CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Interferon beta 1aWiki

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Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug1822 Placebo Wiki 0.06

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D007239 Infection NIH 0.06

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 A Randomised Double-blind Placebo-controlled Trial to Determine the Safety and Efficacy of Inhaled SNG001 (IFN-β1a for Nebulisation) for the Treatment of Patients With Confirmed SARS-CoV-2 Infection

SNG001 is an inhaled drug that contains a antiviral protein called interferon beta (IFN-β). IFN-β in produced in the lungs during viral lung infections. It has been shown that older people and people with some chronic diseases have an IFN-β deficiency. Many viruses inhibit IFN-β as part of their strategy to evade the immune system. Addition of IFN-β in vitro protects lung cells from viral infection. IFN-β protects cells against the MERS and SARS coronaviruses (close relatives of SARS-CoV-2, the virus that causes COVID-19). SNG001 is an inhaled formulation of interferon beta-1a it is currently in Phase II clinical trials for COPD patients. Synairgen has conducted randomised placebo controlled clinical trials of SNG001 involving >200 asthma and COPD patients. These trials have shown that SNG001 has: - been well tolerated during virus infections - enhanced antiviral activity in the lungs (measured in sputum and blood samples) - provided significant lung function benefit over placebo in asthma in two Phase II trials. Synairgen believes SNG001 could help prevent worsening or accelerate recovery of severe lower respiratory tract illness in COVID-19 patients. Patients who are in hospital or non-hospitalised but are a high risk groups (e.g. elderly or diabetics) will be invited to take part in the trial. The patient would receive either SNG001 or placebo once daily for 14 days. The severity of the patients condition would be recorded on a scale developed by the World Health Organisation and the patient would be asked questions about their breathlessness, cough and sputum every day, as well as assess their general medical condition and safety. If SNG001 proves to be beneficial it would be a major breakthrough for the treatment of COVID-19.

NCT04385095 SARS-CoV-2 Drug: Interferon beta 1a Drug: Placebo
MeSH:Infe Infection

Primary Outcomes

Description: Change in condition measured using the Ordinal Scale for Clinical Improvement during the dosing period - minimum of 0 (patient is well) to a maximum of 8 (death)

Measure: Ordinal Scale for Clinical Improvement

Time: Day 1 to day 28

Secondary Outcomes

Description: Progression to pneumonia as diagnosed by chest x-ray, if no pneumonia is present at time of enrolment

Measure: Progression to pneumonia

Time: Day 2 to day 28

Description: Evolution of pneumonia, as diagnosed by chest x-ray, if pneumonia is present at time of enrolment

Measure: Progression to pneumonia

Time: Day 1 to day 28

Description: Time to clinical improvement

Measure: Time to clinical improvement

Time: Time to hospital discharge OR Time to NEWS2 of ≤ 2 maintained for 24 hours

Description: NEWS2 assessment of acute-illness severity on a scale of 0 ( being well) up to 24 (requiring emergency response)

Measure: National Early Warning Score 2 (NEWS2) assessment of acute-illness severity

Time: Day 1 to day 28

Description: Changes in daily breathlessness, cough and sputum scale (BCSS) on a scale of 0 (no symptoms) up to 4 (severe symptoms)

Measure: Changes in daily breathlessness, cough and sputum scale (BCSS)

Time: Day 1 to day 28

Description: Looking at blood pressure measured in mmHg

Measure: Safety and tolerability - blood pressure II. Viral load

Time: Day 1 to day 28

Description: Looking at heart rate measured in beats per minute

Measure: Safety and tolerability - heart rate II. Viral load

Time: Day 1 to day 28

Description: Looking at temperature measured in degrees Celsius

Measure: Safety and tolerability - temperature II. Viral load

Time: Day 1 to day 28

Description: Looking at respiratory rate measure in breaths per minute

Measure: Safety and tolerability - respiratory rate II. Viral load

Time: Day 1 to day 28

Description: Looking at oxygen levels measured in a %

Measure: Safety and tolerability - oxygen saturation II. Viral load

Time: Day 1 to day 28

Description: Looking at adverse events (numbers and terms)

Measure: Safety and tolerability - adverse events II. Viral load

Time: Day 1 to day 28

Description: Looking at concomitant medications given during treatment

Measure: Safety and tolerability - concomitant medications II. Viral load

Time: Day 1 to day 28


No related HPO nodes (Using clinical trials)