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IBRX ImmunityBio, Inc.
交易中 02-24 10:06:43 EST
10.28
+0.45
+4.57%
最高
10.84
最低
9.95
成交量
1,421万
今开
10.15
昨收
9.83
日振幅
9.01%
总市值
105.67亿
流通市值
34.54亿
总股本
10.28亿
成交额
1.47亿
换手率
4.23%
流通股本
3.36亿
市净率
--
ROE
--
每股收益
0.00
52周最高
--
52周最低
--
市盈率
--
股息
--
股息收益率
--
ROA
--
分时
五日
日K
周K
月K
数据加载中...
北京优虎网络科技有限公司
资讯
新帖
简况
ImmunityBio, Inc. 年营收同比飙升700%,Anktiva®获肺癌适应症扩展批准,并与33国达成全球商业合作及标签扩展计划
美股速递 · 02-23 20:01
ImmunityBio, Inc. 年营收同比飙升700%,Anktiva®获肺癌适应症扩展批准,并与33国达成全球商业合作及标签扩展计划
ImmunityBio携手Biopharma与Cigalah Healthcare在沙特阿拉伯推出Anktiva®,惠及膀胱癌与肺癌患者
美股速递 · 02-20
ImmunityBio携手Biopharma与Cigalah Healthcare在沙特阿拉伯推出Anktiva®,惠及膀胱癌与肺癌患者
ImmunityBio携手新分销伙伴拓展Anktiva®欧盟市场 并成立爱尔兰子公司支持欧洲上市
美股速递 · 02-19
ImmunityBio携手新分销伙伴拓展Anktiva®欧盟市场 并成立爱尔兰子公司支持欧洲上市
ImmunityBio获欧盟委员会批准Anktiva®联合BCG治疗非肌层浸润性膀胱癌原位癌,全球准入范围扩至33国
美股速递 · 02-18
ImmunityBio获欧盟委员会批准Anktiva®联合BCG治疗非肌层浸润性膀胱癌原位癌,全球准入范围扩至33国
Immunitybio, Inc.盘中异动 早盘股价大涨5.47%
市场透视 · 02-17
Immunitybio, Inc.盘中异动 早盘股价大涨5.47%
ImmunityBio启动ANKTIVA®联合CAR-NK细胞疗法2期临床试验,探索无化疗方案治疗惰性淋巴瘤
美股速递 · 02-02
ImmunityBio启动ANKTIVA®联合CAR-NK细胞疗法2期临床试验,探索无化疗方案治疗惰性淋巴瘤
ImmunityBio, Inc.临床试验:三名受试者出现疑似与实验疗法相关的严重不良事件
美股速递 · 01-23
ImmunityBio, Inc.临床试验:三名受试者出现疑似与实验疗法相关的严重不良事件
ImmunityBio公布:接受Anktiva®联合CAR-NK无化疗疗法的复发性胶质母细胞瘤患者中位总生存期尚未达到,淋巴细胞减少症得以逆转
美股速递 · 01-23
ImmunityBio公布:接受Anktiva®联合CAR-NK无化疗疗法的复发性胶质母细胞瘤患者中位总生存期尚未达到,淋巴细胞减少症得以逆转
异动解读 | ImmunityBio盘中大跌10.11%,因FDA要求提供膀胱癌药物更广泛应用信息
异动解读 · 01-21
异动解读 | ImmunityBio盘中大跌10.11%,因FDA要求提供膀胱癌药物更广泛应用信息
异动解读 | ImmunityBio盘前大跌5.09%,因FDA要求提供膀胱癌药物更广泛应用信息
异动解读 · 01-21
异动解读 | ImmunityBio盘前大跌5.09%,因FDA要求提供膀胱癌药物更广泛应用信息
异动解读 | ImmunityBio夜盘大跌5.25%,因FDA要求提供膀胱癌药物更广泛应用信息
异动解读 · 01-21
异动解读 | ImmunityBio夜盘大跌5.25%,因FDA要求提供膀胱癌药物更广泛应用信息
异动解读 | ImmunityBio盘中大涨31.34%,因膀胱癌药物Anktiva获FDA进一步审核
异动解读 · 01-20
异动解读 | ImmunityBio盘中大涨31.34%,因膀胱癌药物Anktiva获FDA进一步审核
异动解读 | ImmunityBio盘中大涨29.50%,多款癌症疗法临床试验数据积极
异动解读 · 01-16
异动解读 | ImmunityBio盘中大涨29.50%,多款癌症疗法临床试验数据积极
ImmunityBio股价盘前飙升23.8%,公司公布罕见血癌疗法积极数据
美股速递 · 01-16
ImmunityBio股价盘前飙升23.8%,公司公布罕见血癌疗法积极数据
ImmunityBio推进一线BCG初治NMIBC项目 患者入组超预期且Anktiva®联合BCG中期分析结果积极
美股速递 · 01-16
ImmunityBio推进一线BCG初治NMIBC项目 患者入组超预期且Anktiva®联合BCG中期分析结果积极
FDA要求的中期分析显示:Anktiva联合BCG疗法显著延长完全缓解持续时间
美股速递 · 01-16
FDA要求的中期分析显示:Anktiva联合BCG疗法显著延长完全缓解持续时间
Immunitybio, Inc.盘中异动 股价大涨5.30%
市场透视 · 01-15
Immunitybio, Inc.盘中异动 股价大涨5.30%
沙特FDA加速批准ImmunityBio的Anktiva®联合检查点抑制剂治疗转移性非小细胞肺癌
美股速递 · 01-14
