Last reviewed · How we verify

SAXAGLIPTIN

FDA-approved active Small molecule Quality 6/100

Saxagliptin is a marketed drug with a key composition patent expiring in 2028. Its primary strength lies in its established market presence and revenue generation. The primary risk is the potential increase in competition following the patent expiry in 2028.

At a glance

Generic nameSAXAGLIPTIN
Drug classSodium-Glucose Cotransporter 2 Inhibitor [EPC]
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

Serious adverse events

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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