Viral PneumoniaPhase 2INVENTNCT06999603
Phase 2 Study of Inhaled SNG001 in Mechanically Ventilated Patients With Respiratory Viral Infection
A Phase 2 study testing SNG001 in people with Viral Pneumonia, run by Synairgen Research Ltd. at 10 sites in 2 countries.
Trial summary
The goal of this Phase 2 study is to assess the safety, antiviral biomarker responses and efficacy of SNG001 when given to patients requiring invasive mechanical ventilation due to a respiratory virus infection. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Viral Pneumonia
- What is being tested?
- SNG001
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 11 participants
- Where
- 10 sitesin 2 countries
- Study dates
- 2 Sep 2025to 13 Mar 2026
- Phase
- Phase 2
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Part 1 Inclusion Criteria:
To be eligible for randomisation into Part 1 of this study, each participant must fulfil the following criteria:
- Informed consent or legal representative's consent obtained.
- Patients ≥50 years of age at the time of consent.
- Patient admitted to the ICU and requiring invasive mechanical ventilation (IMV) due to a respiratory virus infection.
- Presence of Influenza A (Flu A), Influenza B (Flu B), respiratory syncytial virus (RSV), rhinovirus (RV), adenovirus, parainfluenza, human metapneumovirus (HMPV), or coronaviruses (including SARS-COV-2 and seasonal coronaviruses) in a nose swab sample, confirmed by a positive virus test using a Sponsor approved rapid POC test (e.g., reverse transcription polymerase chain reaction [RT-PCR]).
- Time from intubation to administration of first dose of study medication ≤48 hours.
- Women of childbearing potential must have a negative pregnancy test. For this study, women of childbearing potential are defined as women <55 years old.
Part 1 Exclusion Criteria:
A participant must not be randomised into Part 1 of the study if they meet any of the following criteria:
- Expected termination of IMV within 24 hours from the time of randomisation
- Life expectancy <24 hours.
- Liver failure (Child-Pugh C).
- Severe congestive heart failure (New York Heart Association [NYHA] IV).
- Receipt of lung transplant.
- Known or suspected active tuberculosis, or infection with other mycobacteria
- Known or suspected active systemic fungal infection.
- Anticipated transfer to another hospital which would prevent the participant from continuing in the study and completing protocol assessments.
- Need for long-term mechanical ventilation prior to ICU admission.
- Use of inhaled sedation.
- Presence of tracheostomy or laryngectomy.
- Requirement for airway pressure release ventilation mode.
- History of hypersensitivity to natural or recombinant IFNβ or to any of the excipients in the drug preparation.
- Any condition, including findings in the patient's medical history or in the pre-randomisation study assessments that in the opinion of the Investigator, constitute a risk or a contraindication for participation in the study or that could interfere with the study objectives, conduct, or evaluation.
- Participation in previous clinical studies of SNG001.
- Current or previous participation in another clinical study where the participant has received a dose of an Investigational Medicinal Product (IMP) containing small molecules within 30 days or 5 half-lives (whichever is longer) prior to entry into this study or containing biologicals within 3 months prior to entry into this study.
- Known or suspected pregnancy.
- Females who are breast-feeding or lactating.
- Immunocompromising condition, including:
- Established acquired immune deficiency syndrome (AIDS) defined as a cluster of differentiation 4 (CD4) count <200 cells/microL, and/or the presence of any AIDS-defining condition;
- Haematological malignancy;
- Bone marrow transplantation; or
- Immunosuppressive therapy, including:
- Cancer therapy (e.g. chemo-, radio-, immuno-, hormone or other types of therapy), immune-cell depleting therapy, immunosuppressive therapy for autoimmune disorders, medications for prevention of organ transplantation rejection, administered within 6 months prior to randomisation; or
- Corticosteroids >20 mg of prednisone or equivalent per day administered continuously for >14 days prior to randomisation.
- Severe chronic lung disease requiring home oxygen therapy, including chronic obstructive pulmonary disease, asthma, cystic fibrosis, or pulmonary fibrosis.
