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Therma Bright Milestone Payments Bring Ownership in Inretio to 7.5%

Therma Bright Milestone Payments Bring Ownership in Inretio to 7.5%

Therma Bright 里程碑付款使Inretio的所有權達到7.5%
newsfile ·  2023/04/21 19:16

Toronto, Ontario--(Newsfile Corp. - April 21, 2023) - Therma Bright Inc. (TSXV: THRM) (OTCQB: TBRIF) ("Therma Bright" or the "Company"), developer and investor in a range of leading-edge, proprietary diagnostic and medical device technologies, is pleased to announce that further to its news releases of January 19 and March 6, 2023, relating to its acquisition of up to 25% of Inretio Inc., it has now paid the portion of the purchase price comprised of US$500,000 in Therma Bright shares, being 6,766,500 common shares of Therma Bright. In accordance with TSX Venture Exchange requirements, these shares were issued at a deemed price of CAD$0.10/share. The shares are subject to a hold period expiring August 1, 2023, in accordance with applicable securities laws and the policies of the TSX Venture Exchange. These issued shares, along with USD$250,000 in cash payments previously made to Inretio, increases Therma Bright's ownership interest in Inretio to 7.5%.

安大略省多倫多--(Newsfile Corp.——2023年4月21日)——Therma Bright Inc.(多倫多證券交易所股票代碼:THRM)(OTCQB:TBRIF)(“Therma Bright” 或 “公司”),一系列前沿的專有診斷和醫療設備技術的開發商和投資者,欣然宣佈,繼2023年1月19日和3月6日發佈的有關其收購Intherma Bright高達25%股份的新聞稿之後 Retio Inc.,它現已支付了收購價格中包括50萬美元Therma Bright股票的部分,即Therma Bright的6,766,500股普通股。根據多倫多證券交易所風險交易所的要求,這些股票的發行價格爲每股0.10加元。根據適用的證券法和多倫多證券交易所風險交易所的政策,這些股票的持有期將於 2023 年 8 月 1 日到期。這些已發行的股票,加上此前向Inretio支付的25萬美元現金,使Therma Bright在Inretio的所有權益增加到7.5%。

On February 23, 2023, Therma Bright shared that Inretio received very encouraging results with its PREVA mechanical thrombectomy device for the treatment of ischemic stroke from a study that was conducted at the Shamir Medical Center's Research Unit, which is known across the world for its innovative and breakthrough research in Israel. The PREVA device has been undergoing a Good Laboratory Practise (GLP) animal study which is essential before initiating studies on patients. The study is proceeding as planned and the results of the GLP study are a positive sign for the device's future development and potential regulatory approval and commercialization. The study is expected to be completed during the second quarter of 2023, at which point Inretio plans to submit the data, as well as mechanical verification and validation (V&V) testing data, to the Israeli Ministry of Health for Clinical Trial clearance in humans, which will be a significant milestone towards commercialization.

2023年2月23日,Therma Bright分享說,Inretio在沙米爾醫學中心研究部進行的一項研究中,其用於治療缺血性中風的PREVA機械血栓切除裝置獲得了非常令人鼓舞的結果,該研究以其在以色列的創新和突破性研究而聞名於世。PREVA設備正在進行一項良好實驗室規範(GLP)動物研究,這在開始對患者進行研究之前至關重要。該研究正在按計劃進行,GLP研究的結果對該設備的未來發展以及潛在的監管批准和商業化是一個積極的信號。該研究預計將於2023年第二季度完成,屆時Inretio計劃向以色列衛生部提交數據以及機械驗證和驗證(V&V)測試數據,以供人體臨牀試驗批准,這將是邁向商業化的重要里程碑。

"This is a significant milestone for Therma Bright as it now owns 7.5% of Inretio, a company which is on track to enter human studies," shared Rob Fia, CEO of Therma Bright. "Thrombectomy involves removing a clot from a blood vessel, most commonly from the brain or heart, as stroke and myocardial infarction remain two of the leading causes of death worldwide," added Rob Fia.

Therma Bright首席執行官羅布·菲亞分享說:“對於Therma Bright來說,這是一個重要的里程碑,因爲它現在擁有Inretio7.5%的股份,該公司有望進入人體研究。”羅布·菲亞補充說:“血栓切除術包括切除血管中的血塊,最常見的是從大腦或心臟中切除血塊,因爲中風和心肌梗塞仍然是全球兩個主要的死因。”

About Inretio

關於 Inretio

Inretio was born out of the need for improving stroke care and reducing thrombectomy complications. Inretio has set itself the goal of reducing stroke's burden and patients' suffering, by being a leader in the neurovascular field, and bringing value to physicians with simple, yet innovative solutions. For further information, go to .

