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Clinical study of switching from pemafibrate IR to XR

Clinical study of switching from pemafibrate IR to XR - Clinical study of switching from pemafibrate IR to XR

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000053992
Enrollment
50
Registered
2024-03-28
Start date
2023-07-01
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

Hypertriglyceridemia while taking pemafibrate IR

Interventions

None listed

Sponsors

Sekino Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Triglyceridemia while taking pemafibrate IR

Exclusion criteria

Exclusion criteria: Patients who were deemed not appropriate to participate in this study by doctor

Design outcomes

Primary

MeasureTime frame
TG

Secondary

MeasureTime frame
1) LDL, HDL, T-cho 2) sCr, eGFR , AST, ALT 3)Remnant-Like Particle, fatty acid fractionation 4) oxidized LDL, hs-CPR 5) side effects

Countries

Japan

Contacts

Public ContactMitsue Akiyama

Sekino Laboratory Department of Research

skn-np@sekino-hospital.com03-3986-5501

Outcome results

None listed

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