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Biodexa Pharmaceuticals Q4 2025 Earnings Results & Report

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$0.46 -0.06 (-12.13%)
Closing price 10/9/2026 04:00 PM Eastern
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$0.46 0.00 (-0.04%)
As of 10/9/2026 07:39 PM Eastern
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Biodexa Pharmaceuticals beat analyst earnings expectations in its Q4 2025 results, released March 27, 2026. The company reported EPS of $3.5250 versus the -$0.0066 consensus estimate.

Earnings Announcement Details

Quarter
Q4 2025
Report Date
Time
Before Market Opens
Conference Call
8:00 AM ET

Biodexa Pharmaceuticals EPS Results

Actual EPS
$3.5250
Consensus EPS
-$0.0066
Beat/Miss
Beat by +$3.5316
One Year Ago EPS
N/A

Biodexa Pharmaceuticals Revenue Results

Actual Revenue
N/A
Expected Revenue
N/A
Beat/Miss
N/A
YoY Revenue Growth
N/A

Earnings Documents

Biodexa Pharmaceuticals Q4 2025 Earnings FAQ

Biodexa Pharmaceuticals (NASDAQ:BDRX) reported earnings of $3.5250 per share for Q4 2025, beating the consensus estimate of -$0.0066. The report was announced on Friday, March 27, 2026.

Biodexa Pharmaceuticals Earnings Headlines

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About Biodexa Pharmaceuticals

Biodexa Pharmaceuticals (NASDAQ:BDRX) plc, formerly known as Midatech Pharma plc, is a biopharmaceutical company focused on developing medicines for diseases with significant unmet medical needs. The company’s work has centered on oncology, rare diseases and conditions that are difficult to treat with conventional drug-delivery methods.

Biodexa’s development programs have included MTX110, a proprietary aqueous formulation of panobinostat being investigated for direct administration into brain tumors, including diffuse intrinsic pontine glioma. The company has also developed drug-delivery technologies intended to improve the administration, absorption and targeting of therapeutics.

Its technology portfolio has included Q-Sphera, a platform designed to produce long-acting injectable medicines, along with other delivery approaches for localized or sustained drug release. Biodexa is headquartered in the United Kingdom and has conducted development activities in the United States and other international markets. The company’s programs remain subject to clinical, regulatory and commercial development requirements.

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