Country for PR: China
Contributor: PR Newswire Asia (China)
Friday, January 21 2022 - 08:30
AsiaNet
Hinova Announces First Patient Dosed in a Phase I Clinical Trial of HP518, an orally bioavailable Chimeric Degrader targeting Androgen Receptor for Prostate Cancer Treatment
MELBOURNE, Australia, Jan. 21, 2022 /PRNewswire-Asianet/ --

Hinova Pharmaceuticals Inc., a clinical-stage biopharmaceutical company focused 
on developing novel therapeutics for cancers and metabolic diseases through 
targeted protein degradation technologies, announced that the first patient 
with metastatic castration-resistant prostate cancer (mCRPC) has been 
successfully dosed in a Phase I clinical trial of HP518, a highly selective and 
orally bioavailable chimeric degrader targeting androgen receptor (AR). The 
ongoing open-label Phase I study in Australia will evaluate the safety, 
pharmacokinetics, and anti-tumor activity of HP518 in patients with mCRPC.

HP518 has been discovered and developed by Hinova's targeted protein 
degradation drug discovery platform. It has the potential to overcome the drug 
resistance of prostate cancer due to some specific AR mutations.

Chimeric degraders are bifunctional small molecules that promote degradation of 
target proteins with high potency and high selectivity. This technology has the 
potential to target non-druggable targets and to overcome the drug resistance 
issue of traditional small molecule drugs.

"This is a significant milestone in the progress of our efforts from drug 
discovery to the clinical study," said Yuanwei Chen, Ph.D., President and CEO 
of Hinova. "We are excited about it and dedicated to bringing new treatment 
options to patients worldwide!"

Through the targeted protein degradation drug discovery platform, Hinova can 
screen protein degradation activity rapidly and accomplish efficient design and 
optimization of chimeric degraders. Furthermore, Hinova has profound experience 
in chemical manufacturing control of Chimeric degrader compounds.

About HP518

In 2019, the number of new cases of prostate cancer worldwide reached 1.3 
million. AR is a validated therapeutic target to treat prostate cancer. HP518, 
is an orally bioavailable chimeric degrader targeting AR, with the potential to 
overcome the drug resistance of prostate cancer due to some specific AR 
mutations. In discovery and preclinical studies, HP518 showed high degradation 
activity against wild type AR and some specific AR mutants that are resistant 
to enzalutamide, and excellent antitumor activity in xenograft mouse models. 
HP518 is highly selective for AR.

About Hinova

Hinova is an international and clinical-stage biopharmaceutical company focused 
on developing novel therapeutics for cancers and metabolic diseases. Hinova has 
committed to the discovery and development of innovative medicines for patients 
globally through deuteration and targeted protein degradation technologies.

Source: Hinova Pharmaceuticals Inc.