沙特FDA加速批准ImmunityBio的Anktiva®联合检查点抑制剂治疗转移性非小细胞肺癌
ImmunityBio公司Anktiva针对BCG初治NMIBC患者的随机试验入组进度超前 预计2026年第二季度完成全部入组
美股速递 · 01-14
ImmunityBio公司Anktiva针对BCG初治NMIBC患者的随机试验入组进度超前 预计2026年第二季度完成全部入组
沙特药监局加速批准ImmunityBio的Anktiva®用于治疗伴有原位癌的非肌层浸润性膀胱癌
美股速递 · 01-14
沙特药监局加速批准ImmunityBio的Anktiva®用于治疗伴有原位癌的非肌层浸润性膀胱癌
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公司概况
公司名称:
ImmunityBio, Inc.
所属市场:
NASDAQ
上市日期:
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主营业务:
ImmunityBio, Inc.于2002年10月7日在伊利诺伊州ZelleRx Corporation公司的名义下注册成立,于2010年1月22日,公司更名为Conkwest股份有限公司。ImmunityBio是一家领先的晚期免疫治疗公司,可激活先天和适应性免疫系统,以治疗肿瘤学和传染病领域内严重未满足的需求。公司是一家领先的临床剂型的现成自然杀伤细胞疗法生产商,记忆NK细胞,连同抗体细胞因子融合蛋白、白蛋白结合化学免疫调节剂和疫苗载体的综合平台。通过结合这些NK、巨噬细胞和T细胞激活平台,该公司相信ImmunityBio在免疫治疗领域处于领先地位,具有跨越多种肿瘤类型和传染病的后期临床开发。
发行价格:
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Inc.宣布通过新的分销合作扩大其创新药物Anktiva®在欧盟地区的可及性,同时正式成立爱尔兰子公司,为产品在欧洲市场的全面推广提供战略支持。这一系列举措标志着该公司在欧洲商业化布局的重要里程碑。\n新建立的合作伙伴关系将有效提升Anktiva®在欧盟各国的分销效率,确保患者能够及时获得这一前沿疗法。爱尔兰子公司的设立将进一步强化本地化运营能力,为欧洲市场提供更精准的临床支持和商业化服务。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"1157842511","title":"ImmunityBio获欧盟委员会批准Anktiva®联合BCG治疗非肌层浸润性膀胱癌原位癌,全球准入范围扩至33国","url":"https://stock-news.laohu8.com/highlight/detail?id=1157842511","media":"美股速递","labels":["corporation"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1157842511?lang=zh_cn&edition=full","pubTime":"2026-02-18 22:01","pubTimestamp":1771423277,"startTime":"0","endTime":"0","summary":"ImmunityBio, Inc.(纳斯达克代码:IBRX)宣布,其创新疗法Anktiva®(nogapendekin alfa inbakicept)联合卡介苗(BCG)已获得欧盟委员会批准,用于治疗非肌层浸润性膀胱癌(NMIBC)的原位癌(CIS)患者。此项授权标志着该疗法在欧洲经济区(EEA)的30个成员国以及冰岛、列支敦士登和挪威共33个国家获得上市许可,将显著提升全球患者对该前沿治疗方案的获取机会。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"2612414397","title":"Immunitybio, Inc.盘中异动 早盘股价大涨5.47%","url":"https://stock-news.laohu8.com/highlight/detail?id=2612414397","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2612414397?lang=zh_cn&edition=full","pubTime":"2026-02-17 22:30","pubTimestamp":1771338627,"startTime":"0","endTime":"0","summary":"北京时间2026年02月17日22时30分,Immunitybio, Inc.股票出现波动,股价急速上涨5.47%。Immunitybio, Inc.股票所在的生物技术行业中,整体涨幅为0.00%。Immunitybio, Inc.公司简介:ImmunityBio Inc是一家综合性临床阶段生物技术公司,致力于发现、开发和商业化下一代免疫和细胞疗法,以增强自然免疫系统,从而驱动和维持免疫反应。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20260217223027a4ad8529&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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Inc.