Part 2 Inclusion Criteria:
To be eligible for randomisation into Part 2 of this study, each participant must fulfil the following criteria:
1.a Patients ≥18 and <50 years of age at the time of consent, with an immunocompromising condition, including:
- Solid tumour malignancy undergoing cancer therapy (e.g. chemo-, radio-, immuno-, hormone or other types of therapy);
- Haematological malignancy in remission, with or without maintenance therapy;
- Immunosuppressive therapy for autoimmune disease;
- Therapy for prevention of organ transplant rejection;
- Corticosteroids >20 mg of prednisone or equivalent per day, administered continuously for >14 days prior to randomisation or
- b Patients ≥50 years of age at the time of consent, with or without an immunocompromising condition (as defined above).
- Patient admitted to the ICU and requiring IMV due to a respiratory virus infection.
- Presence of Flu A, Flu B, RSV, RV, adenovirus, parainfluenza, HMPV, or coronaviruses (including SARS-COV-2 and seasonal coronaviruses) in a Lower Respiratory Tract sample, confirmed by a positive virus test using a Sponsor approved rapid POC test (e.g., RT-PCR).
- Time from intubation to administration of first dose of study medication ≤48 hours.
- Informed consent or legal representative's consent obtained.
- Women of childbearing potential must have a negative pregnancy test. For this study, women of childbearing potential are defined as women <55 years old.
Part 2 Exclusion Criteria:
A participant must not be randomised into Part 2 of the study if they meet any of the following criteria:
- Expected termination of IMV within 24 hours from the time of randomisation.
- Life expectancy <24 hours.
- Liver failure (Child-Pugh C).
- Severe congestive heart failure (NYHA IV).
- Receipt of lung transplant.
- Known or suspected active tuberculosis, or infection with other mycobacteria.
- Known or suspected systemic fungal infection.
- Immunocompromising condition, including:
- Haematological malignancy requiring induction or consolidation therapy within 3 months prior to randomisation;
- Bone marrow transplant within 6 months prior to randomisation;
- Solid organ transplant within 6 months prior to randomisation;
- Corticosteroids >75 mg of prednisone or equivalent per day, administered continuously for >7 days prior to randomisation;
- Methotrexate therapy at randomisation, if the indication is chemotherapy for cancer;
- Chimeric antigen receptor (CAR)-T cell therapy, administered within 3 months prior to randomisation;
- Ibrutinib or alemtuzumab, administered within 3 months prior to randomisation;
- Neutropenia <500/mm3 not due to sepsis;
- Clinical presentation consistent with severe bone marrow suppression or pancytopenia;pancytopenia;
- Established AIDS, defined as a CD4 count <200 cells/microL, and/or the presence of any AIDS-defining condition.
- Anticipated transfer to another hospital which would prevent the participant from continuing in the study and completing protocol assessments.
- Need for long-term mechanical ventilation prior to ICU admission.
- Use of inhaled sedation.
- Presence of tracheostomy or laryngectomy
- History of hypersensitivity to natural or recombinant IFNβ or to any of the excipients in the drug preparation.
- Any condition, including findings in the patient's medical history or in the pre-randomisation study assessments that in the opinion of the Investigator, constitute a risk or a contraindication for participation in the study or that could interfere with the study objectives, conduct, or evaluation.
- Participation in previous clinical studies of SNG001.
- Current or previous participation in another clinical study where the participant has received a dose of an IMP containing small molecules within 30 days or 5 half-lives (whichever is longer) prior to entry into this study or containing biologicals within 3 months prior to entry into this study.
- Known or suspected pregnancy.
- Females who are breast-feeding or lactating.
- Severe chronic lung disease requiring home oxygen therapy, including chronic obstructive pulmonary disease, asthma, cystic fibrosis, or pulmonary fibrosis
Trial locations and contacts
10 sites in 2 countries.
