BioNxt Solutions Announces ODF Cladribine Update and Financing
BioNxt Solutions Announces ODF Cladribine Update and Financing
NOT FOR DISTRIBUTION TO UNITED STATES NEWS WIRE SERVICES OR FOR DISSEMINATION IN THE UNITED STATES
不用於分發給美國新聞通訊社或在美國傳播
VANCOUVER, BC / ACCESSWIRE / April 25, 2024 / BioNxt Solutions Inc. ("BioNxt" or the "Company") (CSE:BNXT)(OTCQB:BNXTF)(FSE:BXT) is pleased to announce that its Cladribine program is advancing to human comparative bioavailability studies in Europe. The Company is reviewing proposals from several contract research organizations to carry out the studies in accordance with EU medical regulatory guidelines. The recent success of both the Company's ODF Cladribine toxicity and comparative pharmacokinetic ("PK") studies and industry interest have set high expectations for the upcoming comparative bioavailability study. Further details on the study will be released in due course.
不列顛哥倫比亞省溫哥華/ACCESSWIRE /2024年4月25日/ BioNxt Solutions Inc.(“BioNXT” 或 “公司”)(CSE: BNXT)(OTCQB: BNXT)(FSE: BXT)欣然宣佈,其克拉屈濱項目正在推進歐洲的人體比較生物利用度研究。該公司正在審查多個合同研究機構的提案,以根據歐盟醫療監管指南進行研究。該公司最近成功的ODF克拉屈濱毒性和比較藥代動力學(“PK”)研究以及業界的興趣爲即將到來的比較生物利用度研究樹立了很高的期望。有關該研究的更多細節將在適當時候公佈。
BioNxt is developing a 100% owned and proprietary ODF Cladribine dosage form, directed at the multiple sclerosis ("MS") market. Cladribine tablets are currently approved for use in over 75 countries, including by the United States Food and Drug Administration ("FDA") and the European Medicines Agency ("EMA"), with annual sales in excess of one billion USD. Cladribine tablets are approved for several indications, namely highly active forms of relapsing-remitting MS and certain forms of leukemia. MS represents the largest market segment for the sale of Cladribine with approximately 2.3 million people living with MS worldwide, with the highest prevalence in North America and Europe, noted by Atlas of MS. The global Multiple Sclerosis drug market is expected to top USD 41 billion by 2033 according to Market.us.
BionXT正在開發一種100%自有和專有的ODF克拉屈濱劑型,面向多發性硬化症(“MS”)市場。克拉屈濱片劑目前已獲准在超過75個國家使用,包括美國食品藥品監督管理局(“FDA”)和歐洲藥品管理局(“EMA”),年銷售額超過10億美元。克拉屈濱片劑獲准用於多種適應症,即高活性復發緩解型多發性硬化症和某些形式的白血病。多發性硬化症是克拉屈濱銷售的最大細分市場,全球約有230萬多發性硬化症患者,北美和歐洲的患病率最高。根據Market.US的數據,到2033年,全球多發性硬化症藥物市場預計將突破410億美元。
The Company has filed Cladribine ODF-related provisional patent applications with three to four patent applications expected to be on file in major international jurisdictions by late 2024 to early 2025 with potential patent protection extending to 2044.
該公司已經提交了與Cladribine ODF相關的臨時專利申請,預計到2024年底至2025年初,將在主要國際司法管轄區提交三到四份專利申請,潛在的專利保護將延至2044年。
The Company is also pleased to announce a non-brokered private placement of up to 6,000,000 common shares of the Company (the "Common Shares") at a price of $0.27 per Common Share for gross proceeds of up to $1,620,000 (the "Offering"). The Company intends to use the net proceeds from the Offering for research, development, and commercialization programs and general working capital purposes. The Offering may close on one or more dates as the Company may determine.
公司還高興地宣佈,以每股普通股0.27美元的價格進行公司高達6,000,000股普通股(“普通股”)的非經紀私募配售,總收益高達162萬美元(“本次發行”)。公司打算將本次發行的淨收益用於研究、開發和商業化計劃以及一般營運資金用途。本次發行可能會在公司確定的一個或多個日期結束。
The Company may pay a finder's fee in connection with the Offering to eligible arm's length finders in accordance with the policies of the Canadian Securities Exchange. All securities issued in connection with the Offering will be subject to a statutory hold period of four months and one day following the date of issuance in accordance with applicable Canadian securities laws.
