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The usefulness of anamorelin for iPPFE

Phase 2
Recruiting
Conditions
idiopathic pleuroparenchymal fibroelastosis
Registration Number
JPRN-jRCTs041220165
Lead Sponsor
Yasui Hideki
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
20
Inclusion Criteria

Patients over 20 years old
Patients diagnosed with iPPFE based on CT imaging and clinical findings
Patients whose consent for this study has been obtained by signing a consent form

Exclusion Criteria

Patients with a history of hypersensitivity to anamorelin
Patients with congestive heart failure
Patients with myocardial infarction or angina pectoris
Patients with severe conduction defects (e.g., complete atrioventricular block)
Patients who have received or are currently taking the following drugs within 1 week prior to the start of study treatment: clarithromycin, indinavir, itraconazole, nelfinavir, saquinavir, telaprevir, voriconazole, ritonavir-containing products, cobicistat-containing products
Patients with hepatic dysfunction of moderate severity or greater (Child-Pugh classification B and C)
Patients with difficulty in oral intake of food due to obstruction of the gastrointestinal tract or other organic abnormality of the gastrointestinal tract
Patients with diabetes mellitus who have poor glycemic control despite the use of oral diabetes medications or insulin
Pregnant or nursing mothers
Patients who are deemed inappropriate by the principal investigator (or sub-investigator)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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