Sharp Therapeutics Corp. Reports Third Quarter 2025 Results and Development Update
Rhea-AI Summary
Sharp Therapeutics (OTCQB: SHRXF; TSXV: SHRX) released condensed interim consolidated financial statements for the three and nine months ended September 30, 2025 and related MD&A.
The company reported it increased R&D spending by 34% versus the comparable quarter in 2024 to advance its Gaucher, Niemann Pick C and Progranulin programs and is targeting entry into Phase I clinical trials in 2026. Sharp describes itself as a pre-clinical small-molecule therapeutics developer using computationally optimized libraries and high-throughput screening.
Positive
- R&D spend up 34% vs comparable quarter 2024
- Targeting Phase I clinical trial entry in 2026
- Advancing three named programs: Gaucher, Niemann Pick C, Progranulin
Negative
- Company is in a pre-clinical stage; no human trial data yet
Pittsburgh, Pennsylvania and Toronto, Ontario--(Newsfile Corp. - November 26, 2025) - Sharp Therapeutics Corp. (TSXV: SHRX) (OTCQB: SHRXF) ("Sharp" or the "Company"), announces the release of its condensed interim consolidated financial statements for the three and nine months ended September 30, 2025, and related management discussion and analysis. All dollar figures are in United States dollars, unless otherwise stated.
Scott Sneddon, Sharp's Chief Executive Officer, stated: "Our Q3 financial results show our continued investment in research and development programs, mainly our Gaucher, Niemann Pick C and Progranulin programs. We spent
About Sharp Therapeutics Corp.
First-Choice Therapies for Genetic Diseases
Sharp Therapeutics is a pre-clinical stage company developing first-choice small-molecule therapeutics for genetic diseases. The Company's discovery platform combines novel high throughput screening technologies, with compound libraries computational optimized based on the physics and biology of cellular trafficking defects and allosteric activation of proteins. The platform produces small molecule compounds that restore activity in mutated proteins giving the potential to treat genetic disorders with conventional pill-based medicines.
For additional information on Sharp, please visit: www.sharptx.com.
Sharp Therapeutics Corp.
Scott Sneddon, PhD, JD
CEO/CSO
Email: scott@sharptx.com
Caution Regarding Forward-Looking Information
Certain statements contained in this press release constitute "forward-looking information" as such term is defined in applicable Canadian securities legislation. The words "may", "would", "could", "should", "potential", "will", "seek", "intend", "plan", "anticipate", "believe", "estimate", "expect" and similar expressions are intended to identify forward-looking information. All statements other than statements of historical fact may be forward-looking information. Such statements reflect Sharp's current views and intentions with respect to future events, and current information available to Sharp, and are subject to certain risks, uncertainties and assumptions. Many factors could cause the actual results, performance or achievements that may be expressed or implied by such forward-looking information to vary from those described herein should one or more of these risks or uncertainties materialize. Should any factor affect Sharp in an unexpected manner, or should assumptions underlying the forward-looking information prove incorrect, the actual results or events may differ materially from the results or events predicted. Any such forward-looking information is expressly qualified in its entirety by this cautionary statement. Moreover, Sharp does not assume responsibility for the accuracy or completeness of such forward-looking information. The forward-looking information included in this press release is made as of the date of this press release and Sharp undertakes no obligation to publicly update or revise any forward-looking information, other than as required by applicable law.
Neither 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 release.

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