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TC BioPharm Announces Closing of Upsized $6.0 Million Public Offering

TC BioPharm Announces Closing of Upsized $6.0 Million Public Offering

TC BioPharm宣布完成扩大规模的600万美元公开发行
PR Newswire ·  08/28 17:15

EDINBURGH, Scotland, Aug. 28, 2024 /PRNewswire/ -- TC BioPharm (Holdings) PLC ("TC BioPharm" or the "Company") (NASDAQ: TCBP) a clinical stage biotechnology company developing platform allogeneic gamma-delta T cell therapies for cancer and other indications, today announced the closing of its previously announced public offering, upsized to 6,000,000 shares of its American Depository Shares ("ADSs")(or pre-funded warrants in lieu thereof), together with Series H warrants ("Series G Warrants") to purchase up to 6,000,000 ADSs at a combined public offering price of $1 per ADS (or pre-funded warrant in lieu thereof) and associated Series H Warrant. The Series H Warrants have an exercise price of £0.76 per ADS, are exercisable upon issuance and will expire one year from the date of issuance. Each ADS represents two hundred ordinary shares of the Company.

2024年8月28日,苏格兰爱丁堡 /美通社/ - 肿瘤细胞生物制品(持股)股份有限公司(“肿瘤细胞生物制品”或“本公司”)(纳斯达克:TCBP)是一家临床阶段的生物技术公司,开发用于癌症和其他适应症的平台性异基因伽马-渔砍细胞疗法,宣布其之前宣布的公开发行发行,上限为600万股美国存托凭证(ADS)(或优先认购权证的抵换),连同购买高品系列认购权证的H系列权证.W)至多可购买600万股美国存托凭证,合并公开发行价格为每股1美元(或抵换的优先认购权证)和相关H系列认购权证。H系列认购权证的行权价为每股0.76英镑,行使权在发行后可行使,将于发行日起一年后到期.每个ADS代表公司两百股普通股。

The gross proceeds to the Company from the offering are $6.0 million, before deducting offering expenses payable by the Company. The Company intends to use the net proceeds from this offering to support its upcoming clinical trial focusing on relapse/refractory Acute Myeloid Leukemia, for market awareness and for continuing operating expenses and working capital.

本次发行给本公司带来的总收益为600万美元,扣除由本公司支付的发行费用。本公司打算将本次发行的净收益用于支持即将进行的关注复发/难治性急性髓细胞白血病的临床试验,并用于市场知名度以及继续营业费用和运营资本。

The securities described above are being offered by the Company pursuant to a registration statement on Form F-1 (File No. 333-281613) previously filed with and declared effective by the U.S. Securities and Exchange Commission ("SEC") on August 28, 2024 and an additional registration statement on Form F-1 filed pursuant to Rule 462(b) which became automatically effective on August 28, 2024. . The offering was made only by means of a prospectus, which is part of the effective registration statement. A final prospectus relating to the offering will be filed with the SEC. Electronic copies of the final prospectus may be obtained for free on the SEC's website located at http://www.sec.gov.

上述证券由公司根据在2024年8月28日以前向美国证券交易委员会(“SEC”)注册委员会提交的F-1表格注册申报(文件号333-281613)和根据规则462(b)提交的额外注册申报书注册(自2024年8月28日起自动生效)。本次发行仅通过一份作为有效注册申报书的一部分的招股说明书进行。有关招股说明书的最终版本将在SEC进行注册。可以免费从位于http://www.sec.gov的SEC网站上获取最终招股说明书的电子副本。

This press release does not constitute an offer to sell or the solicitation of an offer to buy any of the securities described herein, nor shall there be any sale of these securities in any state or other jurisdiction in which such an offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or other jurisdiction.

本新闻稿并非对所述证券的销售要约,也不构成对任何国家或其他司法管辖区内其中类似要约、招揽或销售的邀请或要约。在任何该等国家或其他司法管辖区内,如未在适用的证券法规下进行登记或合规资格审查,则不得销售该等证券。

Forward-Looking Statements

前瞻性声明

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this Current Report on Form 8-K that do not relate to matters of historical fact should be considered forward-looking statements, including without limitation statements regarding the Company's intent or ability to affect any budget savings or execute on any M&A or capital raising strategy. These statements are based on management's current assumptions and are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause the Company's actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. For other important factors that could cause actual results to differ materially from the forward-looking statements in this Current Report on Form 8-K, please see the risks and uncertainties identified under the heading "Risk Factors" in our Annual Report on Form 10-K for the year ended December 31, 2023, and our other reports filed with the SEC, all of which is available on the Company's Investor Relations website at and on the SEC website at www.sec.gov. All forward-looking statements reflect the Company's beliefs and assumptions only as of the date of this press release. The Company undertakes no obligation to update forward-looking statements to reflect future events or circumstances.

本新闻稿包含根据1995年私人证券诉讼改革法而作出的前瞻性声明。本公司在此次上报的Form 8-k表格的所有声明都不属于历史事实,应当作为前瞻性声明。这些声明基于管理层的当前假设且既不是承诺也不是保证,而涉及已知和未知的风险、不确定性和其他重要因素,可能导致本公司的实际结果、表现或成就与前瞻性声明所暗示的任何未来结果、表现或成就有着实质性的不同。请参阅我们于2023年12月31日结束的第10-K份年度报告中所識别的“风险因素”和其他有关该等前瞻性声明可能导致实际结果与当前报告所暗示的不同的重要因素,以及我们向SEC提交的其他报告,所有这些报告都可以通过公司的投资者关系网站和SEC网站上查阅。所有前瞻性声明仅反映本公司的信念和假设,仅在本新闻稿发出之日有效。本公司不承诺更新前瞻性声明以反映任何未来事件或情况。

About TC BioPharm (Holdings) PLC

关于TC BioPharm (Holdings) PLC

TC BioPharm is a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of gamma-delta T cell therapies for the treatment of cancer with human efficacy data in acute myeloid leukemia. Gamma-delta T cells are naturally occurring immune cells that embody properties of both the innate and adaptive immune systems and can intrinsically differentiate between healthy and diseased tissue. TC BioPharm is the leader in developing gamma-delta T cell therapies, and the first company to conduct phase II/pivotal clinical studies in oncology. The Company is conducting two investigator-initiated clinical trials for its unmodified gamma-delta T cell product line - Phase 2b/3 pivotal trial in treatment of acute myeloid leukemia using the Company's proprietary allogeneic CryoTC technology to provide frozen product to clinics worldwide.

TC BioPharm是一家临床阶段的生物制药公司,专注于发现、开发和商业化用于治疗癌症的γ-δ T细胞疗法,产品在急性髓系白血病方面已有人类有效性数据。γ-δ T细胞是天然存在的免疫细胞,具有先天免疫系统和适应性免疫系统的特性,并且能够本身区分健康组织和疾病组织。TC BioPharm是开发γ-δ T细胞疗法的领先者,也是在肿瘤学领域进行Ⅱ期/关键性临床研究的第一家公司。该公司正在进行两项研究者发起的临床试验,针对其未改编的γ-δ T细胞产品线进行——使用公司专有的异基因CryoTC技术,在全球为诊所提供冷冻产品的Ⅱb/Ⅲ关键性试验中,治疗急性髓系白血病。

SOURCE TC BioPharm

消息来源:TC BioPharm

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