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NASDAQ:TRAW

Traws Pharma Q3 2025 Earnings Results & Report

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$0.28 +0.03 (+13.92%)
Closing price 11/12/2026 03:59 PM Eastern
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$0.28 -0.01 (-2.74%)
As of 11/12/2026 07:59 PM Eastern
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Traws Pharma beat analyst earnings expectations in its Q3 2025 results, released November 13, 2025. The company reported EPS of -$0.34 versus the -$9.16 consensus estimate.

Earnings Announcement Details

Quarter
Q3 2025
Time
Before Market Opens
Conference Call
7:00 AM ET

Traws Pharma EPS Results

Actual EPS
-$0.34
Consensus EPS
-$9.16
Beat/Miss
Beat by +$8.82
One Year Ago EPS
N/A
EPS Beat Rate
7 of last 8 quarters

Traws Pharma Revenue Results

Actual Revenue
N/A
Expected Revenue
$60 thousand
Beat/Miss
N/A
YoY Revenue Growth
N/A

Traws Pharma Q3 2025 Earnings FAQ

Traws Pharma (NASDAQ:TRAW) reported earnings of -$0.34 per share for Q3 2025, beating the consensus estimate of -$9.16. The report was announced on Thursday, November 13, 2025.

Traws Pharma Earnings Headlines

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About Traws Pharma

Traws Pharma (NASDAQ:TRAW) is a clinical-stage biotechnology company focused on developing antiviral medicines for respiratory viral infections, including influenza and COVID-19. The company’s approach includes developing therapies designed to act against viral replication and host-cell pathways involved in disease progression.

Traws Pharma’s pipeline includes zapnometinib, an investigational oral host-directed antiviral designed to inhibit the MEK signaling pathway, which may support treatment across multiple strains of influenza and coronaviruses. The company is also developing additional antiviral candidates, including tivoxavir marboxil, an investigational treatment intended to target influenza virus replication. These products remain under clinical development and have not been approved for commercial use.

The company was formed through the combination of Onconova Therapeutics, Inc. and Traws Pharma, LLC and adopted the Traws Pharma name in 2024. Its shares trade on the Nasdaq Capital Market under the symbol “TRAW.” Traws Pharma is headquartered in the United States and is focused on advancing its antiviral programs through clinical development and potential regulatory approval.

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