(纳斯达克代码:IBRX)近日宣布启动一项2期临床研究,评估其核心产品ANKTIVA®(通用名resq215b)与嵌合抗原受体自然杀伤细胞(CAR-NK)疗法联合用于惰性淋巴瘤治疗的潜力。该试验的创新之处在于采用完全无化疗的治疗策略,旨在通过生物免疫疗法精准靶向肿瘤细胞,减少传统化疗带来的毒副作用。若研究结果积极,有望为惰性淋巴瘤患者提供更安全、耐受性更高的治疗选择。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"1198499689","title":"ImmunityBio, Inc.临床试验:三名受试者出现疑似与实验疗法相关的严重不良事件","url":"https://stock-news.laohu8.com/highlight/detail?id=1198499689","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1198499689?lang=zh_cn&edition=full","pubTime":"2026-01-23 20:03","pubTimestamp":1769169797,"startTime":"0","endTime":"0","summary":"在ImmunityBio, Inc.进行的一项临床研究中,有三名参与试验的受试者报告出现了严重不良事件。目前,这些事件被怀疑与该公司所研发的实验性疗法存在关联。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"1154477526","title":"ImmunityBio公布:接受Anktiva®联合CAR-NK无化疗疗法的复发性胶质母细胞瘤患者中位总生存期尚未达到,淋巴细胞减少症得以逆转","url":"https://stock-news.laohu8.com/highlight/detail?id=1154477526","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1154477526?lang=zh_cn&edition=full","pubTime":"2026-01-23 20:01","pubTimestamp":1769169688,"startTime":"0","endTime":"0","summary":"ImmunityBio公司最新报告显示,在采用Anktiva®联合CAR-NK细胞疗法的复发性胶质母细胞瘤患者中,中位总生存期数据尚未达到可统计的终点。这一无化疗治疗方案不仅展现出延长生存期的潜力,更值得注意的是,患者先前存在的淋巴细胞减少症出现了显著逆转。\n该疗法通过激活患者自身的免疫系统对抗肿瘤,为传统治疗手段效果有限的脑癌患者提供了新的希望。淋巴细胞计数的恢复表明免疫功能得到改善,这可能为提升抗肿瘤疗效奠定基础。\n研究结果凸显了Anktiva®与CAR-NK联合疗法的双重优势:既可能延长生存期,又能逆转化疗常见副作用带来的免疫抑制状态。这一突破性进展为晚期脑癌治疗开辟了全新路径。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"1124337225","title":"异动解读 | ImmunityBio盘中大跌10.11%,因FDA要求提供膀胱癌药物更广泛应用信息","url":"https://stock-news.laohu8.com/highlight/detail?id=1124337225","media":"异动解读","labels":["movement"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1124337225?lang=zh_cn&edition=full","pubTime":"2026-01-21 22:33","pubTimestamp":1769005984,"startTime":"0","endTime":"0","summary":"ImmunityBio, Inc.(IBRX)今日盘中股价大跌10.11%,引发了市场的广泛关注。消息面上,美国食品和药物管理局(FDA)要求该公司提供更多信息,以支持其膀胱癌药物Anktiva在更广泛患者群体中的使用申请。这一请求可能引发了投资者对审批进程延迟或额外要求的担忧,从而导致股价大幅下跌。ImmunityBio表示,FDA并未要求进行新的临床试验,但需要补充某些信息以支持重新提交的申请。公司计划在未来30天内提交所需信息。","market":"nz","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"movement","news_rank":0,"length":0,"strategy_id":0,"source":"ai_movement_cn","symbols":["IBRX"],"gpt_icon":0},{"id":"1123640335","title":"异动解读 | ImmunityBio盘前大跌5.09%,因FDA要求提供膀胱癌药物更广泛应用信息","url":"https://stock-news.laohu8.com/highlight/detail?id=1123640335","media":"异动解读","labels":["movement"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1123640335?lang=zh_cn&edition=full","pubTime":"2026-01-21 21:24","pubTimestamp":1769001860,"startTime":"0","endTime":"0","summary":"ImmunityBio, Inc.