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Hit Tumors* Hard With TheraSphere

Interventional Oncology / Cancer Therapies & Ablation / TheraSphere
TheraSphere receives FDA Approval.

TheraSphere receives FDA Approval!

After 20 years as a humanitarian exemption device (HDE), the FDA grants TheraSphere pre-market approval, making TheraSphere the only Y-90 therapy indicated for HCC. This means institutional review board (IRB) approval of TheraSphere is no longer required by the FDA. 

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The TARGET Study.

The TARGET Study

The TARGET Study is a global, real-world data set across 8 countries demonstrating the reproducibility of treatment with TheraSphere Y-90 glass microspheres, confirmed by Simplicit90Y™ Personalized Dosimetry Software.

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Proven. Personalized. Precise.
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Strike first with three distinct advantages. We have a proven therapy to fight primary liver cancer.1 We deploy a custom personalized dose to extend life, to improve life. We act with expert precision.

 
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Your patients are fighting for more than their survival. They’re fighting for their quality of life. TheraSphere is uniquely able to help you strike first on both fronts.

 
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Glass Matters With Y-90

Give your patients a fighting chance with TheraSphere Y-90 Glass Microspheres. These precision-manufactured glass microspheres are the most powerful radiation therapy on the market.
 

1. Salem R, Gabr A, Riaz A, et al. Institutional decision to adopt Y-90 as primary treatment for HCC informed by a 1,000-patient 15-year experience. Hepatology. 2017 Dec 1. 

*Refers to HCC or associated tumors

 
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