ClinicalTrials.gg
RecruitingNCT03630211SScUpdated Aug 14, 2026

Autologous Stem Cell Transplantation in Patients With Systemic Sclerosis

A Phase 2 interventional study of Cyclophosphamide and Mesna in Systemic Sclerosis, Diffuse Sclerosis Systemic and Interstitial Lung Disease, sponsored by Paul Szabolcs. Recruiting at 3 sites in United States. Open to participants aged 8 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-08-14.

Sponsored by Paul Szabolcs · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2018; still recruiting 8 years 3 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
8
Allocation
Not applicable
Ages
8 Years to 60 Years
Sex
All
01

Study summary

The purpose of this study is to determine whether a regimen of high-dose immunoablative therapy will demonstrate safety that is consistent or improved with other published regimens in SSc patients, while maintaining a treatment effect.

Read the detailed description

This is a single center, phase II trial where after a process of stem cell mobilization and conditioning, subjects receive a CD34-selected autologous peripheral blood stem cell rescue. By virtue of positive selection for the stem/progenitor cell marker of CD34, the graft will be depleted for T, B and NK lymphocytes and other immune cells such as monocytes that may be pathogenic. This is an open label study and there will be no randomization or blinding as a part of this study.

The proposed regimen of high-dose immunoablative therapy will demonstrate safety that is consistent or improved with other published regimens in SSc patients, while maintaining a treatment effect.

The primary objectives of this study are to determine the safety and treatment effect of high-dose immunoablative therapy followed by transplantation of CD34+ positively selected peripheral blood stem cells (PBSC) for systemic scleroderma (SSc) patients using a regimen designed to maximize patient safety while also aiming to eradicate autoreactive clones responsible for the disease. Safety will be determined by monitoring for death of any cause, and severe or life-threatening infections. Treatment effect will be determined by assessing event-free survival in comparison to a SSc observational cohort control group treated with standard of care medication (mycophenolate mofetil) at 12 and 36 months post hematopoietic stem cell transplant (HSCT). Enrolled subjects will be followed for survival, secondary malignancies, and SSC activity at least yearly up to 36 months post-HSCT.

The secondary objectives of this study are to:

  • To assess cutaneous disease response to high dose immunosuppressive therapy (HDIT) by comparing pre- and post-transplant measurements of the modified Rodnan skin score (mRSS).
  • To assess pulmonary disease response by longitudinally tracking FVC (pulmonary function test) and DLCO (diffusing capacity of the lung for carbon monoxide) yearly up to 36 months post-HSCT.
  • To evaluate the treatment effect on disease activity/progression, as indicated by severity measures of cardiac, pulmonary, musculoskeletal, gastrointestinal, vascular and renal organ involvement, and need for concomitant disease-modifying antirheumatic drugs (DMARD) use.
  • To evaluate quality of life by comparing pre- and post-transplant quality of life measurements. These measurements will include the Scleroderma Health Assessment Questionnaire (SHAQ), the Medical Outcomes Study Questionnaire Short Form 36 Health Survey (SF-36) and the Scleroderma Skin Patient Reported Outcome (SSPRO) pre- and post-mobilization.
02

Conditions studied

  • Systemic Sclerosis
  • Diffuse Sclerosis Systemic
  • Interstitial Lung Disease
  • Pulmonary Hypertension

Keywords

  • Stem Cell Transplantation
  • Systemic Sclerosis
  • Scleroderma
  • Interstitial Lung Disease
  • ILD (Interstitial Lung Disease)
  • Pulmonary Hypertension
  • BMT ( bone marrow transplantation)
  • Autologous
03

In context

Scleroderma, Systemic

610 studies on the registry are indexed under Scleroderma, Systemic; 218 are open to participants now.

This study's planned enrollment of 8 is below the median of 37 across 446 interventional studies indexed under Scleroderma, Systemic.

Browse Scleroderma, Systemic studies →

Lead sponsor

Paul Szabolcs is the lead sponsor of 9 studies on the registry; 9 are open to participants now.

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

04

Who can participate

Ages eligible
8 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Cohort 1: Children, Adolescents and Young Adults (Cohort 1)

Inclusion:

Individuals must meet all the following criteria to be eligible for this study.