Inretio的誕生是出於改善中風護理和減少血栓切除術併發症的需求。Inretio爲自己設定了減少中風負擔和患者痛苦的目標,成爲神經血管領域的領導者,並通過簡單而創新的解決方案爲醫生帶來價值。欲瞭解更多信息,請訪問。

About Therma Bright Inc.

關於 Therma Bright Inc

Therma Bright, is a developer and partner in a range of leading edge, proprietary diagnostic and medical device technologies focused on providing consumers and medical professionals with quality, innovative solutions that address some of today's most important medical and healthcare challenges. Therma Bright is the developer of the smart-enabled AcuVid COVID-19 Rapid Antigen Saliva Test, currently undergoing regulatory review. Therma Bright Inc. trades on the TSXV (TSXV: THRM) (OTCQB: TBRIF) (FSE: JNX). Visit: .

Therma Bright 是一系列前沿專有產品的開發商和合作夥伴診斷和醫療設備技術專注於爲消費者和醫療專業人員提供優質、創新的解決方案,以應對當今一些最重要的醫療和醫療保健挑戰。Therma Bright是支持智能的AcuViD COVID-19 快速抗原唾液測試的開發者,該測試目前正在接受監管審查。Therma Bright Inc.在多倫多證券交易所(多倫多證券交易所股票代碼:THRM)(OTCQB:TBRIF)(FSE:JNX)上交易。訪問:。

Therma Bright Inc.
Rob Fia, CEO
rfia@thermabright.com
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Therma Bright公司
首席執行官 Rob Fia
rfia@thermabright.com
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FORWARD LOOKING STATEMENTS

前瞻性陳述

Certain statements in this news release constitute "forward-looking" statements. These statements relate to future events such as development and commercialization of medical devices as described in the news release. All such statements involve substantial known and unknown risks, uncertainties and other factors which may cause the actual results to vary from those expressed or implied by such forward-looking statements. Forward-looking statements involve significant risks and uncertainties, they should not be read as guarantees of future performance or results, and they will not necessarily be accurate indications of whether or not such results will be achieved. Actual results could differ materially from those anticipated due to a number of factors and risks. Although the forward-looking statements contained in this news release are based upon what management of the Company believes are reasonable assumptions on the date of this news release, the Company cannot assure investors that actual results will be consistent with these forward-looking statements. The forward-looking statements contained in this press release are made as of the date hereof and the Company disclaims any intention or obligation to update or revise any forward-looking statements whether as a result of new information, future events or otherwise, except as required under applicable securities regulations.

本新聞稿中的某些陳述構成 “前瞻性” 陳述。這些聲明涉及未來事件,例如新聞稿中描述的醫療器械的開發和商業化。所有此類陳述都涉及重大的已知和未知風險、不確定性和其他因素,這些因素可能導致實際結果與此類前瞻性陳述所表達或暗示的結果有所不同。前瞻性陳述涉及重大風險和不確定性,不應將其視爲未來表現或業績的保證,也不一定能準確表明此類結果是否會實現。由於多種因素和風險,實際結果可能與預期結果存在重大差異。儘管本新聞稿中包含的前瞻性陳述基於公司管理層在本新聞稿發佈之日認爲合理的假設,但公司無法向投資者保證實際業績將與這些前瞻性陳述一致。本新聞稿中包含的前瞻性陳述自本文發佈之日起作出,除非適用的證券法規要求,否則公司不打算或有義務更新或修改任何前瞻性陳述,無論是由於新信息、未來事件還是其他原因。

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this press release.

多倫多證券交易所風險投資交易所及其監管服務提供商(該術語在多倫多證券交易所風險投資交易所的政策中定義)均不對本新聞稿的充分性或準確性承擔責任。

This press release is not an offer of the securities for sale in the United States. The securities have not been registered under the U.S. Securities Act of 1933, as amended, and may not be offered or sold in the United States absent registration or an exemption from registration. This press 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 any state in which such offer, solicitation or sale would be unlawful.

本新聞稿不是在美國出售證券的要約。這些證券尚未根據經修訂的1933年《美國證券法》進行註冊,未經註冊或免於註冊,不得在美國發行或出售。本新聞稿不構成出售要約或招攬買入要約,也不得在任何此類要約、招攬或出售爲非法的州出售證券。

To view the source version of this press release, please visit

要查看本新聞稿的源版本,請訪問

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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