Optimal Conditioning Regimen for Autologous Transplantation of Relapsing Remitting Multiple Sclerosis
Primary Purpose
Multiple Sclerosis, Relapsing-Remitting
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Autologous hematopoietic stem cell transplantation
Cyclophosphamide/ATG
Cyclophosphamide/Rituximab
Sponsored by
About this trial
This is an interventional treatment trial for Multiple Sclerosis, Relapsing-Remitting focused on measuring Autologous Hematopoietic Stem Cell Transplant
Eligibility Criteria
Inclusion Criteria:
- Age 18-58 years old
- MRI T2 hyperintense lesions with at least 1 lesion in two or more of the following locations: periventricular, cortical or juxtacortical, infratentorial, or 1 spinal lesion
- Since diagnosis a new MRI T2 lesion or since diagnosis a gadolinium positive lesion and at least one T2 weighted lesion
RRMS with a history of:
- 2 or more "active flares" in the prior 12 months despite either copaxone or interferon; or
- 1 or more "active flares" in the prior year despite a 2nd or 3rd generation DMT; or
- Active secondary progressive MS (aSPMS) with 2 or more gadolinium enhancing lesions with at least 1 gadolinium enhancing lesion > 5 mm in longest dimension within the last 9 months
Exclusion Criteria:
- CIS- clinically isolated lesion
- isolated optic neuritis
- Primary progressive MS b) Nonactive SPSM (defined as no new or enhancing lesions in last 12 months)
- spasticity or clinical stiffness of leg(s) unless there is documented new MRI enhancement within the past 12 months.
- hyperreflexia or clonus
- other immune neurologic disease such as NMO, CIDP, Stiff person syndrome, myasthenia gravis
- genetic neurologic diseases such as CMT or spinal cerebellar degeneration
- another autoimmune diagnosis such as systemic lupus erythematosus, systemic sclerosis, Behcets, or crohn's disease, etc (with the exception of hypo or hyperthyroidism or history of ITP or AIHA that is in remission)
- insulin dependent diabetes mellitus
- sickle cell disease
- thalassemia major
- porphyria
- a current or prior cancer / malignancy except for cutaneous basal cell carcinoma or carcinoma in situ (completely excised)
Hepatic:
- Liver function test (AST or ALT) > 2 x upper limit of normal or
- bilirubin > 2.0 mg /dl
Pulmonary:
- DLCO < 60% of normal or;
- Asthma not easily corrected with bronchodilator therapy or;
- Pulmonary artery hypertension (pulmonary artery systolic pressure (PASP) > 40 mmHg on echocardiogram or by cardiac catheterization a mean pulmonary artery pressure (mPAP) > 25 mmHg; a cardiac catheterization for pulmonary artery pressures is only performed if clinically indicated)
Renal:
- creatinine > 2.0 mg/dl, or
- nephrotic syndrome
Cardiac:
- Acute myocardial infarction (AMI) within the last year, and if history of AMI not being approved by cardiology as low risk or not at increased risk for another AMI: or
- Persistent arrythmia not controlled with medication;
- Any patient requiring medication for an arrhythmia must be pre-approved by cardiology, or
- left ventricular ejection fraction < 45%
Hematology
- Hereditary coagulopathy or currently receiving anticoagulation therapy
- platelets < 100,000
- myelodysplastic syndrome
Infection:
- HIV,
- hepatitis B
- hepatitis C
- positive quantiferon gold (tuberculosis test) (may start HSCt once seen by ID and started on anti-tuberculous therapy, that will be continued throughout transplant, if asymptomatic),
d) active infection at time of hospital admission (except UTI)
- EDSS < 2.0 at time of enrollment or insurance submission
- Inability to comprehend or give or sign informed consent
- Pregnancy (positive serum or urine HCG test) or breast feeding
- Failure to comprehend infertility as a complication.
- Failure to offer sperm or oocyte collection and storage
- Before HSCT failure to be Free of alemtuzumab for 12 months
- Before HSCT failure to be Free of natalizumab for 5 months
- Before HSCT failure to be Free of rituximab or ocrelizumab for 5 months
- Before HSCT failure to be Free of fingolimod for 3 months
- Before HSCT failure to be Free of dimethyl fumarate (tecfidera) for 3 months
- Before HSCT failure of teriflunomide to have plasma levels < 0.02 mg/L after either oral cholestyramine or activated charcoal clearance.