  1. Patient, parent, or legal guardian must have given written . For patients ≥ 168 years of age who are developmentally able, assent or affirmation will be obtained.
  2. Age 8-24, inclusive, at time of consent.
  3. Diagnosed with Systemic Sclerosis (SSc) at the age of ≤19.
  4. Failure to respond, specifically no improvement or progression of disease, to at least 2 disease-modifying antirheumatic drugs (DMARDS) within 12 months of consent with any of the following conditions:

    1. Progression of skin thickening over the past 6 months or Modified Rodnan skin score (mRSS) ≥ 20
    2. Progression of ILD within 18 months prior to consent. Progression to be determined by either of the following:

      • CT scan showing increased ground glass opacities or reticulations OR
      • Pulmonary function testing (PFTs) showing a decrease in FVC% or DLCO% predicted value of ≥10%.
    3. Myositis - CPK > 2x or MRI consistent with myositis
    4. Childhood Myositis Assessment Score \< 30
    5. Arthritis
    6. Digital tip ulcerations
  5. Cardiology clearance to undergo stem cell transplantation (documented in subject's medical chart)
  6. Negative for (HIV), virus and virus, all confirmed by PCR testing.
  7. Negative pregnancy test for females. who have reached menarche.

87. All females of and sexually active males must agree to use an FDA approved method of for up to 24 months after BMT or for as long as they are taking any medication that may harm a pregnancy, an unborn child or may cause a birth defect.

Exclusion:

Individuals who meet any of these criteria are not eligible for this study.

  1. FVC \<35%, determined by pulmonary function tests for those able to complete spirometry adequately (per investigator's determination)
  2. O2 sat \<92% at rest in room air
  3. Estimated \<40 mL/min,using Cockcroft-Gault formula based on actual body weight.
  4. Active, untreated SSc renal crisis at the time of consent.
  5. > 4x upper limit of normal.
  6. Active, uncontrolled infection that would be a to safe use of high-dose therapy or cyclophosphamide.
  7. Hematologic abnormalities as defined by any of the following peripheral blood counts:

    1. ANC \< 1500 cell/µL.
    2. \< 100,000 cells/ µL.
    3. \< 9.0 g/dL.
  8. within 2 years prior to enrollment, excluding adequately treated squamous cell cancer, basal cell carcinoma or carcinoma in situ. Treatment should have been completed with cure/remission status documented for at least 2 years.
  9. Past or current medical problems or findings from medical history, physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.

Cohort 2 for Adults

Inclusion:

Individuals must meet all the following criteria to be eligible for this study.

  1. Patient, parent, or legal guardian must have given written informed consent. For patients ≥ 16 years of age who are developmentally able, assent or affirmation will be obtained.
  2. Age 1618-705560, inclusive, at time of consent. Patients up to age 24, diagnosed with SSc at age ≤ 19, will be included in Cohort 1 and evaluated according to the Pediatric and Young Adult criteria listed in sections 3.1.1 and 3.1.2.
  3. Diagnosed with Systemic Sclerosis (SSc), according to the 2013 ACR/EULAR criteria (van den Hoogen et al., 2013).
  4. All patients must meet either the following skin or ILD criteria. Disease duration is defined as time from first non-Raynaud symptom.

    Skin Criteria: Diffuse SSc, defined by presence of proximal skin thickening and:

    A. If disease duration is of \<2 years, patients must have a calculated mortality risk prediction score which places them in the intermediate or high- risk category (Domsic et al., 2016). Refer to Appendix 5 for calculation criteria.

    B. If disease duration is of >2 years, patients must have evidence of active cutaneous disease based upon 1) a worsening Modified Rodnan Skin Score (MRSS) in the preceding three months or 2) the presence of palpable tendon friction rubs.

    ILD Criteria:

    A. The presence of recognized fibrosis on imaging of \<2 years AND either > 10% of lung involvement by CT scan or FVC% pred \<80% or B. Fibrosis on imaging of any duration with a decline in FVC% pred of ≥10% over the preceding 12-18 months.

