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Phase 3 N=70 Randomized Quadruple-blind Treatment

A Phase II/III Study of Sargramostim

COVID-19

Enrolled (actual)
70
Serious AEs
2.9%
Results posted
Jul 2024
Primary outcome: Primary: 2-rank Improvement on a 7-point Ordinal Scale — 9; 8 Number of Days

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Sargramostim (Drug); Placebo (Drug)
Age
Adult, Older Adult · 20+ yrs
Sex
All
Sponsor
Nobelpharma
Primary completion
Oct 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
2-rank Improvement on a 7-point Ordinal Scale
9; 8
SECONDARY
Changes From Baseline in Alveolar-arterial Oxygen Partial Pressure Gradient (A-aDO)
SECONDARY
Number of Days Until Discharge From Baseline
SECONDARY
Proportion of Subjects Whose Category Has Shifted to Category 1 or 2

Summary

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.

Eligibility Criteria

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.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04642950). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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