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NCT02903914 · OUTCOME

AUC0-tau of INCB001158 Following Multiple Escalating Doses for Part 1A

Arginase Inhibitor INCB001158 as a Single Agent and in Combination With Immune Checkpoint Therapy in Patients With Advanced/Metastatic Solid Tumors · Source last updated 2025-08-05

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

Measure
GEOMETRIC_MEAN
Unit
hours x ng/mL
Interval / dispersion
Geometric Coefficient of Variation
Time frame
Cycle 1 Day 15: predose; 0.5, 1, 2, 4, 6, 8, and 12 hours post-dose

What was measured

AUC0-tau was defined as the area under the concentration-time curve from dosing (time 0) of INCB001158 to the end of the dosing period.

Analysis population: PK Population. Only participants with available data were analyzed.

Groups in this outcome

Part 1A: INCB001158 50 mg

INCB001158 was administered orally at 50 milligrams (mg) twice daily (BID) in participants with advanced/metastatic solid tumors.

Part 1A: INCB001158 75 mg

INCB001158 was administered orally at 75 mg BID in participants with advanced/metastatic solid tumors.

Part 1A: INCB001158 100 mg

INCB001158 was administered orally at 100 mg BID in participants with advanced/metastatic solid tumors.

Part 1A: INCB001158 150 mg

INCB001158 was administered orally at 150 mg BID in participants with advanced/metastatic solid tumors.

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

Analysis denominator · Participants

GroupSource count
Part 1A: INCB001158 50 mg6
Part 1A: INCB001158 75 mg4
Part 1A: INCB001158 100 mg4
Part 1A: INCB001158 150 mg6

Reported measurements

Source class 1
Values in hours x ng/mL · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
Part 1A: INCB001158 50 mg82500.27Not reportedNot reportedNot reported
Part 1A: INCB001158 75 mg166000.39Not reportedNot reportedNot reported
Part 1A: INCB001158 100 mg183000.34Not reportedNot reportedNot reported
Part 1A: INCB001158 150 mg297000.31Not reportedNot reportedNot reported

Source statistical analyses

Group order, estimate direction, methods and comments are retained. No treatment ranking is inferred.

  1. group Ids
    1. OG000
    2. OG001
    3. OG002
    4. OG003
    non Inferiority Type
    OTHER
    p Value
    0.1705
    statistical Comment
    1-factor ANOVA of log-transformed, dose-normalized data (factor = dose)
    statistical Method
    ANOVA
  2. ci Lower Limit
    0.863
    ci Num Sides
    TWO_SIDED
    ci Pct Value
    90
    ci Upper Limit
    1.359
    group Ids
    1. OG002
    2. OG003
    non Inferiority Type
    OTHER
    param Type
    pairwise GMR
    param Value
    1.083
  3. ci Lower Limit
    0.719
    ci Num Sides
    TWO_SIDED
    ci Pct Value
    90
    ci Upper Limit
    1.132
    group Ids
    1. OG000
    2. OG002
    non Inferiority Type
    OTHER
    param Type
    pairwise GMR
    param Value
    0.902
  4. ci Lower Limit
    0.945
    ci Num Sides
    TWO_SIDED
    ci Pct Value
    90
    ci Upper Limit
    1.554
    group Ids
    1. OG001
    2. OG002
    non Inferiority Type
    OTHER
    param Type
    pairwise GMR
    param Value
    1.212
Complete source fields
analyses
  1. group Ids
    1. OG000
    2. OG001
    3. OG002
    4. OG003
    non Inferiority Type
    OTHER
    p Value
    0.1705
    statistical Comment
    1-factor ANOVA of log-transformed, dose-normalized data (factor = dose)
    statistical Method
    ANOVA
  2. ci Lower Limit
    0.863
    ci Num Sides
    TWO_SIDED
    ci Pct Value
    90
    ci Upper Limit
    1.359
    group Ids
    1. OG002
    2. OG003
    non Inferiority Type
    OTHER
    param Type
    pairwise GMR
    param Value
    1.083
  3. ci Lower Limit
    0.719
    ci Num Sides
    TWO_SIDED
    ci Pct Value
    90
    ci Upper Limit
    1.132
    group Ids
    1. OG000
    2. OG002
    non Inferiority Type
    OTHER
    param Type
    pairwise GMR
    param Value
    0.902
  4. ci Lower Limit
    0.945
    ci Num Sides
    TWO_SIDED
    ci Pct Value
    90
    ci Upper Limit
    1.554
    group Ids
    1. OG001
    2. OG002
    non Inferiority Type
    OTHER
    param Type
    pairwise GMR
    param Value
    1.212
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        0.27
        value
        8250
      2. group Id
        OG001
        spread
        0.39
        value
        16600
      3. group Id
        OG002
        spread
        0.34
        value
        18300
      4. group Id
        OG003
        spread
        0.31
        value
        29700
denoms
  1. counts
    1. group Id
      OG000
      value
      6
    2. group Id
      OG001
      value
      4
    3. group Id
      OG002
      value
      4
    4. group Id
      OG003
      value
      6
    units
    Participants
description
AUC0-tau was defined as the area under the concentration-time curve from dosing (time 0) of INCB001158 to the end of the dosing period.
dispersion Type
Geometric Coefficient of Variation
groups
  1. description
    INCB001158 was administered orally at 50 milligrams (mg) twice daily (BID) in participants with advanced/metastatic solid tumors.
    id
    OG000
    title
    Part 1A: INCB001158 50 mg
  2. description
    INCB001158 was administered orally at 75 mg BID in participants with advanced/metastatic solid tumors.
    id
    OG001
    title
    Part 1A: INCB001158 75 mg
  3. description
    INCB001158 was administered orally at 100 mg BID in participants with advanced/metastatic solid tumors.
    id
    OG002
    title
    Part 1A: INCB001158 100 mg
  4. description
    INCB001158 was administered orally at 150 mg BID in participants with advanced/metastatic solid tumors.
    id
    OG003
    title
    Part 1A: INCB001158 150 mg
param Type
GEOMETRIC_MEAN
population Description
PK Population. Only participants with available data were analyzed.
reporting Status
POSTED
time Frame
Cycle 1 Day 15: predose; 0.5, 1, 2, 4, 6, 8, and 12 hours post-dose
title
AUC0-tau of INCB001158 Following Multiple Escalating Doses for Part 1A
type
SECONDARY
unit Of Measure
hours x ng/mL

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