A Study of ZSP1273 Tablets in Patients With Acute Uncomplicated Influenza A

Guangdong Raynovent Biotech Co., Ltd750 enrolled

Overview

This is a multi-center, randomized, double-blind, placebo-controlled, and active controlled clinical trial to assess the efficacy and safety of ZSP1273 tablets in the treatment of Acute Uncomplicated influenza A.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

750

Conditions

Influenza A

Interventions

ZSP1273 600 mgDRUG

3 X 200-mg tablet taken orally

Placebo to OseltamivirDRUG

Placebo capsules matching oseltamivir2 X 75-mg

Oseltamivir(oral)DRUG

2 X 75-mg tablet taken orally

Eligibility

Sex: ALLMin age: 18 YearsMax age: 64 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Patients who are able to understand the study and comply with all study procedures, and willing to provide written informed consent/assent prior to the predose examinations appropriately. 2. Male or female patient s aged ≥ 18 to ≤ 64 years at the time of signing the informed consent/assent form 3. Patients with a diagnosis of influenza virus infection confirmed by all of the following * Positive Rapid Antigen Test (RAT) with throat swabs;and * Fever ≥ 38ºC (axillary) in the predose examinations or \> 4 hours after dosing of antipyretics if they were taken;and * At least one of the following general systemic symptoms associated with influenza are present with a severity of moderate or greater I. Headache II. Feverishness or chills III. Muscle or joint pain IV. Fatigue * At least one of the following respiratory symptoms associated with influenza are present with a severity of moderate or greater I. Cough II. Sore throat III. Nasal congestion 4. The time interval between the onset of symptoms and the predose examinations is 48 hours or less. The onset of symptoms is defined as either * Time of the first increase in body temperature (an increase of at least 1ºC from normal body temperature) * Time when the patient experiences at least one general or respiratory symptom 5. Women of childbearing potential (WOCBP) who agree to use a highly effective method of contraception for 3 months after the first dose of ZSP1273 or oseltamivir Exclusion Criteria: 1. Patients with severe influenza virus infection requiring inpatient treatment 2. Patients aged ≥ 18 years with known allergy to oseltamivir (Tamiflu) or ZSP1273 3. Patients unable to swallow tablets or capsules or any medical history in gastrointestinal that interferes with the absorption of drugs 4. Patients who have received antiviral medication including peramivir, laninamivir, oseltamivir, zanamivir, rimantadine, umifenovir, or amantadine within 7 days prior to the predose examinations 5. Patients who have received Chinese patent medicine or herbal medicine with antiviral effect within 7 days prior to the predose examinations 6. Patients who have received Anti-influenzal prescription within 7 days prior to the predose examinations 7. Subject who produces purulent sputum or has suppurative tonsillitis. 8. White blood cells(WBC)\>10.0×109/L at screening. 9. Chest X - ray examination confirmed bronchitis,pneumonia,pleural effusion or pulmonary interstitial lesions. 10. Patients who have experienced respiratory tract infection,Otitis media,nasosinusitis. 11. Patients with severe or uncontrollable underlying diseases:blood disorders,severe chronic obstructive pulmonary disease(COPD),liver disorders(ALT or AST≥3 ULN,total bilirubin≥1.5 ULN),kidney disorders(serum creatinine\>177μmol/L or 2mg/dL),chronic congestive heart failure(NYHA III-IV),mental disorders 12. Immunodeficiency,including malignant tumor,organ or marrow transplant,human immunodeficiency virus \[HIV\] infection,or patients receiving immunosuppressant therapy 3 months prior to enrollment. 13. Concomitant therapy with aspirin or salicylic acid. 14. Patients weighing \< 40 kg or morbid obesity(Body mass index \[BMI\]≥30kg/m2) 15. Known history of alcohol abuse or drug abuse 16. Pregnancy or breastfeeding at screening and during the study.All female subjects of childbearing potential must have a negative urine pregnancy test at screening and during the trial. 17. Have received any other investigational products within 3 months prior to dosing. 18. Patients who, in the opinion of the investigator, would be unlikely to comply with required study visits, self-assessments, and interventions

Locations (76)

Outcomes

Primary Outcomes

Time to Alleviation of Symptoms in Participants Randomized to ZSP1273 or Placebo

Participants assessed the severity of seven influenza-associated symptoms (cough, sore throat, headache, nasal congestion, feverishness or chills, muscle or joint pain, and fatigue) on a 4-point scale (with 0 indicating no symptoms, 1 mild symptoms, 2 moderate symptoms, and 3 severe symptoms). Time to alleviation of symptoms was defined as the time from the start of the study treatment to the time when all seven influenza-related symptoms were assessed by the participant as absent (0) or mild (1) for at least 21.5 hours. Time to alleviation of symptoms was analyzed using the Kaplan-Meier(KM) method; participants who did not experience alleviation of symptoms were censored at the last observation time point

Time frame: Up to 14 days after first dose

Time to Alleviation of Symptoms in Participants Randomized to ZSP1273 or Oseltamivir

Time frame: Up to 14 days after first dose

Secondary Outcomes

Percentage of Participants With Positive Influenza Virus Titer at Each Time Point in Participants Randomized to ZSP1273 or Placebo

Virus titer was quantified from nasopharyngeal swabs by tissue culture methods.