(IBRX)今日盘前股价大跌5.09%,引起了市场的广泛关注。消息面上,美国食品和药物管理局(FDA)要求该公司提供更多信息,以支持其膀胱癌药物Anktiva在更广泛患者群体中的使用申请。这一请求可能引发了投资者对审批进程延迟或额外要求的担忧,从而导致股价下跌。ImmunityBio表示,FDA并未要求进行新的临床试验,但需要补充某些信息以支持重新提交的申请。公司计划在未来30天内提交所需信息。","market":"sg","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"movement","news_rank":0,"length":0,"strategy_id":0,"source":"ai_movement_cn","symbols":["IBRX"],"gpt_icon":0},{"id":"1160682901","title":"异动解读 | ImmunityBio夜盘大跌5.25%,因FDA要求提供膀胱癌药物更广泛应用信息","url":"https://stock-news.laohu8.com/highlight/detail?id=1160682901","media":"异动解读","labels":["movement"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1160682901?lang=zh_cn&edition=full","pubTime":"2026-01-21 09:32","pubTimestamp":1768959164,"startTime":"0","endTime":"0","summary":"ImmunityBio, Inc.(IBRX)今日夜盘股价大跌5.25%,引起了市场的关注。消息面上,美国食品和药物管理局(FDA)要求该公司提供更多信息,以支持其膀胱癌药物Anktiva在更广泛患者群体中的使用申请。这一请求可能引发了投资者对审批进程延迟或额外要求的担忧,从而导致股价下跌。ImmunityBio表示,FDA并未要求进行新的临床试验,但需要补充某些信息以支持重新提交的申请。公司计划在未来30天内提交所需信息。","market":"nz","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"movement","news_rank":0,"length":0,"strategy_id":0,"source":"ai_movement_cn","symbols":["IBRX"],"gpt_icon":0},{"id":"1176958641","title":"异动解读 | ImmunityBio盘中大涨31.34%,因膀胱癌药物Anktiva获FDA进一步审核","url":"https://stock-news.laohu8.com/highlight/detail?id=1176958641","media":"异动解读","labels":["movement"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1176958641?lang=zh_cn&edition=full","pubTime":"2026-01-20 23:10","pubTimestamp":1768921821,"startTime":"0","endTime":"0","summary":"ImmunityBio(IBRX)今日盘中股价大幅上涨31.34%,成为市场焦点。消息面上,该公司宣布准备重新向美国食品药品监督管理局(FDA)提交申请,寻求批准其膀胱癌药物Anktiva用于更广泛的患者群体。FDA要求提供更多信息但未要求新试验,公司计划30天内完成提交。长期数据显示,几乎所有接受Anktiva联合卡介苗治疗的患者存活至少三年,超80%保留膀胱避免手术。这一进展显著提升了市场对药物商业化前景的预期。","market":"nz","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"c6432e252784cc64192d8c0a1d7cc58c","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"movement","news_rank":0,"length":0,"strategy_id":0,"source":"ai_movement_cn","symbols":["IBRX"],"gpt_icon":0},{"id":"1182603474","title":"异动解读 | ImmunityBio盘中大涨29.50%,多款癌症疗法临床试验数据积极","url":"https://stock-news.laohu8.com/highlight/detail?id=1182603474","media":"异动解读","labels":["movement"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1182603474?lang=zh_cn&edition=full","pubTime":"2026-01-16 23:14","pubTimestamp":1768576471,"startTime":"0","endTime":"0","summary":"ImmunityBio, Inc.