Skip to content

Senicapoc in patients with Progressive Fibrotic ILD (Interstitial Lung Disease) or IPF (Idiopathic Pulmonary Fibrosis) to prevent progression.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-511131-97-00
Acronym
FIBROPOC
Enrollment
100
Registered
2024-08-30
Start date
2025-08-10
Completion date
Unknown
Last updated
2024-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Progressive Fibrotic Interstitial Lung Disease

Brief summary

Rate of decline of FVC (in mL) over a period of 26 weeks

Detailed description

Absolute decline in percent predicted forced vital capacity (%FVC) over 13 and 26 weeks, All-cause mortality., Chance in Vas of dyspnea, All-cause non-elective hospitalizations, Respiratory-related mortality, Acute exacerbations (as evaluated by the investigator), Changes in quality of life, assessed by the EQ-5D, Amount and type of adverse events., Changes in quality of life, assessed by the SGRQ-I and K-BILD total score. (Danish and UK sites only)

Interventions

DRUGPLACEBO

Sponsors

Lillebaelt Hospital
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Secondary

MeasureTime frame
Absolute decline in percent predicted forced vital capacity (%FVC) over 13 and 26 weeks, All-cause mortality., Chance in Vas of dyspnea, All-cause non-elective hospitalizations, Respiratory-related mortality, Acute exacerbations (as evaluated by the investigator), Changes in quality of life, assessed by the EQ-5D, Amount and type of adverse events., Changes in quality of life, assessed by the SGRQ-I and K-BILD total score. (Danish and UK sites only)

Primary

MeasureTime frame
Rate of decline of FVC (in mL) over a period of 26 weeks

Countries

Denmark, Estonia

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026