Calquence shows long-term efficacy and tolerability in MCL
Patients with relapsed or refractory mantle cell lymphoma (MCL) treated with AstraZeneca’s Calquence remained progression free for a median of 22 months
Read Moreby Selina McKee | Dec 7, 2020 | News | 0
Patients with relapsed or refractory mantle cell lymphoma (MCL) treated with AstraZeneca’s Calquence remained progression free for a median of 22 months
Read Moreby Selina McKee | Nov 27, 2018 | News | 0
Kyowa Hakko Kirin (Kyowa Kirin) has received marketing authorisation Europe for use of Poteligeo to treat Mycosis Fungoides and Sézary Syndrome.
Read Moreby Selina McKee | Jul 10, 2018 | News | 0
A late-stage trial of Servier and CTI BioPharma’s Pixuvri in combination with Roche’s MabThera has failed to hit targets in B-cell non-Hodgkin lymphoma, putting its conditional approval in Europe in jeopardy.
Read Moreby Selina McKee | May 25, 2018 | News | 0
Adding Arzerra to treatment with Treanda has failed to significantly extend progression-free survival in patients with indolent B cell non-Hodgkin’s lymphoma.
Read Moreby Selina McKee | Sep 18, 2017 | News | 0
US regulators have issued an accelerated approval for Bayer’s relapsed follicular lymphoma therapy Aliqopa.
Read Moreby Selina McKee | Aug 29, 2017 | News | 0
Gilead Sciences is buying Kite Pharma in a deal worth $11.9 billion, securing itself access to the latter’s experimental CAR-T therapy axicabtagene ciloleucel and wider cancer pipeline.
Read Moreby Selina McKee | Aug 1, 2017 | News | 0
Kite Pharma has submitted the first CAR-T cell therapy in Europe, seeking permission to market its axicabtagene ciloleucel (axi-cel) to treat patients with three subtypes of aggressive non-Hodgkin lymphoma (NHL).
Read Moreby Selina McKee | Feb 23, 2017 | News | 0
Mundipharma is gearing up to launch biosimilar Truxima in seven European markets for the treatment of certain cancers and inflammatory conditions, after Celltrion bagged a regulatory approval for the drug.
Read Moreby Selina McKee | Oct 13, 2016 | News | 0
Cost regulators for the NHS in England and Wales have turned down Janssen’s Imbruvica for treating some people with Waldenstrom’s macroglobulinaemia (WM) – a rare type of slow growing non-Hodgkin’s lymphoma.
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