Phase II \& Phase III: This is a pragmatic, adaptive, randomized, multicenter phase II/III study evaluating IFX-1 for the treatment of COVID-19 related severe pneumonia. The study consists of two parts: Phase II, an open-label, randomized, 2-arm phase evaluating best supportive care (BSC) + IFX-1 (Arm A) and BSC alone (Arm B); and Phase III, a double-blind, placebo-controlled, randomized phase comparing standard of care (SOC) + IFX-1 (Arm A) versus SOC + placebo-to-match (Arm B)
The phase II and Phase III portions enrolled patients subsequently. 1st patient was enrolled in the phase III portion on 1st October 2020.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
399
Phase II study part: IFX-1 + BSC
Phase II study part: BSC
Phase III study part: IFX-1 + SOC
Phase II: Relative Change From Baseline in Oxygenation Index in Supine Position at Day 5 (FAS)
Relative change (%) from baseline in Oxygenation Index (OI; partial pressure of oxygen in the arterial blood (PaO2) / fractional inspired oxygen (FiO2)) in supine position for ≥2 hours at day 5 (FAS)
Time frame: Baseline and Day 5
Phase III: 28-day All-cause Mortality (FAS)
Number and percentage of deaths (all-cause) until Day 28 (FAS)
Time frame: Day 28
Phase II: All-cause 28-day Mortality (FAS)
Number and percentage of deaths (all-cause) until Day 28 (FAS)
Time frame: Day 28
Phase II: Early Response at Day 7 After Enrollment
Number of patients (%) achieving an early response at day 7 after enrollment (FAS)
Time frame: Day 7
Phase II: Late Response Until Day 28 After Enrollment
Number of patients (%) reaching a late response until day 28 (FAS)
Time frame: Baseline until Day 28
Phase II: Relative Change From Baseline in Oxygenation Index in Supine Position (FAS)
Relative change (%) from baseline in Oxygenation Index (OI) in supine position for ≥2 hours at days 3, 7, 9, 11, and 15 (FAS)
Time frame: Baseline, Day 3, Day 7, Day 9, Day 11, Day 15
Phase III: 60-day All-cause Mortality (FAS)
Number and percentage of deaths (all-cause) until Day 60 (FAS)
Time frame: Day 60
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Phase III study part: Placebo + SOC
InflaRx Site #1107
Aalst, Belgium
InflaRx Site #1102
Brussels, Belgium
InflaRx Site #1104
Leuven, Belgium
InflaRx Site #1106
Lodelinsart, Belgium
InflaRx Site #1101
Yvoir, Belgium
InflaRx Site #0301
Belo Horizonte, Brazil
InflaRx Site #0302
Campinas, Brazil
InflaRx Site #0305
Criciúma, Brazil
InflaRx Site #0308
Curitiba, Brazil
InflaRx Site #0304
Porto Alegre, Brazil
...and 38 more locations
Phase III: Percentage of Patients With an Improvement in the 8-point Ordinal Scale (FAS)
Percentage of patients with an improvement in the 8-point ordinal scale (Day 15, Day 28), the scale ranges from 0 = 'No clinical or virological evidence of infection' to 8 = 'Death' with higher scores meaning greater limitation and ventilation/organ support
Time frame: Day 15, Day 28
Phase III: Percentage of Patients Developing Acute Kidney Failure Until Day 28 (FAS)
Percentage of patients developing acute kidney failure (estimated glomerular filtration rate \[eGFR\] \< 15 mL/min/1.73m², assessed by the Chronic Kidney Disease Epidemiology Collaboration \[CKD-EPI\] equation requiring race information) until Day 28 (FAS)
Time frame: Day 28
Phase III: Percentage of Patients Free of Any Renal Replacement Therapy Within 28 Days Upon Randomization (FAS)
Percentage of patients free of any renal replacement therapy (RRT) within 28 days upon randomization (FAS), number of patients free of any RRT = number of patients - number of patients with RRT initiated after randomization until Day 28
Time frame: Day 28