10 sites in 2 countries
United States5 sites
Emory University
Atlanta, Georgia, 30308
Northwestern University
Chicago, Illinois, 60611
Sinai-Grace Hospital
Detroit, Michigan, 48235
Oregon Health & Science University (OHSU)
Portland, Oregon, 97239-3098
Mercy St. Vincent Medical Center
Toledo, Ohio, 43608
United Kingdom5 sites
Aberdeen Royal Infirmary
Aberdeen, AB25 2ZN
Bradford Royal Infirmary
Bradford, BD9 6RJ
University College London Hospital
London, NW1 2PG
Royal Free Hospital
London, NW3 2QG
Southampton General Hospital
Southampton, SO16 6YD
About this study
Official title: A Phase 2, Two-part Study to Assess the Safety, Antiviral Biomarker Responses, and Efficacy of Inhaled SNG001 for the Treatment of Patients With a Confirmed Respiratory Virus Infection Undergoing Invasive Mechanical Ventilation
The goal of this Phase 2 study is to assess the safety, antiviral biomarker responses and efficacy of SNG001 when given to patients requiring invasive mechanical ventilation due to a respiratory virus infection. Its ability to speed up virus clearance and reduce mortality, compared with standard of care, will be studied.
The study is split into two parts. All participants will receive standard of care in addition to SNG001 or placebo.
Read more
In Part 1, the safety of SNG001 will be assessed. Participants of 50 years and older will receive study drug or placebo once a day for up to 14 days, whilst in hospital.
In Part 2, the primary objective will be the efficacy of SNG001. Participants between 18 and 50 years with an immunocompromising condition and patients over 50 years (with or without an immunocompromising condition) will receive study drug once a day for up to 14 days, whilst in hospital.
- Conditions
- Viral Pneumonia
- Being tested
- SNG001, Placebo
- Keywords
- Influenza, Respiratory Syncytial Virus, Rhinovirus, Adenovirus, Human Metapneumovirus, Coronavirus, Intubated, Mechanically ventilated, Interferon, Intensive care, SARS-CoV-2, Parainfluenza
- Medical subject headings
- Pneumonia, Viral, Influenza, Human, Adenoviridae Infections, Coronavirus Infections, Paramyxoviridae Infections
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SNG001Drug
SNG001 nebuliser solution is presented as a ready-to-use aqueous solution (neutral pH) in glass syringes containing drug product solution of IFNβ 1a.
PlaceboDrug
The placebo nebuliser solution is presented in glass syringes containing solution containing the same formulation as the study medication but without IFNβ 1a (i.e., only the excipients of the SNG001 solution).
| Study group | Role | What they receive |
|---|---|---|
| Part 1 Safety Evaluation of SNG001 | Experimental | Participants will inhale a dose of SNG001 via the nebuliser, once a day for up to 14 days. A first, single syringe, low-dose cohort may be followed by an optional second cohort utilising a two-syringe dose. Receives: Drug: SNG001 |
| Part 1 Safety Evaluation of SNG001 (Placebo) | Placebo comparator | Participants will inhale a dose of placebo matched to SNG001 (only excipients of the SNG001 solution) via the nebuliser, once a day for up to 14 days. Receives: Drug: Placebo |
| Part 2 Efficacy Evaluation of SNG001 | Experimental | Participants will inhale the higher (two-syringe) dose of SNG001 via the nebuliser, once a day for up to 14 days. Receives: Drug: SNG001 |
| Part 2 Efficacy evaluation of SNG001 (Placebo) | Placebo comparator | Participants will inhale a dose of placebo matched to SNG001 (only excipients of the SNG001 solution) via the nebuliser, once a day for up to 14 days Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Part 1: AE and SAE Severity
The occurrence and severity of AEs and serious adverse events (SAEs), including pre-specified respiratory and cardiovascular deteriorations.
Measured: Up to 28 days from randomisation
Part 2: All-cause Mortality
All deaths recorded on study
Measured: Within 28 days from randomisation
Secondary outcomes (11)
Part 2: AE and SAE Severity
The occurrence and severity of AEs and SAEs, including pre-specified respiratory and cardiovascular deteriorations.
