Clinical trials: Acute, Uncomplicated Human Influenza
Influenza, Acute Respiratory Viral Infections
Study to Assess Efficacy and Safety of XC221 200 mg in the Treatment of Influenza or Other ARVI
The innovative drug XC221 is planned for use in treatment of acute respiratory viral infections in a double-blind, randomized, placebo-controlled, comparative multicenter study assessing the safety, tolerability and efficacy of…
- Trial name
- NCT03830905
- Testing
- XC221
- Where
- 16 sites in Russia
- Volunteers
- 120 people
- Sponsor
- PHARMENTERPRISES LLC
Influenza
Intramuscular Peramivir for the Treatment of Uncomplicated Influenza
This is a multinational, randomized, double-blind study comparing the efficacy and safety of two single dose regimens of peramivir administered intramuscularly versus placebo in adults with uncomplicated acute influenza.
- Trial name
- NCT00486980
- Testing
- Peramivir 150mg, Peramivir 300mg
- Sponsor
- BioCryst Pharmaceuticals
Influenza A
Study of ZSP1273 in Patients With Acute Uncomplicated Influenza A
The purpose of this study is to evaluate the antiviral effect, as measured by the time to alleviation of influenza symptoms and viral titer in nasopharyngeal secretions in adults with acute uncomplicated influenza A following…
- Trial name
- NCT04024137
- Testing
- ZSP1273 200 mg, ZSP1273-400 mg, ZSP1273-600 mg
- Where
- 26 sites in China
- Volunteers
- 172 people
- Sponsor
- Guangdong Raynovent Biotech Co., Ltd
Influenza
A Clinical Study on the Safety and Efficacy of GP681 Tablets in the Treatment of Uncomplicated Acute Influenza
Analyse the time of flu symptom relief in adults with uncomplicated acute influenza,to evaluate the antiviral effects of high and low doses of GP681 tablets, and explore the optimal dose for phase III clinical trials.
- Trial name
- NCT04736758
- Testing
- GP681 tablet, GP681 Simulant
- Where
- China
- Volunteers
- 216 people
- Sponsor
- Jiangxi Qingfeng Pharmaceutical Co. Ltd.
Influenza A
A Study of MHAA4549A as Monotherapy for Acute Uncomplicated Seasonal Influenza A in Otherwise Healthy Adults
This is a Phase 2, randomized, double-blind, placebo-controlled single dose study in otherwise healthy adults with acute uncomplicated seasonal influenza A to assess the safety and tolerability, efficacy, and pharmacokinetics of…
- Trial name
- NCT02623322
- Testing
- MHAA4549A
- Where
- 80 sites in United States, Canada and 5 more
- Volunteers
- 124 people
- Sponsor
- Genentech, Inc.
Influenza
To Assess the Efficacy of GP681 Tablet Versus Placebo in Patients With Acute Uncomplicated Influenza Virus Infection
This study will evaluate the efficacy, safety, and population pharmacokinetics of a single, oral dose of GP681 compared with placebo in patients aged 12 to 65 years with acute uncomplicated influenza virus infection
- Trial name
- NCT05474755
- Testing
- GP681 40mg
- Where
- China
- Volunteers
- 591 people
- Sponsor
- Jiangxi Qingfeng Pharmaceutical Co. Ltd.
Influenza
A Phase 2a to Evaluate the Safety of MEDI8852 in Adults With Uncomplicated Influenza
The purpose of this study is to evaluate safety and tolerability of a single dose of MEDI8852 when given with oseltamivir, the safety and tolerability of oseltamivir alone, and the safety and tolerability of a single dose of…
- Trial name
- MEDI8852 (NCT02603952)
- Testing
- Oseltamivir, MEDI8852
- Where
- 31 sites in United States, South Africa
- Volunteers
- 126 people
- Sponsor
- MedImmune LLC
Influenza A
Study of Acute Uncomplicated Seasonal Influenza A in Adult Subjects
The purpose of this study is to evaluate the antiviral effect, as measured by viral titer in nasal secretions in adults with acute uncomplicated seasonal influenza A following administration of VX-787.
- Trial name
- NCT02342249
- Testing
- VX-787 300 mg, VX-787 600 mg, Oseltamivir 75 mg
- Where
- 176 sites in United States, Belgium and 7 more
- Volunteers
- 292 people
- Sponsor
- Janssen Research & Development, LLC
Influenza A
Efficacy and Safety of ZSP1273 in Children 12-17 Years Old With Influenza A
This trial is conducted in China. This is a multi-center, randomized, double-blind, placebo-controlled clinical trial to assess the efficacy and safety of ZSP1273 in the treatment of Acute Uncomplicated influenza A in adolescents.
- Trial name
- NCT07229820
- Testing
- ZSP1273
- Where
- China
- Volunteers
- 157 people
- Sponsor
- Guangdong Raynovent Biotech Co., Ltd