Result of General Meeting
Biodexa Pharmaceuticals (NASDAQ: BDRX), a clinical stage biopharmaceutical company, announced that shareholders approved both resolutions at its General Meeting held on November 22, 2024. The approved resolutions will only reduce the nominal (par) value per ordinary share, with no change to the number of outstanding ordinary shares. The complete text of the resolutions can be found in the Notice of the General Meeting on the company's website.
Biodexa Pharmaceuticals (NASDAQ: BDRX), una società biofarmaceutica in fase clinica, ha annunciato che gli azionisti hanno approvato entrambe le risoluzioni durante l'Assemblea Generale tenutasi il 22 novembre 2024. Le risoluzioni approvate ridurranno solo il valore nominale (par) per azione ordinaria, senza modifiche al numero di azioni ordinarie in circolazione. Il testo completo delle risoluzioni è disponibile nell'Avviso dell'Assemblea Generale sul sito web della società.
Biodexa Pharmaceuticals (NASDAQ: BDRX), una compañía biofarmacéutica en etapa clínica, anunció que los accionistas aprobaron ambas resoluciones en su Junta General celebrada el 22 de noviembre de 2024. Las resoluciones aprobadas solo reducirán el valor nominal (par) por acción ordinaria, sin cambiar el número de acciones ordinarias en circulación. El texto completo de las resoluciones se puede encontrar en el Aviso de la Junta General en el sitio web de la compañía.
Biodexa Pharmaceuticals (NASDAQ: BDRX), 임상 단계의 생물 의약품 회사는 2024년 11월 22일 개최된 정기 주주 총회에서 주주들이 두 가지 결의를 모두 승인했다고 발표했습니다. 승인된 결의안은 보통주당 명목 가치(액면가)만을 줄이며, 발행된 보통주 수에는 변동이 없습니다. 결의안의 전체 텍스트는 회사 웹사이트의 정기 총회 공고에서 확인할 수 있습니다.
Biodexa Pharmaceuticals (NASDAQ: BDRX), une société bio-pharmaceutique en phase clinique, a annoncé que les actionnaires ont approuvé les deux résolutions lors de son Assemblée Générale tenue le 22 novembre 2024. Les résolutions approuvées ne feront que réduire la valeur nominale (par) par action ordinaire, sans changer le nombre d'actions ordinaires en circulation. Le texte complet des résolutions est disponible dans l'Avis de l'Assemblée Générale sur le site Web de la société.
Biodexa Pharmaceuticals (NASDAQ: BDRX), ein biopharmazeutisches Unternehmen in klinischer Phase, gab bekannt, dass die Aktionäre beide Beschlüsse auf der Hauptversammlung vom 22. November 2024 genehmigt haben. Die genehmigten Beschlüsse reduzieren nur den Nennwert (Stück) je Stammaktie, ohne die Anzahl der ausgegebenen Stammaktien zu verändern. Der vollständige Text der Beschlüsse ist in der Mitteilung zur Hauptversammlung auf der Website des Unternehmens zu finden.
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Insights
This general meeting announcement reflects a technical adjustment to share structure rather than a substantive business change. The reduction in nominal (par) value of shares is primarily an administrative move that doesn't affect the company's market capitalization, operations, or shareholder value. For a small-cap biotech company with a market cap of
November 22, 2024
Biodexa Pharmaceuticals PLC
(“Biodexa” or the “Company”)
Result of General Meeting
Biodexa Pharmaceuticals PLC (“Biodexa” or the “Company”) (NASDAQ: BDRX), a clinical stage biopharmaceutical company developing a pipeline of innovative products for the treatment of diseases with unmet medical needs announces, announces that at its General Meeting held earlier today, both resolutions put to the Company’s shareholders were duly passed.
The full text of, inter alia, the resolutions proposed and passed at the Annual General Meeting and General Meeting can be found in the Notice of the General Meeting on the Company's website at: https://biodexapharma.com/investors/corporate-governance/#agms.
The effect of the resolutions is solely to reduce the nominal, or par, value per ordinary share. There is no change to the number of ordinary shares outstanding.
About Biodexa Pharmaceuticals PLC
Biodexa Pharmaceuticals PLC (listed on NASDAQ: BDRX) is a clinical stage biopharmaceutical company developing a pipeline of innovative products for the treatment of diseases with unmet medical needs. The Company’s lead development programs include eRapa, under development for Familial Adenomatous Polyposis and Non-Muscle Invasive Blader Cancer; tolimidone, under development for the treatment of type 1 diabetes; and MTX110, which is being studied in aggressive rare/orphan brain cancer indications.
eRapa is a proprietary oral tablet formulation of rapamycin, also known as sirolimus. Rapamycin is an mTOR (mammalian Target Of Rapamycin) inhibitor. mTOR has been shown to have a significant role in the signalling pathway that regulates cellular metabolism, growth and proliferation and is activated during tumorigenesis.
Tolimidone is an orally delivered, potent and selective inhibitor of Lyn kinase. Lyn is a member of the Src family of protein tyrosine kinases, which is mainly expressed in hematopoietic cells, in neural tissues, liver, and adipose tissue. Tolimidone demonstrates glycaemic control via insulin sensitization in animal models of diabetes and has the potential to become a first in class blood glucose modulating agent.
MTX110 is a solubilized formulation of the histone deacetylase (HDAC) inhibitor, panobinostat. This proprietary formulation enables delivery of the product via convection-enhanced delivery (CED) at chemotherapeutic doses directly to the site of the tumor, by-passing the blood-brain barrier and potentially avoiding systemic toxicity.
Biodexa is supported by three proprietary drug delivery technologies focused on improving the bio-delivery and bio-distribution of medicines. Biodexa’s headquarters and R&D facility is in Cardiff, UK. For more information visit www.biodexapharma.com.
Forward-Looking Statements
Certain statements in this announcement may constitute “forward-looking statements” within the meaning of legislation in the United Kingdom and/or United States. Such statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995 and are based on management’s belief or interpretation. All statements contained in this announcement that do not relate to matters of historical fact should be considered forward-looking statements. In certain cases, forward-looking statements can be identified by the use of words such as “plans”, “expects” or “does not anticipate”, or “believes”, or variations of such words and phrases or statements that certain actions, events or results “may”, “could”, “would”, “might” or “will be taken”, “occur” or “be achieved.” Forward-looking statements and information are subject to various known and unknown risks and uncertainties, many of which are beyond the ability of the Company to control or predict, that may cause their actual results, performance or achievements to be materially different from those expressed or implied thereby, and are developed based on assumptions about such risks, uncertainties and other factors set out herein.
Reference should be made to those documents that Biodexa shall file from time to time or announcements that may be made by Biodexa in accordance with the rules and regulations promulgated by the SEC, which contain and identify other important factors that could cause actual results to differ materially from those contained in any projections or forward-looking statements. These forward-looking statements speak only as of the date of this announcement. All subsequent written and oral forward-looking statements by or concerning Biodexa are expressly qualified in their entirety by the cautionary statements above. Except as may be required under relevant laws in the United States, Biodexa does not undertake any obligation to publicly update or revise any forward-looking statements because of new information, future events or events otherwise arising.
FAQ
What resolutions were passed at Biodexa Pharmaceuticals (BDRX) General Meeting on November 22, 2024?
Does the November 22, 2024 Biodexa (BDRX) General Meeting result affect the number of outstanding shares?