Influenza
Conditions
Keywords
severe influenza, arbidol, oseltamivir, ordinal scale
Brief summary
This is a multicenter, randomised, double-blind, controlled study to assess the efficacy and safety of arbidol plus oseltamivir, compared with oseltamivir alone in approximately 200 hospitalized adults and adolescent patients with confirmed severe influenza. Patients should be randomised as soon as possible after screening (no later than 12 hours), providing they are within 7 days of symptom onset. Patients will be assigned in a 1:1 ratio to receive an arbidol plus oseltamivir, or oseltamivir plus placebo. Rescreening of patients who fail to meet the inclusion and exclusion criteria will be permitted only once, providing the time from symptom onset to randomization is still within 7 days. Arbidol/placebo will be administrated as 200mg TID from Days 1-7. Oseltamivir will be administered as 75mg twice daily from Days 1-7 (dose to be adjusted for renal impairment). Oseltamivir could be continued till influenza PCR negative. Both drugs, along with the corresponding placebo for arbidol, will be started at the time of randomization.
Interventions
DRUGArbidol
Oseltamivir plus Arbidol will be administrated from Days 1-7.
DRUGPlacebos
Oseltamivir plus placebos will be administrated from Days 1-7.
Sponsors
University of Oxford
Peking University
National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention
Capital Medical University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Hospitalized males or females with a positive antigen or PCR test for influenza virus infection 2. Age ≥16 years at the time of signing Informed Consent Form 3. Arterial oxygen saturation (SaO2)/ pulse oxygen saturation (SPO2) ≤94% in room air condition 4. ≤ 7 days since symptom onset. 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- ≥38℃); Time when the patient experiences at least one general or respiratory symptom. 5. Willingness to use contraception for 7 days after the end of treatment
Exclusion criteria
1. Physicians make a decision that trial involvement is not in patients' best interest, or any condition that does not allow the protocol to be followed safely. 2. Patient refusal to accept invasive organ support treatment if needed 3. More than 3 consecutive doses of NAIs within 2 days before enrolment (including oseltamivir, zanamivir, peramivir) 4. Women who are pregnant (including a positive pregnancy test at enrolment), breastfeeding, or within 2 weeks post-partum. The following female subjects do not need to undergo a pregnancy test at enrolment: a. Postmenopausal (defined as cessation of regular menstrual periods for 2 years or more and confirmed by a follicle-stimulating hormone test) women. b. Women who are surgically sterile by hysterectomy, bilateral oophorectomy, or tubal ligation. 5. Any condition requiring renal replacement therapy 6. Severe liver disease (Child-Pugh score ≥ C) 7. A history of hypersensitivity to arbidol or oseltamivir (Tamiflu®) 8. Currently or have been involved in another anti-influenza treatment trial in the last 28 days 9. Patients who, in the opinion of the investigator, would be unlikely to comply with required study visits, self-assessments, and interventions
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The primary efficacy endpoint was time to clinical status improvement (the event) up to 28 days | 28 days | the event defined as seven-category ordinal scale of clinical status after enrolment decrease by two category or discharged |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Day 28 mortality rate | 28 days | — |
| Proportion of Clinical Improvement (≥2-category decline / discharge with improvement) at Days 7, 14, and 28 since arbidol initiation | Up to 28 days | — |
| Proportion of Patients at Each Category of the 7-category Ordinal Scale at Days 7, 14, and 28 | up to 28 days | — |
| Time to decline of one category on the seven-category ordinal scale of clinical status lasting for 48h, or hospital discharge within 28 days, days | Up to 28 days | the event defined as seven-category ordinal scale of clinical status after enrolment decrease by one category or discharged |
| Incidence of Secondary Infection, Secondary Aspergillus and Bacterial Infection | Up to 28 days | — |
| Patients Requiring Continuous Renal Replacement Therapy (CRRT) After Treatment | Up to 28 days | — |
| Duration of Mechanical Ventilation (days), Oxygen Therapy (days), Hospitalization (days), Time from Randomization to Discharge (days), Time from Randomization to Death (days) | Up to 28 days | — |
Countries
China
Outcome results
None listed