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NCT02003625 · OUTCOME

Numbers of Circulating CD34+ Cells on the First Day of Apheresis

Meloxicam vs Placebo for Mobilization · Source last updated 2020-05-18

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

Measure
MEDIAN
Unit
Cells per microliter
Interval / dispersion
Full Range
Time frame
3 days after starting treatment (or 9 days for multiple myeloma patients that received cyclophosphamide)

What was measured

Numbers of circulating CD34+ cells on the first day of apheresis

Groups in this outcome

A. GCSF + Placebo

GCSF + Placebo Patients in this group will receive GCSF 10 ug/kg s.c. daily, beginning 4 days prior to the 1st apheresis \[days -4, -3, -2, -1\] and continued on daily GCSF for a total of 4 apheresis or until ≥ 5 x 10\^6 CD34+ cells/kg are collected. They will also receive oral placebo for 5 days on days -6 through -2. Patients will undergo apheresis for 300 minutes to achieve approximately 3 to 4 whole blood volumes processed. This is a standard institutional protocol for autologous HSPC collection at the MGH. GCSF Placebo

B. GCSF + Meloxicam

B. GCSF + meloxicam: Patients in this group will be treated with meloxicam and GCSF in an approximate two-day staggered dose schedule as described in our preclinical studies. Meloxicam will be given orally at a dose of 15 mg/day for 5 days (days -6 through -2). GCSF at 10 ug/kg/day subcutaneously will be started on day -4 and continued daily for a total of 4 apheresis or until ≥ 5 x 10\^6 CD34+ cells/kg are collected. GCSF meloxicam

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

Analysis denominator · Participants

GroupSource count
A. GCSF + Placebo15
B. GCSF + Meloxicam15

Reported measurements

Source class 1
Values in Cells per microliter · Interval/dispersion: Full Range
GroupValueSpreadLowerUpperComment
A. GCSF + Placebo26Not reported8.38148.81Not reported
B. GCSF + Meloxicam30.7Not reported1461.6Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        8.38
        upper Limit
        148.81
        value
        26
      2. group Id
        OG001
        lower Limit
        14
        upper Limit
        61.6
        value
        30.7
denoms
  1. counts
    1. group Id
      OG000
      value
      15
    2. group Id
      OG001
      value
      15
    units
    Participants
description
Numbers of circulating CD34+ cells on the first day of apheresis
dispersion Type
Full Range
groups
  1. description
    GCSF + Placebo Patients in this group will receive GCSF 10 ug/kg s.c. daily, beginning 4 days prior to the 1st apheresis \[days -4, -3, -2, -1\] and continued on daily GCSF for a total of 4 apheresis or until ≥ 5 x 10\^6 CD34+ cells/kg are collected. They will also receive oral placebo for 5 days on days -6 through -2. Patients will undergo apheresis for 300 minutes to achieve approximately 3 to 4 whole blood volumes processed. This is a standard institutional protocol for autologous HSPC collection at the MGH. GCSF Placebo
    id
    OG000
    title
    A. GCSF + Placebo
  2. description
    B. GCSF + meloxicam: Patients in this group will be treated with meloxicam and GCSF in an approximate two-day staggered dose schedule as described in our preclinical studies. Meloxicam will be given orally at a dose of 15 mg/day for 5 days (days -6 through -2). GCSF at 10 ug/kg/day subcutaneously will be started on day -4 and continued daily for a total of 4 apheresis or until ≥ 5 x 10\^6 CD34+ cells/kg are collected. GCSF meloxicam
    id
    OG001
    title
    B. GCSF + Meloxicam
param Type
MEDIAN
reporting Status
POSTED
time Frame
3 days after starting treatment (or 9 days for multiple myeloma patients that received cyclophosphamide)
title
Numbers of Circulating CD34+ Cells on the First Day of Apheresis
type
PRIMARY
unit Of Measure
Cells per microliter

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

Preserved source evidence · Not medical advice