Measured: Up to 42 days from randomisation
Part 2: Change in mSOFA From Baseline
Change from baseline in modified Sequential Organ Failure Assessment (mSOFA) score during ICU (intensive Care Unit) stay.
Measured: Up to 14 days
Part 2: Time to Extubation
Time to extubation.
Measured: Up to 28 days from randomisation
Part 2: Number of Ventilator Free Days
Ventilator-free days over 28 days from randomisation
Measured: Up to 28 days from randomisation
Part 2: Duration of Stay in ICU
Duration of ICU stay measured from time of admission until discharge.
Measured: Up to 28 days from randomisation
Part 2: Duration of Stay in Hospital
Duration of hospital stay measured from time of admission until discharge.
Measured: Up to 28 days from randomisation
Part 2: Change in OSCI From Baseline
Change in Ordinal Scale for Clinical Improvement (OSCI) score from baseline to 7, 10, 14 and 28 days post randomisation.
Measured: Up to 28 days from randomisation
Part 2: Time to First Negative Virus Test
Time to first negative virus test in tracheal aspirates.
Measured: Up to 14 days from randomisation
Part 2: Change in IFNβ Levels From Baseline
Change from baseline in levels of IFNβ dependent biomarkers in tracheal aspirates
Measured: Up to 14 days from randomisation
Part 2: No Organ Support
Alive and free of organ support
Measured: At 28 days from randomisation and at 28 days post final dose
Part 2: All Cause Mortality
All deaths recorded post final dose
Measured: Within 28 days post final dose
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 May 2025
- Study start2 Sep 2025
- Primary completion13 Mar 2026
- Study completion13 Mar 2026
Why it stopped: Study was stopped due to significantly low patient recruitment rate.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Viral PneumoniaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Model description
- Part 1 of this study will include a low-dose (one syringe) first cohort, followed by an optional second cohort utilising a two-syringe dose. Part 2 will commence following the conclusion of Part 1 and will utilise the two-syringe dose. Both Part 1 and Part 2 of the study will be randomised, double-blind and placebo-controlled.
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 11 participants (actual)
Sponsor and investigators
- Lead sponsor
- Synairgen Research Ltd.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06999603
- Sponsor's protocol ID
- SG021
- Other IDs
- 2024-520375-27-00, U1111-1317-0525, ISRCTN30482473
- Acronym
- INVENT
- Status last verified
- Aug 2026
- First submitted
- 22 May 2025
- Last updated
- 14 Sep 2026
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 14 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 2, Two-part Study to Assess the Safety, Antiviral Biomarker Responses, and Efficacy of Inhaled SNG001 for the Treatment of Patients With a Confirmed Respiratory Virus Infection Undergoing Invasive Mechanical Ventilation
- ClinicalTrials.gov ID
- NCT06999603
- Acronym / sponsor ID
- INVENT / SG021
- Conditions
- Viral Pneumonia
- Keywords
- Influenza, Respiratory Syncytial Virus, Rhinovirus, Adenovirus, Human Metapneumovirus, Coronavirus, Intubated, Mechanically ventilated
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Study was stopped due to significantly low patient recruitment rate.
- Enrolment
- 11 participants (actual)
- Lead sponsor
- Synairgen Research Ltd.Industry (pharma, biotech, devices)
- Study start
- 2 Sep 2025 (actual)
- Primary completion
- 13 Mar 2026 (actual)
- Study completion
- 13 Mar 2026 (actual)
- First posted
- 31 May 2025 (actual)
- Results
- Posted 14 Sep 2026
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this Phase 2 study is to assess the safety, antiviral biomarker responses and efficacy of SNG001 when given to patients requiring invasive mechanical ventilation due to a respiratory virus infection. Its ability to speed up virus clearance and reduce mortality, compared with standard of care, will be studied.
The study is split into two parts. All participants will receive standard of care in addition to SNG001 or placebo.
