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To evaluate the exploratory clinical trial of homoharringtonine in the treatment of adult COVID-19 patients

To evaluate the exploratory clinical trial of homoharringtonine in the treatment of adult COVID-19 patients

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045993
Enrollment
Unknown
Registered
2021-05-01
Start date
2021-03-09
Completion date
Unknown
Last updated
2021-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

experimental group:Nebulized inhalation of homoharringtonine+Basic treatment
control group:Basic treatment

Sponsors

Beijing Ditan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 50 years; 2. RT-PCR method detects the positive of new coronavirus nucleic acid; 3. The time between the first positive nucleic acid test or the first appearance of clinical symptoms is no more than 5 days after enrollment; 4. The informed consent form has been signed.

Exclusion criteria

Exclusion criteria: 1. Known or suspected allergy to the components of homoharringtonine; 2. According to the current trial implementation of the latest version of the "New Coronavirus Infection Pneumonia Diagnosis and Treatment Plan", the patient is diagnosed as a critically ill patient with novel coronavirus pneumonia; 3. Combined with severe liver disease (TBIL >= 2 ULN, ALT, AST >=5 ULN; 4. Patients with severe renal insufficiency (glomerular filtration rate <= 60 mL/min/1.73m2) or who are receiving continuous renal replacement therapy, hemodialysis, and peritoneal dialysis; 5. Patients who have severe breathing difficulties and cannot complete the self-aerosolized drug inhalation; 6. Patients with hematological tumors; 7. Patients who have used antiviral drugs in the past 2 months, such as interferon, lopinavir, ritonavir, remdesivir, etc., are receiving other antiviral drugs; 8. Women who are pregnant or breastfeeding or have a birth plan during the trial period and within 6 months after the end of the trial; 9. Are participating in other clinical trials or are using experimental drugs; 10. Rehabilitation plasma therapy for patients with COVID-19; 11. Are using Chinese medicine for treatment; 12. Patients with diabetes, hypertension and obese people; 13. According to the judgment of the investigator, there are other circumstances that are not suitable for participating in this trial.

Design outcomes

Primary

MeasureTime frame
Viral load;

Secondary

MeasureTime frame
Ratio of light to ordinary to heavy duty;Proportion of heavy to critical loads;Time of nucleic acid negative reaction of novel coronavirus;

Countries

China

Contacts

Public ContactZhang Fujie

Beijing Ditan Hospital, Capital Medical University

Treatment@chinaaids.cn+86 13001953958

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026