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MAIA Biotechnology's Lung Cancer Drug Shows Promising Long-Term Benefits In Advanced Patients

MAIA Biotechnology's Lung Cancer Drug Shows Promising Long-Term Benefits In Advanced Patients

MAIA生物技术的肺癌药物在晚期患者中显示出有希望的长期益处
Benzinga ·  07/23 10:38

On Tuesday, MAIA Biotechnology Inc (NASDAQ:MAIA) announced treatment updates from its Phase 2 THIO-101 trial of THIO sequenced with Regeneron Pharmaceuticals Inc's (NASDAQ:REGN) cemiplimab (Libtayo) for advanced non-small-cell-lung-cancer patients who failed two or more standard-of-care therapy regimens.

MAIA生物技术公司(纳斯达克股票代码:MAIA)在周二公布了从其第二期THIO-101试验的治疗更新中获得的消息,该试验将THIO与再生元制药公司(纳斯达克股票代码:REGN)的Cemiplimab(Libtayo)用于治疗晚期非小细胞肺癌患者,其治疗失败了两个或更多的标准疗法方案。

The trial's therapeutic regimen is cycled every three weeks, with THIO 180mg administered in 60mg incremental doses on days 1, 2 and 3, followed by immune activation on day 4 (no dosing), and cemiplimab 350mg administered on day 5.

该试验的治疗方案每三周循环一次,在第1、2和3天分3次口服THIO 180mg,第4天进行免疫激活(不用药物),第5天注射Cemiplimab 350mg。

As of the latest clinical cutoff date, June 12, 2024:

截至2024年6月12日最新的临床截止日期,仍有6名患者在治疗中,在接受至少12个月的治疗后。

  • Six patients remain on treatment following at least 12 months of therapy.
  • Treatment with THIO followed by cemiplimab has been well tolerated throughout the trial, with much lower toxicity than standard-of-care treatments.
  • Continuing treatment past 12 months demonstrates safety, efficacy and ongoing benefit from MAIA's novel telomere targeting NSCLC therapy.
  • 在至少接受12个月治疗后,有6名患者仍在接受治疗。
  • 与标准治疗相比,THIO后随Cemiplimab的治疗在整个试验期间都很耐受,毒副反应明显降低。
  • 延续治疗超过12个月,可以证明MAIA的新型端粒靶向NSCLC疗法有安全性、疗效和持续的好处。

"Our longest treated patient so far has completed 21 cycles of THIO sequenced with a CPI, and six patients who have crossed the 12-month survival follow-up are continuing the treatment," said Vlad Vitoc, chairman and chief executive officer of MAIA.

MAIA的董事长兼首席执行官Vlad Vitoc表示:“到目前为止,我们最长治疗的患者完成了THIO和CPI 21个疗程的顺序治疗,六名已经接受了12个月以上的随访,继续治疗。”

In June, MAIA Biotechnology shared new efficacy data from its Phase 2 THIO-101 study of THIO.

今年6月,MAIA生物技术公司分享了THIO-101第二期研究的新的疗效数据。

Updated results show a favorable overall response rate (ORR) of 38% and a disease control rate (DCR) of 85% from THIO + CPI in third-line treatment:

更新后的结果显示,第三线治疗中THIO + CPI显示出38%的相对疗效率(ORR)和85%的疾病控制率(DCR):

  • The disease control rate (DCR) was 85% for THIO vs. standard of care DCR of 25–35% for chemotherapy.
  • 65% of patients crossed the 5.8-month overall survival (OS) threshold.
  • 85% of patients crossed the 2.5-month progression-free survival (PFS) threshold.
  • Median survival follow-up time is currently 9.1 months (n=20)
  • THIO的疾病控制率(DCR)为85%,化疗的标准疾病控制率(DCR)为25-35%。
  • 65%的患者跨越了5.8个月的总生存期(OS)门槛。
  • 85%的患者跨越了2.5个月的无进展生存期(PFS)门槛。
  • 目前的中位生存期为9.1个月(n=20)。

Price Action: MAIA stock is down 14.25% at $3.31 at last check Tuesday.

价格变动:截至上周二的最后查看,MAIA股票下跌了14.25%,至3.31美元。

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Image created using artificial intelligence via Midjourney.

图像由Midjourney通过人工智能创建。

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