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Study identifier: NCT06577558 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy and Safety of SR1375 in Adult Patients With CAP

Condition: Community-acquired Pneumonia  ·  Sponsor: Shanghai SIMR Biotechnology Co., Ltd.

PhasePhase 2
Planned participants240
Who can joinAll sexes, 18 Years to 85 Years
Healthy volunteersNo

About this study

This is a phase 2 study to evaluate the efficacy and safety of SR1375 in hospitalized adult patients with CAP. Patients will receive SR1375 or placebo for 8 weeks. The study duration for each patient is up to 10 weeks.

This description comes directly from the study's public registry record.

Talk to the study team

Wang, PhD  ·  (086)021-68161783  ·  fwang@simrbio.com

Always discuss trial participation with your own doctor first.

Locations (29)

Fuyang People's HospitalFuyang, Anhui, ChinaRecruiting
Peking University Third HospitalBeijing, Beijing Municipality, ChinaRecruiting
Zhangzhou HospitalZhangzhou, Fujian, ChinaRecruiting
Gaozhou People's HospitalGaozhou, Guangdong, ChinaRecruiting
The First Affiliated Hospital of Sun Yat-sen UniversityGuangzhou, Guangdong, ChinaRecruiting
The Third Affiliated Hospital of Southern Medical UniversityGuangzhou, Guangdong, ChinaRecruiting
Nanfang HospitalGuangzhou, Guangdong, ChinaRecruiting
The First Affiliated Hospital of Shantou University Medical CollegeShantou, Guangdong, ChinaRecruiting
Yulin First People's HospitalYulin, Guangxi, ChinaRecruiting
The First Hospital of Hebei Medical UniversityShijiazhuang, Hebei, ChinaRecruiting
Daqing Longnan HospitalDaqing, Heilongjiang, ChinaRecruiting
Daqing People's HospitalDaqing, Heilongjiang, ChinaRecruiting

+ 17 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06577558