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Liposomal doxorubicin hydrochloride

Cephalon, Inc. · FDA-approved active Small molecule Quality 19/100

Liposomal doxorubicin hydrochloride, marketed by Cephalon, Inc., is an established oncology treatment with a key composition patent expiring in 2028. Its liposome-encapsulated formulation provides targeted delivery to cancer cells, enhancing efficacy and reducing systemic toxicity compared to conventional doxorubicin. The primary competitive threat comes from Doxil (Janssen Pharmaceuticals) and Caelyx (Pfizer), which also offer liposomal formulations of doxorubicin.

At a glance

Generic nameLiposomal doxorubicin hydrochloride
Also known asMyocet®
SponsorCephalon, Inc.
Drug classAntineoplastic agent
TargetDNA and topoisomerase II
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Approved indications

No approved indications tracked.

Pipeline indications

Common side effects

No common side effects on file.

Drug interactions

Key clinical trials

Patents

PatentExpiryType
US7897765B2

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
FDA Orange BookPatents + exclusivity

Competitive intelligence

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