- Prior mitoxantrone
- Prior cladribine
Sites / Locations
- Scripps Green HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Cyclophosphamide/ATG Conditioning Regimen
Cyclophosphamide/Rituximab Conditioning Regimen
Arm Description
Cyclophosphamide (200 mg /kg) / rabbit antithymocyte globulin (6.0 mg/kg)
Cyclophosphamide (200 mg/kg) / rituximab (1000 mg).
Outcomes
Primary Outcome Measures
Durability of remission between two arms
Defined as the time to first confirmed acute relapse or 5 years after treatment which ever comes first
Secondary Outcome Measures
Neurologic Disability
Defined by change in EDSS (Expanded Disability Status Scale, ranges from 0 to 10 with 0 normal and 10 worst)
Quality of Life
Defined by the SF-36 questionnaire (scale of 0 to 100, lower score corresponds with more disability)
Safety
Defined by mortality (treatment related and all causes), during HSCT at first 100 days, one year, and last evaluation up to 5 years
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05482542
Brief Title
Optimal Conditioning Regimen for Autologous Transplantation of Relapsing Remitting Multiple Sclerosis
Official Title
Optimal Conditioning Regimen Protocol for Autologous Hematopoietic Stem Cell Transplantation of Relapsing Remitting Multiple Sclerosis
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2023 (Anticipated)
Primary Completion Date
July 1, 2027 (Anticipated)
Study Completion Date
July 1, 2027 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Scripps Health
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is designed to compare two non-myeloablative conditioning regimens (combination of chemotherapy and immune specific proteins against immune cells) for relapsing remitting multiple sclerosis (RRMS). The two conditioning regimens are the most commonly used world wide in clinical practice for the treatment of multiple sclerosis (MS). The first investigational conditioning regimen is cyclophosphamide (chemotherapy) and rATG (rabbit anti-thymocyte globulin, a protein against immune cells). The second investigational conditioning regimen includes the same dose of cyclophosphamide (chemotherapy) and rituximab (a protein against immune cells). Both cyclophosphamide and either rATG or rituximab are given to kill immune cells that are thought to be causing MS, followed by return of one's own previously collected blood stem cells (autologous stem cell transplant) to hasten recovery. The goal of this study is to assess the difference of these treatments in terms of toxicity and efficacy.
Detailed Description
Autologous hematopoietic stem cell transplantation (HSCT) in patients with active relapsing remitting multiple sclerosis (RRMS) halts disease progression, improves neurologic disability and quality of life, and provides a prolonged drug-free remission. A "position paper" by neurologists and hematologists under the American Society of Transplant and Cellular Therapy (ASTCT) has recommended autologous HSCT as standard of care, clinical evidence available, for treatment-refractory relapsing MS with high risk of future disability. Similarly, the EBMT has recommended the use of HSCT as "standard or care" for patients with highly active RRMS failing at least one DMT. Currently, the optimal conditioning regimen in terms of safety and efficacy is unknown. Herein, we will compare the two most commonly used regimens cyclophosphamide/ATG, or cyclophosphamide/rituximab in terms of safety and efficacy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Relapsing-Remitting
Keywords
Autologous Hematopoietic Stem Cell Transplant
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Cyclophosphamide/ATG Conditioning Regimen
Arm Type
Other
Arm Description
Cyclophosphamide (200 mg /kg) / rabbit antithymocyte globulin (6.0 mg/kg)
Arm Title
Cyclophosphamide/Rituximab Conditioning Regimen
Arm Type
Other
Arm Description
Cyclophosphamide (200 mg/kg) / rituximab (1000 mg).
Intervention Type
Other
Intervention Name(s)
Autologous hematopoietic stem cell transplantation
Intervention Description
Autologous hematopoietic stem cell transplantation
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide/ATG
Intervention Description
Cyclophosphamide/ATG
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide/Rituximab
Intervention Description
Cyclophosphamide/Rituximab
Primary Outcome Measure Information:
Title
Durability of remission between two arms
Description
Defined as the time to first confirmed acute relapse or 5 years after treatment which ever comes first
Time Frame
Time to first confirmed acute relapse or 5 years after treatment which ever comes first
Secondary Outcome Measure Information:
Title
Neurologic Disability
Description
Defined by change in EDSS (Expanded Disability Status Scale, ranges from 0 to 10 with 0 normal and 10 worst)
Time Frame
From initiation of study to completion, up until 5 years after treatment
Title
Quality of Life
Description
Defined by the SF-36 questionnaire (scale of 0 to 100, lower score corresponds with more disability)
Time Frame
From initiation of study to completion, up until 5 years after treatment
Title
Safety
Description
Defined by mortality (treatment related and all causes), during HSCT at first 100 days, one year, and last evaluation up to 5 years
Time Frame
From initiation of study to completion, up until 5 years after treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
58 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18-58 years old
MRI T2 hyperintense lesions with at least 1 lesion in two or more of the following locations: periventricular, cortical or juxtacortical, infratentorial, or 1 spinal lesion
Since diagnosis a new MRI T2 lesion or since diagnosis a gadolinium positive lesion and at least one T2 weighted lesion
RRMS with a history of:
2 or more "active flares" in the prior 12 months despite either copaxone or interferon; or
1 or more "active flares" in the prior year despite a 2nd or 3rd generation DMT; or
Active secondary progressive MS (aSPMS) with 2 or more gadolinium enhancing lesions with at least 1 gadolinium enhancing lesion > 5 mm in longest dimension within the last 9 months
Exclusion Criteria:
CIS- clinically isolated lesion
isolated optic neuritis
Primary progressive MS b) Nonactive SPSM (defined as no new or enhancing lesions in last 12 months)
spasticity or clinical stiffness of leg(s) unless there is documented new MRI enhancement within the past 12 months.
