Study of Efficacy and Safety of LEE011 in Men and Postmenopausal Women With Advanced Breast Cancer. · Source last updated 2023-11-30
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
Measure
GEOMETRIC_MEAN
Unit
ng/mL
Interval / dispersion
Geometric Coefficient of Variation
Time frame
Cycle 1 and Cycle 2 at Day 15 pre-dose and at 2, 4, and 6 hours post-dose. Cycle = 28 days
What was measured
Blood samples were collected to assess the concentration by time point for LEQ803, a metabolite of ribociclib. Participants were classified into the following dose groups at each timepoint: 1) ribociclib 600 mg: consisted of all participants who provided evaluable concentrations after receiving at least 10 consecutive daily ribociclib doses of 600 mg immediately prior to the blood collection without a dose change or interruption. 2) ribociclib 400 mg: consisted of all participants who provided evaluable concentrations after receiving at least 10 consecutive daily ribociclib doses of 400 mg immediately prior to the blood collection without a dose change or interruption. 3) ribociclib 200 mg: consisted of all participants who provided evaluable concentrations after receiving at least 10 consecutive daily ribociclib doses of 200 mg immediately prior to the blood collection without a dose change or interruption.
Analysis population: All participants with at least one evaluable ribociclib concentration. Number analyzed indicated the number of participants with an evaluable ribociclib concentration at the specified time point.
Groups in this outcome
Ribociclib + Fulvestrant
Ribociclib was administered orally at a daily dose of 600mg for 21 consecutive days within a 28-day cycle. This treatment was combined with fulvestrant, which was administered via intramuscular injections of 500mg every 28 days starting on Day 1 of each cycle. Additionally, an extra dose of fulvestrant was given on Day 15 of Cycle 1.
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
Ribociclib + Fulvestrant
253
Reported measurements
Cycle 1 Day 15 predose (ribociclib 600 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
253
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
75.6
50.4
Not reported
Not reported
Not reported
Cycle 1 Day 15 predose (ribociclib 400 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
0
Cycle 1 Day 15 predose (ribociclib 200 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
0
Cycle 1 Day 15 2 hours post-dose (ribociclib 600 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
102
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
134
44.5
Not reported
Not reported
Not reported
Cycle 1 Day 15 2 hours post-dose (ribociclib 400 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
0
Cycle 1 Day 15 2 hours post-dose (ribociclib 200 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
0
Cycle 1 Day 15 4 hours post-dose (ribociclib 600 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
107
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
137
42.0
Not reported
Not reported
Not reported
Cycle 1 Day 15 4 hours post-dose (ribociclib 400 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
0
Cycle 1 Day 15 4 hours post-dose (ribociclib 200 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
0
Cycle 1 Day 15 6 hours post-dose (ribociclib 600 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
92
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
128
42.4
Not reported
Not reported
Not reported
Cycle 1 Day 15 6 hours post-dose (ribociclib 400 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
0
Cycle 1 Day 15 6 hours post-dose (ribociclib 200 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
0
Cycle 2 Day 15 predose (ribociclib 600 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
177
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
72.7
62.9
Not reported
Not reported
Not reported
Cycle 2 Day 15 predose (ribociclib 400 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
7
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
46.2
52.3
Not reported
Not reported
Not reported
Cycle 2 Day 15 predose (ribociclib 200 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
0
Cycle 2 Day 15 2 hours post-dose (ribociclib 600 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
75
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
126
56.4
Not reported
Not reported
Not reported
Cycle 2 Day 15 2 hours post-dose (ribociclib 400 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
7
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
70.8
68.5
Not reported
Not reported
Not reported
Cycle 2 Day 15 2 hours post-dose (ribociclib 200 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
1
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
36.0
Not reported
Not reported
Not reported
Not reported
