Skip to content
← Full study record

NCT02663518 · OUTCOME

Part 1: Area Under the Plasma Concentration Time Curve From Time Zero to 168 (AUC[0-168]) of TTI-621

A Trial of PF-07901800 (TTI-621) for Patients With Hematologic Malignancies and Selected Solid Tumors · Source last updated 2024-05-10

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

Measure
MEAN
Unit
Nanogram*hour/milliliter
Interval / dispersion
Standard Deviation
Time frame
Part 1: Pre-dose, end of infusion (EOI), 2, 4, 24, 72, 168 hours post dose on Week 1

Analysis population: PK evaluable set included treated participants with adequate blood sampling to estimate at least one pharmacokinetic PK parameter. Here, "Number of Participants Analyzed" refers to participants evaluable for this outcome measure.

Groups in this outcome

Part 1: Ontorpacept (PF-07901800/TTI-621) 0.05 mg/kg

Participants with advanced relapsed or refractory lymphomas received TTI-621 0.05 mg/kg infusion once weekly until disease progression, unacceptable toxicity, or other reasons for treatment discontinuation occurred.

Part 1: Ontorpacept (PF-07901800/TTI-621) 0.1 mg/kg

Participants with advanced relapsed or refractory lymphomas received TTI-621 0.1 mg/kg infusion once weekly until disease progression, unacceptable toxicity, or other reasons for treatment discontinuation occurred.

Part 1: Ontorpacept (PF-07901800/TTI-621) 0.2 mg/kg

Participants with advanced relapsed or refractory lymphomas received TTI-621 0.2 mg/kg infusion once weekly until disease progression, unacceptable toxicity, or other reasons for treatment discontinuation occurred.

Part 1: Ontorpacept (PF-07901800/TTI-621) 0.3 mg/kg

Participants with advanced relapsed or refractory lymphomas received TTI-621 0.3 mg/kg infusion once weekly until disease progression, unacceptable toxicity, or other reasons for treatment discontinuation occurred.

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 1: Ontorpacept (PF-07901800/TTI-621) 0.05 mg/kg1
Part 1: Ontorpacept (PF-07901800/TTI-621) 0.1 mg/kg2
Part 1: Ontorpacept (PF-07901800/TTI-621) 0.2 mg/kg5
Part 1: Ontorpacept (PF-07901800/TTI-621) 0.3 mg/kg4

Reported measurements

Source class 1
Values in Nanogram*hour/milliliter · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Part 1: Ontorpacept (PF-07901800/TTI-621) 0.05 mg/kg1200.722Not reportedNot reportedNot reportedNot reported
Part 1: Ontorpacept (PF-07901800/TTI-621) 0.1 mg/kg6178.488844.463Not reportedNot reportedNot reported
Part 1: Ontorpacept (PF-07901800/TTI-621) 0.2 mg/kg18873.9396213.503Not reportedNot reportedNot reported
Part 1: Ontorpacept (PF-07901800/TTI-621) 0.3 mg/kg36782.7008700.626Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        1200.722
      2. group Id
        OG001
        spread
        844.463
        value
        6178.488
      3. group Id
        OG002
        spread
        6213.503
        value
        18873.939
      4. group Id
        OG003
        spread
        8700.626
        value
        36782.700
denoms
  1. counts
    1. group Id
      OG000
      value
      1
    2. group Id
      OG001
      value
      2
    3. group Id
      OG002
      value
      5
    4. group Id
      OG003
      value
      4
    units
    Participants
dispersion Type
Standard Deviation
groups
  1. description
    Participants with advanced relapsed or refractory lymphomas received TTI-621 0.05 mg/kg infusion once weekly until disease progression, unacceptable toxicity, or other reasons for treatment discontinuation occurred.
    id
    OG000
    title
    Part 1: Ontorpacept (PF-07901800/TTI-621) 0.05 mg/kg
  2. description
    Participants with advanced relapsed or refractory lymphomas received TTI-621 0.1 mg/kg infusion once weekly until disease progression, unacceptable toxicity, or other reasons for treatment discontinuation occurred.
    id
    OG001
    title
    Part 1: Ontorpacept (PF-07901800/TTI-621) 0.1 mg/kg
  3. description
    Participants with advanced relapsed or refractory lymphomas received TTI-621 0.2 mg/kg infusion once weekly until disease progression, unacceptable toxicity, or other reasons for treatment discontinuation occurred.
    id
    OG002
    title
    Part 1: Ontorpacept (PF-07901800/TTI-621) 0.2 mg/kg
  4. description
    Participants with advanced relapsed or refractory lymphomas received TTI-621 0.3 mg/kg infusion once weekly until disease progression, unacceptable toxicity, or other reasons for treatment discontinuation occurred.
    id
    OG003
    title
    Part 1: Ontorpacept (PF-07901800/TTI-621) 0.3 mg/kg
param Type
MEAN
population Description
PK evaluable set included treated participants with adequate blood sampling to estimate at least one pharmacokinetic PK parameter. Here, "Number of Participants Analyzed" refers to participants evaluable for this outcome measure.
reporting Status
POSTED
time Frame
Part 1: Pre-dose, end of infusion (EOI), 2, 4, 24, 72, 168 hours post dose on Week 1
title
Part 1: Area Under the Plasma Concentration Time Curve From Time Zero to 168 (AUC[0-168]) of TTI-621
type
SECONDARY
unit Of Measure
Nanogram*hour/milliliter

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

Preserved source evidence · Not medical advice