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Macrolide Antibiotic

Carrimycin for COVID-19

Phase 3
Waitlist Available
Research Sponsored by Shenyang Tonglian Group CO., Ltd
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from baseline (day -4 to day -1) days 3, 7, 10, 14 and 28 after treatment
Awards & highlights

Summary

This trial is testing carrimycin in hospitalized patients with severe COVID-19 to see if it can help fight the virus and improve their condition.

Eligible Conditions
  • COVID-19

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from baseline (day -4 to day -1) days 3, 7, 10, 14 and 28 after treatment
This trial's timeline: 3 weeks for screening, Varies for treatment, and from baseline (day -4 to day -1) days 3, 7, 10, 14 and 28 after treatment for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Time to patient not requiring supplemental oxygen up to 28 days after randomisation
Secondary study objectives
Change from baseline in respiratory rate
Change from baseline in temperature
Changes from baseline in sequential organ failure assessment (SOFA) score
+9 more

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: CarrimycinExperimental Treatment1 Intervention
Patients will receive oral dose of 400 mg carrimycin once-daily and SOC for 14 days.
Group II: PlaceboPlacebo Group1 Intervention
Patients will receive oral dose of Placebo once-daily and SOC for 14 days.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Carrimycin
2019
Completed Phase 1
~10

Find a Location

Who is running the clinical trial?

Shenyang Tonglian Group CO., LtdLead Sponsor
1 Previous Clinical Trials
520 Total Patients Enrolled
1 Trials studying COVID-19
520 Patients Enrolled for COVID-19
~21 spots leftby Sep 2025
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