Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
DAN-405 is a preclinical antibody-drug conjugate being developed by Dantari as a targeted high-capacity drug conjugate against prostate-specific membrane antigen (PSMA) for the treatment of castration-resistant prostate cancer. It uses a PSMA-targeting antibody linked to a highly loaded tubulin-inhibiting cytotoxic payload, with a drug–antibody ratio of approximately 60 enabled by Dantari’s Targeted High-capacity Drug Conjugate (T-HDC) platform.[1][3][7] By binding PSMA on prostate cancer cells and delivering a large quantity of tubulin inhibitor intracellularly, DAN-405 is intended to induce mitotic arrest and apoptosis while limiting systemic exposure, but it has not yet entered clinical trials and remains in preclinical development.[1][3][7]
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 DAN-405.