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Phio Pharmaceuticals Announces Positive Recommendation From Safety Monitoring Committee (SMC) of Phase 1b Clinical Study of Phio's Lead Compound PH-762

Phio Pharmaceuticals Announces Positive Recommendation From Safety Monitoring Committee (SMC) of Phase 1b Clinical Study of Phio's Lead Compound PH-762

Phio Pharmicals 宣佈安全監測委員會 (SMC) 對 Phio 的先導化合物 PH-762 的 1b 期臨床研究提出積極建議
Phio Pharmaceuticals ·  05/28 12:00
  • Intratumoral PH-762 has encouraging safety profile in the initial cohort

  • Escalation to proceed to next dose concentration

  • 腫瘤內pH-762在最初的隊列中有令人鼓舞的安全性表現。

  • 逐步提高到下一個劑量濃度。

Marlborough, Massachusetts–(Newsfile Corp. – May 28, 2024) – Phio Pharmaceuticals Corp. (NASDAQ: PHIO), a clinical stage biotechnology company whose proprietary INTASYL siRNA gene silencing technology is designed to make immune cells more effective in killing tumor cells, today announced that a Safety Monitoring Committee (SMC) reviewed safety data from the first dose cohort treated in the Phase 1b clinical trial with Phio's lead compound PH-762. Based on these findings, the SMC recommended the escalation to the next dose concentration.

瑪爾伯勒,馬薩諸塞州-(新聞稿公司-2024年5月28日)-Phio生物製藥公司(NASDAQ:PHIO)是一家臨床階段的生物技術公司,其專有的INTASYL siRNA基因沉默技術旨在使免疫細胞更有效地殺滅腫瘤細胞,今天宣佈,一個安全監測委員會(SMC)查閱了在Phio的首席複合物PH-762的1b期臨床試驗中接受治療的第一劑量隊列的安全數據。根據這些發現,SMC建議提高下一劑量濃度。

Phio's ongoing Phase 1b clinical study (NCT 06014086) is designed to evaluate the safety and tolerability of neoadjuvant use of intratumoral PH-762 in Stages 1, 2 and 4 cutaneous squamous cell carcinoma, Stage 4 melanoma and Stage 4 Merkel cell carcinoma.

Phio正在進行的1b期臨床研究(NCT 06014086)旨在評估劑量給藥的腫瘤內PH-762在1級、2級和4級皮膚鱗癌、4級黑色素瘤和4級默克爾細胞癌中的安全性和耐受性 。

There have been no dose-limiting toxicities, or clinically relevant treatment-emergent adverse events in the initial cohort receiving intratumoral PH-762. The intratumoral injections have been well tolerated. The SMC has recommended dose escalation and enrollment of the next planned cohort in the clinical study.

在接受腫瘤內PH-762的初始隊列中,沒有劑量限制的毒性或臨床相關的治療新出現的不良事件。腫瘤內注射耐受性良好。安全部建議升級劑量,並在臨床試驗中招募下一個計劃隊列。

"Safety and efficacy data from our clinical trial will establish the roadmap for continued development of PH-762," said Mary Spellman MD, Phio's acting Chief Medical Officer. "We are pleased with continued interest in the potential therapy and look forward to continued enrollment in the clinical study."

"我們的臨床試驗的安全性和有效性數據將爲PH-762的持續開發制定路線圖,"Phio的代理首席醫學官Mary Spellman MD說:"我們爲潛在療法的持續關注感到高興,並期待在臨床試驗中持續招募。"

About Phio Pharmaceuticals Corp.

關於Phio Pharmaceuticals Corp.

Phio Pharmaceuticals Corp. (Nasdaq: PHIO) is a clinical stage biotechnology company whose proprietary INTASYL siRNA gene silencing technology is designed to make immune cells more effective in killing tumor cells. INTASYL is the only self-delivering RNAi technology focused on immuno-oncology therapeutics. INTASYL drugs precisely target specific proteins that reduce the body's ability to fight cancer, without the need for specialized formulations or drug delivery systems.

