Aprepitant- and Olanzapine- Containing Anti-emetic Regimens With High Dose Melphalan
Primary Purpose
Nausea, Vomiting
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Aprepitant
Olanzapine
Aprepitant plus Olanzapine
Sponsored by
About this trial
This is an interventional supportive care trial for Nausea focused on measuring autologous, myeloma, transplant
Eligibility Criteria
Inclusion Criteria:
- Autologous transplant containing high dose melphalan as part of the conditioning regimen (single or 2 day melphalan; BEAM [carmustine, etoposide, cytarabine, melphalan])
- able to tolerate oral medications
Exclusion Criteria:
- Nausea/vomiting within 12 hours before planned high dose conditioning chemotherapy
- Any anti-emetic treatment within 24 hours before planned high dose conditioning chemotherapy
- Pregnancy
- Baseline corrected QT interval (QTc) > 500 ms
- History of seizures
- History of central nervous system (CNS) disease
- Human immunodeficiency virus (HIV)
Sites / Locations
- Rush University Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Experimental
Experimental
Arm Label
Aprepitant
Olanzapine
Aprepitant plus olanzapine
Arm Description
aprepitant plus standard anti-emetic regimen
olanzapine plus standard anti-emetic regimen
aprepitant and olanzapine plus standard anti-emetic regimen
Outcomes
Primary Outcome Measures
complete response (CR)
no emesis and no rescue anti-emetic therapy
Secondary Outcome Measures
Acute complete response
no emesis or rescue therapy
Delayed complete response
no emesis or rescue therapy
Very delayed complete response
no emesis or rescue therapy
Mucositis/Significant mucositis
Time to neutrophil engraftment
Time to platelet engraftment
Full Information
NCT ID
NCT02939287
First Posted
October 18, 2016
Last Updated
December 20, 2022
Sponsor
Rush University Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT02939287
Brief Title
Aprepitant- and Olanzapine- Containing Anti-emetic Regimens With High Dose Melphalan
Official Title
Aprepitant- and Olanzapine- Containing Regimens for Prevention of Acute and Delayed Nausea and Vomiting Associated With High Dose Melphalan and BEAM in Autologous Stem Cell Transplant Patients
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
September 23, 2017 (Actual)
Primary Completion Date
December 30, 2021 (Actual)
Study Completion Date
December 1, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rush University Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to help answer the following research question:
Whether administration of an aprepitant containing regimen, an olanzapine containing regimen or regimen containing both will prevent nausea and vomiting better for patients undergoing an autologous stem cell transplant with melphalan chemotherapy. Both of these medications are approved by the United States Food and Drug Administration (FDA) for nausea and vomiting.
Participants will be randomly assigned to one of the 3 treatment groups:
Arm A: aprepitant containing anti-emetic therapy
Arm B: olanzapine containing anti-emetic therapy
Arm C: Aprepitant plus olanzapine containing anti-emetic therapy
Detailed Description
This is a multi-center, randomized, non-inferiority phase 3 study conducted to determine an appropriate anti-emetic regimen for patients receiving melphalan for an autologous stem cell transplant (SCT). Candidates for this trial will include patients aged 18-80 years with hematologic malignancies receiving high dose melphalan as part of a conditioning regimen for an autologous stem cell transplant. Patients will be enrolled in 3 arms. Patients in Arm A will receive an aprepitant containing anti-emetic regimen. Patients in Arm B will receive an olanzapine containing anti-emetic regimen. Patients in Arm C will receive an aprepitant plus olanzapine containing anti-emetic regimen. Patients must be able to tolerate oral medications.
Patients will be carefully monitored for rates of emesis, nausea, and mucositis. Any adverse events will be recorded. Impact on quality of life will also be assessed. A total of 184 patients will be accrued to each arm. It is anticipated that the accrual period will last approximately 2-3 years. The primary endpoint of this study is a complete response, defined as no emesis and no rescue therapy within 120 hours of melphalan administration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nausea, Vomiting
Keywords
autologous, myeloma, transplant
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
429 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Aprepitant
Arm Type
Active Comparator
Arm Description
aprepitant plus standard anti-emetic regimen
Arm Title
Olanzapine
Arm Type
Experimental
Arm Description
olanzapine plus standard anti-emetic regimen
Arm Title
Aprepitant plus olanzapine
Arm Type
Experimental
Arm Description
aprepitant and olanzapine plus standard anti-emetic regimen
Intervention Type
Drug
Intervention Name(s)
Aprepitant
Other Intervention Name(s)
Emend
Intervention Description
Add aprepitant to anti-emetic regimen
Intervention Type
Drug
Intervention Name(s)
Olanzapine
Other Intervention Name(s)
Zyprexa
Intervention Description
add olanzapine to anti-emetic regimen
Intervention Type
Drug
Intervention Name(s)
Aprepitant plus Olanzapine
Other Intervention Name(s)
Emend, Zyprexa
Intervention Description
add aprepitant and olanzapine to anti-emetic regimen
Primary Outcome Measure Information:
Title
complete response (CR)
Description
no emesis and no rescue anti-emetic therapy
Time Frame
within 120 hours following melphalan administration
Secondary Outcome Measure Information:
Title
Acute complete response
Description
no emesis or rescue therapy
Time Frame
0 to 24 hours
Title
Delayed complete response
Description
no emesis or rescue therapy
Time Frame
25-120 hours
Title
Very delayed complete response
Description
no emesis or rescue therapy
Time Frame
121-168 hours
Title
Mucositis/Significant mucositis
Time Frame
up to 14 days
Title
Time to neutrophil engraftment
Time Frame
up to 14 days
Title
Time to platelet engraftment
Time Frame
up to 30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Autologous transplant containing high dose melphalan as part of the conditioning regimen (single or 2 day melphalan; BEAM [carmustine, etoposide, cytarabine, melphalan])
able to tolerate oral medications
Exclusion Criteria:
Nausea/vomiting within 12 hours before planned high dose conditioning chemotherapy
Any anti-emetic treatment within 24 hours before planned high dose conditioning chemotherapy
Pregnancy
Baseline corrected QT interval (QTc) > 500 ms
History of seizures
History of central nervous system (CNS) disease
Human immunodeficiency virus (HIV)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathryn Schultz, PharmD
Organizational Affiliation
Rush University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rush University Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Links:
URL
http://www.nccn.org/professionals/physician_gls/pdf/antiemesis.pdg
Description
National Comprehensive Cancer Network Anti-emesis Guidelines
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Aprepitant- and Olanzapine- Containing Anti-emetic Regimens With High Dose Melphalan
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