Kevzara fails in PhIII COVID-19 trial
Sanofi and Regeneron do not anticipate carrying out further research on Kevzara in COVID-19
Read Moreby Selina McKee | Sep 1, 2020 | News | 0
Sanofi and Regeneron do not anticipate carrying out further research on Kevzara in COVID-19
Read Moreby Selina McKee | Jul 3, 2020 | News | 0
The drug failed to show any significant benefit in patient requiring mechanical ventilation
Read Moreby Selina McKee | Apr 10, 2018 | News | 0
Scottish cost regulators have approved funding for five new therapies on the NHS, offering new treatment options for a range of conditions.
Read Moreby Selina McKee | Nov 2, 2017 | News | 0
The National Institute for Health and Care Excellence has issued final guidance backing Sanofi’s Kevzara as a new treatment option for adults with severe, active rheumatoid arthritis (RA).
Read Moreby Selina McKee | Sep 22, 2017 | News | 0
Some patients with rheumatoid arthritis living in England and Wales should get ‘routine’ NHS access to Sanofi’s Kevzara after cost regulators issued draft guidelines deeming the drug cost effective.
Read Moreby Selina McKee | Jun 27, 2017 | News | 0
Sanofi and Regeneron’s Kevzara has been approved by European regulators to treat moderately to severely active rheumatoid arthritis (RA) in adult patients.
Read Moreby Selina McKee | May 23, 2017 | News | 0
Sanofi and Regeneron’s Kevzara has been cleared in the US to treat moderately to severely active rheumatoid arthritis (RA) in adult patients.
Read Moreby Selina McKee | Oct 31, 2016 | News | 0
US regulators are refusing to approve Sanofi and Regeneron’s sarilumab to treat patients with rheumatoid arthritis until certain manufacturing issues are addressed.
Read Moreby Selina McKee | Aug 2, 2016 | News | 0
European regulators have agreed to review Regeneron and Sanofi’s application to market the biologic sarilumab as a treatment for rheumatoid arthritis.
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