Sanofi/Regeneron’s Libtayo shows benefit in BCC
BCC marks the second non-melanoma skin cancer for which Libtayo has demonstrated first-in-class data, the firms note
Read Moreby Selina McKee | May 5, 2020 | News | 0
BCC marks the second non-melanoma skin cancer for which Libtayo has demonstrated first-in-class data, the firms note
Read Moreby Selina McKee | Jul 3, 2019 | News | 0
Around 560 patients per year with cutaneous squamous cell carcinoma are thought to be eligible for treatment with the drug in England
Read Moreby Anna Smith | Jul 2, 2019 | News | 0
The European Commission has granted conditional marketing authorisation for the drug for patients who are not candidates for curative surgery or curative radiation.
Read Moreby Selina McKee | Oct 1, 2018 | News | 0
Sanofi and Regeneron’s imunotherapy Libtayo has been cleared in the US to treat patients with certain forms of cutaneous squamous cell carcinoma (CSCC).
Read Moreby Selina McKee | Apr 30, 2018 | News | 0
US regulators are undertaking a priority review of Sanofi and Regeneron’s cemiplimab for the treatment of patients with metastatic cutaneous squamous cell carcinoma (CSCC), or those with locally advanced CSCC who are not candidates for surgery.
Read Moreby Selina McKee | Apr 3, 2018 | News | 0
European regulators have agreed to review Sanofi and Regeneron’s Dupixent for asthma and cemiplimab for advanced cutaneous squamous cell carcinoma.
Read Moreby Selina McKee | Jan 9, 2018 | News | 0
Sanofi and Regeneron are boosting their investment in development programmes for the PD-1 antibody cemiplimab in oncology and dupilumab in Type 2 (tissue specific) allergic diseases.
Read Moreby Selina McKee | Dec 14, 2017 | News | 0
Sanofi and Regeneron are gearing up to file their experimental PD-1 inhibitor cemiplimab on both sides of the Atlantic following the drug’s success in clinical trials.
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