Cycle 2 Day 15 4 hours post-dose (ribociclib 600 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
79
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
134
44.9
Not reported
Not reported
Not reported
Cycle 2 Day 15 4 hours post-dose (ribociclib 400 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
7
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
79.3
67.2
Not reported
Not reported
Not reported
Cycle 2 Day 15 4 hours post-dose (ribociclib 200 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
1
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
41.9
Not reported
Not reported
Not reported
Not reported
Cycle 2 Day 15 6 hours post-dose (ribociclib 600 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
69
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
122
60.1
Not reported
Not reported
Not reported
Cycle 2 Day 15 6 hours post-dose (ribociclib 400 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
5
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
72.3
75.4
Not reported
Not reported
Not reported
Cycle 2 Day 15 6 hours post-dose (ribociclib 200 mg)
Analysis denominator · Participants
Group
Source count
Ribociclib + Fulvestrant
1
Values in ng/mL · Interval/dispersion: Geometric Coefficient of Variation
Group
Value
Spread
Lower
Upper
Comment
Ribociclib + Fulvestrant
38.3
Not reported
Not reported
Not reported
Not reported
Complete source fields
classes
categories
measurements
group Id
OG000
spread
50.4
value
75.6
denoms
counts
group Id
OG000
value
253
units
Participants
title
Cycle 1 Day 15 predose (ribociclib 600 mg)
denoms
counts
group Id
OG000
value
0
units
Participants
title
Cycle 1 Day 15 predose (ribociclib 400 mg)
denoms
counts
group Id
OG000
value
0
units
Participants
title
Cycle 1 Day 15 predose (ribociclib 200 mg)
categories
measurements
group Id
OG000
spread
44.5
value
134
denoms
counts
group Id
OG000
value
102
units
Participants
title
Cycle 1 Day 15 2 hours post-dose (ribociclib 600 mg)
denoms
counts
group Id
OG000
value
0
units
Participants
title
Cycle 1 Day 15 2 hours post-dose (ribociclib 400 mg)
denoms
counts
group Id
OG000
value
0
units
Participants
title
Cycle 1 Day 15 2 hours post-dose (ribociclib 200 mg)
categories
measurements
group Id
OG000
spread
42.0
value
137
denoms
counts
group Id
OG000
value
107
units
Participants
title
Cycle 1 Day 15 4 hours post-dose (ribociclib 600 mg)
denoms
counts
group Id
OG000
value
0
units
Participants
title
Cycle 1 Day 15 4 hours post-dose (ribociclib 400 mg)
denoms
counts
group Id
OG000
value
0
units
Participants
title
Cycle 1 Day 15 4 hours post-dose (ribociclib 200 mg)
categories
measurements
group Id
OG000
spread
42.4
value
128
denoms
counts
group Id
OG000
value
92
units
Participants
title
Cycle 1 Day 15 6 hours post-dose (ribociclib 600 mg)
denoms
counts
group Id
OG000
value
0
units
Participants
title
Cycle 1 Day 15 6 hours post-dose (ribociclib 400 mg)
denoms
counts
group Id
OG000
value
0
units
Participants
title
Cycle 1 Day 15 6 hours post-dose (ribociclib 200 mg)
denoms
counts
group Id
OG000
value
253
units
Participants
description
Blood samples were collected to assess the concentration by time point for LEQ803, a metabolite of ribociclib. Participants were classified into the following dose groups at each timepoint: 1) ribociclib 600 mg: consisted of all participants who provided evaluable concentrations after receiving at least 10 consecutive daily ribociclib doses of 600 mg immediately prior to the blood collection without a dose change or interruption. 2) ribociclib 400 mg: consisted of all participants who provided evaluable concentrations after receiving at least 10 consecutive daily ribociclib doses of 400 mg immediately prior to the blood collection without a dose change or interruption. 3) ribociclib 200 mg: consisted of all participants who provided evaluable concentrations after receiving at least 10 consecutive daily ribociclib doses of 200 mg immediately prior to the blood collection without a dose change or interruption.
dispersion Type
Geometric Coefficient of Variation
groups
description
Ribociclib was administered orally at a daily dose of 600mg for 21 consecutive days within a 28-day cycle. This treatment was combined with fulvestrant, which was administered via intramuscular injections of 500mg every 28 days starting on Day 1 of each cycle. Additionally, an extra dose of fulvestrant was given on Day 15 of Cycle 1.
id
OG000
title
Ribociclib + Fulvestrant
param Type
GEOMETRIC_MEAN
population Description
All participants with at least one evaluable ribociclib concentration. Number analyzed indicated the number of participants with an evaluable ribociclib concentration at the specified time point.
reporting Status
POSTED
time Frame
Cycle 1 and Cycle 2 at Day 15 pre-dose and at 2, 4, and 6 hours post-dose. Cycle = 28 days