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
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.
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.
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 →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.
Failure is defined by (one or more of the following) (not caused by unrelated conditions):
Exclusion Criteria:
Significant end organ damage such as (not caused by IIM):
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
Autologous hematopoietic stem cell transplantation
Also known as: Cytoxan
Survival
Survival
Time frame: up to 5 years
| Milestone | Hematopoietic Stem Cell Transplantation |
|---|---|
| Started | 7 |
| Completed | 3 |
| Not completed | 4 |
| Withdrew: Lack of efficacy | 4 |
Survival
| Participants | Hematopoietic Stem Cell Transplantation |
|---|---|
| Survival | 7 |
Collected over 6 months, 1 year, then yearly up to 5 years post transplant. Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Hematopoietic Stem Cell Transplantation | 0/7 (0%) | 0/7 (0%) | 4/7 (57.1%) |
| Event | Hematopoietic Stem Cell Transplantation |
|---|---|
| SinusitisInfections and infestations | 2/7 |
| Viral infectionGeneral disorders | 1/7 |
| hypokalemiaGeneral disorders | 1/7 |
| Age, Categorical(Participants) | Hematopoietic Stem Cell Transplantation |
|---|---|
| <=18 years | 0 |
| Between 18 and 65 years | 7 |
| >=65 years | 0 |
| Age, Continuous(years) | Hematopoietic Stem Cell Transplantation |
|---|---|
| Mean | 37 ± 8 |
| Sex: Female, Male(Participants) | Hematopoietic Stem Cell Transplantation |
|---|---|
| Female | 7 |
| Male | 0 |
| Region of Enrollment(Participants) | Hematopoietic Stem Cell Transplantation |
|---|---|
| United States | 7 |
Plan to share: No
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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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