NCT01546038 · OUTCOME

Tmax of Glasdegib in Participants Receiving Glasdegib and Decitabine at Phase 1B on Cycle 1/Day 10 and Cycle 2/Day 1

A Study To Evaluate PF-04449913 With Chemotherapy In Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome · Source last updated 2020-03-03

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

Measure: MEDIAN
Unit: Hours
Interval / dispersion: Full Range
Time frame: Pre-dose, 0.5, 1, 2, 4, 6 and 24 hours post-dose on Cycle 1/Day 10; pre-dose, 0.5, 1, 2, 6 and 24 hours post-dose on Cycle 2/Day 1

Analysis population: Dose compliant group:Participants who had at least 4 days of uninterrupted dosing for a multiple dose PK assessment were considered to be at steady state,part of the "dose compliant" group.

Groups in this outcome

Phase 1B: Glasdegib 100 mg + Decitabine

Participants received oral doses of glasdegib tablets 100 mg starting on Day 2 of Cycle 1 for PK assessment purposes and thereafter QD and continuously for 28-day cycles (starting on Day 1 for all other cycles). Decitabine was given at a dose of 20 mg/m\^2 as an intravenous (IV) infusion over 1 hour on Days 1-5 of the 28-day cycles.

Phase 1B: Glasdegib 200 mg + Decitabine

Participants received oral doses of glasdegib tablets 200 mg starting on Day 2 of Cycle 1 for PK assessment purposes and thereafter QD and continuously for 28-day cycles (starting on Day 1 for all other cycles). Decitabine was given at a dose of 20 mg/m\^2 as an IV infusion over 1 hour on Days 1-5 of the 28-day cycles.In March 2013, all active participants receiving glasdegib 200 mg were required to reduce dose to 100 mg. Participants who had glasdegib dose reduction were reported as the starting glasdegib dose level received. Two (2) participants in this cohort had dose reduction to 100 mg starting from Cycle 1/Day 24 and Cycle 5/Day 1, respectively.

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

Analysis denominator · Participants

Group	Source count
Phase 1B: Glasdegib 100 mg + Decitabine	4
Phase 1B: Glasdegib 200 mg + Decitabine	3

Reported measurements

Cycle 1/Day 10

Analysis denominator · Participants

Group	Source count
Phase 1B: Glasdegib 100 mg + Decitabine	3
Phase 1B: Glasdegib 200 mg + Decitabine	3

Values in Hours · Interval/dispersion: Full Range
Group	Value	Spread	Lower	Upper	Comment
Phase 1B: Glasdegib 100 mg + Decitabine	2.00	Not reported	0.500	24.0	Not reported
Phase 1B: Glasdegib 200 mg + Decitabine	2.05	Not reported	1.00	5.97	Not reported

Cycle 2/Day 1

Analysis denominator · Participants

Group	Source count
Phase 1B: Glasdegib 100 mg + Decitabine	3
Phase 1B: Glasdegib 200 mg + Decitabine	2

Values in Hours · Interval/dispersion: Full Range
Group	Value	Spread	Lower	Upper	Comment
Phase 1B: Glasdegib 100 mg + Decitabine	1.03	Not reported	0.567	2.00	Not reported
Phase 1B: Glasdegib 200 mg + Decitabine	NA	Not reported	NA	NA	Based on pre-specified criteria, statistical analysis was not performed if fewer than 3 participants have reportable parameter values.

Complete source fields

classes

categories
measurements
group Id
OG000
lower Limit
0.500
upper Limit
24.0
value
2.00
group Id
OG001
lower Limit
1.00
upper Limit
5.97
value
2.05
denoms
counts
group Id
OG000
value
3
group Id
OG001
value
3
units
Participants
title
Cycle 1/Day 10
categories
measurements
group Id
OG000
lower Limit
0.567
upper Limit
2.00
value
1.03
comment
Based on pre-specified criteria, statistical analysis was not performed if fewer than 3 participants have reportable parameter values.
group Id
OG001
lower Limit
NA
upper Limit
NA
value
NA
denoms
counts
group Id
OG000
value
3
group Id
OG001
value
2
units
Participants
title
Cycle 2/Day 1

denoms

counts
group Id
OG000
value
4
group Id
OG001
value
3
units
Participants

dispersion Type

Full Range

groups

description
Participants received oral doses of glasdegib tablets 100 mg starting on Day 2 of Cycle 1 for PK assessment purposes and thereafter QD and continuously for 28-day cycles (starting on Day 1 for all other cycles). Decitabine was given at a dose of 20 mg/m\^2 as an intravenous (IV) infusion over 1 hour on Days 1-5 of the 28-day cycles.
id
OG000
title
Phase 1B: Glasdegib 100 mg + Decitabine
description
Participants received oral doses of glasdegib tablets 200 mg starting on Day 2 of Cycle 1 for PK assessment purposes and thereafter QD and continuously for 28-day cycles (starting on Day 1 for all other cycles). Decitabine was given at a dose of 20 mg/m\^2 as an IV infusion over 1 hour on Days 1-5 of the 28-day cycles.In March 2013, all active participants receiving glasdegib 200 mg were required to reduce dose to 100 mg. Participants who had glasdegib dose reduction were reported as the starting glasdegib dose level received. Two (2) participants in this cohort had dose reduction to 100 mg starting from Cycle 1/Day 24 and Cycle 5/Day 1, respectively.
id
OG001
title
Phase 1B: Glasdegib 200 mg + Decitabine

param Type

MEDIAN

population Description

Dose compliant group:Participants who had at least 4 days of uninterrupted dosing for a multiple dose PK assessment were considered to be at steady state,part of the "dose compliant" group.

reporting Status

POSTED

time Frame

Pre-dose, 0.5, 1, 2, 4, 6 and 24 hours post-dose on Cycle 1/Day 10; pre-dose, 0.5, 1, 2, 6 and 24 hours post-dose on Cycle 2/Day 1

title

Tmax of Glasdegib in Participants Receiving Glasdegib and Decitabine at Phase 1B on Cycle 1/Day 10 and Cycle 2/Day 1

type

SECONDARY

unit Of Measure

Hours

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Preserved source evidence · Not medical advice