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Recruiting NCT07743996

NCT07743996 Emotional and Social Experiences of Antifibrotic (AF) Therapy Among Idiopathic Pulmonary Fibrosis (IPF)/Progressive Pulmonary Fibrosis (PPF) Patients: A Real-World Study

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Clinical Trial Summary
NCT ID NCT07743996
Status Recruiting
Phase
Sponsor Boehringer Ingelheim
Condition Idiopathic Pulmonary Fibrosis
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2026-08-01
Primary Completion 2026-09-30

Eligibility & Interventions

Sex All sexes
Min Age 40 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2026-08-01 with a primary completion date of 2026-09-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This is a cross-sectional study that will be conducted across Japan using an online patient-reported outcome questionnaire. This study tries to find out the attitudes toward and experiences of the emotional and/or social impact of side effects associated with antifibrotic (AF) treatment among Japanese patients with Idiopathic Pulmonary Fibrosis (IPF)/Progressive Pulmonary Fibrosis (PPF), and how are these attitudes associated with patients' individual characteristics.

Eligibility Criteria

Inclusion Criteria: 1. Patients with IPF aged 40 years or older who received nintedanib or pirfenidone within the previous 4 weeks, or patients with PPF aged 18 years or older who received nintedanib within the previous 4 weeks 2. Patients capable of responding to a self-administered questionnaire Exclusion Criteria: 1. Patients treated with nerandomilast (including clinical trials) 2. Patients with PPF treated with pirfenidone 3. Patients currently hospitalized 4. Patients with malignant tumors

Contact & Investigator

Central Contact

Boehringer Ingelheim

✉ clintriage.rdg@boehringer-ingelheim.com

📞 1-800-243-0127

Frequently Asked Questions

Who can join the NCT07743996 clinical trial?

This trial is open to participants of all sexes, aged 40 Years or older, studying Idiopathic Pulmonary Fibrosis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07743996 currently recruiting?

Yes, NCT07743996 is actively recruiting participants. Contact the research team at clintriage.rdg@boehringer-ingelheim.com for enrollment information.

Where is the NCT07743996 trial being conducted?

This trial is being conducted at Tokyo, Japan.

Who is sponsoring the NCT07743996 clinical trial?

NCT07743996 is sponsored by Boehringer Ingelheim. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology