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TerminatedNCT00278564Updated Aug 6, 2018Results posted

Stem Cell Transplantation in Idiopathic Inflammatory Myopathy Diseases

A Phase 1 interventional study of Hematopoietic stem cell transplantation and Cyclophosphamide in MYOPATHY, sponsored by Northwestern University. Terminated at 1 site in United States. Open to participants aged 16 Years to 65 Years. Per ClinicalTrials.gov, last updated 2018-08-06.

Sponsored by Northwestern University · Phase 1, Interventional, and Treatment

Why this study was terminated
high relapse rate
Phase
Phase 1
Study type
Interventional
Enrollment
7
Allocation
Not applicable
Ages
16 Years to 65 Years
Sex
All
01

Study summary

Myositis is a disease, believed to be due to immune cells, cells which normally protect the body, but are now attacking the muscles and other organ systems within body. As a result, the affected muscles and organs fail to work properly causing weakness, difficulty swallowing, skin rash, respiratory problems, heart problems, joint stiffness, soft tissue calcification and vasculitis (blood circulation problems). The likelihood of progression of this disease is high. This study is designed to examine whether treating patients with high dose cyclophosphamide (a drug which reduces the function of the immune system) and ATG (a protein that kills the immune cells that are thought to be causing this disease), followed by return of previously collected blood stem cells will stop the progression of myositis.

Read the detailed description

Conditioning Regimen (In order to assure sterility testing, a minimum of 14 days will be required between stem cell collection and starting the conditioning regimen).

The conditioning regimen is outlined in below:

Cyclophosphamide 50 mg/kg/day will be given IV over 1 hour in 250 cc of normal saline on day -5, -4, -3, and -2. If actual weight is \< ideal weight, cyclophosphamide will be given based on actual weight. If actual weight is > ideal weight, cyclophosphamide will be given as adjusted ideal weight. Adjusted ideal weight = ideal weight + 40% (actual weight minus ideal weight).

Mesna 50mg/kg/day will be given IV over 24 hours in 250 cc of normal saline or D5W starting at 10AM each dose. Weight base is calculated same as cyclophosphamide as above.

1ATG (rabbit) 0.5 mg/kg on day -6 and 1mg/kg on day -5, -4, -3, -2 and -1 (total 5.5mg/kg, no dose adjustment) will be given IV over 10 hours in 250 cc of normal saline beginning at least 1 hour after infusion of cyclophosphamide. Premedicate with acetaminophen 650 mg po and diphenhydramine 25 mg po/IV 30 minutes before the infusion.

Methylprednisolone- A suggested dose of 250mg IV should be administered 30 minutes before each ATG infusion.

Hydration- A suggested rate of 125 cc/hr NS should be given starting 6 hours before the first cyclophosphamide dose and continued until 24 hours after the last cyclophosphamide dose. The rate of hydration will be aggressively adjusted. BID weights will be obtained. Amount of fluid can be modified based on patient's fluid status. Minimum target urine output is 2 liters/m2/day

G-CSF 5 mcg/kg/day will be given subcutaneously and continued until the absolute neutrophil counts reaches at least 500/µl.

Rituxan 500 mg will be given IV on the day before the first dose of ATG and the day after stem cell infusion.

02

Conditions studied

  • MYOPATHY
03

In context

Muscular Diseases

280 studies on the registry are indexed under Muscular Diseases; 63 are open to participants now.

This study's enrollment of 7 is below the median of 34 across 157 interventional studies indexed under Muscular Diseases.

Browse Muscular Diseases studies →

Lead sponsor

Northwestern University is the lead sponsor of 1,396 studies on the registry; 199 are open to participants now.

Of its 102 completed or terminated interventional studies of FDA-regulated products, 73 (72%) have results posted.

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

04

Who can participate

Ages eligible
16 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Age ≥ 16 years and ≤ 65 years at the time of pretransplant evaluation.
  2. An established diagnosis of polymyositis, dermatomyositis, juvenile polymyositis/dermatomyositis, and myositis associated with other collagen diseases. Diagnosis requires electrophysiological studies and histopathologic features. MRI evidence of muscle inflammation or histological evidence of active myositis is mandatory at entry. If patient had dermatomyositis/polymyositis associated with malignancy, the patient has to be free of malignancy for 5 years and considered to be cured.
  3. Patients who failed conventional treatment of at least 3 months duration including high-dose corticosteroids (equivalent dosage of prednisone >1.0 mg/kg/day to start), and must also have failed two or more of the followings: cyclophosphamide, azathioprine, 6-MP, methotrexate, tacrolimus, cyclosporin A, mycophenolate mofetil, TNF inhibitor (e.g. etanercept), IVIG or any other immunosuppressive drugs or immune modulating drugs.
  4. Failure is defined by (one or more of the following) (not caused by unrelated conditions):

    • Persistent muscle weakness (grade 4/5 or worse by MRC) with elevation of muscle derived enzymes (CPK, aldolase)
    • Worsening pulmonary function especially %VC or DLCo > 15% over 12 months indicating active alveolitis.
    • Abnormal EKG or echocardiographic evidence of cardiomyopathy.
    • Presence of progressive joint contracture, progressive calcinosis, vasculitis, or skin ulcers in juvenile dermatomyositis/polymyositis.

