Press Releases May 27, 2026 08:00 AM

CDT Announces Canadian Patent for AZD5904 in Male Infertility

CDT Equity Inc. Secures Canadian Patent for AZD5904, Reinforcing Global Intellectual Property in Male Infertility Treatment

By Hana Yamamoto CDT

CDT Equity Inc. announced that the patent for AZD5904 in treating male infertility has been granted in Canada, completing patent approvals in all major pharmaceutical markets. This strengthens the company's intellectual property portfolio for AZD5904, a drug originally licensed from AstraZeneca, addressing a significant unmet need in the $4.4 billion global male infertility market. CDT is advancing discussions on licensing and strategic partnerships while leveraging its platform to foster innovation and shareholder value.

CDT Announces Canadian Patent for AZD5904 in Male Infertility
CDT

Key Points

  • CDT received Canadian patent approval for AZD5904, completing coverage in all key markets.
  • AZD5904 targets male infertility, a $4.4 billion market with currently no approved drug therapies.
  • The firm is actively pursuing licensing and strategic partnerships to further develop AZD5904.
  • The biopharmaceutical company employs AI and asset repositioning to accelerate novel treatment development.

NAPLES, Fla. and CAMBRIDGE, United Kingdom, May 27, 2026 (GLOBE NEWSWIRE) -- CDT Equity Inc. (Nasdaq: CDT) (“CDT” or the “Company”), today announces that the patent covering the use of AZD5904 in male infertility has now been granted in Canada, completing the approval of this patent in all key pharmaceutical target markets.

CDT believes that the extensive geographical coverage of this patent combined with its more recent composition of matter application provides a strong IP position for development of AZD5904 in male infertility as discussions continue regarding potential licensing and strategic partnering opportunities.

Originally licensed from AstraZeneca, AZD5904 benefits from an extensive clinical safety package alongside pre-clinical validation in an area of significant unmet medical need and a continually growing market.

“Globally, the male infertility market is estimated at approximately USD $4.4 billion annually, representing a significant area of unmet medical need with no approved drug therapies specifically addressing male infertility,” said Dr. Joanne Holland, Chief Scientific Officer of CDT. “The Canadian approval further strengthens the global positioning of AZD5904 as we continue advancing partnering and future development discussions.”

About CDT Equity Inc.

CDT Equity Inc. (NASDAQ: CDT) is a data-driven biopharmaceutical development company focused on identifying, enhancing, and advancing high-potential therapeutic assets through scientific innovation and strategic partnerships. Originally established as Conduit Pharmaceuticals, the company has evolved into a broader, more agile platform that leverages artificial intelligence, solid-form chemistry, and efficient asset repositioning to accelerate the development of novel treatments. Looking ahead, CDT are committed to creating shareholder value through licensing, strategic M&A, and positioning the company as a platform for transformative innovation.

Cautionary Statement Regarding Forward-Looking Statements

This press release contains certain forward-looking statements within the meaning of the federal securities laws. All statements other than statements of historical facts contained in this press release, including statements regarding CDT's future results of operations and financial position, CDT's business strategy, prospective product candidates, product approvals, research and development cost timing and likelihood of success, plans and objectives of management for future operations, future results of current and anticipated studies and business endeavors with third parties, and future results of current and anticipated product candidates, are forward-looking statements. These forward-looking statements generally are identified by the words “believe,” “project,” “expect,” “anticipate,” “estimate,” “intend,” “strategy,” “future,” “opportunity,” “plan,” “may,” “should,” “will,” “would,” “will be,” “will continue,” “will likely result,” and similar expressions. These forward-looking statements are subject to a number of risks, uncertainties and assumptions, including, but not limited to; the effect that the reverse stock split may have on the price of the Company’s common stock; the ability or inability to maintain the listing of CDT's securities on Nasdaq; the ability to recognize the anticipated benefits of the business combination completed in September 2023, which may be affected by, among other things, competition; the ability of the combined company to grow and manage growth economically and hire and retain key employees; the risks that CDT's product candidates in development fail clinical trials or are not approved by the U.S. Food and Drug Administration or other applicable authorities on a timely basis or at all; changes in applicable laws or regulations; the possibility that CDT may be adversely affected by other economic, business, and/or competitive factors; and other risks and uncertainties identified in other filings made by CDT with the U.S. Securities and Exchange Commission. Moreover, CDT operates in a very competitive and rapidly changing environment. Because forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified and some of which are beyond CDT's control, you should not rely on these forward-looking statements as predictions of future events.

Forward-looking statements speak only as of the date they are made. Readers are cautioned not to put undue reliance on forward-looking statements, and except as required by law, CDT assumes no obligation and does not intend to update or revise these forward-looking statements, whether as a result of new information, future events, or otherwise. CDT gives no assurance that it will achieve its expectations.

Investors
CDT Equity Inc.
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Risks

  • The drug candidate AZD5904 may fail clinical trials or not receive regulatory approval, impacting commercialization.
  • Market and regulatory changes could adversely affect CDT's business strategy and financial performance.
  • Competition in the biopharmaceutical sector may hinder growth prospects and the ability to maintain Nasdaq listing.

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