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Emergency application of therapeutic monoclonal antibodies against SARS-COV-2

Emergency application of therapeutic monoclonal antibodies against SARS-COV-2

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046965
Enrollment
Unknown
Registered
2021-06-05
Start date
2021-05-27
Completion date
Unknown
Last updated
2022-01-18

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

Intervention group:therapeutic monoclonal antibodies

Sponsors

The Third People's Hospital of Shenzhen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. At least 18 years of age; 2. Within 7 days of screening, SARS-CoV-2 infection is clearly identified by PCR testing; 3. Male or female (contraceptive or infertile).

Exclusion criteria

Exclusion criteria: 1. Patients with COVID-19 recurrence; 2. When screening, meet any of the following: (1) Stroke; (2) Meningitis; (3) Encephalitis; (4) Myelitis; (5) Myocardial ischemia; (6) Myocarditis; (7) Pericarditis; (8) Congestive heart failure (NYHA class III-IV); (9) Arterial or deep vein thrombosis, pulmonary embolism; 3. Have a history of severe allergic reactions, including systemic urticaria, angioedema, hypersensitivity reactions; 4. Chronic active liver disease; 5. Have received COVID-19 convalescence plasma and SARS-CoV-2 antibody treatment; 6. Have received other investigational drugs for the treatment of SARS-CoV-2; 7. The history of drug abuse within 1 year before screening; 8. The research doctor judges that there is any situation that is not suitable for participating in the project.

Design outcomes

Primary

MeasureTime frame
SARS-CoV-2 RNA quantification;

Countries

China

Contacts

Public ContactZhang Zheng

The Third People's Hospital of Shenzhen

zhangzheng1975@aliyun.com+86 13927461302

Outcome results

None listed

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