Skip to content

Clinical study of novel coronavirus (SARS-Cov-2) infection treated with aerosol inhalation (IFN-? plus anti-inflammatory factor TFF2)

Clinical study of novel coronavirus (SARS-Cov-2) infection treated with aerosol inhalation (IFN-? plus anti-inflammatory factor TFF2)

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030262
Enrollment
Unknown
Registered
2020-02-26
Start date
2020-02-11
Completion date
Unknown
Last updated
2020-05-18

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

Group 1:Standard therapy plus aerosol inhalation for 3 times (once for every day)
Group 2:Standard therapy plus aerosol inhalation for 3 times (once for every 2 days)
Third group:Standard therapy
Fourth group:Standard therapy plus aerosol inhalation for 6 times (once for every day)

Sponsors

Shanghai Public Health Clinical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 18 to 70 years old; 2. According with the clinical diagnosis of viral pneumonia symptoms,including fever, Low white blood cells or platelets infiltration shadow in CT; 3. Positive result for nucleic acid of 2019-nCov; 4. Patients can receive aerosol inhalation 5. Consent to sign a written informed statement prior to the beginning of the study.

Exclusion criteria

Exclusion criteria: 1. Pneumonia caused by other viruses, except for 2019-nCov; 2. Clear bacterial infection; 3. Subjects who have used antiviral drugs and may need another antiviral treatment during the study; 4. There are serious non-infectious pulmonary diseases, including tuberculosis, pulmonary edema and pulmonary embolism; 5. Severe liver and kidney dysfunction; 6. Participating in other clinical studies within 30 days before administration; 7. Allergic to type 1 interferon; 8. Pregnant or lactating women; 9.In any other case, if the investigator thinks it is not suitable for the trial, or it may increase the risk of the subject or interfere with the clinical trial.

Design outcomes

Primary

MeasureTime frame
Viral load;Clinical features;Inflammation;Pulmonary imaging;In-hospital days;

Secondary

MeasureTime frame
routine blood test;routine urine test;blood biochemical;

Countries

China

Contacts

Public ContactJianqing Xu

Shanghai Public Health Clinical Center

xujianqing@shphc.org.cn+86 18964630206

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026