Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SID530 is a novel **parenteral formulation of docetaxel** that contains hydroxypropyl-beta-cyclodextrin (HP-β-CD) as a solubilizing agent. This formulation was developed to be comparable to Taxotere, the original docetaxel formulation, in terms of pharmacokinetics and is administered intravenously. Comparative studies in nonhuman primates show that SID530 achieves **bioequivalence with Taxotere** based on similar pharmacokinetic parameters (Cmax, Tmax, AUC), indicating comparable distribution and plasma profile. The inclusion of hydroxypropyl-beta-cyclodextrin is aimed at improving the solubility and potentially reducing formulation-related toxicities typical of polysorbate 80-based docetaxel products[1].
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 docetaxel hydroxypropyl-beta-cyclodextrin formulation.