanAll
Biopharma will be eligible to receive potentially up to $81 million in
development, regulatory and sales milestones as well as tiered royalties on net
sales of both products.
Meanwhile, for the HL036 eye drop, HanAll
Biopharma and Daewoong Pharmaceutical completed the first Phase 3 clinical
trial(VELOS-2) in the U.S. last year and are planning to start a second Phase 3
clinical trial in the third quarter of this year.