Time frame: Days 2, 4, 6

Percentage of Participants With Positive Influenza Virus Titer at Each Time Point in Participants Randomized to ZSP1273 or Oseltamivir

Data from ClinicalTrials.gov

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Placebo capsules matching ZSP1273 600 mg

The First Affiliated Hospital of bengbu medical college

Bengbu, Anhui, China

Xuancheng People's Hospital

Xuancheng, Anhui, China

Beijing Chaoyang Hospital,Capital Medical University

Beijing, Beijing Municipality, China

Beijing Ditan Hospital Capital Medical University

Beijing, Beijing Municipality, China

Peking University Third Hospital

Beijing, Beijing Municipality, China

People's Hospital of Cuanjiang, Chongqing

Chongqing, Chongqing Municipality, China

Third Military Medical University

Chongqing, Chongqing Municipality, China

Quanzhou First Hospital

Quanzhou, Fujian, China

Fujian Provincal Hospital

Xiamen, Fujian, China

Xiamen Hospital of T.C.M

Xiamen, Fujian, China

...and 66 more locations

Virus titer was quantified from nasopharyngeal swabs by tissue culture methods.

Time frame: Days 2, 4, 6

Percentage of Participants With Positive Influenza Virus by RT-PCR at Each Time Point in Participants Randomized to ZSP1273 or Placebo

Influenza virus ribonucleic acid (RNA) was quantified from nasopharyngeal swabs.

Time frame: Days 2, 4, 6

Percentage of Participants With Positive Influenza Virus by RT-PCR at Each Time Point in Participants Randomized to ZSP1273 or Oseltamivir

Influenza virus ribonucleic acid (RNA) was quantified from nasopharyngeal swabs.

Time frame: Days 2, 4, 6

Change From Baseline in Virus Titer at Each Time Point in Participants Randomized to ZSP1273 or Placebo

Virus titer was quantified from nasopharyngeal swabs.

Time frame: Days 2, 4, 6

Change From Baseline in Virus Titer at Each Time Point in Participants Randomized to ZSP1273 or Oseltamivir

Virus titer was quantified from nasopharyngeal swabs.

Time frame: Days 2, 4, 6

Change From Baseline in Virus RNA (RT-PCR) at Each Time Point in Participants Randomized to ZSP1273 or Placebo

Nasopharyngeal swabs were obtained for viral quantitation.

Time frame: Days 2, 4, 6

Change From Baseline in Virus RNA (RT-PCR) at Each Time Point in Participants Randomized to ZSP1273 or Oseltamivir

Nasopharyngeal swabs were obtained for viral quantitation.

Time frame: Days 2, 4, 6

Area Under the Curve (AUC) Adjusted by Baseline in Influenza Virus Titer in Participants Randomized to ZSP1273 or Placebo

This endpoint was defined as AUC of change from Baseline in virus titer from Day 1 to Day 5. AUC was calculated using the trapezoidal method

Time frame: Up to 6 days after first dose

Area Under the Curve (AUC) Adjusted by Baseline in Influenza Virus Titer in Participants Randomized to ZSP1273 or Oseltamivir

This endpoint was defined as AUC of change from Baseline in virus titer from Day 1 to Day 5. AUC was calculated using the trapezoidal method

Time frame: Up to 6 days after first dose

Time to Cessation of Viral Shedding Determined by Virus Titer in Participants Randomized to ZSP-1273 or Placebo

Time frame: Up to 6 days after first dose

Time to Cessation of Viral Shedding Determined by Virus Titer in Participants Randomized to ZSP1273 or Oseltamivir

Time frame: Up to 6 days after first dose

Time to Cessation of Viral Shedding Determined by Virus RNA in Participants Randomized to ZSP1273 or Placebo

Time frame: Up to 6 days after first dose

Time to Cessation of Viral Shedding Determined by Virus RNA in Participants Randomized to ZSP1273 or Oseltamivir

Time frame: Up to 6 days after first dose

Percentage of Participants Whose Symptoms Were Alleviated at Each Time Point in Participants Randomized to ZSP1273 or Placebo

Time frame: Up to 14 days after first dose

Percentage of Participants Whose Symptoms Were Alleviated at Each Time Point in Participants Randomized to ZSP1273 or Oseltamivir

Time frame: Up to 14 days after first dose

Time to Alleviation of the Four Systemic Symptoms in Participants Randomized to ZSP1273 or Placebo

Participants assessed the severity of seven influenza-associated symptoms (cough, sore throat, headache, nasal congestion, feverishness or chills, muscle or joint pain, and fatigue) on a 4-point scale (with 0 indicating no symptoms, 1 mild symptoms, 2 moderate symptoms, and 3 severe symptoms). Time to alleviation of the 4 systemic symptoms was defined as the time between the initiation of the study treatment to the time when all 4 systemic symptoms (headache, feverishness or chills, muscle or joint pain, and fatigue) were assessed by the participant as 0 (None) or 1 (Mild) for a duration of at least 21.5 hours. Time to alleviation of the 4 systemic symptoms was analyzed using KM methods; participants who did not experience alleviation of symptoms were censored at the last observation time point.

