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A Randomized, Double-blind, Placebo-controlled, Multicenter and Phase Ⅱa Clinical Trial for the Effectiveness and Safety of Baicalein Tablets in the Treatment of Improve Other Aspects of Healthy Adult With Influenza Fever

Primary Purpose

Influenza

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Baicalein Tablets 400mg
Baicalein Tablets 600mg
blank control 0mg
Sponsored by
CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Influenza

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1.Meet the diagnostic criteria for influenza(non-severe); 2.Fever to take medicine for the first time, The patient's maximum temperature (axillary temperature) is over 38℃; 3.The rapid virus antigen test of nasal swab was positive; 4.Course of disease ≤ 24 hours(The definition of course of disease is the time from fever to take investigational product for the first time); 5.Aged 18 to 65 years old(include 18 and 65), all genders; 6.Sign the informed consent form.

Exclusion Criteria:

  • 1.The patients with severe influenza or complication (e.g. secondary bacterial pneumonia, pneumonia caused by other pathogens or other viral pneumonia); 2.The patients with other acute upper respiratory tract infection (e.g. acute pharyngitis, tonsillitis, rhinitis and nasosinuitis); 3.Allergic to baicalin and its analogue, Paracetamol tablets, or allergic people; 4.Patients with any of the following risk factors:

    1. Residents living in long-term care facilities (e.g. welfare house, sanatorium);
    2. Combined with chronic respiratory diseases (e.g. bronchial asthma, chronic obstrctive palmonary diseases);
    3. Combined with chronic cardiovascular disease (e.g. congenital heart disease, congestive heart failure, or coronary artery disease, but doesnt include hypertension without any other cardio-related symptoms);
    4. Combined with hematological system diseases (e.g. chronic myelogenous leukemia, lymphocytic leukemia, myelodysplastic syndrome, aplastic anemia);
    5. Neurodevelopmental disorders, include cerebrum, spinal cord, Peripheral nerve and muscle disorders (e.g. cerebral palsy, epilepsy[epileptic seizure disorder], stroke, dysgnosia, Moderate to severe dysplasia, myodystrophy, or spinal cord injury);
    6. Poor control of chronic metabolic and endocrine diseases;
    7. Immunosuppression (long-term use of immunosuppressant, immunocom promise caused by infection by HIV or malignant tumour);
    8. Obese people[BMI>30, BMI=Weight(kg)/Height(m2)] 5.Long-term take aspirin under 19 years old; 6.White blood cell count>11.0×109/L, or the proportion of neutrophils >80%, or need systemic antibacterial therapy; 7.24 hours before the visit, the patients have received antiviral treatment for influenza; 8.The patients have received Influenza vaccine or research monoclonal antibody in a year; 9.ALT and AST is equal or greater than 1.5 times of upper limit of normal, Scr is greater than upper limit of normal; 10.Suspected or really have a history of alcohol or drug abuse; 11.Gestation (have a positive pregnancy test), lactating women, or have a family planning within the next 6 months; 12.The patients have participated in other clinical trials within 3 months; 13.The investigator considers it inappropriate to participate in this clinical trial.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Placebo Comparator

    Arm Label

    low-dose group

    high-dose group

    placebo group

    Arm Description

    Baicalein Tablets group

    Baicalein Tablets group

    control group

    Outcomes

    Primary Outcome Measures

    The time of fever relieving
    After the first dose, the time of subjects' armpit temperature reduced to 37.3℃, and no longer increases in 24h.

    Secondary Outcome Measures

    symptom alleviating time of influenza
    The area under the curve (AUC) of the decline in the subjects' influenza symptom total score.
    Percentage of subjects with influenza complications Percentage of subjects with influenza complications
    Percentage of subjects with influenza complications, e.g. be hospitalized, death, sinusitis, otitis media, bronchitis, pneumonia, and so on.
    Percentage of antipyretic drugs used
    Percentage of the subjects used paracetamol.
    Percentage of virus positive to negative
    Percentage of subjects' influenza virus positive change to negative

    Full Information

    First Posted
    December 12, 2018
    Last Updated
    February 4, 2019
    Sponsor
    CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03830684
    Brief Title
    A Randomized, Double-blind, Placebo-controlled, Multicenter and Phase Ⅱa Clinical Trial for the Effectiveness and Safety of Baicalein Tablets in the Treatment of Improve Other Aspects of Healthy Adult With Influenza Fever
    Official Title
    A Randomized, Double-blind, Placebo-controlled, Multicenter and Phase Ⅱa Clinical Trial for the Effectiveness and Safety of Baicalein Tablets in the Treatment of Improve Other Aspects of Healthy Adult With Influenza Fever
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 1, 2019 (Anticipated)
    Primary Completion Date
    May 31, 2019 (Anticipated)
    Study Completion Date
    October 31, 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study in order to evaluate the Baicalein Tablets' safety and efficiency for audit with influenza
    Detailed Description
    This study in order to evaluate the Baicalein Tablets' safety and efficiency for audit with influenza, The trial designed by randomized, double-blind, placebo-controlled, multicenter and optimal efficiency. Subjects will be randomly assigned to low-dose group, high-dose group or placebo group as 1:1:1 proportionally, planned to enroll 180 subjects, each group enroll 60 subjects. The primary indicator is the time of fever relieving, comparison after the second visit. The secondary indicator are symptom alleviating time of influenza, percentage of subjects with influenza complications, percentage of antipyretic drugs used, percentage of virus positive to negative, comparison at the end of the experiment.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Influenza