Phio Pharmaceuticals Corp.(Nasdaq:PHIO)是一家處於臨床階段的生物技術公司,其專有的INTASYL siRNA基因沉默技術旨在使免疫細胞更有效地殺死腫瘤細胞。INTASYL是唯一專注於免疫腫瘤學治療的自交付RNAi技術。INTASYL藥物精確地靶向特定蛋白質,降低機體抗癌能力,無需專門的製劑或藥物輸送系統。

For additional information, visit the Company's website, www.phiopharma.com.

欲了解更多信息,請訪問公司網站:www.phiopharma.com.

Forward-Looking Statements

前瞻性聲明

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words such as "intends," "believes," "anticipates," "indicates," "plans," "expects," "suggests," "may," "would," "should," "potential," "designed to," "will," "ongoing," "estimate," "forecast," "target," "predict," "could" and similar references, although not all forward-looking statements contain these words. These statements are based only on our current beliefs, expectations and assumptions and are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of our control. Our actual results may differ materially from those indicated in the forward-looking statements as a result of a number of important factors, including, but not limited to, the impact to our business and operations by inflationary pressures, rising interest rates, recession fears, the development of our product candidates, results from our preclinical and clinical activities, our ability to execute on business strategies, our ability to develop our product candidates with collaboration partners, and the success of any such collaborations, the timeline and duration for advancing our product candidates into clinical development, the timing or likelihood of regulatory filings and approvals, the success of our efforts to commercialize our product candidates if approved, our ability to manufacture and supply our product candidates for clinical activities, and for commercial use if approved, the scope of protection we are able to establish and maintain for intellectual property rights covering our technology platform, our ability to obtain future financing, market and other conditions and those identified in our Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q under the caption "Risk Factors" and in other filings the Company periodically makes with the SEC. Readers are urged to review these risk factors and to not act in reliance on any forward-looking statements, as actual results may differ from those contemplated by our forward-looking statements. Phio does not undertake to update forward-looking statements to reflect a change in its views, events or circumstances that occur after the date of this release, except as required by law.

本新聞稿包含根據1995年《私人證券訴訟改革法》的前瞻性聲明。儘管並非所有前瞻性聲明都包含這些單詞,但是可以通過單詞"意圖"、"相信"、"預計"、"表明"、"計劃"、"期望"、"建議"、"可能"、"會"、"應該"、"潛在"、"旨在"、"將"、"正在進行"、"估計"、"預測"、"目標"、"預測"、"可能"等參考詞語進行識別。這些聲明僅基於我們當前的信仰、期望和假設,並且因困難預測和我們無法控制的固有不確定性、風險和情況的變化而面臨着天然的不確定性。由於多種重大因素,我們實際的結果可能與前瞻性聲明中指示的結果有所不同,其中包括但不限於通貨膨脹壓力、利率上升、經濟衰退擔憂、產品候選的發展結果、我們的臨床和臨床活動結果、我們落實業務戰略的能力,我們能否與合作伙伴共同開發產品候選及其成功,將我們的產品候選加速到臨床開發階段的時間或持續時間,提出監管申請和獲得批准的時間或可能性,如果獲得批准,成功投放市場的能力,製造和爲臨床活動提供及批准後的商業使用提供我們的產品候選的能力,我們能夠爲覆蓋技術平台的知識產權建立和維護的保護範圍,我們能夠獲得未來的融資,市場和其他條件,以及我們每年提交給SEC的年度報告10-K和後續季度報告10-Q中在"風險因素"中標識的條件和其他文件中發現的條件。敬請讀者仔細閱讀這些風險因素,並不依賴於任何前瞻性聲明,因爲實際結果可能與我們的前瞻性聲明所考慮的有所不同。Phio不承擔更新前瞻性聲明以反映本發佈日期後發生的觀點、事件或情況的責任,除非法律要求。

Contact:
Phio Pharmaceuticals Corp.
ir@phiopharma.com

聯繫方式:
Phio Pharmaceuticals Corp.
ir@phiopharma.com

PR Contact
Michael Adams
Bridge View Media
adams@bridgeviewmedia.com

公關聯繫方式
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Bridge View Media
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To view the source version of this press release, please visit https://www.newsfilecorp.com/release/210357

要查看此新聞發佈的源版本,請訪問 https://www.newsfilecorp.com/release/210357

譯文內容由第三人軟體翻譯。


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