deltatrials
Completed PHASE3 INTERVENTIONAL 2-arm NCT04732949

Study to Assess Efficacy and Safety of Inhaled Interferon-β Therapy for COVID-19 (SPRINTER)

A Randomised, Double-blind, Placebo-controlled, Phase III Trial to Determine the Efficacy and Safety of Inhaled SNG001 for the Treatment of Patients Hospitalised Due to Moderate COVID-19

Sponsor: Synairgen Research Ltd.

Interventions Placebo SNG001
Updated 12 times since 2021 Last updated: Mar 24, 2023 Started: Jan 12, 2021 Primary completion: Dec 15, 2021 Completion: Feb 10, 2022
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Listed as NCT04732949, this PHASE3 trial focuses on COVID-19 and Severe Acute Respiratory Syndrome Coronavirus 2 and remains completed. Sponsored by Synairgen Research Ltd., it has been updated 12 times since 2021, reflecting substantial change activity. This study is part of the global effort to build evidence for infectious disease interventions.

Study Description(click to expand)

Eligible patients with SARS-CoV-2 infection confirmed by a positive virus test and who are hospitalised due to COVID-19 and require oxygen therapy, will be randomised in a 1:1 ratio to receive SNG001 two syringes or placebo two syringes. SNG001 or placebo will be administered via the Ultra nebuliser. Patients will receive a dose of SNG001 or placebo once a day for 14 days and will be followed up for up to 90 days after the first dose of study medication. Study data will be collected from patients daily, as per the study schedule.

Eligible patients with SARS-CoV-2 infection confirmed by a positive virus test and who are hospitalised due to COVID-19 and require oxygen therapy, will be randomised in a 1:1 ratio to receive SNG001 two syringes or placebo two syringes. SNG001 or placebo will be administered via the Ultra nebuliser. Patients will receive a dose of SNG001 or placebo once a day for 14 days and will be followed up for up to 90 days after the first dose of study medication. Study data will be collected from patients daily, as per the study schedule.

Status Flow

~Mar 2021 – ~Apr 2021 · 31 days · monthly snapshotRecruiting~Apr 2021 – ~Jun 2021 · 2 months · monthly snapshotRecruiting~Jun 2021 – ~Sep 2021 · 3 months · monthly snapshotRecruiting~Sep 2021 – ~Nov 2021 · 2 months · monthly snapshotRecruiting~Nov 2021 – ~Dec 2021 · 30 days · monthly snapshotRecruiting~Dec 2021 – ~Apr 2022 · 4 months · monthly snapshotRecruiting~Apr 2022 – ~Apr 2023 · 12 months · monthly snapshotCompleted~Apr 2023 – ~Jul 2024 · 15 months · monthly snapshotCompleted~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotCompleted~Sep 2024 – ~Sep 2025 · 12 months · monthly snapshotCompleted~Sep 2025 – present · 7 months · monthly snapshotCompleted~Jan 2026 – present · 3 months · monthly snapshotCompleted

Change History

12 versions recorded
  1. Jan 2026 — Present [monthly]

    Completed PHASE3

  2. Sep 2025 — Present [monthly]

    Completed PHASE3

  3. Sep 2024 — Sep 2025 [monthly]

    Completed PHASE3

  4. Jul 2024 — Sep 2024 [monthly]

    Completed PHASE3

  5. Apr 2023 — Jul 2024 [monthly]

    Completed PHASE3

Show 7 earlier versions
  1. Apr 2022 — Apr 2023 [monthly]

    Completed PHASE3

    Status: RecruitingCompleted

  2. Dec 2021 — Apr 2022 [monthly]

    Recruiting PHASE3

  3. Nov 2021 — Dec 2021 [monthly]

    Recruiting PHASE3

  4. Sep 2021 — Nov 2021 [monthly]

    Recruiting PHASE3

  5. Jun 2021 — Sep 2021 [monthly]

    Recruiting PHASE3

  6. Apr 2021 — Jun 2021 [monthly]

    Recruiting PHASE3

  7. Mar 2021 — Apr 2021 [monthly]

    Recruiting PHASE3

    First recorded

Jan 2021

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Synairgen Research Ltd.
Data source: Synairgen Research Ltd.

For direct contact, visit the study record on ClinicalTrials.gov .