今日盘中大涨29.50%,创下近期新高。消息面上,公司公布了多款癌症疗法的积极临床试验数据。其中,针对一线BCG初治非肌层浸润性膀胱癌的Anktiva与BCG联合疗法中期分析结果积极,患者入组人数超出预期。公司还公布了罕见血癌疗法的积极数据,进一步提振了投资者信心。这些突破性成果不仅展现了ImmunityBio在癌症治疗领域的创新能力,也为后续监管审批和商业化奠定了坚实基础。","market":"nz","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"movement","news_rank":0,"length":0,"strategy_id":0,"source":"ai_movement_cn","symbols":["IBRX"],"gpt_icon":0},{"id":"1189285578","title":"ImmunityBio股价盘前飙升23.8%,公司公布罕见血癌疗法积极数据","url":"https://stock-news.laohu8.com/highlight/detail?id=1189285578","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1189285578?lang=zh_cn&edition=full","pubTime":"2026-01-16 20:20","pubTimestamp":1768566020,"startTime":"0","endTime":"0","summary":"ImmunityBio, Inc. (纳斯达克代码: IBRX) 股价在盘前交易时段大幅攀升23.8%,此前该公司公布了其针对一种罕见血癌的疗法的临床试验结果。\n这一显著涨幅反映了市场对该疗法积极数据的乐观反应。公司披露的详细结果显示,其在研疗法在临床试验中取得了令人鼓舞的成效,为治疗这种罕见血液癌症带来了新的希望。\n消息公布后,投资者信心得到提振,推动该股在盘前交易中表现强劲。市场正密切关注该疗法的后续进展及其对ImmunityBio未来业绩的潜在影响。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"1152780615","title":"ImmunityBio推进一线BCG初治NMIBC项目 患者入组超预期且Anktiva®联合BCG中期分析结果积极","url":"https://stock-news.laohu8.com/highlight/detail?id=1152780615","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1152780615?lang=zh_cn&edition=full","pubTime":"2026-01-16 20:09","pubTimestamp":1768565391,"startTime":"0","endTime":"0","summary":"ImmunityBio公司宣布,其针对一线BCG初治非肌层浸润性膀胱癌的研发项目取得显著进展。目前患者入组人数已超出预期目标,同时Anktiva®与BCG联合疗法的中期分析显示出积极结果。这一里程碑为后续临床开发奠定了坚实基础。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"1117568591","title":"FDA要求的中期分析显示:Anktiva联合BCG疗法显著延长完全缓解持续时间","url":"https://stock-news.laohu8.com/highlight/detail?id=1117568591","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1117568591?lang=zh_cn&edition=full","pubTime":"2026-01-16 20:03","pubTimestamp":1768565029,"startTime":"0","endTime":"0","summary":"ImmunityBio, Inc.近期公布的一项由美国食品药品监督管理局(FDA)要求进行的中期分析结果显示,其研发的Anktiva联合BCG(卡介苗)治疗方案在临床试验中表现出统计学上显著的更长完全缓解持续时间。\n这一发现为膀胱癌等疾病的治疗提供了新的希望,凸显了联合疗法在提升患者临床获益方面的潜力。数据进一步证实,Anktiva与BCG的组合可能改善患者的长期治疗效果,为后续监管审批和临床应用奠定重要基础。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"2603962227","title":"Immunitybio, Inc.