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NASDAQ:SMMT

Summit Therapeutics Q2 2026 Earnings Report

Summit Therapeutics logo
$13.81 +0.05 (+0.36%)
Closing price 07/17/2026 04:00 PM Eastern
Extended Trading
$13.92 +0.11 (+0.83%)
As of 07/17/2026 07:06 PM Eastern
Extended trading is trading that happens on electronic markets outside of regular trading hours. This is a fair market value extended hours price provided by Massive. Learn more.

Summit Therapeutics EPS Results

Actual EPS
N/A
Consensus EPS
-$0.26
Beat/Miss
N/A
One Year Ago EPS
N/A

Summit Therapeutics Revenue Results

Actual Revenue
N/A
Expected Revenue
$0.11 million
Beat/Miss
N/A
YoY Revenue Growth
N/A

Summit Therapeutics Announcement Details

Quarter
Q2 2026
Time
After Market Closes
Conference Call Date
Thursday, July 23, 2026
Conference Call Time
4:30PM ET

Conference Call Resources

Summit Therapeutics Earnings Headlines

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About Summit Therapeutics

Summit Therapeutics (NASDAQ:SMMT) is a clinical‐stage biotechnology company dedicated to the discovery and development of precision medicines for serious and life‐threatening diseases. The company applies a targeted approach to drug design, focusing on novel mechanisms of action that differentiate its candidates from existing therapies.

Summit’s lead asset, ridinilazole (formerly SMT19969), is being developed to treat Clostridioides difficile infections and has received both Fast Track and Qualified Infectious Disease Product designations from the U.S. Food and Drug Administration. Alongside its infectious disease program, Summit has explored small‐molecule therapies for rare genetic disorders, leveraging its drug discovery capabilities to identify compounds that modulate disease‐relevant pathways.

Founded in 2003 and headquartered in Oxford, England, Summit maintains operations in North America to support clinical development and regulatory activities across the United States and Europe. The company’s management team brings extensive experience in biopharmaceutical research, clinical operations, and commercialization strategy, with a commitment to advancing its pipeline toward regulatory approval and broad patient access.

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