{"id":24391,"date":"2022-11-11T14:29:00","date_gmt":"2022-11-11T06:29:00","guid":{"rendered":"https:\/\/flcube.com\/?p=24391"},"modified":"2025-01-31T14:32:16","modified_gmt":"2025-01-31T06:32:16","slug":"beigenes-brukinsa-receives-marketing-approval-in-brazil","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=24391","title":{"rendered":"BeiGene&#8217;s Brukinsa Receives Marketing Approval in Brazil"},"content":{"rendered":"\n<p>China-based biotech BeiGene Inc. (<a href=\"https:\/\/www.google.com\/finance\/quote\/6160:HKG\">HKG: 6160<\/a>, <a href=\"https:\/\/www.google.com\/finance\/quote\/688235:SHA\">SHA: 688235<\/a>, NASDAQ: BGNE) has announced that it has received marketing approval in Brazil for its Bruton&#8217;s tyrosine kinase (BTK) inhibitor Brukinsa (zanubrutinib). The in-house developed drug is now approved for the treatment of Waldenstr\u00f6m\u2019s macroglobulinemia (WM) and relapsed\/refractory (r\/r) marginal zone lymphoma (MZL) in patients who have previously received at least one anti-CD20 therapy. This approval expands the drug&#8217;s indications in Brazil, where it was previously approved for the treatment of mantle cell lymphoma (MCL).<\/p>\n\n\n\n<p><strong>Global Regulatory Progress<\/strong><br>Brukinsa is currently awaiting regulatory decisions for over 40 filings around the globe. The drug has already received approvals in more than 55 countries and regions, including the United States, China, the European Union, Switzerland, Great Britain, Canada, Australia, and other international markets. In 2020, Brukinsa was added to China\u2019s National Reimbursement Drug List (NRDL), further enhancing its accessibility to patients in need.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>China-based biotech BeiGene Inc. (HKG: 6160, SHA: 688235, NASDAQ: BGNE) has announced that it has&#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":[2092,16,847,846,15,848,33],"class_list":["post-24391","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-beone-medicines","tag-cancer","tag-hkg-6160","tag-nasdaq-bgne","tag-product-approvals","tag-sha-688235","tag-tkis-egfr-vegf-btk-etc"],"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>BeiGene&#039;s Brukinsa Receives Marketing Approval in Brazil - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"China-based biotech BeiGene Inc. (HKG: 6160, SHA: 688235, NASDAQ: BGNE) has announced that it has received marketing approval in Brazil for its Bruton&#039;s tyrosine kinase (BTK) inhibitor Brukinsa (zanubrutinib). The in-house developed drug is now approved for the treatment of Waldenstr\u00f6m\u2019s macroglobulinemia (WM) and relapsed\/refractory (r\/r) marginal zone lymphoma (MZL) in patients who have previously received at least one anti-CD20 therapy. This approval expands the drug&#039;s indications in Brazil, where it was previously approved for the treatment of mantle cell lymphoma (MCL).\" \/>\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=24391\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"BeiGene&#039;s Brukinsa Receives Marketing Approval in Brazil\" \/>\n<meta property=\"og:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. FLCUBE delivers reliable data, news, and intelligence to broaden your horizons and sharpen your decision-making. 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(HKG: 6160, SHA: 688235, NASDAQ: BGNE) has announced that it has received marketing approval in Brazil for its Bruton's tyrosine kinase (BTK) inhibitor Brukinsa (zanubrutinib). The in-house developed drug is now approved for the treatment of Waldenstr\u00f6m\u2019s macroglobulinemia (WM) and relapsed\\\/refractory (r\\\/r) marginal zone lymphoma (MZL) in patients who have previously received at least one anti-CD20 therapy. 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