Time frame: Up to 14 days after first dose

Time to Alleviation of the Four Systemic Symptoms in Participants Randomized to ZSP1273 or Oseltamivir

Participants assessed the severity of seven influenza-associated symptoms (cough, sore throat, headache, nasal congestion, feverishness or chills, muscle or joint pain, and fatigue) on a 4-point scale (with 0 indicating no symptoms, 1 mild symptoms, 2 moderate symptoms, and 3 severe symptoms). Time to alleviation of the 4 systemic symptoms was defined as the time between the initiation of the study treatment to the time when all 4 systemic symptoms (headache, feverishness or chills, muscle or joint pain, and fatigue) were assessed by the participant as 0 (None) or 1 (Mild) for a duration of at least 21.5 hours. Time to alleviation of the 4 systemic symptoms was analyzed using KM methods; participants who did not experience alleviation of symptoms were censored at the last observation time point.

Time frame: Up to 14 days after first dose

Time to Alleviation of the Three Respiratory Symptoms in Participants Randomized to ZSP1273 or Placebo

* Participants assessed the severity of seven influenza-associated symptoms (cough, sore throat, headache, nasal congestion, feverishness or chills, muscle or joint pain, and fatigue) on a 4-point scale (with 0 indicating no symptoms, 1 mild symptoms, 2 moderate symptoms, and 3 severe symptoms). Time to alleviation of the 3 respiratory symptoms was defined as the time from the start of study treatment to the time when all 3 respiratory symptoms (cough, sore throat and nasal congestion) were assessed by the participant as absent (0) or mild (1) for at least 21.5 hours * Time to alleviation of the 3 respiratory symptoms was analyzed using the KM method; participants who did not experience alleviation of symptoms were censored at the last observation time point

Time frame: Up to 14 days after first dose

Time to Alleviation of the Three Respiratory Symptoms in Participants Randomized to ZSP1273 or Oseltamivir

Time frame: Up to 14 days after first dose

Change From Baseline in Composite Symptom Score at Each Time Point in Participants Randomized to ZSP1273 or Placebo

Time frame: Up to 14 days after first dose

Change From Baseline in Composite Symptom Score at Each Time Point in Participants Randomized to ZSP1273 or Oseltamivir

Time frame: Up to 14 days after first dose

Time to Resolution of Fever in Participants Randomized to ZSP1273 or Placebo

* Time to resolution of fever was defined as the time between the initiation of the study treatment and the resolution of fever. The resolution of fever was defined as the time when the participant's self-measured axillary temperature became less than 37ºC and was maintained at less than 37ºC for a duration of at least 12 hours * Time to resolution of fever was analyzed using KM methods; participants who did not experience resolution of fever by the last observation time point were censored at that time point

Time frame: Up to 14 days after first dose

Time to Resolution of Fever in Participants Randomized to ZSP1273 or Oseltamivir

Time frame: Up to 14 days after first dose

Percentage of Participants Reporting Normal Temperature at Each Time Point in Participants Randomized to ZSP1273 or Placebo

Defined as the percentage of patients whose axillary temperature dropped to less than 37ºC after the initiation of study treatment

Time frame: Up to 14 days after first dose

Percentage of Participants Reporting Normal Temperature at Each Time Point in Participants Randomized to ZSP1273 or Oseltamivir

Defined as the percentage of patients whose axillary temperature dropped to less than 37ºC after the initiation of study treatment

Time frame: Up to 14 days after first dose

Time to Alleviation of Individual Symptoms in Participants Randomized to ZSP1273 or Placebo

Time frame: Up to 14 days after first dose

Time to Alleviation of Individual Symptoms in Participants Randomized to ZSP1273 or Oseltamivir

Time frame: Up to 14 days after first dose

Time to Return to Preinfluenza Health Status in Participants Randomized to ZSP1273 or Placebo

Time frame: Up to 14 days after first dose

Time to Return to Preinfluenza Health Status in Adults Randomized to ZSP1273 or Oseltamivir

Defined as the time between the initiation of the study treatment and the return to normal activities of daily life. The return to normal activities of daily life is defined as the time when the subject assesses his/her activities as 10.Subjects with a baseline self-rated daily activity score of 10 are not included in this analysis.

Time frame: Up to 14 days after first dose

Percentage of Participants With Influenza-related Complications in Participants Randomized to ZSP1273 or Placebo

Time frame: Up to 14 days after first dose

Percentage of Participants With Influenza-related Complications in Participants Randomized to ZSP1273 or Oseltamivir

Time frame: Up to 14 days after first dose

Change in EQ-5D-5L

Defined as the change from baseline in the index value and that in EQ VAS score as calculated from the EQ-5D-5L questionnaire.

Time frame: Up to 14 days after first dose