Skip to main content
OpenTrials
Completed

NCT Number: NCT04642950

A Phase II/III Study of Sargramostim

This is a randomized, placebo-controlled, double-blind, group comparison, multicenter study to evaluate the efficacy and safety of inhalation administration of sargramostim for 5 days, in principle (up to 10 days) as Add-on treatment to the standard treatment in COVID-19 patients.

Completed

Looking for future studies?

Notify Me

Key information

Age range

20 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

IUHW Narita Hospital, Narita, Chiba, Japan

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Japanese male or female subjects who have been confirmed to meet all the following criteria.

  • Hospitalized patients under treatment who were severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2] positive by polymerase chain reaction (PCR) test.
  • Patients with clinically diagnosed pneumonia and a percutaneous oxygen saturation [SpO2] of 93% or less on breathing of room air at bed rest.
  • Patients for whom written informed consent has been obtained from those themselves or the legally acceptable representatives.
  • Patients aged 20 years or older and younger than 85 years at the time of obtaining informed consent.

Exclusion criteria

Subjects who meet any of the following criteria will be excluded. Unless otherwise stated, the following criteria refer to those at the time of screening.

  • Patients who have been participating in other intervention studies, such as studies on unapproved pharmacotherapy, within 90 days prior to screening.
  • Patients who have experienced off-label use of approved drugs (including those for COVID-19 treatment other than steroids as standard treatment) within 7 days prior to screening.
  • Patients who are not expected to survive longer than 24 hours after commencement of study drug administration.
  • Patients who are using invasive ventilator or extracorporeal membrane oxygenation (ECMO).
  • Patients who have a chronic respiratory disease requiring continuous home oxygen therapy or ventilator use.
  • Patients with an underlying condition that is considered very unlikely to withdraw ventilator (e.g., motor neuron disease, Duchenne muscular dystrophy, rapidly progressive interstitial pulmonary fibrosis).
  • Patients who have a disease including bronchial asthma, lower respiratory tract infections, and interstitial lung diseases that may affect the assessment of the clinical study, since before the symptom onset of COVID-19.
  • Patients who have a disease including leukemia and leukocytosis that causes leukocytosis.
  • Patients who have a chronic kidney disease requiring dialysis.
  • Patients who have severe liver failure (Child Pugh grade C).
  • Patients aged 80 years or older with any of heart failure, cerebrovascular disease, obesity (BMI 30 or higher), dyslipidemia, hypertension or diabetes.

Treatment and study plan

Sargramostim

Drug

250 μg/vial of sargramostim will be dissolved in 4 mL of physiological saline and 125 μg of which will be administered using inhaler twice daily in approximately 10-15 minutes.

Other names: Leukine

Placebo

Drug

2 mL of physiological saline will be administered using inhaler twice daily in approximately 10-15 minutes.

Primary outcomes

  1. 2-rank Improvement on a 7-point Ordinal Scale

    Time frame: Period until Day 28 (including the case after discharge).

    Number of days to achieve at least 2-rank improvement on a 7-point ordinal scale from baseline until Day 28.

Secondary outcomes

  1. Changes From Baseline in Alveolar-arterial Oxygen Partial Pressure Gradient (A-aDO)

    Time frame: Period until Day 28 (including the case after discharge).

    Changes from baseline in alveolar-arterial oxygen partial pressure gradient (A-aDO) on Day 5 and at the end of administration.

  2. Number of Days Until Discharge From Baseline

    Time frame: Period until Day 28 (including the case after discharge).

    Number of days until discharge from baseline (days of shifting to Category 7 on a 7-point ordinal scale).

  3. Proportion of Subjects Whose Category Has Shifted to Category 1 or 2

    Time frame: Period until Day 28 (including the case after discharge).

    Proportion of subjects whose category has shifted to Category 1 or 2 on a 7-point ordinal scale from baseline until Day 28

Sponsors and collaborators

Lead sponsor

Nobelpharma

Industry

Registry information

Official study title

A Phase II/III Study of Sargramostim in Patients With Coronavirus Disease-2019 (COVID-19)

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Nov 24, 2020
Registry last updated
Jul 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.