Eleven medicines backed for EU approval
Recommendations include the first antibody-drug conjugate for multiple myeloma patients with limited treatment options
Read Moreby Selina McKee | Jul 27, 2020 | News | 0
Recommendations include the first antibody-drug conjugate for multiple myeloma patients with limited treatment options
Read Moreby Selina McKee | Jun 29, 2020 | News | 0
The recommendations include a conditional approval for Gilead’s Veklury (remdesivir) for COVID-19
Read Moreby Selina McKee | Jun 3, 2020 | News | 0
Tecentriq in combination with Avastin is the first and only cancer immunotherapy regimen cleared to treat unresectable or metastatic liver cancer
Read Moreby Selina McKee | Dec 17, 2018 | News | 0
The European Medicines Agency’s human medicines committee (CHMP) has put forward seven medicines for approval in the region.
Read Moreby Selina McKee | Sep 24, 2018 | News | 0
Bayer and Novartis have lost a landmark case in the UK seeking to prevent the off-label use of Roche’s Avastin to treat wet AMD, a leading cause of sight loss in the elderly.
Read Moreby Selina McKee | Jan 22, 2018 | News | 0
European regulators have issued a green light for Amgen and Allergan’s Mvasi, marking the first biosimilar of Roche’s Avastin to be approved in the region.
Read Moreby Selina McKee | Jan 4, 2018 | News | 0
AstraZeneca has expanded its agreement with US group Myriad Genetics to identify women with advanced ovarian cancer most likely to benefit from its medicines.
Read Moreby Selina McKee | Dec 11, 2017 | News | 0
Roche unit Genentech has announced that a Phase III study assessing a combination of Tecentriq and Avastin for advanced or metastatic renal cell carcinoma achieved its co-primary endpoint of progression-free survival.
Read Moreby Selina McKee | Dec 7, 2017 | News | 0
Roche group Genentech has announced full US approval for Avastin for the treatment of adults with glioblastoma that progressed following prior therapy.
Read Moreby Selina McKee | Nov 13, 2017 | News | 0
The European Medicines Agency’s Committee for Medicinal Products for Human Use has put 10 medicines forward for approval in the region, including new options for multiple sclerosis, eosinophilic esophagitis and eosinophilic asthma.
Read Moreby Selina McKee | Oct 27, 2017 | News | 0
US regulators are reviewing a potential new indication for Avastin as a first-line option for advanced ovarian cancer, filed by Roche group Genentech.
Read Moreby Selina McKee | Dec 7, 2016 | News | 0
The US Food and Drug Administration has approved Roche-group Genentech’s application to market Avastin for patients with a specific type of ovarian cancer.
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