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WithdrawnNCT05482542Updated Nov 9, 2023

Optimal Conditioning Regimen for Autologous Transplantation of Relapsing Remitting Multiple Sclerosis

An interventional study of Autologous hematopoietic stem cell transplantation and Cyclophosphamide/ATG in Multiple Sclerosis, Relapsing-Remitting, sponsored by Scripps Health. Withdrawn at 1 site in United States. Open to participants aged 18 Years to 58 Years. Per ClinicalTrials.gov, last updated 2023-11-09.

Sponsored by Scripps Health · Not applicable, Interventional, and Treatment

Why this study was withdrawn
lack of funding for support staff
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
18 Years to 58 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Multiple Sclerosis, Relapsing-Remitting

Keywords

  • Autologous Hematopoietic Stem Cell Transplant
03

In context

Multiple Sclerosis, Relapsing-Remitting

615 studies on the registry are indexed under Multiple Sclerosis, Relapsing-Remitting; 80 are open to participants now.

Browse Multiple Sclerosis, Relapsing-Remitting studies →

Lead sponsor

Scripps Health is the lead sponsor of 48 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 58 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age 18-58 years old
  2. 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
  3. Since diagnosis a new MRI T2 lesion or since diagnosis a gadolinium positive lesion and at least one T2 weighted lesion
  4. RRMS with a history of:

    1. 2 or more "active flares" in the prior 12 months despite either copaxone or interferon; or
    2. 1 or more "active flares" in the prior year despite a 2nd or 3rd generation DMT; or
    3. 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

Exclusion Criteria:

  1. CIS- clinically isolated lesion
  2. isolated optic neuritis
  3. Primary progressive MS b) Nonactive SPSM (defined as no new or enhancing lesions in last 12 months)
  4. spasticity or clinical stiffness of leg(s) unless there is documented new MRI enhancement within the past 12 months.
  5. hyperreflexia or clonus
  6. other immune neurologic disease such as NMO, CIDP, Stiff person syndrome, myasthenia gravis
  7. genetic neurologic diseases such as CMT or spinal cerebellar degeneration
  8. 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)
  9. insulin dependent diabetes mellitus
  10. sickle cell disease
  11. thalassemia major
  12. porphyria
  13. a current or prior cancer / malignancy except for cutaneous basal cell carcinoma or carcinoma in situ (completely excised)
  14. Hepatic:

    1. Liver function test (AST or ALT) > 2 x upper limit of normal or
    2. bilirubin > 2.0 mg /dl
  15. Pulmonary:

    1. DLCO \< 60% of normal or;
    2. Asthma not easily corrected with bronchodilator therapy or;
    3. 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)
  16. Renal:

    1. creatinine > 2.0 mg/dl, or
    2. nephrotic syndrome
  17. Cardiac:

    1. 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
    2. Persistent arrythmia not controlled with medication;
    3. Any patient requiring medication for an arrhythmia must be pre-approved by cardiology, or
    4. left ventricular ejection fraction \< 45%
  18. Hematology

    1. Hereditary coagulopathy or currently receiving anticoagulation therapy
    2. platelets \< 100,000
    3. myelodysplastic syndrome
  19. Infection:

    1. HIV,
    2. hepatitis B
    3. hepatitis C
    4. 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)

  20. EDSS \< 2.0 at time of enrollment or insurance submission
  21. Inability to comprehend or give or sign informed consent
  22. Pregnancy (positive serum or urine HCG test) or breast feeding
  23. Failure to comprehend infertility as a complication.
  24. Failure to offer sperm or oocyte collection and storage
  25. Before HSCT failure to be Free of alemtuzumab for 12 months
  26. Before HSCT failure to be Free of natalizumab for 5 months
  27. Before HSCT failure to be Free of rituximab or ocrelizumab for 5 months
  28. Before HSCT failure to be Free of fingolimod for 3 months
  29. Before HSCT failure to be Free of dimethyl fumarate (tecfidera) for 3 months
  30. Before HSCT failure of teriflunomide to have plasma levels \< 0.02 mg/L after either oral cholestyramine or activated charcoal clearance.
  31. Prior mitoxantrone
  32. Prior cladribine
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Other
    Cyclophosphamide/ATG Conditioning Regimen

    Cyclophosphamide (200 mg /kg) / rabbit antithymocyte globulin (6.0 mg/kg)

    Other: Autologous hematopoietic stem cell transplantation · Drug: Cyclophosphamide/ATG

  • Other
    Cyclophosphamide/Rituximab Conditioning Regimen

    Cyclophosphamide (200 mg/kg) / rituximab (1000 mg).

    Other: Autologous hematopoietic stem cell transplantation · Drug: Cyclophosphamide/Rituximab

Interventions

  • OtherAutologous hematopoietic stem cell transplantation

    Autologous hematopoietic stem cell transplantation

  • DrugCyclophosphamide/ATG

    Drug pages: Cyclophosphamide · Antilymphocyte Serum

    Cyclophosphamide/ATG

  • DrugCyclophosphamide/Rituximab

    Cyclophosphamide/Rituximab

06

What researchers measure

Primary outcomes

  1. Durability of remission between two arms

    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 outcomes

  1. Neurologic Disability

    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

07

Study locations

1 site
  • Scripps Green Hospital
    La Jolla, California 92037, United States
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jan 2023 (actual). Primary completion is estimated for Jul 2027, 54 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 12, 2022
First posted
Aug 1, 2022
StartActual
Jan 1, 2023
Primary completionEst.
Jul 1, 2027
CompletionEst.
Jul 1, 2027
Last update
Nov 9, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 9, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05482542
Lead sponsor
Scripps Health
Responsible party
Sponsor
First posted
Aug 1, 2022
Start date
Jan 1, 2023
Primary completion
Jul 1, 2027 (estimated)
Completion
Jul 1, 2027 (estimated)
Last update
Nov 9, 2023

Study contacts

David J Hermel, MD
principal investigator · Scripps Health

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Dec 2022. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drugs tested here: Cyclophosphamide · Antilymphocyte Serum

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