EU expands scope of Imbruvica to include untreated CLL patients
Treatment naïve patients lived longer without disease progression with the Imbruvica-based regimen than those given a chemotherapy-based one
Read Moreby Selina McKee | Sep 8, 2020 | News | 0
Treatment naïve patients lived longer without disease progression with the Imbruvica-based regimen than those given a chemotherapy-based one
Read Moreby Anna Smith | Aug 14, 2019 | News | 0
The approval follows the Positive Opinion from the European Medicines Agency’s CHMP, and marks the fifth European approval in as many years.
Read Moreby Selina McKee | Jul 12, 2018 | News | 0
AbbVie and Johnson & Johnson’s Imbruvica has failed to meet its key target in a late stage study assessing its use in patients with treatment-naïve diffuse large B-cell lymphoma.
Read Moreby Selina McKee | May 25, 2018 | News | 0
A combination of AbbVie/Johnson & Johnson’s Imbruvica and Roche’s Gazyva has taken a step closer to becoming first chemotherapy-free CD20 combination for first-line treatment of chronic lymphocytic leukaemia (CLL), after showing promise in a late-stage clinical trial.
Read Moreby Selina McKee | Feb 1, 2018 | News | 0
Janssen’s Imbruvica will be routinely available on the NHS to treat certain patients with mantle cell lymphoma (MCL), after cost regulators issued a final green light for the drug.
Read Moreby Selina McKee | Dec 15, 2017 | News | 0
It is looking likely that a subgroup of patients with mantle cell lymphoma (MCL) will get routine access to Janssen’s Imbruvica on the NHS.
Read Moreby Selina McKee | Aug 3, 2017 | News | 0
The US Food and Drug Administration has expanded the scope of Johnson & Johnson/AbbVie’s Imbruvica to include the treatment of adult patients with chronic graft versus host disease (cGVHD) after failure of one or more treatments, marking the first therapy specifically approved for the condition in the US.
Read Moreby Selina McKee | Apr 11, 2017 | News | 0
Scotland will become the first UK nation to routinely offer HIV pre-exposure prophylaxis to all eligible patients after the Scottish Medicines Consortium backed the use of Gilead’s Truvada alongside four other new therapies to be funded by the NHS.
Read Moreby Selina McKee | Apr 5, 2017 | News | 0
US regulators have agreed to review AbbVie and Janssen’s Imbruvica for previously treated chronic graft-versus-host-disease (cGVHD), a severe, potentially life-threatening consequence of stem cell or bone marrow transplant.
Read Moreby Selina McKee | Jan 26, 2017 | News | 0
Cost regulators for the NHS in England and Wales have now published final guidelines endorsing Janssen’s Imbruvica to treat some patients with chronic lymphocytic leukaemia (CLL).
Read Moreby Selina McKee | Jan 20, 2017 | News | 0
Janssen and AbbVie’s Imbruvica has been cleared by regulators in the US to treat certain patients with marginal zone lymphoma (MZL), a rare form of non-Hodgkin’s lymphoma.
Read Moreby Selina McKee | Nov 25, 2016 | News | 0
It is looking likely that Janssen’s Imbruvica will be available to treat some people with chronic lymphocytic leukaemia (CLL) routinely on the NHS, after cost regulators issued draft guidelines endorsing its use.
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