hyperreflexia or clonus
other immune neurologic disease such as NMO, CIDP, Stiff person syndrome, myasthenia gravis
genetic neurologic diseases such as CMT or spinal cerebellar degeneration
another autoimmune diagnosis such as systemic lupus erythematosus, systemic sclerosis, Behcets, or crohn's disease, etc (with the exception of hypo or hyperthyroidism or history of ITP or AIHA that is in remission)
insulin dependent diabetes mellitus
sickle cell disease
thalassemia major
porphyria
a current or prior cancer / malignancy except for cutaneous basal cell carcinoma or carcinoma in situ (completely excised)
Hepatic:
Liver function test (AST or ALT) > 2 x upper limit of normal or
bilirubin > 2.0 mg /dl
Pulmonary:
DLCO < 60% of normal or;
Asthma not easily corrected with bronchodilator therapy or;
Pulmonary artery hypertension (pulmonary artery systolic pressure (PASP) > 40 mmHg on echocardiogram or by cardiac catheterization a mean pulmonary artery pressure (mPAP) > 25 mmHg; a cardiac catheterization for pulmonary artery pressures is only performed if clinically indicated)
Renal:
creatinine > 2.0 mg/dl, or
nephrotic syndrome
Cardiac:
Acute myocardial infarction (AMI) within the last year, and if history of AMI not being approved by cardiology as low risk or not at increased risk for another AMI: or
Persistent arrythmia not controlled with medication;
Any patient requiring medication for an arrhythmia must be pre-approved by cardiology, or
left ventricular ejection fraction < 45%
Hematology
Hereditary coagulopathy or currently receiving anticoagulation therapy
platelets < 100,000
myelodysplastic syndrome
Infection:
HIV,
hepatitis B
hepatitis C
positive quantiferon gold (tuberculosis test) (may start HSCt once seen by ID and started on anti-tuberculous therapy, that will be continued throughout transplant, if asymptomatic),
d) active infection at time of hospital admission (except UTI)
EDSS < 2.0 at time of enrollment or insurance submission
Inability to comprehend or give or sign informed consent
Pregnancy (positive serum or urine HCG test) or breast feeding
Failure to comprehend infertility as a complication.
Failure to offer sperm or oocyte collection and storage
Before HSCT failure to be Free of alemtuzumab for 12 months
Before HSCT failure to be Free of natalizumab for 5 months
Before HSCT failure to be Free of rituximab or ocrelizumab for 5 months
Before HSCT failure to be Free of fingolimod for 3 months
Before HSCT failure to be Free of dimethyl fumarate (tecfidera) for 3 months
Before HSCT failure of teriflunomide to have plasma levels < 0.02 mg/L after either oral cholestyramine or activated charcoal clearance.
Prior mitoxantrone
Prior cladribine
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
RRMS Coordinator
Phone
858-554-9100
Email
BurtRRMSTrial@scrippshealth.org
First Name & Middle Initial & Last Name or Official Title & Degree
Richard R Burt, MD
Phone
858-554-9100
Email
Burt.Richard@scrippshealth.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David J Hermel, MD
Organizational Affiliation
Scripps Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Scripps Green Hospital
City
La Jolla
State/Province
California
ZIP/Postal Code
92037
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
RRMS Coordinator
Phone
858-554-9100
Email
BurtRRMSTrial@scrippshealth.org
12. IPD Sharing Statement
Learn more about this trial
Optimal Conditioning Regimen for Autologous Transplantation of Relapsing Remitting Multiple Sclerosis
We'll reach out to this number within 24 hrs