Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CPO-140 is a liposomal formulation of the anthracycline antineoplastic agent doxorubicin, developed by CONJ Biotherapeutics. Doxorubicin exerts its cytotoxic effects by intercalating into DNA and inhibiting the enzyme topoisomerase II, which prevents the religation of DNA strands and leads to DNA damage and apoptosis. The liposomal delivery system is designed to optimize the pharmacokinetic profile of doxorubicin, potentially enhancing its accumulation in tumor tissues through the enhanced permeability and retention (EPR) effect while minimizing systemic toxicities, particularly cardiotoxicity. CPO-140 is being developed as a potential generic or improved formulation (ANDA/NDA pathway) for the treatment of various solid and liquid tumors and is currently in the Pre-NDA/ANDA stage.
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 CPO-140.