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The content of this website has been produced in line with the INLYTA® (axitinib) Summary of Product Characteristics for Great Britain. 
Prescribing Information for INLYTA® (axitinib) click here.  Prescribing Information for SUTENT® (sunitinib malate) click here. Adverse event reporting information can be found at the bottom of the page.

INLYTA® (axitinib)

INLYTA® is indicated for the treatment of adult patients with advanced renal cell carcinoma (aRCC) after failure of prior treatment with sunitinib or a cytokine.1

 Dosing & half-life

INLYTA® has a flexible dosing regimen and short half-life that could help you manage some adverse reactions.1

 More information Loading Clinical study data

INLYTA® is an established second line mRCC therapy that continues to deliver efficacy outcomes for patients.1–7

 See the dataLoading Safety information

​​​​​​INLYTA® has a well-characterised safety and tolerability profile.1, 4-7

 Learn moreLoadingINLYTA® dosing and half-life video

An animated video describing the INLYTA® dosing and half-life information.

References

INLYTA® Summary of Product Characteristics for Great Britain click here. INLYTA® Summary of Product Characteristics for Northern Ireland click here.Hu-Lowe DD et al. Clin Cancer Res 2008;14:7272–7283. Escudier B, Gore M. Drugs R D 2011;11:113–126.Rini BI, et al. Lancet 2011;378:1931-1939.Melichar B, et al. Efficacy and tolerability of axitinib in metastatic renal cell carcinoma (mRCC): comparison of Czech clinical registry and AXIS trial data. ECC. 25–29 September 2015. Vienna, Austria. Poster: 2615.Rossetti S, et al. Activity of second line axitinib in metastatic renal cell carcinoma (mRCC) patients treated with sunitinib: results from SAX Italian real world trial. ASCO. 2–6 June 2017. Chicago, USA. Abstract: e16054.Matias M, et al. Eur J Cancer 2017;79:185–192.
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