NCT02773030 · OUTCOME

Overall Survival for Cohort D, Cohort H2 and Cohort I

A Study to Determine Dose, Safety, Tolerability and Efficacy of CC-220 Monotherapy, and in Combination With Other Treatments in Subjects With Multiple Myeloma · Source last updated 2026-03-20

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

Measure: MEDIAN
Unit: Weeks
Interval / dispersion: Full Range
Time frame: On Average of (Cohort D: 81.14 Cohort H2: 91.54 Cohort I: 74.20)Weeks

What was measured

Time from first dose of IP to death due to any cause Data will be collected and analyzed per Cohort Totals.

Analysis population: Safety Population for Cohort D, Cohort H2 and Cohort I - as per protocol, the individual arms in the cohort would be combined for OS presentation

Groups in this outcome

Cohort D: Total

CC220

Cohort H2

CC220 + DEX

Cohort I

CC220 + DEX

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
Cohort D: Total	107
Cohort H2	5
Cohort I	41

Reported measurements

Source class 1

Values in Weeks · Interval/dispersion: Full Range
Group	Value	Spread	Lower	Upper	Comment
Cohort D: Total	44.29	Not reported	1.9	228.0	Not reported
Cohort H2	103.43	Not reported	19.9	147.0	Not reported
Cohort I	60.43	Not reported	6.6	210.6	Not reported

Complete source fields

classes

categories
measurements
group Id
OG000
lower Limit
1.9
upper Limit
228.0
value
44.29
group Id
OG001
lower Limit
19.9
upper Limit
147.0
value
103.43
group Id
OG002
lower Limit
6.6
upper Limit
210.6
value
60.43

denoms

counts
group Id
OG000
value
107
group Id
OG001
value
5
group Id
OG002
value
41
units
Participants

description

Time from first dose of IP to death due to any cause Data will be collected and analyzed per Cohort Totals.

dispersion Type

Full Range

groups

description
CC220
id
OG000
title
Cohort D: Total
description
CC220 + DEX
id
OG001
title
Cohort H2
description
CC220 + DEX
id
OG002
title
Cohort I

param Type

MEDIAN

population Description

Safety Population for Cohort D, Cohort H2 and Cohort I - as per protocol, the individual arms in the cohort would be combined for OS presentation

reporting Status

POSTED

time Frame

On Average of (Cohort D: 81.14 Cohort H2: 91.54 Cohort I: 74.20)Weeks

title

Overall Survival for Cohort D, Cohort H2 and Cohort I

type

SECONDARY

unit Of Measure

Weeks

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

Preserved source evidence · Not medical advice