盘中异动 股价大涨5.30%","url":"https://stock-news.laohu8.com/highlight/detail?id=2603962227","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2603962227?lang=zh_cn&edition=full","pubTime":"2026-01-15 22:32","pubTimestamp":1768487535,"startTime":"0","endTime":"0","summary":"北京时间2026年01月15日22时32分,Immunitybio, Inc.股票出现波动,股价快速拉升5.30%。Immunitybio, Inc.股票所在的生物技术行业中,整体涨幅为0.24%。Immunitybio, Inc.公司简介:ImmunityBio Inc是一家综合性临床阶段生物技术公司,致力于发现、开发和商业化下一代免疫和细胞疗法,以增强自然免疫系统,从而驱动和维持免疫反应。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN2026011522321597a1fc59&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, .wx-sou","directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN2026011522321597a1fc59&s=b","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tencent","symbols":["BK4139","IBRX"],"gpt_icon":0},{"id":"1151783482","title":"沙特FDA加速批准ImmunityBio的Anktiva®联合检查点抑制剂治疗转移性非小细胞肺癌","url":"https://stock-news.laohu8.com/highlight/detail?id=1151783482","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1151783482?lang=zh_cn&edition=full","pubTime":"2026-01-14 21:36","pubTimestamp":1768397772,"startTime":"0","endTime":"0","summary":"沙特食品药品监督管理局(FDA)已对ImmunityBio, Inc.(纳斯达克代码:IBRX)旗下免疫疗法药物Anktiva®授予加速审批资格,批准其与检查点抑制剂联合用于治疗转移性非小细胞肺癌(NSCLC)患者。此项决定标志着该创新组合疗法在沙特阿拉伯监管流程中的关键进展,为晚期肺癌患者提供了新的潜在治疗选择。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"1121956771","title":"ImmunityBio公司Anktiva针对BCG初治NMIBC患者的随机试验入组进度超前 预计2026年第二季度完成全部入组","url":"https://stock-news.laohu8.com/highlight/detail?id=1121956771","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1121956771?lang=zh_cn&edition=full","pubTime":"2026-01-14 21:33","pubTimestamp":1768397603,"startTime":"0","endTime":"0","summary":"ImmunityBio公司宣布,其针对BCG初治型非肌层浸润性膀胱癌患者开展的Anktiva随机试验,目前患者入组进度较原计划大幅超前。根据最新时间表,这项重要临床研究预计将于2026年第二季度完成全部患者招募工作。\n该试验旨在评估Anktiva在BCG未接受过的NMIBC患者群体中的疗效与安全性。研究进度的加速推进,为早日获得关键临床数据奠定了坚实基础,也反映出医疗界对该创新疗法的积极参与和高度期待。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IBRX","BK4139"],"gpt_icon":0},{"id":"1159820089","title":"沙特药监局加速批准ImmunityBio的Anktiva®用于治疗伴有原位癌的非肌层浸润性膀胱癌","url":"https://stock-news.laohu8.com/highlight/detail?id=1159820089","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1159820089?lang=zh_cn&edition=full","pubTime":"2026-01-14 21:30","pubTimestamp":1768397421,"startTime":"0","endTime":"0","summary":"沙特食品和药物管理局(Saudi FDA)已对ImmunityBio, Inc.(纳斯达克代码:IBRX)旗下创新疗法Anktiva®予以加速审批通过。该药物获批适应症为伴随原位癌(Carcinoma 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