LONDON, July 8 -- The government of the United Kingdom issued the following news:

The Medicines and Healthcare products Regulatory Agency (MHRA) has today (8 July 2026) approved the medicinenerandomilast (Jascayd)to treatadults with a lung disease called Idiopathic Pulmonary Fibrosis (IPF) and Progressive Pulmonary Fibrosis (PPF).

IPF and PPF are conditions where the lung tissue becomes scarred over timeand as a result breathing becomes increasingly difficult.

The active ingredient,nerandomilast, helpstoregulate the immune system and reduces tissue scarringonthe lungs.

The medicine can only be obtained with a prescription and should be taken exactly as your doctor or pharmacist has prescribed. The recommended dose is an 18mg tablet taken orally twice a day.

Julian Beach, MHRA Executive Director, Healthcare Quality and Access, said:

"Nerandomilastprovides a new treatment option for adultswithIPF and PPF. 

"This approval reflects the MHRA's commitment to ensuring patients can access safe and effective medicines where there is an unmet clinical need. 

"As with any medicine, the MHRA will keep the safety and effectiveness of nerandomilast under close review."

The most common side effectsofnerandomilast,which may affect more than 1 in 10 people,arediarrhoeaand weight loss.

Anyone who suspects they are having a side effect from this medicine are encouraged to talk to their doctor, pharmacist or nurse and report it directly to the Yellow Card scheme, either through the website(https://yellowcard.mhra.gov.uk/) or by searching the Google Play or Apple App stores for MHRA Yellow Card. 

Notes to editors  

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Thenew marketingauthorisationwasgranted on8 July 2026 to Boehringer Ingelheim Limited International GmbH. 

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More information can be found in the Summary of Product Characteristics and Patient Information leaflets which will be published on theMHRA Products websitewithin 7 days of approval.  

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For more information aboutidiopathic pulmonary fibrosis, visit:Idiopathic pulmonary fibrosis - NHS

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The Medicines and Healthcare products Regulatory Agency (MHRA)is responsible forregulating all medicines and medical devices in the UK by ensuring they work and are acceptably safe.  All our work is underpinned by robust and fact-based judgements to ensure that the benefits justify any risks.  

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The MHRA is an executive agency of the Department of Health and Social Care.  

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For media enquiries, please contact thenewscentre@mhra.gov.uk, or call on 020 3080 7651.

Disclaimer: Curated by HT Syndication.