Tryptamine Therapeutics Advances Psilocin-Based IV Infusion To Phase 2 Clinical Trials
Tryptamine Therapeutics Advances Psilocin-Based IV Infusion To Phase 2 Clinical Trials
Tryptamine Therapeutics Ltd (OTC:TYPTF) has announced that its lead asset, TRP-8803, a psilocin-based IV infusion, will progress to Phase 2 clinical trials following a successful Phase 1b study. TRP-8803 demonstrated significant advantages over oral psilocybin, including rapid onset, precise control of the psychedelic state and the ability to halt treatment if adverse events occur, enhancing patient safety.
Tryptamine Therapeutics Ltd (OTC:TYPTF)宣佈,其主力資產TRP-8803,一種基於哌幻基的靜脈注射液,將在成功進行第10億階段研究後進入第2期臨床試驗。TRP-8803相對口服哌喹比有顯著優勢,包括快速發作、對迷幻狀態的精確控制以及在出現不良事件時停止治療的能力,提高了患者的安全性。
Phase 1b Achievements
第10億階段成就
TRP-8803 was well-tolerated across all tested doses—low, mid and high—demonstrating its safety profile. The study identified optimal doses and infusion rates that maintained psilocin blood levels within the therapeutic range. Additionally, TRP-8803 achieved steady and controlled blood levels, outperforming oral psilocybin formulations in terms of consistency.
TRP-8803在所有經過測試的劑量(低、中、高)中都具有良好的耐受性,表現出其安全性。該研究確定了維持哌幻血藥濃度在治療範圍內的最佳劑量和輸注速率。此外,TRP-8803實現了穩定和受控的血藥濃度,表現出在一致性方面優於口服哌喹製劑。
Participants experienced a rapid onset of the psychedelic state, much faster than the typical one- to two-hour delay with oral psilocybin. "To have achieved these positive results from our Phase 1b for TRP-8803 study so quickly has exceeded all expectations," said Tryptamine CEO Jason Carroll.
參與者體驗到了快速的迷幻狀態發作,比口服哌喹通常需要一到兩個小時的延遲快得多。Tryptamine首席執行官傑森·卡羅爾表示:「能夠如此迅速地從我們對TRP-8803進行的第10億階段研究中取得這些積極結果已經超出了所有的預期。」
Path To Phase 2
第2期之路
Armed with a robust proprietary dataset, Tryptamine is preparing to advance TRP-8803 to active patient studies. Phase 2 trials will target specific therapeutic indications, with planning already underway. Carroll highlighted the importance of these findings, stating, "Tryp has now established the strong foundations essential to advance our world-first trials for IV-infused psilocin to the highest standards of safety, quality and integrity."
憑藉強大的專有數據集,Tryptamine正準備將TRP-8803推進至積極的患者研究。第2期試驗將針對特定的治療指標,計劃已經在進行中。卡羅爾強調了這些發現的重要性,稱:「Tryp現已確立了推進IV注射哌幻進行世界首例試驗所必不可少的堅實基礎,達到最高安全、質量和完整性標準。」
TRP-8803: A Transformative Approach
TRP-8803:一種變革性方法
TRP-8803 offers multiple advantages over traditional oral psilocybin. It provides faster onset, precise control over treatment duration and reversibility, enabling clinicians to halt therapy immediately if necessary. These features make the treatment safer and more commercially viable while reducing the overall duration of therapy. By promoting neuroplasticity, TRP-8803 aims to drive adaptive structural and functional changes in the brain, solidifying Tryptamine's position at the forefront of psychedelic medical innovation.
TRP-8803相對傳統口服哌喹具有多重優勢。它提供更快的發作時間、對治療時間的精確控制和可逆性,使臨床醫生可以立即停止療法。這些特點使治療更安全、更具商業可行性,同時縮短了整體療程時間。通過促進神經可塑性,TRP-8803旨在驅動大腦的適應性結構和功能變化,鞏固Tryptamine在迷幻醫學創新前沿的地位。
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譯文內容由第三人軟體翻譯。