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The department conducted an intake study: "Treatment for mother has been recommended.
The majority of patients (91.0%) received study treatment as outpatients.
In total, 28 IPF patients were randomized to study treatment.
a One randomized patient did not receive study treatment.
Discontinues study treatment for 7 or more consecutive days.
To study treatment outcome using the modified technique: Cavaterm™ plus.
Investigators judged 9 of the 14 TEAEs as being possibly related to the study treatment and the other five as not being related to the study treatment.
Patients who failed the study treatment were given rescue treatment.
*Including initial study treatment.
All patients discontinued study treatment.
Study treatment was extremely safe.
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