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A Phase III study of Solithromycin in patients with community-acquired pneumonia

Phase 3
Conditions
Community-acquired pneumonia
Registration Number
JPRN-jRCT2080223384
Lead Sponsor
Toyama Chemical Co., Ltd.(Current FUJIFILM Toyama Chemical Co., Ltd.)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1.Age: 20 years of age and older (at the time of obtaining informed consents)
2.Gender : Both
3.Inpatient/Outpatient status: Either
4.No history of hospitalization or hospitalization in a long-term care facility within 2 weeks before the onset of pneumonia
5.Confirmed clear infiltrative shadow by chest X-ray or CT within 48 hours prior to the first administration of the study drug
6.Signed the informed consent form by patients or patients' legal representatives
7.Others

Exclusion Criteria

1.Having improvement of clinical symptoms due to pneumonia by other systemic antibiotics
2.Having a history of allergy to macrolide or quinolone antibiotics
3.Others

Study & Design

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