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NCT02004522 · OUTCOME

Number of Subjects With Samples Available for Duvelisib Pharmacokinetics (PK)

A Phase 3 Study of Duvelisib Versus Ofatumumab in Patients With Relapsed or Refractory CLL/SLL (DUO) · Source last updated 2023-09-21

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

Measure
NUMBER
Unit
participants
Interval / dispersion
Not reported
Time frame
Cycle 2, Cycle 3, and Cycle 7

What was measured

Number of subjects with samples available for duvelisib Pharmacokinetics (PK)

Analysis population: Intent to Treat for duvelisib patients, no PK samples were collected for ofatumumab patients.

Groups in this outcome

Duvelisib

Duvelisib is administered orally and supplied as 5 mg and 25 mg formulated capsules.

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

Analysis denominator · Participants

GroupSource count
Duvelisib160

Reported measurements

Source class 1
Values in participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Duvelisib158Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        158
denoms
  1. counts
    1. group Id
      OG000
      value
      160
    units
    Participants
description
Number of subjects with samples available for duvelisib Pharmacokinetics (PK)
groups
  1. description
    Duvelisib is administered orally and supplied as 5 mg and 25 mg formulated capsules.
    id
    OG000
    title
    Duvelisib
param Type
NUMBER
population Description
Intent to Treat for duvelisib patients, no PK samples were collected for ofatumumab patients.
reporting Status
POSTED
time Frame
Cycle 2, Cycle 3, and Cycle 7
title
Number of Subjects With Samples Available for Duvelisib Pharmacokinetics (PK)
type
SECONDARY
unit Of Measure
participants

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice