A Study of Efficacy and Safety of Azvudine vs. Nirmatrelvir-Ritonavir in the Treatment of COVID-19 Infection

COVID-19 Clinical Trial

Official title:

A Prospective Multicenter, Randomized, Controlled Clinical Trial of the Safety and Efficacy of Azvudine vs. Nirmatrelvir-Ritonavir in Hospitalized Patients With Moderate to Severe COVID-19 Infection

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05697055
• Other study ID #: SWYX2023022
• Status: Recruiting
• Phase: Phase 4
• Start date: January 21, 2023
• Est. completion date: July 21, 2023

Study information

• Verified date: February 2023
• Source: Shandong Provincial Hospital
• Contact: Bing Leng
• Phone: +86531-68776461
• Email: taozilb[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The COVID-19 pandemic has become a major public health challenge, and the treatment options for the disease are currently limited. The commonly used oral small-molecule anti-COVID-19 drugs in China are Nirmatrelvir-Ritonavir and Azvudine. These drugs have been tested in pre-marketing clinical trials in patients with non-severe COVID-19 infection and have demonstrated therapeutic effects in inhibiting virus transmission and preventing disease progression. However, until now, the efficacy and safety of these drugs in patients with moderate to severe COVID-19 infections remains unclear. Therefore, this study is aiming to compare the efficacy and safety of Azvudine and Nirmatrelvir-Ritonavir in moderate to severe COVID-19 infections. This study will be a multicenter, randomized, controlled clinical trial study in patients hospitalized with moderate to severe COVID-19 infections. Recovery of clinical symptoms, nucleic acid negative conversion, improvement in oxygenation index, and imaging improvement will be used as study endpoints.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 410
• Est. completion date: July 21, 2023
• Est. primary completion date: May 21, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Hospitalized patients of =18 years old, regardless of gender or race;

2. Patients who have a positive SARS-CoV-2 test result;

3. Diagnosed with moderate or severe COVID-19 infection according to the diagnostic criteria from the "Diagnosis and treatment program trial version 10 guidelines" issued by the National Health Commission of the People's Republic of China. Including:

?Moderate: continuous high fever for more than 3 days or/and cough, shortness of breath, etc., but the breathing frequency (RR) is less than 30 times/minute, and the oxygen saturation when inhaling air at rest is > 93%. Imaging shows the characteristic manifestations of COVID-19 pneumonia.

? Severe: Adults meet any of the following requirements: A, shortness of breath, RR= 30 times/minute; B, the oxygen saturation when inhaling air at rest is = 93%; C, Arterial partial oxygen pressure (PaO2)/ Fraction of inspiration O2 (FiO2) =300mmHg (1mmHg=0.133kPa), and PaO2/FiO2 should be corrected according to the following formula for areas above 1000 m :PaO2/FiO2× [760/ atmospheric pressure (mmHg)]; D, the clinical symptoms were gradually aggravated, and the lung imaging showed that the lesion progressed significantly within 24 ~ 48 hours > 50%.

4. Join this study voluntarily.

5. Each subject must sign an informed consent form (ICF) indicating that he/she understands the purpose and procedure of the study and is willing to participate in the study. Considering the patient's condition, the ICF may be signed by the legal representative.

Exclusion Criteria:

1. Allergic to the drugs involved;

2. Pregnancy or lactation;

3. Diagnosed or suspected critical COVID-19 infection;

4. Child-Pugh C of liver function or estimated glomerular filtration rate (eGFR) less than 30mL/min during screening;

5. Receive SARS-CoV-2 monoclonal antibody therapy or other antiviral therapy;

6. The subject and/or authorized family members refused to receive anti-COVID-19 treatment;

7. Any life-threatening disease or organ system dysfunction that the researcher thinks can harm the safety of the subjects and expose the research results to unnecessary risks; drug addicts, uncontrolled mental illness or cognitive dysfunction.

8. Join other similar clinical researchers within 3 months;

9. Patients who were not considered suitable for inclusion by the researchers (such as patients who were expected to be unable to adhere to the treatment due to financial problems).

Related Conditions & MeSH terms

• COVID-19

Intervention

Drug:
• Azvudine
5mg orally, once a day, for no more than 14 days
• Nirmatrelvir-Ritonavir
Nirmatrelvir 300mg combined with Ritonavir 100mg every 12 hours for 5 days. For patients with 30= eGFR < 60 ml/min, it should be reduced to150mg/100mg Nirmatrelvir-Ritonavir every 12 hours for 5 days

Locations

Country	Name	City	State
China	Shandong Provincial Hospital	Jinan	Shandong

Sponsors (6)

Lead Sponsor	Collaborator
Shandong Provincial Hospital	Central hospital Affiliated to Shandong First Medical University, Gansu Provincial Hospital, Rizhao People's Hospital, The Affiliated Hospital Of Southwest Medical University, The Second Affiliated Hospital of Shandong First Medical University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time and proportion of patients with COVID-19 infection to have sustained clinical recovery		Up to 28 days
Secondary	Proportion of progression to critical COVID-19 and death from any cause		Up to 28 days
Secondary	Time of COVID-19 related symptom score and World Health Organization (WHO) clinical progress scale score. Time and proportion of clinical recovery, symptom resolution and regression of major symptoms		Up to 28 days
Secondary	Time and proportion of the nucleic acid negative conversion		Days 3, 6, 9, 12, 15, 18, 21, 24, 27
Secondary	Time and proportion of chest CT image improvement		Days 6, 12, 18, 24
Secondary	Time and proportion of oxygenation index improvement		Up to 28 days
Secondary	Length of stay		Up to 28 days