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Regeneron and Sanofi bust into new I-O market with FDA nod for Libtayo in basal cell carcinoma


Feb 10, 2021 10:55am
In a phase 2 trial, the response rate to Libtayo was 21% in metastatic basal cell carcinoma and 29% in locally advanced disease.(Sanofi Genzyme/Regeneron)
Regeneron and Sanofi’s anti-PD-1 cancer drug Libtayo has been pegged as an immuno-oncology laggard in diseases such as lung cancer, where well-established players like Merck’s Keytruda rule the market. But there’s one area where Regeneron and Libtayo can claim a lead: skin cancer.
In that department, the FDA has added another jewel to Regeneron and Sanofi’s crown, approving Libtayo to treat patients with advanced basal cell carcinoma (BCC). It’s the first immunotherapy drug cleared by the FDA to treat that disease, and it comes two years after Libtayo’s first approval in metastatic cutaneous squamous cell carcinoma. ....

Merck Keytruda , Bristol Myers Squibb Opdivo Yervoy , European Society Of Clinical Oncology , European Society , Clinical Oncology , Bristol Myers Squibb , Regeneron Pharmaceuticals , Pd 1 L1 , Checkpoint Inhibitors , Skin Cancer , Immuno Oncology , ஐரோப்பிய சமூகம் ஆஃப் மருத்துவ புற்றுநோயியல் , ஐரோப்பிய சமூகம் , மருத்துவ புற்றுநோயியல் , பிரிஸ்டல் மைஸ் ஸ்க்விப்ப் , பி.டி. எல்1 , தோல் புற்றுநோய் , இம்யூனோ புற்றுநோயியல் ,