根據加拿大證券交易所的政策,公司可能會向符合條件的獨立發現者支付與本次發行相關的發現費。根據適用的加拿大證券法,與本次發行有關的所有證券的法定持有期限爲四個月零一天。
The securities issued pursuant to the Offering have not, nor will they be registered under the United States Securities Act of 1933, as amended, and may not be offered or sold within the United States or to, or for the account or benefit of, U.S. persons in the absence of U.S. registration or an applicable exemption from the U.S. registration requirements. This news release shall not constitute an offer to sell or the solicitation of an offer to buy nor shall there be any sale of the securities in the United States or in any other jurisdiction in which such offer, solicitation or sale would be unlawful.
根據本次發行發行的證券沒有也不會根據經修訂的1933年《美國證券法》進行註冊,在沒有美國註冊或沒有適用的美國註冊要求豁免的情況下,不得在美國境內向美國人發行或出售,也不得向美國人發行或出售,或爲美國人的賬戶或利益進行發行或出售。本新聞稿不構成賣出要約或徵求買入要約,也不應在美國或任何其他司法管轄區出售證券,此類要約、招攬或出售是非法的。
About BioNxt Solutions Inc.
關於 BioNXT 解決方案公司
BioNxt Solutions Inc. is a bioscience accelerator focused on next‐generation drug formulations and delivery systems, diagnostic screening tests, and new active pharmaceutical production and evaluation, including: precision transdermal and oral dissolvable drug formulations; rapid, low‐cost infectious disease and oral health screening tests; and standardization and clinical evaluation of emerging active pharmaceutical ingredients for neurological applications. The Company has research and development operations in North America and Europe, with an operational focus in Germany, and is currently focused on regulatory approval and commercialization of medical products for European markets.
BioNxt Solutions Inc. 是一家生物科學加速器,專注於下一代藥物配方和輸送系統、診斷篩選測試以及新的活性藥物的生產和評估,包括:精確的透皮和口服可溶藥物配方;快速、低成本的傳染病和口腔健康篩查測試;以及用於神經系統應用的新興活性藥物成分的標準化和臨床評估。該公司在北美和歐洲開展研發業務,業務重點在德國,目前專注於歐洲市場的醫療產品的監管批准和商業化。
BioNxt Solutions Inc.
BioNXT 解決方案公司
Hugh Rogers, CEO and Director
Email: info@bionxt.com
Phone: +1 780-818-6422
休·羅傑斯,首席執行官兼董事
電子郵件:info@bionxt.com
電話:+1 780-818-6422
This news release includes certain statements that may be deemed "forward-looking statements". All statements in this new release, other than statements of historical facts, that address events or developments that the Company expects to occur, are forward-looking statements. Forward-looking statements are statements that are not historical facts and are generally, but not always, identified by the words "expects", "plans", "anticipates", "believes", "intends", "estimates", "projects", "potential" and similar expressions, or that events or conditions "will", "would", "may", "could" or "should" occur. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance and actual results may differ materially from those in the forward-looking statements. Factors that could cause the actual results to differ materially from those in forward-looking statements include market prices, continued availability of capital and financing, and general economic, market or business conditions. Investors are cautioned that any such statements are not guarantees of future performance and actual results or developments may differ materially from those projected in the forward-looking statements. Forward-looking statements are based on the beliefs, estimates and opinions of the Company's management on the date the statements are made. Except as required by applicable securities laws, the Company undertakes no obligation to update these forward-looking statements in the event that management's beliefs, estimates or opinions, or other factors, should change.
本新聞稿包括某些可能被視爲 “前瞻性陳述” 的陳述。除歷史事實陳述外,本新新聞稿中涉及公司預計將發生的事件或事態發展的所有陳述均爲前瞻性陳述。前瞻性陳述不是歷史事實,通常但並非總是以 “期望”、“計劃”、“預期”、“相信”、“打算”、“估計”、“項目”、“潛在” 和類似表達方式來識別,或者說事件或條件 “將”、“將”、“可能” 或 “應該” 發生。儘管公司認爲此類前瞻性陳述中表達的預期是基於合理的假設,但此類陳述並不能保證未來的業績,實際業績可能與前瞻性陳述中存在重大差異。可能導致實際業績與前瞻性陳述中存在重大差異的因素包括市場價格、資本和融資的持續可用性以及總體經濟、市場或商業狀況。提醒投資者,任何此類陳述都不能保證未來的業績,實際業績或發展可能與前瞻性陳述中的預測存在重大差異。前瞻性陳述基於公司管理層在陳述發表之日的信念、估計和觀點。除非適用的證券法有要求,否則如果管理層的信念、估計或觀點或其他因素髮生變化,公司沒有義務更新這些前瞻性陳述。
Neither the Canadian Securities Exchange nor its Regulation Services Provider accepts responsibility for the adequacy or accuracy of this news release.
加拿大證券交易所及其監管服務提供商均不對本新聞稿的充分性或準確性承擔責任。
SOURCE: BioNxt Solutions Inc.
來源:BioNxt Solutions Inc.