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TACT

University of Oxford · FDA-approved active Small molecule Quality 7/100

TACT, developed by the University of Oxford, is a marketed small molecule that binds to specific biological targets to treat its primary indication. The key composition patent for TACT is set to expire in 2028, which currently provides a strong barrier to generic competition. The primary risk for TACT is the potential loss of market exclusivity and revenue following the patent expiry in 2028.

At a glance

Generic nameTACT
SponsorUniversity of Oxford
ModalitySmall molecule
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

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