Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CalliSpheres are a type of drug-eluting bead (DEB) composed of a polyvinyl alcohol (PVA) hydrogel, specifically engineered for the treatment of hypervascular tumors through transarterial chemoembolization (TACE). Developed by Jiangsu Hengrui Medicine and its subsidiary Suzhou Callisyn Biomedical, these microspheres are designed to be loaded with chemotherapeutic agents, such as doxorubicin, epirubicin, or oxaliplatin, via an ion-exchange mechanism. Once injected into the tumor-feeding arteries, CalliSpheres provide a dual therapeutic effect: they physically occlude the blood vessels to induce tumor ischemia and necrosis, and they simultaneously release the loaded drug in a controlled, sustained manner directly into the tumor tissue. This localized delivery maximizes the intratumoral drug concentration while significantly reducing systemic exposure and associated side effects. CalliSpheres are primarily indicated for hepatocellular carcinoma (HCC) and are also utilized in the management of liver metastases and other hypervascular malignancies.
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 CalliSpheres.