Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AP5346 (ProLindac) is a third-generation polymer-conjugated platinum-based chemotherapeutic agent designed for the treatment of various cancers. It consists of diaminocyclohexane (DACH)-platinum—the active moiety in oxaliplatin—covalently bound to a water-soluble hydroxypropylmethacrylamide (HPMA) copolymer via a pH-sensitive linker. This design enables targeted delivery and controlled release of the cytotoxic platinum compound preferentially within the acidic microenvironment typical of tumors. The mechanism involves DNA binding and crosslinking, leading to inhibition of DNA replication and transcription, ultimately triggering apoptosis in cancer cells. Preclinical and clinical studies have shown efficacy at least equal to or superior to oxaliplatin with improved tolerability. The drug was developed by Abeona Therapeutics and reached phase II clinical trials for solid tumors including recurrent ovarian cancer but has since been discontinued[1][3][4][5].
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 AP5346.