PharmAbcine signs a license agreement with Wincal Biopharm to expand
indications of PharmAbcine's existing assets to non-oncology areas
DAEJEON, South Korea, June 3, 2020 /PRNewswire/ -- PharmAbcine (KOSDAQ: 208340), a clinical-stage biotechnology company,
announced today that the company entered into a license agreement with Wincal Biopharm ("Wincal"), a wholly owned US subsidiary of PharmAbcine, so that Wincal can expand the commercial value of PharmAbcine's existing and future assets through R&D efforts. Under this agreement, Wincal will use PharmAbcine's assets to develop new platforms that can enhance biological activities of traditional
antibody therapeutic to target broader disease areas.
"This agreement will finally allow us to unlock the full potential of our assets," said Dr. Jinsan Yoo, CEO of PharmAbcine. "We have long been aware of non-oncology potential of our assets but we could not do much about it due to limited resources. The biggest challenge
was to hire R&D experts in Korea due mainly to a shortage arising from a bio venture boom in recent years. We believe that this arrangement will enable us to get access to the talent pool, resources, and collaborative opportunity in the US."
Wincal's efforts will be spearheaded by Dr. Tae-Weon Lee, Chief Scientific Officer and a founding member of Wincal. Dr. Lee has over
20 years of pharmaceutical industry experience in overseeing drug discovery efforts and supporting scientific collaborative efforts with
academics and pharmaceutical companies. Before joining Wincal, he was a director and a principal investigator leading the diabetes and heart failure drug discovery program at Amgen.
"Our team with years of big pharma drug discovery experiences is devoted to bringing a new cure for vascular diseases. We are
developing an innovative eye-drop technology to deliver therapeutic antibodies to treat ophthalmological diseases such as age-related
macular degeneration, diabetic retinopathy, and diabetic macula edema. In addition, we are building a new platform to treat pulmonary
edema (acute lung injury and acute respiratory distress syndrome), as well as plaque-induced vascular aneurysm (thoracic aortic
aneurysm and abdominal aortic aneurysm)," said Dr Lee.
About PharmAbcine Inc.
PharmAbcine is a clinical-stage biotech company focusing on the development of fully human antibody therapeutics to treat neovascular disorders, tumors, and other medically unmet diseases. It provides therapeutic antibodies for a wide spectrum of indications from
oncology, immuno-oncology, ophthalmology, respiratory, to renal pathology.
PharmAbcine's leading pipeline, olinvacimab, an anti-VEGFR2 neutralizing fully human IgG, is currently in a phase II study for
bevacizumab-nonresponding rGBM (recurrent glioblastoma multiforme) patients in both US and Australia. In collaboration with MERCK, olinvacimab plus pembrolizumab Phase Ib trials for mTNBC and rGBM are on-going.
PharmAbcine has its own HuPhage library and innovative selection system. PharmAbcine's advanced 3G expression system
accommodates high levels of antibody production with high reproducibility. With its highly advanced technology platforms, it provides high-quality antibody generation services. The high standards have allowed PharmAbcine to expand co-development opportunities with not
only existing but also potential partners.
Additional information about PharmAbcine can be found on our website at http://www.pharmabcine.com.