Overview

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

Status:
Not yet recruiting
Trial end date:
2022-06-01
Target enrollment:
0
Participant gender:
All
Summary
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.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Guangdong Raynovent Biotech Co., Ltd
Treatments:
Oseltamivir
Criteria
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