ImmunityBio Reports ANKTIVA Plus BCG Achieves 96% Three-Year Survival in BCG-Unresponsive Bladder Cancer

Reuters

2025/12/16

ImmunityBio Reports ANKTIVA Plus BCG Achieves 96% Three-Year Survival in BCG-Unresponsive Bladder Cancer

ImmunityBio, Inc. announced new clinical study results demonstrating that treatment with ANKTIVA® (nogapendekin alfa inbakicept-pmln) in combination with Bacillus Calmette-Guérin $(BCG)$ shows a 96% bladder cancer-specific survival rate at three years in patients with BCG-unresponsive high-grade papillary-only non-muscle invasive bladder cancer (NMIBC). The findings, published in the January 2026 edition of The Journal of Urology, also indicate favorable outcomes in disease-free survival, progression-free survival, and high rates of cystectomy avoidance, with the median to cystectomy not yet reached. Safety data revealed a 3% incidence of grade 3 treatment-related adverse events, with no grade 4 or 5 events reported. ANKTIVA is currently approved in the U.S., U.K., and has conditional marketing authorization in the EU for BCG-unresponsive NMIBC with carcinoma in situ, with or without papillary tumors.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Immunitybio Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20251216185945) on December 16, 2025, and is solely responsible for the information contained therein.

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The findings, published in the January 2026 edition of The Journal of Urology, also indicate favorable outcomes in disease-free survival, progression-free survival, and high rates of cystectomy avoidance, with the median to cystectomy not yet reached. Safety data revealed a 3% incidence of grade 3 treatment-related adverse events, with no grade 4 or 5 events reported. ANKTIVA is currently approved in the U.S., U.<a href=\"https://laohu8.com/S/TKKD.SI\">K</a>., and has conditional marketing authorization in the EU for BCG-unresponsive NMIBC with carcinoma in situ, with or without papillary tumors.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<em>Disclaimer: <span>This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Immunitybio Inc. published the original content used to generate this news brief via Business Wire (Ref. 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The findings, published in the January 2026 edition of The Journal of Urology, also indicate favorable outcomes in disease-free survival, progression-free survival, and high rates of cystectomy avoidance, with the median to cystectomy not yet reached. Safety data revealed a 3% incidence of grade 3 treatment-related adverse events, with no grade 4 or 5 events reported. ANKTIVA is currently approved in the U.S., U.<a href=\"https://laohu8.com/S/TKKD.SI\">K</a>., and has conditional marketing authorization in the EU for BCG-unresponsive NMIBC with carcinoma in situ, with or without papillary tumors.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<em>Disclaimer: <span>This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Immunitybio Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20251216185945) on December 16, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"BK4139","symbol_name":"生物科技","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251216:nNDL6Qm9P:1","article_id":"2591803539","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2591803539","pubTimestamp":1765893704,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"ImmunityBio, Inc. announced new clinical study results demonstrating that treatment with ANKTIVA  in combination with Bacillus Calmette-Guérin  shows a 96% bladder cancer-specific survival rate at three years in patients with BCG-unresponsive high-grade papillary-only non-muscle invasive bladder cancer . The findings, published in the January 2026 edition of The Journal of Urology, also indicate favorable outcomes in disease-free survival, progression-free survival, and high rates of cystectomy avoidance, with the median to cystectomy not yet reached. Safety data revealed a 3% incidence of grade 3 treatment-related adverse events, with no grade 4 or 5 events reported. ANKTIVA is currently approved in the U.S., U.K., and has conditional marketing authorization in the EU for BCG-unresponsive NMIBC with carcinoma in situ, with or without papillary tumors.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. 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The findings, published in the January 2026 edition of The Journal of Urology, also indicate favorable outcomes in disease-free survival, progression-free survival, and high rates of cystectomy avoidance, with the median to cystectomy not yet reached. Safety data revealed a 3% incidence of grade 3 treatment-related adverse events, with no grade 4 or 5 events reported. ANKTIVA is currently approved in the U.S., U.K., and has conditional marketing authorization in the EU for BCG-unresponsive NMIBC with carcinoma in situ, with or without papillary tumors.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Immunitybio Inc. published the original content used to generate this news brief via Business Wire (Ref. 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