News

EU green light for Takeda’s Alunbrig

EU green light for Takeda’s Alunbrig

Takeda’s Alunbrig has been approved in Europe as a treatment for a specific group of lung cancer patients, but access to the drug in the UK remains uncertain.

US approves first ever TRK inhibitor

US approves first ever TRK inhibitor

Bayer and Loxo Oncology’s Vitrakvi has become the first ever TRK inhibitor to be approved in the US, having been cleared to treat advanced solid tumours harbouring an NTRK gene fusion.

First children set to receive Novartis’ Kymriah

First children set to receive Novartis’ Kymriah

The first children to receive Novartis’ Kymriah – a ‘game-changing’ CAR-T therapy for cancer – will start treatment at Great Ormond Street Hospital in London this week, NHS England has announced.

Join the medical & scientific community at the MSEA awards 2018

Join the medical & scientific community at the MSEA awards 2018

The first edition of the PharmaTimes Medical & Scientific Excellence Awards will take place on Thursday 6th December – the competition will take place during the day, with the dinner and awards ceremony following in the evening at The Sofitel Hotel, Gatwick.

EU OKs Mundipharma’s Neulasta biosimilar

EU OKs Mundipharma’s Neulasta biosimilar

The Mundipharma network of independent associated companies says European regulators have approved use of Pelmeg, a biosimilar of Amgen’s white blood cell booster Neulasta.

Cell and Gene Therapy Catapult addresses sector skills gap

Cell and Gene Therapy Catapult addresses sector skills gap

The Cell and Gene Therapy (CGT) Catapult has launched the first Advanced Therapy Medicinal Products (ATMP) focused apprenticeship programme, developed in partnership with The Medicine Manufacturing Industry Partnership (MMIP).