{"id":20039,"date":"2023-04-06T22:36:00","date_gmt":"2023-04-06T14:36:00","guid":{"rendered":"https:\/\/flcube.com\/?p=20039"},"modified":"2024-12-27T22:39:25","modified_gmt":"2024-12-27T14:39:25","slug":"haisco-pharmaceutical-gets-cde-approval-for-hsk38008-prostate-cancer-clinical-study","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=20039","title":{"rendered":"Haisco Pharmaceutical Gets CDE Approval for HSK38008 Prostate Cancer Clinical Study"},"content":{"rendered":"\n<p>Haisco Pharmaceutical Group Co., Ltd (<a href=\"https:\/\/www.google.com\/finance\/quote\/002653:SHE\">SHE: 002653<\/a>) has announced receiving approval from the Center for Drug Evaluation (CDE) to conduct a clinical study for its Category 1 chemical drug, HSK38008 oral preparation, in the treatment of prostate cancer.<\/p>\n\n\n\n<p><strong>HSK38008: An Androgen Mutant AR-V7 Oral Degradation Agent<\/strong><br>HSK38008 is an androgen mutant AR-V7 oral degradation agent that has the capability to degrade the splicing variant of the androgen receptor through the proteasome pathway. By blocking the transmission of the androgen receptor signal pathway, HSK38008 inhibits the growth and proliferation of prostate cancer cells. This novel approach offers a potential new treatment option for patients with prostate cancer.<\/p>\n\n\n\n<p><strong>Preclinical Efficacy and Comparison with Other Drugs<\/strong><br>In preclinical studies using the AR-V7 mutated 22RV1 castrated mouse transplanted tumor model, HSK38008 demonstrated dose-dependent inhibition of tumor growth. The drug showed significantly better efficacy compared to the AR PROTAC drug ARV-110 and the AR inhibitor enzalutamide. These results highlight HSK38008&#8217;s potential as a more effective treatment in the fight against prostate cancer.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Haisco Pharmaceutical Group Co., Ltd (SHE: 002653) has announced receiving approval from the Center for&#8230;<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"googlesitekit_rrm_CAownpewDA:productID":"","_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[7,11],"tags":[16,62,139,929,70],"class_list":["post-20039","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-cancer","tag-clinical-trial-approval-initiation","tag-haisco-pharmaceutical","tag-she-002653","tag-tpd"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v23.6 (Yoast SEO v27.5) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Haisco Pharmaceutical Gets CDE Approval for HSK38008 Prostate Cancer Clinical Study - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Haisco Pharmaceutical Group Co., Ltd (SHE: 002653) has announced receiving approval from the Center for Drug Evaluation (CDE) to conduct a clinical study for its Category 1 chemical drug, HSK38008 oral preparation, in the treatment of prostate cancer.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/flcube.com\/?p=20039\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Haisco Pharmaceutical Gets CDE Approval for HSK38008 Prostate Cancer Clinical Study\" \/>\n<meta property=\"og:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. 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