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    180 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    low-dose group
    Arm Type
    Experimental
    Arm Description
    Baicalein Tablets group
    Arm Title
    high-dose group
    Arm Type
    Experimental
    Arm Description
    Baicalein Tablets group
    Arm Title
    placebo group
    Arm Type
    Placebo Comparator
    Arm Description
    control group
    Intervention Type
    Drug
    Intervention Name(s)
    Baicalein Tablets 400mg
    Intervention Description
    4 Baicalein Tablets and 2 placebo per time, three times a day
    Intervention Type
    Drug
    Intervention Name(s)
    Baicalein Tablets 600mg
    Intervention Description
    6 Baicalein Tablets per time, three times a day
    Intervention Type
    Drug
    Intervention Name(s)
    blank control 0mg
    Intervention Description
    6 placebo per time, three times a day
    Primary Outcome Measure Information:
    Title
    The time of fever relieving
    Description
    After the first dose, the time of subjects' armpit temperature reduced to 37.3℃, and no longer increases in 24h.
    Time Frame
    day 3
    Secondary Outcome Measure Information:
    Title
    symptom alleviating time of influenza
    Description
    The area under the curve (AUC) of the decline in the subjects' influenza symptom total score.
    Time Frame
    day 3 and day 5
    Title
    Percentage of subjects with influenza complications Percentage of subjects with influenza complications
    Description
    Percentage of subjects with influenza complications, e.g. be hospitalized, death, sinusitis, otitis media, bronchitis, pneumonia, and so on.
    Time Frame
    day 3 and day 5
    Title
    Percentage of antipyretic drugs used
    Description
    Percentage of the subjects used paracetamol.
    Time Frame
    day 3 and day 5
    Title
    Percentage of virus positive to negative
    Description
    Percentage of subjects' influenza virus positive change to negative
    Time Frame
    day 3 and day 5

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: 1.Meet the diagnostic criteria for influenza(non-severe); 2.Fever to take medicine for the first time, The patient's maximum temperature (axillary temperature) is over 38℃; 3.The rapid virus antigen test of nasal swab was positive; 4.Course of disease ≤ 24 hours(The definition of course of disease is the time from fever to take investigational product for the first time); 5.Aged 18 to 65 years old(include 18 and 65), all genders; 6.Sign the informed consent form. Exclusion Criteria: 1.The patients with severe influenza or complication (e.g. secondary bacterial pneumonia, pneumonia caused by other pathogens or other viral pneumonia); 2.The patients with other acute upper respiratory tract infection (e.g. acute pharyngitis, tonsillitis, rhinitis and nasosinuitis); 3.Allergic to baicalin and its analogue, Paracetamol tablets, or allergic people; 4.Patients with any of the following risk factors: Residents living in long-term care facilities (e.g. welfare house, sanatorium); Combined with chronic respiratory diseases (e.g. bronchial asthma, chronic obstrctive palmonary diseases); Combined with chronic cardiovascular disease (e.g. congenital heart disease, congestive heart failure, or coronary artery disease, but doesnt include hypertension without any other cardio-related symptoms); Combined with hematological system diseases (e.g. chronic myelogenous leukemia, lymphocytic leukemia, myelodysplastic syndrome, aplastic anemia); Neurodevelopmental disorders, include cerebrum, spinal cord, Peripheral nerve and muscle disorders (e.g. cerebral palsy, epilepsy[epileptic seizure disorder], stroke, dysgnosia, Moderate to severe dysplasia, myodystrophy, or spinal cord injury); Poor control of chronic metabolic and endocrine diseases; Immunosuppression (long-term use of immunosuppressant, immunocom promise caused by infection by HIV or malignant tumour); Obese people[BMI>30, BMI=Weight(kg)/Height(m2)] 5.Long-term take aspirin under 19 years old; 6.White blood cell count>11.0×109/L, or the proportion of neutrophils >80%, or need systemic antibacterial therapy; 7.24 hours before the visit, the patients have received antiviral treatment for influenza; 8.The patients have received Influenza vaccine or research monoclonal antibody in a year; 9.ALT and AST is equal or greater than 1.5 times of upper limit of normal, Scr is greater than upper limit of normal; 10.Suspected or really have a history of alcohol or drug abuse; 11.Gestation (have a positive pregnancy test), lactating women, or have a family planning within the next 6 months; 12.The patients have participated in other clinical trials within 3 months; 13.The investigator considers it inappropriate to participate in this clinical trial.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Kun Lou
    Phone
    0311-67808817
    Email
    loukun@mail.ecspc.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Qingquan Liu, Professor
    Organizational Affiliation
    Beijing Chinese Medicine Hospital affiliated to Capital Medical University
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    A Randomized, Double-blind, Placebo-controlled, Multicenter and Phase Ⅱa Clinical Trial for the Effectiveness and Safety of Baicalein Tablets in the Treatment of Improve Other Aspects of Healthy Adult With Influenza Fever

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