In Part 1, the safety of SNG001 will be assessed. Participants of 50 years and older will receive study drug or placebo once a day for up to 14 days, whilst in hospital.
In Part 2, the primary objective will be the efficacy of SNG001. Participants between 18 and 50 years with an immunocompromising condition and patients over 50 years (with or without an immunocompromising condition) will receive study drug once a day for up to 14 days, whilst in hospital.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- Double blind (participant, investigator)
- Number of arms
- 4
- Model description
- Part 1 of this study will include a low-dose (one syringe) first cohort, followed by an optional second cohort utilising a two-syringe dose. Part 2 will commence following the conclusion of Part 1 and will utilise the two-syringe dose. Both Part 1 and Part 2 of the study will be randomised, double-blind and placebo-controlled.
| Arm | Type | Receives |
|---|---|---|
| Part 1 Safety Evaluation of SNG001 | Experimental | Drug: SNG001Participants will inhale a dose of SNG001 via the nebuliser, once a day for up to 14 days. A first, single syringe, low-dose cohort may be followed by an optional second cohort utilising a two-syringe dose. |
| Part 1 Safety Evaluation of SNG001 (Placebo) | Placebo comparator | Drug: PlaceboParticipants will inhale a dose of placebo matched to SNG001 (only excipients of the SNG001 solution) via the nebuliser, once a day for up to 14 days. |
| Part 2 Efficacy Evaluation of SNG001 | Experimental | Drug: SNG001Participants will inhale the higher (two-syringe) dose of SNG001 via the nebuliser, once a day for up to 14 days. |
| Part 2 Efficacy evaluation of SNG001 (Placebo) | Placebo comparator | Drug: PlaceboParticipants will inhale a dose of placebo matched to SNG001 (only excipients of the SNG001 solution) via the nebuliser, once a day for up to 14 days |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| SNG001SNG001 nebuliser solution is presented as a ready-to-use aqueous solution (neutral pH) in glass syringes containing drug product solution of IFNβ 1a. | Drug | Part 1 Safety Evaluation of SNG001, Part 2 Efficacy Evaluation of SNG001 |
| PlaceboThe placebo nebuliser solution is presented in glass syringes containing solution containing the same formulation as the study medication but without IFNβ 1a (i.e., only the excipients of the SNG001 solution). | Drug | Part 1 Safety Evaluation of SNG001 (Placebo), Part 2 Efficacy evaluation of SNG001 (Placebo) |
Primary outcome
Part 1: AE and SAE Severity
Time frame: Up to 28 days from randomisation
The occurrence and severity of AEs and serious adverse events (SAEs), including pre-specified respiratory and cardiovascular deteriorations.
Part 2: All-cause Mortality
Time frame: Within 28 days from randomisation
All deaths recorded on study
11 secondary outcomes
Part 2: AE and SAE Severity
Time frame: Up to 42 days from randomisation
Part 2: Change in mSOFA From Baseline
Time frame: Up to 14 days
Part 2: Time to Extubation
Time frame: Up to 28 days from randomisation
Part 2: Number of Ventilator Free Days
Time frame: Up to 28 days from randomisation
Part 2: Duration of Stay in ICU
Time frame: Up to 28 days from randomisation
Part 2: Duration of Stay in Hospital
Time frame: Up to 28 days from randomisation
Part 2: Change in OSCI From Baseline
Time frame: Up to 28 days from randomisation
Part 2: Time to First Negative Virus Test
Time frame: Up to 14 days from randomisation
Part 2: Change in IFNβ Levels From Baseline
Time frame: Up to 14 days from randomisation
Part 2: No Organ Support
Time frame: At 28 days from randomisation and at 28 days post final dose
Part 2: All Cause Mortality
Time frame: Within 28 days post final dose
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Sep 2026.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
10 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing SNG001 in people with Viral Pneumonia, run by Synairgen Research Ltd. at 10 sites in 2 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 14 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 10 sites in United States, United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 14 Sep 2026). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Part 1: AE and SAE Severity (time frame: Up to 28 days from randomisation). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Sep 2026.