Jan/Feb 2026 • PharmaTimes Magazine • 9
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The MHRA has authorised GSK’s Nucala (mepolizumab) in the UK as an add-on maintenance treatment for adults with uncontrolled COPD of an eosinophilic phenotype who are already receiving triple therapy with an inhaled corticosteroid, a long-acting beta2 agonist and a long-acting muscarinic antagonist.
The decision follows results from two placebo-controlled phase 3 studies, MATINEE and METREX, which demonstrated that mepolizumab significantly reduced the annualised rate of moderate or severe exacerbations and extended the time to first exacerbation once treatment had begun. The safety profile was consistent with what is already known for the medicine.
Professor Mona Bafadhel, Director of King’s Centre for Lung Health and Chair of Respiratory Medicine at King’s College London, said: “For people living with COPD, managing exacerbations is an ongoing challenge that significantly impacts their lives, with almost a quarter of hospitalised patients being re-admitted within 30 days. The approval of mepolizumab provides us with a new treatment option that can help people with eosinophilic COPD by reducing the frequency of their exacerbations.”
Dr Joanne Hunt, Medical Head, Specialty, GSK UK, said: “At GSK, we’re committed to redefining respiratory care through innovation. If recommended by the National Institute for Health and Care Excellence (NICE), mepolizumab will be administered every four weeks to significantly reduce the rate of moderate/severe exacerbations and delay the time to first moderate/severe exacerbation once commenced on treatment.”
Bial has introduced a new sublingual formulation of apomorphine in the UK, offering a fresh treatment option for adults with Parkinson’s disease who experience intermittent OFF episodes that are not adequately controlled by oral medication.
Around 166,000 people in the UK are estimated to live with Parkinson’s, many of whom experience OFF periods when levodopa becomes insufficient during the day.
These episodes can cause the return of symptoms such as stiffness, tremors and difficulty moving, affecting independence and quality of life. Rescue therapies that act quickly are therefore considered an important complement to standard treatment.
Tom Foltynie, Consultant Neurologist and Professor of Neurology at the National Hospital for Neurology & Neurosurgery, Queen Square, London, said: “Motor fluctuations are a major concern for patients as Parkinson’s progresses. Oral doses of Levodopa can take an hour before they start to take effect, and some doses fail completely because of slow stomach emptying or competition for absorption from dietary protein.
“Identifying other mechanisms of administration for dopaminergic therapies is therefore of major importance and we look forward to assessing the benefits of sublingual apomorphine in our PD patients experiencing this problem,” he added.
Camille Carroll, Consultant Neurologist and Professor of Clinical Neuroscience at the Translational and Clinical Research Institute at Newcastle and Faculty of Health, University of Plymouth, said: “I am delighted to see Kynmobi becoming available as another therapeutic option in the UK for Parkinson’s disease.”
Johnson & Johnson has submitted a Type II variation application to the European Medicines Agency for an extension of indication for teclistamab in combination with subcutaneous daratumumab for adults with relapsed or refractory multiple myeloma who have received at least one prior therapy.
The company said the two immunotherapies act in a complementary way by targeting BCMA and CD38 to activate the immune system earlier in the treatment pathway.
Modus Therapeutics has announced that the first patient has been dosed in part 2 of its ongoing phase 2a clinical study evaluating sevuparin for the treatment of chronic kidney disease (CKD) with anaemia.
The company confirmed that the initiation of part 2 was preceded by a protocol amendment submitted during the summer of 2025 to finalise dose selection.
Zenas BioPharma has announced positive findings from its phase 3 INDIGO trial evaluating obexelimab in patients with immunoglobulin G4-related disease (IgG4-RD), reporting a statistically significant reduction in flare risk and favourable safety outcomes.
The company said the study met its primary endpoint, with obexelimab delivering a 56% reduction in the risk of IgG4-RD flare compared with placebo during the 52-week controlled period.
Lindus Health and Quotient Sciences have announced a strategic partnership to enable enhanced patient recruitment and streamlined pathways for clinical trials. The partnership will address the industry challenge posed by biotechnology and pharmaceutical companies needing to engage with multiple vendors across preclinical and clinical phases, causing inefficiencies and operational delays. Quotient’s expertise in early clinical and drug development will be integrated with Lindus’ expertise in patient recruitment and later-stage trial delivery.
Responding to the Health Services Safety Investigations Body’s new report on corridor care, Rory Deighton, from the NHS Confederation, said: “Corridor care has gone from being a last resort during the busiest periods of winter to an increasingly common way of managing the rising demand the NHS is facing. We know that corridor care is undignified, unsafe and frustrating for patients and their families, and leaves NHS staff with the moral injury of being unable to provide the quality of care they would like to.”
Recent NHS doctor strikes have again centred on disputes over pay, working conditions and staffing pressures.
Resident doctors in England staged a five day walkout in December 2025, one of the largest in NHS history, with around 95,000 staff absences reported.