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MOVENTIG

MOVENTIG is indicated for the treatment of opioid-induced constipation (OIC) in adult patients who have had an inadequate response to laxative(s).1

Adverse Events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse Events should also be reported to Kyowa Kirin International UK NewCo Ltd, known as Grünenthal Meds on +44 (0)1896 664000, email PVUK@grunenthalmeds.com

Click here for Prescribing Information.

Efficacy of MOVENTIG in treating opioid-induced constipation (OIC)2

The efficacy of MOVENTIG has been compared in clinical trials to placebo in treating patients suffering from OIC who have had an inadequate response to laxative therapy.

Pooled data from two randomised, double-blind, placebo-controlled trials were analysed. The patients were experiencing non-cancer pain, aged 18-84 with OIC and had inadequate response to laxatives (defined as concurrent OIC symptoms of at least moderate severity while taking at least one laxative class for a minimum of four days during the pre-study period).1 Patients were randomised to receive MOVENTIG 12.5mg, 25mg or placebo. Assessments included response rate, time to first post-dose spontaneous bowel movement, number of spontaneous bowel movements (SBMs), OIC symptoms and patient-reported outcomes over 12 weeks.

MOVENTIG (naloxegol) is indicated for the treatment of opioid-induced constipation (OIC) in adult patients who have had an inadequate response to laxative(s). For advice on the responsible use of opioids to treat pain, please click here

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  • References

    1. MOVENTIG Summary of Product Characteristics.

    2. Tack J, et al. UEG. 2015;3(5):471-480.

    KKI/INT/MOV/0115 November 2023