A Study to Evaluate the Efficacy and Safety of DXP604 in Patients With Mild to Moderate COVID-19

NCT05381519 | Unknown Phase 2 DMC

• 1 other identifier: DXP604-201
• Study Type: interventional
• Target: 50
• Locations: 0 countries
• Sites: N/A

Brief Summary

A phase II, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of DXP604 in patients with mild to moderate COVID-19. By determination of severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) virus in nasopharyngeal swab samples by reverse transcription quantitative polymerase chain reaction (RT-qPCR) from baseline (2 h ± 30 min before dosing) to Viral load changes on day 8,to evaluate the efficacy of DXP604 monotherapy in patients with mild to moderate coronavirus disease 2019 (COVID-19). It was assumed that the difference in viral load change of SARS-CoV-2 virus from baseline (2 h ± 30 min before administration) to day 8 in nasopharyngeal swab samples by RT-qPCR between the experimental drug group and the placebo group was -1.00 log10 copies/mL.The null and alternative hypotheses comparing the experimental drug group with the placebo group are set as follows: H0：µ1 = µ2 H1：µ1 ≠ µ2

Conditions

COVID-19

Outcome Measures

Primary Outcomes (1)

• viral load of SARS-CoV-2 virus in nasopharyngeal swab samples

  determination of changes in viral load of SARS-CoV-2 virus in nasopharyngeal swab samples from baseline (2 h ± 30 min before dosing) to day 8

  from baseline (2 h ± 30 min before dosing) to day 8

Study Arms (2)

DXP604

EXPERIMENTAL

1800mg，IVgtt

Biological: DXP604

placebo

PLACEBO COMPARATOR

IVgtt

Biological: DXP604

Interventions

DXP604 BIOLOGICAL

1800mg，IVgtt

DXP604; placebo

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• The age of the subjects when signing the ICF is 18 to 70 years old (including 18 and 70 years old), male or female;
• Possess venous access conditions, allowing drug administration and blood sample collection according to the research protocol;
• SARS-CoV-2 positive in any laboratory-confirmed sample within 96 hours before screening;
• According to the National Health Commission of the People's Republic of China (NHC) "New Coronary Virus Pneumonia Diagnosis and Treatment Program", the ninth revised version of the trial was clinically classified as mild/ordinary patients;
• There is at least one factor that may lead to a high risk of severe/critical COVID-19: ① age \> 60 years; ② cardiovascular and cerebrovascular diseases (including hypertension), chronic lung diseases (chronic obstructive pulmonary disease, chronic obstructive pulmonary disease, Moderate to severe asthma), diabetes, chronic liver, kidney disease, tumor and other basic diseases; ③ immunodeficiency (such as AIDS patients, long-term use of corticosteroids or other immunosuppressive drugs lead to immunosuppression); ④ obesity (physical constitution) index ≥ 30); ⑤ Heavy smokers.
• Symptoms of COVID-19 ≤ 5 days before randomization; such as fever, cough, shortness of breath, sore throat, diarrhea, vomiting, and dysgeusia;
• Agree to collect nasopharyngeal swabs, saliva and venous blood;
• The subjects can communicate well with the researcher, understand and comply with the requirements of this study, and understand and sign the ICF.

You may not qualify if:

• Severe COVID-19 patients who meet any of the following:
• Shortness of breath, respiratory rate ≥ 30 times/min;
• In resting state, blood oxygen saturation (SpO2) ≤ 93% when inhaling air;
• Arterial blood oxygen partial pressure PaO2/inhaled oxygen concentration (FiO2)≤300mmHg (1mmHg=0.133kPa); Note: For areas with high altitude (over 1000 meters above sea level), the following formula should be used to correct PaO2/FiO2: PaO2/FiO2×\[760/air pressure (mmHg)\];
• The clinical symptoms are progressively worsened, and lung imaging shows that the lesion progresses significantly within 24 to 48 hours by \>50%;
• Critically ill patients with COVID-19 who meet any of the following:
• Respiratory failure occurs and requires mechanical ventilation;
• Shock occurs;
• Complicated with other organ failure requires ICU monitoring and treatment;
• Those who are known to be allergic to the test drug and its components;
• Hemodynamic instability within 24 hours before treatment allocation requires the use of vasopressors;
• Suspected or confirmed serious, active bacterial, fungal, viral or other infections (except for COVID-19) that the investigator believes may pose a risk when taking interventions;
• Any comorbidities requiring surgery within 7 days prior to screening, or comorbidities deemed life-threatening within 29 days prior to screening;
• Any serious concomitant systemic disease, condition or disorder that the investigator believes should be prevented from participating in this study;
• Patients with positive anti-SARS-CoV-2 immunoglobulin G (IgG) and IgG\>10;

Sponsors & Collaborators

• Wuhan Institute of Biological Products Co., Ltd: lead

MeSH Terms

Conditions

COVID-19

Interventions

DXP-604

Condition Hierarchy (Ancestors)

Pneumonia, Viral; Pneumonia; Respiratory Tract Infections; Infections; Virus Diseases; Coronavirus Infections; Coronaviridae Infections; Nidovirales Infections; RNA Virus Infections; Lung Diseases; Respiratory Tract Diseases

Central Study Contacts

jin ronghua, Bachelor

CONTACT

010-84322000; bjdtyyll@163.com

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 16, 2022
• First Posted: May 19, 2022
• Study Start: May 1, 2022
• Primary Completion: June 1, 2022
• Study Completion: September 1, 2022
• Last Updated: May 19, 2022

Record last verified: 2022-05

Data Sharing

• IPD Sharing: Will not share