Indaptus Therapeutics Provides 2025 Outlook, Launching Decoy20 Combination Cohort With BeiGene's Tislelizumab, Expanding Clinical Sites Beyond 8, Updating Higher Dose Cohort, First Patient Dosed In Combination, Focus On Cancer Challenges
Indaptus Therapeutics Provides 2025 Outlook, Launching Decoy20 Combination Cohort With BeiGene's Tislelizumab, Expanding Clinical Sites Beyond 8, Updating Higher Dose Cohort, First Patient Dosed In Combination, Focus On Cancer Challenges
2025 Outlook
2025年展望
Jeffrey Meckler, CEO of Indaptus Therapeutics, commented, "As we enter 2025, we remain committed to advancing Decoy20 through clinical trials and exploring its combination potential with BeiGene's tislelizumab. We are excited about the progress we made in 2024 and optimistic about the transformative potential of our platform to address some of the most challenging cancers."
Indaptus Therapeutics的首席执行官Jeffrey Meckler评论道:"随着我们进入2025年,我们仍然致力于通过临床试验推进Decoy20,并探索其与百济神州的tislelizumab的联合潜力。我们对2024年取得的进展感到兴奋,并对我们平台在应对一些最具挑战性的癌症方面的变革潜力持乐观态度。"
Indaptus intends to maintain its commitment to robust data generation, with plans to share new findings at leading scientific forums as they become available, while actively pursuing opportunities to expand the applications of its Decoy platform.
Indaptus打算继续致力于稳健的数据生成,计划在新的发现可用时在领先的科学论坛上分享,同时积极寻求机会扩大其Decoy平台的应用。
The Company currently anticipates that it will achieve the following milestones in the first half of 2025:
公司目前预计在2025年上半年实现以下里程碑:
- Launch of Combination Cohort: The Company plans to open an amendment to its clinical trial to include a combination cohort evaluating Decoy20 in conjunction with the PD-1 checkpoint inhibitor, tislelizumab.
- Expansion of Clinical Sites: Building on its progress in 2024, the Company intends to increase the number of participating clinical sites beyond the eight active locations at the end of last year, enabling broader patient enrollment.
- Higher Dose Cohort Update: The Company plans to provide an update on the patients treated in the higher dose expansion cohort, providing insights into safety and immune activation at this dose level.
- First Patient Dosed in Combination Cohort: The Company aims to start dosing the first patients in the combination cohort, marking an important step in evaluating Decoy20's synergistic potential with checkpoint inhibitors.
- 联合队列的启动:公司计划开放临床试验的修订,增加一个联合队列,评估与PD-1检查点抑制剂tislelizumab联合使用的Decoy20。
- 临床地点扩展:基于2024年取得的进展,公司打算在去年的八个活跃地点之外增加参与的临床地点数量,从而使更多患者能够入组。
- 高剂量组更新:公司计划提供高剂量扩展组中接受治疗患者的更新,提供关于该剂量水平的安全性和免疫激活的见解。
- 联合队列首位患者给药:公司旨在开始对联合队列的首批患者进行给药,这标志着评估Decoy20与检查点抑制剂协同潜力的重要一步。
The company believes these milestones, if achieved, will represent significant advancements in the clinical development of Decoy20 and the broader Decoy platform.
公司认为,如果这些里程碑能够实现,将代表Decoy20及更广泛的Decoy平台在临床开发方面的重要进展。
译文内容由第三方软件翻译。