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A Randomized, Double-blinded, Placebo-controlled, Parallel-treatment Group, Adaptive Design, Multi-center, Phase 2b/3 Trial to Evaluate Efficacy and Safety of NuSepin® Intravenous Infusion in COVID-19 Pneumonia Patients
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NuSepin® 0.2 mg/kg | Active Comparator | NuSepin® 0.2 mg/kg in 100mL NS bid |
|
| NuSepin® 0.4 mg/kg | Active Comparator | NuSepin® 0.4 mg/kg in 100mL NS bid |
|
| Placebo | Placebo Comparator | Normal saline (NS) 100mL bid |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| NuSepin® 0.2 mg/kg | Drug | NuSepin® 0.2 mg/kg in 100mL NS bid |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Time to improvement of at least 2 categories relative to the first dosing date of the Investigational Medicinal Product (randomization date) on an 8-point ordinal scale (WHO 8-point ordinal scale) of clinical status up to day 29 [Phase 2b] | Day 29 | |
| Time to discharge relative to the first dosing date of the IMP (randomization date) [Phase 3] | Day 29 |
| Measure | Description | Time Frame |
|---|---|---|
| WHO 8-point ordinal scale | The proportion of subjects with categories of 2 or less (outpatient condition); and 3 or less (hospitalized, no oxygen treatment) at day 8, 15 and 29 and etc. | Day 29 |
| NEWS 2 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Seung-Yong Seong, Dr. | Shaperon Inc. | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Gachon University Gil Medical Center | Recruiting | Incheon | Namdong-gu | 21565 | South Korea |
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| NuSepin® 0.4 mg/kg |
| Drug |
NuSepin® 0.4 mg/kg in 100mL NS bid |
|
| Placebo | Drug | Normal saline (NS) 100mL bid |
|
Time to normalization of vital signs that lasts 24 hours or more (score 0 on NEWS2 that lasts 24 hours or more) and etc.
| Day 29 |
| the use of ventilatory assistance | The proportion of subjects undergoing a ventilatory assistance (facial mask, low-flow oxygen cannula, high-flow oxygen cannula, Non-invasive ventilation, Invasive Mechanical Ventilation/ECMO) at day 8, day 15, and day 29; and the days of each ventilatory assistance since the first dosing date of IMP (randomization date) up to day 29 | Day 29 |
| Hospitalization and ICU Admission | Proportion of subjects transferred to ICU and the duration of ICU admission (date of admission to ICU ~ discharge date) since the first dosing date of IMP (randomization date) up to day 29 and etc. | Day 29 |
| Survival | All-cause mortality; follow-up until discharge, or up to 60 days for patients who are still hospitalized at day 29 of the first IMP dosing (randomization date) | Day 29 |
| biomarkers | Proportions of subjects whose inflammatory-related biomarkers at baseline, day 4, day 8, day 15, day 29 are within the normal range (① TNF-α, ② IL-1β, ③ IL-6, ④ IL-8 ⑤ IL-18 ⑥ CRP) and etc. | Day 29 |
| Cytokine release syndrome | The proportion of subjects with a decrease of at least 1 category according to an ASTCT Consensus Grading step for Cytokine Release Syndrome | Day 29 |
| Viral burden | Proportion of patients who become negative for viral titer at each assessment time point since the first dosing date of IMP and etc. | Day 29 |
| Compliance | Compliance of the study drugs (days of dosing with the study drugs and total dose administered) | Day 29 |
| Safety Endpoints | The incidence and characteristics of adverse events after administration of IMP and etc. | Day 29 |