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The comparative use-result survey of TORAYMYXIN (PMX) for acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF)

The comparative use-result survey of TORAYMYXIN (PMX) for acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT2032250211
Enrollment
760
Registered
2025-07-04
Start date
2024-12-10
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF)

Interventions

None listed

Sponsors

Takamatsu Seigo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with AE-IPF who receive PMX treatment for the first time

Exclusion criteria

Exclusion criteria: Patients with AE-IPF who have previously received PMX treatment

Design outcomes

Primary

MeasureTime frame
Survival rate on 4 weeks after AE-IPF

Secondary

MeasureTime frame
1. Survival rate on 12 weeks after AE-IPF (compared to non-PMX treatment patients) 2. Improvement in pulmonary oxygenation (P/F ratio, AaDO2) before and after PMX treatment 3. Improvement of imaging findings in chest X-ray and high-resolution CT (HRCT) 4. Change in serum lactate dehydrogenase (LDH) levels before and after PMX treatment 5. Change in serum C-reactive protein (CRP) levels before and after PMX treatment 6. Duration of mechanical ventilation 7. Change in serum levels of KL-6, SP-D, ferritin, and D-dimer before and after PMX treatment 8. Comparison of efficacy between AE-IPF patients with and without a known triggers

Contacts

Public ContactSeigo Takamatsu

Toray Industries, Inc.

device-safety.toray.mb@mail.toray+81-3-3245-8617

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026