medcelerator · clinician one-pager
New Pill for Scarred-Lung Disease in Adults
Jascayd (nerandomilast) for IPF and PPF
FDA Approved · United States, Canada, United Kingdom, European Union · September 3, 2026
Condition: Pulmonary Fibrosis
Who this is for
Jascayd (nerandomilast) is approved in the United States, Europe and the United Kingdom. It is for adults with idiopathic or progressive pulmonary fibrosis, two types of lung scarring. Health Canada is reviewing it.
Next clinical step
The US Food and Drug Administration (FDA) has approved this medicine. In the United States, the United Kingdom and the European Union, ask your doctor or a specialist whether it suits you. They can write a prescription. Insurance or public drug plan coverage is not guaranteed. In Canada, authorisation is not confirmed; see Possible routes below if any are listed.
Ways to access this treatment
United States · Prescription
US prescription (FDA-labelled)
https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa1b14c6-957f-d326-5099-911bfe33e391
United Kingdom · Prescription
UK prescription (MHRA-authorised)
https://www.gov.uk/government/news/nerandomilast-jascayd-approved-to-treat-adult-patients-with-idiopathic-pulmonary-fibrosis-and-progressive-pulmonary-fibrosis
European Union · Prescription
EU prescription (EC marketing authorisation)
https://www.ema.europa.eu/en/medicines/human/EPAR/jascayd
United States, United Kingdom, European Union, Canada · Recruiting clinical trial
FIBRONEER-ACT: A Study to Test Whether Nerandomilast Helps People With Fibrosing Interstitial Lung Disease at Risk for Disease Progression
Tests this treatment. Nerandomilast vs placebo in fibrosing ILD (FIBRONEER-ACT, phase 3).
https://clinicaltrials.gov/study/NCT07540988
United States, United Kingdom, European Union, Canada · Recruiting clinical trial
A Study to Test Whether Nerandomilast Can Help Slow Down Changes in the Lung in People With a Family History of Pulmonary Fibrosis
Combination or different setting. Relatives with interstitial lung abnormalities (prevention setting), not established IPF/PPF (phase 3).
https://clinicaltrials.gov/study/NCT07201922
United States, United Kingdom, European Union, Canada · Recruiting clinical trial
A Study to Find Out How Nerandomilast is Tolerated, Handled by the Body, and if it Helps Children and Adolescents With Interstitial Lung Disease (FIBRONEER-chILD)
Combination or different setting. Children and adolescents 2-17 with fibrosing ILD; the label is adults (phase 3).
https://clinicaltrials.gov/study/NCT07366034
Search all trials on ClinicalTrials.gov: https://clinicaltrials.gov/search?cond=interstitial%20lung%20disease&intr=nerandomilast&aggFilters=status:rec
Search Health Canada's Clinical Trials Search Portal: https://clinical-trials-search.canada.ca/en/search?search_api_fulltext=nerandomilast
Possible routes (not confirmed)
Canada · Health Canada Special Access Programme (SAP) · Applicability unknown
Health Canada Special Access Programme (manufacturer must agree)
SAP here depends on the manufacturer agreeing to supply; no confirmation for this drug.
https://www.canada.ca/en/health-canada/services/drugs-health-products/special-access/drugs.html
General resources for further research
Canadian Clinical Trial Search Portal (Health Canada)
Health Canada's public search of the drug and biologic clinical trials it has authorised in Canada (phase 1 to 3, since April 2013). Search by condition, drug, or trial status and see where trials are running. It replaced the Health Canada Clinical Trials Database in July 2026. A listing is not enrolment, and Health Canada does not recruit patients: ask your clinician and contact the trial sponsor.
https://clinical-trials-search.canada.ca/en/home
ClinicalTrials.gov
US National Library of Medicine registry of clinical studies. Search by condition, drug, NCT number, and location. A listing is not enrolment, eligibility, or funding. Talk with the trial contact and a clinician before assuming a slot exists.
https://clinicaltrials.gov/
CTIS (EU Clinical Trials Information System)
European Union public portal for clinical trials submitted under the Clinical Trials Regulation. Search by medicine, condition, and member state. A CTIS record is not an EMA marketing authorisation and is not enrolment.
https://euclinicaltrials.eu/
AI-produced discussion aid; not prescribing instructions. Approval does not establish coverage. Full article: https://medcelerator.com/articles/jascayd-nerandomilast-ipf-ppf