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NCT04401579 · OUTCOME

Change From Baseline in Hemoglobin

Adaptive COVID-19 Treatment Trial 2 (ACTT-2) · Source last updated 2022-03-14

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
MEAN
Unit
grams/deciliter (g/dL)
Interval / dispersion
Standard Deviation
Time frame
Days 1, 3, 5, 8, 11, 15 and 29

What was measured

Blood to evaluate hemoglobin was collected at Days 1, 3, 5, 8, and 11 while participants were inpatient, and at Days 15 and 29, with the Day 1 assessment serving as baseline. Participants who had been discharged had blood collected if infection control measures allowed for in-person visits after discharge.

Analysis population: The safety population includes all treated participants with available data at baseline and the post baseline assessment point, analyzed as treated.

Groups in this outcome

Remdesivir Plus Baricitinib

200 mg of Remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of Remdesivir while hospitalized for up to a 10-day total course and 4 mg (2 tablets of 2 mg) of Baricitinib administered orally daily for the duration of the hospitalization up to a 14-day total course.

Remdesivir Plus Placebo

200 mg of Remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of Remdesivir while hospitalized for up to a 10-day total course and 4 mg (2 tablets of 2 mg) of Baricitinib Placebo administered orally daily for the duration of the hospitalization up to a 14-day total course.

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Remdesivir Plus Baricitinib493
Remdesivir Plus Placebo494

Reported measurements

Day 3

Analysis denominator · Participants

GroupSource count
Remdesivir Plus Baricitinib493
Remdesivir Plus Placebo494
Values in grams/deciliter (g/dL) · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Remdesivir Plus Baricitinib-0.461.05Not reportedNot reportedNot reported
Remdesivir Plus Placebo-0.341.51Not reportedNot reportedNot reported
Day 5

Analysis denominator · Participants

GroupSource count
Remdesivir Plus Baricitinib410
Remdesivir Plus Placebo409
Values in grams/deciliter (g/dL) · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Remdesivir Plus Baricitinib-0.621.23Not reportedNot reportedNot reported
Remdesivir Plus Placebo-0.641.13Not reportedNot reportedNot reported
Day 8

Analysis denominator · Participants

GroupSource count
Remdesivir Plus Baricitinib270
Remdesivir Plus Placebo284
Values in grams/deciliter (g/dL) · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Remdesivir Plus Baricitinib-0.931.61Not reportedNot reportedNot reported
Remdesivir Plus Placebo-1.081.47Not reportedNot reportedNot reported
Day 11

Analysis denominator · Participants

GroupSource count
Remdesivir Plus Baricitinib189
Remdesivir Plus Placebo199
Values in grams/deciliter (g/dL) · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Remdesivir Plus Baricitinib-1.291.85Not reportedNot reportedNot reported
Remdesivir Plus Placebo-1.621.88Not reportedNot reportedNot reported
Day 15

Analysis denominator · Participants

GroupSource count
Remdesivir Plus Baricitinib253
Remdesivir Plus Placebo267
Values in grams/deciliter (g/dL) · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Remdesivir Plus Baricitinib-0.961.87Not reportedNot reportedNot reported
Remdesivir Plus Placebo-1.122.38Not reportedNot reportedNot reported
Day 29

Analysis denominator · Participants

GroupSource count
Remdesivir Plus Baricitinib260
Remdesivir Plus Placebo254
Values in grams/deciliter (g/dL) · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Remdesivir Plus Baricitinib-0.541.87Not reportedNot reportedNot reported
Remdesivir Plus Placebo-0.772.25Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        1.05
        value
        -0.46
      2. group Id
        OG001
        spread
        1.51
        value
        -0.34
    denoms
    1. counts
      1. group Id
        OG000
        value
        493
      2. group Id
        OG001
        value
        494
      units
      Participants
    title
    Day 3
  2. categories
    1. measurements
      1. group Id
        OG000
        spread
        1.23
        value
        -0.62
      2. group Id
        OG001
        spread
        1.13
        value
        -0.64
    denoms
    1. counts
      1. group Id
        OG000
        value
        410
      2. group Id
        OG001
        value
        409
      units
      Participants
    title
    Day 5
  3. categories
    1. measurements
      1. group Id
        OG000
        spread
        1.61
        value
        -0.93
      2. group Id
        OG001
        spread
        1.47
        value
        -1.08
    denoms
    1. counts
      1. group Id
        OG000
        value
        270
      2. group Id
        OG001
        value
        284
      units
      Participants
    title
    Day 8
  4. categories
    1. measurements
      1. group Id
        OG000
        spread
        1.85
        value
        -1.29
      2. group Id
        OG001
        spread
        1.88
        value
        -1.62
    denoms
    1. counts
      1. group Id
        OG000
        value
        189
      2. group Id
        OG001
        value
        199
      units
      Participants
    title
    Day 11
  5. categories
    1. measurements
      1. group Id
        OG000
        spread
        1.87
        value
        -0.96
      2. group Id
        OG001
        spread
        2.38
        value
        -1.12
    denoms
    1. counts
      1. group Id
        OG000
        value
        253
      2. group Id
        OG001
        value
        267
      units
      Participants
    title
    Day 15
  6. categories
    1. measurements
      1. group Id
        OG000
        spread
        1.87
        value
        -0.54
      2. group Id
        OG001
        spread
        2.25
        value
        -0.77
    denoms
    1. counts
      1. group Id
        OG000
        value
        260
      2. group Id
        OG001
        value
        254
      units
      Participants
    title
    Day 29
denoms
  1. counts
    1. group Id
      OG000
      value
      493
    2. group Id
      OG001
      value
      494
    units
    Participants
description
Blood to evaluate hemoglobin was collected at Days 1, 3, 5, 8, and 11 while participants were inpatient, and at Days 15 and 29, with the Day 1 assessment serving as baseline. Participants who had been discharged had blood collected if infection control measures allowed for in-person visits after discharge.
dispersion Type
Standard Deviation
groups
  1. description
    200 mg of Remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of Remdesivir while hospitalized for up to a 10-day total course and 4 mg (2 tablets of 2 mg) of Baricitinib administered orally daily for the duration of the hospitalization up to a 14-day total course.
    id
    OG000
    title
    Remdesivir Plus Baricitinib
  2. description
    200 mg of Remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of Remdesivir while hospitalized for up to a 10-day total course and 4 mg (2 tablets of 2 mg) of Baricitinib Placebo administered orally daily for the duration of the hospitalization up to a 14-day total course.
    id
    OG001
    title
    Remdesivir Plus Placebo
param Type
MEAN
population Description
The safety population includes all treated participants with available data at baseline and the post baseline assessment point, analyzed as treated.
reporting Status
POSTED
time Frame
Days 1, 3, 5, 8, 11, 15 and 29
title
Change From Baseline in Hemoglobin
type
SECONDARY
unit Of Measure
grams/deciliter (g/dL)

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Preserved source evidence · Not medical advice