Press Releases June 30, 2026 04:30 PM

Result of Annual General Meeting

Biodexa Pharmaceuticals announces Annual General Meeting results with mixed outcomes on key resolutions

By Maya Rios
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BDRX

Biodexa Pharmaceuticals PLC, a clinical stage biopharmaceutical company listed on NASDAQ under ticker BDRX, announced the results of its re-scheduled Annual General Meeting held on June 30, 2026. Seven ordinary resolutions passed with strong majority support, while certain key resolutions (8, 10, and 11) failed to pass, indicating mixed shareholder sentiment. The company continues to develop innovative therapeutics targeting gastrointestinal cancers and other diseases with unmet medical needs.

Result of Annual General Meeting
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Key Points

  • Seven ordinary resolutions passed with majority approval ranging from 73% to 94%.
  • Resolutions 8, 10, and 11 failed to pass; resolution 11 was contingent on resolution 8.
  • Biodexa's clinical pipeline includes development programs for eRapa, MTX240, and tolimidone targeting gastrointestinal cancers and type 1 diabetes.

June 30, 2026

Biodexa Pharmaceuticals PLC
(“Biodexa” or the “Company”)

Result of Annual General Meeting

Biodexa Pharmaceuticals PLC (Nasdaq: BDRX) (“Biodexa” or “the Company”), a clinical stage biopharmaceutical company developing innovative products focused on the treatment or prevention of gastrointestinal cancers announces that its re-scheduled Annual General Meeting held at 11.00 BST today, ordinary resolutions 1 through 7 passed with majorities of 94%, 73%, 92%, 81%, 81%, 91% and 94%, respectively. Ordinary resolution 8 and special resolution 10 failed to pass. Because resolution 11 was contingent on the passing of resolution 8, resolution 11 also failed to pass.

ENDS

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 Bladder Cancer, MTX240 under development for Gastrointestinal Stromal Tumors (GIST) and tolimidone, under development for the treatment of type 1 diabetes.

eRapa is a proprietary oral capsule 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.

MTX240 is a molecular glue, bringing two intracellular proteins, PDE3a and SLFN12, specifically co-expressed by GIST cancer cells, into close proximity to form a stable complex. This interaction stabilizes SLFN12, enabling it to drive RNase-mediated apoptosis in GIST cells through a mechanism independent of KIT signalling.

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.

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.


Risks

  • Failure of certain shareholder resolutions indicates governance or strategic uncertainties that could impact investor confidence.
  • Clinical-stage status of Biodexa’s products presents inherent development and regulatory risks.
  • Forward-looking statements highlight risks associated with drug development outcomes and market acceptance that could materially affect performance.

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