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NEXAVAR

Nexavar receives final appraisal for primary liver cancer

10 August 2017 | By Dr Zara Kassam (European Pharmaceutical Review)

NICE has released a Final Appraisal Document recommending Nexavar for the treatment of patients with advanced hepatocellular carcinoma...

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Bayer receives EU approval for Regorafenib

8 August 2017 | By Dr Zara Kassam (European Pharmaceutical Review)

Bayer have announced the European Commission has granted marketing authorisation for Stivarga...

news

Bayer and Onyx report Phase 3 study results of NEXAVAR® (sorafenib) as adjuvant treatment for patients with liver cancer who have undergone surgery or local ablation

11 March 2014 | By Amgen

Bayer HealthCare Pharmaceuticals Inc. and Onyx Pharmaceuticals, Inc., announced that a Phase 3 trial evaluating the investigational use of NEXAVAR® (sorafenib) tablets as an adjuvant treatment for patients with hepatocellular carcinoma...

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U.S. FDA Approves NEXAVAR® (sorafenib) for the treatment of patients with locally recurrent or metastatic, progressive, differentiated thyroid carcinoma refractory to radioactive iodine treatment

22 November 2013 | By Amgen

First and only FDA-approved treatment option for patients with this type of thyroid cancer...

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Recommended

NEXAVAR

Nexavar receives final appraisal for primary liver cancer

Bayer receives EU approval for Regorafenib

Bayer and Onyx report Phase 3 study results of NEXAVAR® (sorafenib) as adjuvant treatment for patients with liver cancer who have undergone surgery or local ablation

U.S. FDA Approves NEXAVAR® (sorafenib) for the treatment of patients with locally recurrent or metastatic, progressive, differentiated thyroid carcinoma refractory to radioactive iodine treatment