Exclusion criteria

Exclusion Criteria:

  1. Poor performance (PS) status (ECOG >2) at the time of entry, unless decline of PS is due to the disease itself.
  2. Significant end organ damage such as (not caused by IIM):

    • LVEF \<40% or deterioration of LVEF during exercise test on MUGA or echocardiogram.
    • Untreated life-threatening arrhythmia.
    • Active ischemic heart disease or heart failure.
    • DLCo \<40% or FEV1/FEV \< 50%.
    • Serum creatinine >2.5 or creatinine clearance \<30ml/min.
    • Liver cirrhosis, transaminases >3x of normal limits or bilirubin >2.0 unless due to Gilbert disease.
  3. HIV positive.
  4. Uncontrolled diabetes mellitus, or any other illness that in the opinion of the investigators would jeopardize the ability of the patient to tolerate aggressive treatment.
  5. Prior history of malignancy except localized basal cell or squamous skin cancer. Other malignancies for which the patient is judged to be cured by local surgical therapy, such as (but not limited to) head and neck cancer, or stage I or II breast cancer will be considered on an individual basis.
  6. Positive pregnancy test, inability or unable to pursue effective means of birth control, failure to willingly accept or comprehend irreversible sterility as a side effect of therapy.
  7. Psychiatric illness or mental deficiency making compliance with treatment or informed consent impossible.
  8. Inability to give informed consent.
  9. Major hematological abnormalities such as platelet count less than 100,000/ul, ANC less than 1000/ul.
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
7 participants (actual)

Study arms

  • Experimental
    Hematopoietic stem cell transplantation

    Intervention as hematopoietic stem cells transplantation after conditioning regimen: Autologous hematopoietic stem cells will be injected after conditioning regimen

    Biological: Hematopoietic stem cell transplantation · Drug: Cyclophosphamide · Drug: Mesna · Drug: ATG(rabbit) · Drug: Methylprednisolone · Drug: G-CSF · Drug: Rituxan

Interventions

  • BiologicalHematopoietic stem cell transplantation

    Autologous hematopoietic stem cell transplantation

  • DrugCyclophosphamide

    Also known as: Cytoxan

  • DrugMesna
  • DrugATG(rabbit)
  • DrugMethylprednisolone
  • DrugG-CSF
  • DrugRituxan
06

What researchers measure

Primary outcomes

  1. Survival

    Survival

    Time frame: up to 5 years

07

Results

Posted Aug 6, 2018
Limitations and caveats
Early termination leading to small numbers of subjects analyzed

Participant flow

Participant flow — Overall Study
MilestoneHematopoietic Stem Cell Transplantation
Started7
Completed3
Not completed4
Withdrew: Lack of efficacy4

Outcome measures

PrimarySurvival

Survival

Time frame:
up to 5 years
Reported as:
Count of participants · Participants
Survival
ParticipantsHematopoietic Stem Cell Transplantation
Survival7

Adverse events

Collected over 6 months, 1 year, then yearly up to 5 years post transplant. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Hematopoietic Stem Cell Transplantation0/7 (0%)0/7 (0%)4/7 (57.1%)
Most frequent other events
Most frequent other events
EventHematopoietic Stem Cell Transplantation
SinusitisInfections and infestations2/7
Viral infectionGeneral disorders1/7
hypokalemiaGeneral disorders1/7

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Hematopoietic Stem Cell Transplantation
<=18 years0
Between 18 and 65 years7
>=65 years0
Age, Continuous
Age, Continuous(years)Hematopoietic Stem Cell Transplantation
Mean37 ± 8
Sex: Female, Male
Sex: Female, Male(Participants)Hematopoietic Stem Cell Transplantation
Female7
Male0
Region of Enrollment
Region of Enrollment(Participants)Hematopoietic Stem Cell Transplantation
United States7
08

Study locations

1 site
  • Northwestern University, Feinberg School of Medicine
    Chicago, Illinois 60611, United States
09

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 6, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT00278564
Lead sponsor
Northwestern University
Responsible party
Richard Burt, MD (MD, Northwestern University) — Principal investigator
First posted
Jan 18, 2006
Start date
Sep 2005
Primary completion
Jul 2016
Completion
Jul 2016
Results posted
Aug 6, 2018
Last update
Aug 6, 2018

Study contacts

Richard Burt, MD
principal investigator · Northwestern University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Jun 2017. You cannot join it, but the record below documents what was studied.

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