Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Duomeisu** is a pegylated liposomal formulation of doxorubicin hydrochloride, a cytotoxic anthracycline antibiotic developed by CSPC Pharmaceutical Group Limited (specifically CSPC Ouyi Pharmaceutical). It intercalates into DNA, inhibits topoisomerase II, generates reactive oxygen species, and induces apoptosis, primarily for treating ovarian cancer, breast cancer (including HER2-negative metastatic), lymphoma, multiple myeloma, and other solid tumors. The liposomal encapsulation enhances tumor penetration, prolongs circulation, and reduces cardiotoxicity compared to conventional doxorubicin, with typical dosing at 40 mg/m² intravenously every 28 days. Approved in China since 2012 for AIDS-related Kaposi’s sarcoma and later for additional indications, it has demonstrated efficacy in platinum-resistant ovarian cancer and anthracycline-pretreated breast cancer patients.[1][2][3][4][7][9]
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Duomeisu.