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NCT03215030 · OUTCOME

Part 3: Health Care Utilization: Length of Hospital Stays

A Study of Modakafusp Alfa on Adult Participants With Relapsed/Refractory Multiple Myeloma · Source last updated 2026-01-29

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

Measure
MEDIAN
Unit
days
Interval / dispersion
Full Range
Time frame
Up to 20.5 months in Part 3

Analysis population: The FAS included all participants who received at least 1 dose, even an incomplete dose, of modakafusp alfa, in the Part 3 extension cohorts. Overall number of participants analyzed is the number of participants with data available for analyses.

Groups in this outcome

Part 3 (Dose Extension): Modakafusp Alfa 120 mg

Participants received modakafusp alfa 120 mg, infusion, IV, Q4W, for each 28-day treatment cycle until disease progression or treatment discontinuation.

Part 3 (Dose Extension): Modakafusp Alfa 240 mg

Participants received modakafusp alfa 240 mg, infusion, IV, Q4W, for each 28-day treatment cycle until disease progression or treatment discontinuation.

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 3 (Dose Extension): Modakafusp Alfa 120 mg71
Part 3 (Dose Extension): Modakafusp Alfa 240 mg75

Reported measurements

Source class 1
Values in days · Interval/dispersion: Full Range
GroupValueSpreadLowerUpperComment
Part 3 (Dose Extension): Modakafusp Alfa 120 mg14Not reported2240Not reported
Part 3 (Dose Extension): Modakafusp Alfa 240 mg11Not reported1158Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        2
        upper Limit
        240
        value
        14
      2. group Id
        OG001
        lower Limit
        1
        upper Limit
        158
        value
        11
denoms
  1. counts
    1. group Id
      OG000
      value
      71
    2. group Id
      OG001
      value
      75
    units
    Participants
dispersion Type
Full Range
groups
  1. description
    Participants received modakafusp alfa 120 mg, infusion, IV, Q4W, for each 28-day treatment cycle until disease progression or treatment discontinuation.
    id
    OG000
    title
    Part 3 (Dose Extension): Modakafusp Alfa 120 mg
  2. description
    Participants received modakafusp alfa 240 mg, infusion, IV, Q4W, for each 28-day treatment cycle until disease progression or treatment discontinuation.
    id
    OG001
    title
    Part 3 (Dose Extension): Modakafusp Alfa 240 mg
param Type
MEDIAN
population Description
The FAS included all participants who received at least 1 dose, even an incomplete dose, of modakafusp alfa, in the Part 3 extension cohorts. Overall number of participants analyzed is the number of participants with data available for analyses.
reporting Status
POSTED
time Frame
Up to 20.5 months in Part 3
title
Part 3: Health Care Utilization: Length of Hospital Stays
type
SECONDARY
unit Of Measure
days

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

Preserved source evidence · Not medical advice