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NCT00450814 · OUTCOME

Overall Survival (Phase II)

Vaccine Therapy With or Without Cyclophosphamide in Treating Patients With Recurrent or Refractory Multiple Myeloma · Source last updated 2019-12-16

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

Measure
MEDIAN
Unit
months
Interval / dispersion
95% Confidence Interval
Time frame
Time from registration to death due to any cause, assessed up to 1 year

What was measured

Time from registration to death due to any cause, assessed up to 1 year. The distribution of survival time will be estimated using the method of Kaplan-Meier.

Analysis population: Only phase II patients who completed the study are included in this analysis. Phase II Cohort A and Phase II Cohort B were combined for this analysis due to accrual terminating early in Cohort B.

Groups in this outcome

Phase II (Acetaminophen + Benadryl + MV-NIS)

Patients receive 650 mg Acetaminophen and 50 mg Benadryl orally 30 minutes prior to MV-NIS then receive MV-NIS IV over 1 hour on day 1.

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

Analysis denominator · Participants

GroupSource count
Phase II (Acetaminophen + Benadryl + MV-NIS)15

Reported measurements

Source class 1
Values in months · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Phase II (Acetaminophen + Benadryl + MV-NIS)12.0Not reported5.6NAThe 95% confidence interval upper limit has not been reached. (insufficient number of participants with events)
Complete source fields
classes
  1. categories
    1. measurements
      1. comment
        The 95% confidence interval upper limit has not been reached. (insufficient number of participants with events)
        group Id
        OG000
        lower Limit
        5.6
        upper Limit
        NA
        value
        12.0
denoms
  1. counts
    1. group Id
      OG000
      value
      15
    units
    Participants
description
Time from registration to death due to any cause, assessed up to 1 year. The distribution of survival time will be estimated using the method of Kaplan-Meier.
dispersion Type
95% Confidence Interval
groups
  1. description
    Patients receive 650 mg Acetaminophen and 50 mg Benadryl orally 30 minutes prior to MV-NIS then receive MV-NIS IV over 1 hour on day 1.
    id
    OG000
    title
    Phase II (Acetaminophen + Benadryl + MV-NIS)
param Type
MEDIAN
population Description
Only phase II patients who completed the study are included in this analysis. Phase II Cohort A and Phase II Cohort B were combined for this analysis due to accrual terminating early in Cohort B.
reporting Status
POSTED
time Frame
Time from registration to death due to any cause, assessed up to 1 year
title
Overall Survival (Phase II)
type
SECONDARY
unit Of Measure
months

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

Preserved source evidence · Not medical advice