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NCT03484702 · OUTCOME

Maximum Concentration (Cmax) of JCAR017 by qPCR

Trial to Determine the Efficacy and Safety of JCAR017 in Adult Participants With Aggressive B-Cell Non-Hodgkin Lymphoma · Source last updated 2024-12-27

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

Measure
GEOMETRIC_MEAN
Unit
Copies/ug
Interval / dispersion
Geometric Coefficient of Variation
Time frame
At baseline and up until 24 months post JCAR017 infusion

What was measured

Cmax is the maximum or peak concentration of drug reached in the plasma following a dose of the drug. Quantitative polymerase chain reaction (qPCR) was used to determine Cmax by detecting the JCAR017 transgene. Baseline is defined as the last available recorded value on or prior to the date of JCAR017 infusion.

Analysis population: All participants in the JCAR017 treated set with baseline and on-study PK measurements.

Groups in this outcome

Cohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of Therapy

JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).

Cohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line Therapy

JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).

Cohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2

JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).

Cohort 4: Newly Diagnosed High-Grade B-cell Lymphoma

JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).

Cohort 5: Primary Central Nervous System Lymphoma

JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).

Cohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting

JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).

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

Analysis denominator · Participants

GroupSource count
Cohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of Therapy34
Cohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line Therapy22
Cohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 210
Cohort 4: Newly Diagnosed High-Grade B-cell Lymphoma1
Cohort 5: Primary Central Nervous System Lymphoma5
Cohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting9

Reported measurements

Source class 1
Values in Copies/ug · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
Cohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of Therapy23132.1434.6Not reportedNot reportedNot reported
Cohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line Therapy21960.0278.1Not reportedNot reportedNot reported
Cohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 217337.8894.4Not reportedNot reportedNot reported
Cohort 4: Newly Diagnosed High-Grade B-cell Lymphoma51121.0NANot reportedNot reportedInsufficient number of participants to calculate Geometric Coefficient of Variation.
Cohort 5: Primary Central Nervous System Lymphoma7661.61730.0Not reportedNot reportedNot reported
Cohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting32027.1101.4Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        434.6
        value
        23132.1
      2. group Id
        OG001
        spread
        278.1
        value
        21960.0
      3. group Id
        OG002
        spread
        894.4
        value
        17337.8
      4. comment
        Insufficient number of participants to calculate Geometric Coefficient of Variation.
        group Id
        OG003
        spread
        NA
        value
        51121.0
      5. group Id
        OG004
        spread
        1730.0
        value
        7661.6
      6. group Id
        OG005
        spread
        101.4
        value
        32027.1
denoms
  1. counts
    1. group Id
      OG000
      value
      34
    2. group Id
      OG001
      value
      22
    3. group Id
      OG002
      value
      10
    4. group Id
      OG003
      value
      1
    5. group Id
      OG004
      value
      5
    6. group Id
      OG005
      value
      9
    units
    Participants
description
Cmax is the maximum or peak concentration of drug reached in the plasma following a dose of the drug. Quantitative polymerase chain reaction (qPCR) was used to determine Cmax by detecting the JCAR017 transgene. Baseline is defined as the last available recorded value on or prior to the date of JCAR017 infusion.
dispersion Type
Geometric Coefficient of Variation
groups
  1. description
    JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).
    id
    OG000
    title
    Cohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of Therapy
  2. description
    JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).
    id
    OG001
    title
    Cohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line Therapy
  3. description
    JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).
    id
    OG002
    title
    Cohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2
  4. description
    JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).
    id
    OG003
    title
    Cohort 4: Newly Diagnosed High-Grade B-cell Lymphoma
  5. description
    JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).
    id
    OG004
    title
    Cohort 5: Primary Central Nervous System Lymphoma
  6. description
    JCAR017 was infused at a dose of 100 x 10\^6 JCAR017-positive transfected viable T cells (50 × 10\^6 CD8+ CAR+ T cells and 50 × 10\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).
    id
    OG005
    title
    Cohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
param Type
GEOMETRIC_MEAN
population Description
All participants in the JCAR017 treated set with baseline and on-study PK measurements.
reporting Status
POSTED
time Frame
At baseline and up until 24 months post JCAR017 infusion
title
Maximum Concentration (Cmax) of JCAR017 by qPCR
type
SECONDARY
unit Of Measure
Copies/ug

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice