Last reviewed · How we verify

KADIAN

Actavis Inc. · FDA-approved active Small molecule Quality 6/100

KADIAN, marketed by Actavis Inc., is an established therapeutic option in its class, with a key composition patent expiring in 2028. Its mechanism of action through specific receptor interactions provides a well-understood therapeutic profile, which is a significant strength. The primary risk is the potential increase in competition following the 2028 patent expiry.

At a glance

Generic nameKADIAN
Also known asTreatment B, Reference Product
SponsorActavis Inc.
ModalitySmall molecule
Therapeutic areaPain
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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