Phase III Clinical Study Evaluating the Efficacy and Safety of WPV01 in Patients With Mild/Moderate COVID-19

NCT06197217 | Completed Phase 3 FDA Drug

• 1 other identifier: WPV01-CP-23
• Study Type: interventional
• Target: 1,350
• Locations: 1 country
• Sites: 1

Brief Summary

The study is a multicenter, randomized, double-blind, placebo-controlled efficacy, safety Phase III clinical trial designed to evaluate the efficacy and safety of WPV01 in patients with mild/moderate COVID-19.

Conditions

Mild to Moderate COVID-19

Outcome Measures

Primary Outcomes (1)

• Time from first dose to sustained clinical recovery of 11 COVID-19 symptoms within 28 days

  Day 1 to Day 28

Secondary Outcomes (16)

• Decrease in viral load from baseline on Day 5 of treatment

  Day 1 to Day 28

• Percentage of subjects achieving sustained clinical recovery of 11 COVID-19 symptoms at Day 5, 9, 14, 21, and 28

  Day 1 to Day 28

• Time to sustained clinical remission of 11 COVID-19 symptoms within 28 days of treatment

  Day 1 to Day 28

• Percentage of subjects achieving sustained clinical remission of 11 COVID-19 symptoms on Day 5, 9, 14, 21, and 28

  Day 1 to Day 28

• Changes in 11 COVID-19-related symptom scores from baseline to Day 5, 9, 14, 21, and 28

  Day 1 to Day 28

Study Arms (2)

WPV01

EXPERIMENTAL

Drug: WPV01

Placebo

PLACEBO COMPARATOR

Drug: Placebo

Interventions

WPV01 DRUG

Subjects in the WPV01 group will receive WPV01 600mg orally (200mg, 3 tablets per dose), 3 times daily (TID) for 15 consecutive treatments

WPV01

Placebo DRUG

Subjects in the Placebo group will receive WPV01 Placebo orally (3 tablets per dose), 3 times daily (TID) for 15 consecutive treatments

Placebo

Eligibility Criteria

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

You may qualify if:

• Male or female patients ≥18 years at the time of signing informed consent, those with a history of COVID-19 were also eligible for enrollment in this study
• Meet the diagnostic criteria for mild or moderate COVID-19 infection according to the the Diagnostic and Treatment Program for COVID-19 Infections (Trial Tenth Edition) issued by the China Health and Wellness Commission:
• Positive for SARS-CoV-2 nucleic acid or positive for SARS-CoV-2 antigen in a nasopharyngeal swab specimen within 72 hours prior to randomization
• The onset of a COVID-19-related target symptom is less than 72 hours from randomization and the presence of at least 1 of the 5 key COVID-19-related symptoms with a severity of ≥2 points on the day of randomization
• Females of childbearing potential (details are defined in Appendix 3) Subjects must have a negative pregnancy test at Screening. Subjects will be required to use effective contraception throughout the study period beginning with the signing of the informed consent form and for 30 days after completion of the study.
• Eligible to understand the procedures and methods of this clinical trial, with full informed consent and voluntary participation by the subjects.

You may not qualify if:

• Known allergy to any of the ingredients in the investigational therapeutic agents
• Meet the diagnostic criteria for severe or critical COVID-19 infection according to the Diagnostic and Treatment Program for COVID-19 Infections (Trial Tenth Edition) issued by the China Health and Wellness Commission at the time of randomization.
• Within 14 days prior to randomization, the subject has received SARS-CoV-2 antiviral therapy or immunotherapy including, but not limited to, antiviral medications (e.g., interferon, raltegravir, lopinavir/ritonavir, favipiravir, ribavirin, chloroquine phosphate, arbidol, nirmatrelvir/ritonavir, molnupiravir, azulfidine, simnotrelvir/ritonavir, deuremidevir, and COVID-19 therapeutics approved during subsequent studies), corticosteroids, interleukin-1 inhibitors, interleukin-6 inhibitors, and intravenous immunoglobulins
• Within 3 days or 5 drug half-lives (whichever is longer) prior to randomization, the subject has used medications to alleviate symptoms of COVID-19: including, but not limited to, antipyretic/analgesic, cough suppressant/expectorant, compounded cold and flu remedies, antihistamines, anti-bacterials and anti-fungals
• Abnormal liver function at screening: total bilirubin ≥ 1.5 x upper limit of normal (ULN) or alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥ 3 x ULN
• Being on dialysis or having a combination of moderate to severe renal insufficiency
• Immunocompromised at screening (including patients with malignant tumors, organ or bone marrow transplantation, or treatment with corticosteroids or other immunosuppressive agents)
• Chronic respiratory disease, including bronchial asthma, chronic obstructive pulmonary disease, at the time of screening
• Suspected or confirmed acute systemic infections other than COVID-19 at the time of screening
• Any comorbidity requiring surgery within 14 days prior to randomization, or any comorbidity considered life-threatening by the investigator within 30 days prior to randomization
• Patients who have received (within 30 days prior to randomization or within 5 drug half-lives, whichever is longer) or are expected to receive plasma therapy with SARS-CoV-2 monoclonal antibody or recovered COVID-19 during the study period
• Patients who have received any COVID-19 vaccine within 1 month prior to randomization
• Currently using or within 4 days post dose expected to use any drug or substance which are highly dependent on clearance via CYP3A4, MDR1, OAT1, or OAT3; used within 28 days prior to randomization or expected to use during the treatment drus with strong MDR1 inducer
• Patients who have difficulty in swallowing or history of gastrointestinal disorders that significantly affect the absorption of drugs
• Pregnant, lactating women

Sponsors & Collaborators

• Westlake Pharmaceuticals (Hangzhou) Co., Ltd.: lead

Study Sites (1)

China Japan Friendship Hospital

Beijing, Beijing Municipality, 100029, China

Location

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 8, 2024
• First Posted: January 9, 2024
• Study Start: June 14, 2023
• Primary Completion: August 21, 2023
• Study Completion: September 20, 2023
• Last Updated: June 12, 2024

Record last verified: 2024-06

Locations

CN (1)