  5. Negative for human immunodeficiency virus (HIV), hepatitis B virus and hepatitis C virus, all confirmed by PCR testing.
  6. Negative pregnancy test for females.
  7. All females of childbearing potential and sexually active males must agree to use an FDA approved method of birth control for up to 24 months after BMT or for as long as they are taking any medication that may harm a pregnancy, an unborn child or may cause a birth defect.

Exclusion Criteria Individuals who meet any of these criteria are not eligible for this study.

  1. Moderate to severe cardiac involvement defined by any of the following:

    1. classification of heart failure ≥3.
    2. (LVEF) \<50% as determined by cardiac MRI.
    3. Significant pulmonary hypertension, for subjects ≥ 18 years of age, defined as mean PASP ≥30 mmHg determined by right heart catheterization, or for subjects ≤ 17 years of age, defined as mean PASP >45 mmHg, determined by echocardiogram.
    4. Atrial tachycardia, atrial fibrillation or atrial flutter of ≥1-minute duration, determined by (EKG) or, cardiac event monitor and/or implanted loop recorder (if applicable), or on anti-arrhythmic therapy for the arrhythmias listed above.
    5. Ventricular tachycardia of ≥6 beats at rate of ≥100 beats per minute, determined by EKG or, cardiac event monitor and/or implanted loop recorder (if applicable), or on an anti-arrhythmic therapy for any ventricular arrhythmia.
    6. Left bundle branch block, bifascicular heart block, Mobitz 2 heart block, complete heart block or infarction pattern as determined by EKG or, cardiac event monitor and/or implanted loop recorder
    7. Presence of pacemaker or implantable cardioverter defibrillator.
  2. Moderate to severe pulmonary involvement defined by any of the following:

    1. Hemoglobin-corrected DLCO \<45%, determined by pulmonary function tests.
    2. FVC \<45%, determined by pulmonary function tests.
    3. pO2 \<70 mmHg, determined by an arterial blood gas (not applicable for subjects ≤17 years of age).
    4. pCO2 ≥45 without supplemental O2 determined by an arterial blood gas (not applicable for subjects ≤17 years of age).
    5. O2 sat \<92% at rest without supplemental O2, determined by an arterial blood gas (not applicable for subjects ≤17 years of age).
    6. Six-minute walk (6MW) results \<400 feet.
  3. therapy defined by either of the following:

    1. Subjects who received > 10 mg/day prednisone or equivalent within 30 days prior to start of conditioning regimen on Day -21.
    2. Subjects who have been treated for concurrent illnesses (eg, asthma) with the equivalent of prednisone 1 mg/kg/day or its equivalent for > 5 days on > 2 occasions during the previous 12 months (prior to conditioning) or > 1 occasion in the prior 6 months (prior to conditioning).
  4. Estimated CrCl \<40 mL/min,using Cockcroft-Gault formula based on actual body weight.
  5. Serum creatinine >2.0 mg/dL.
  6. Active, untreated SSc renal crisis at the time of consent.
  7. Dependence on nutritional supplementation/hyperalimentation.
  8. Active gastric antral vascular ectasia (GAVE), defined by a decrease in hemoglobin greater than 1 g/dL in the preceding 60 days, attributed to GAVE.
  9. Active hepatitis defined by any of the following:

    1. AST > 2x upper limit of normal.
    2. ALT > 2x upper limit of normal.
    3. >2x upper limit of normal.
  10. Evidence of moderate to severe periportal fibrosis, determined by liver , if applicable.
  11. Active, uncontrolled infection that would be a contraindication to safe use of high-dose immunosuppressive therapy or cyclophosphamide.
  12. Hematologic abnormalities as defined by any of the following peripheral blood counts:

    1. ANC \< 1500 cell/µL.
    2. Platelets \< 100,000 cells/ µL.
    3. Hemoglobin \< 9.0 g/dL.
  13. Evidence of myelodysplasia (MDS), confirmed by bone marrow aspirate, if applicable.
  14. Malignancy within 2 years prior to enrollment, excluding adequately treated squamous cell cancer, basal cell carcinoma or carcinoma in situ. Treatment should have been completed with cure/remission status documented for at least 2 years, with the exception of hormonal therapy for breast cancer.
  15. Females who are pregnant or who are lactating.
  16. Tobacco use, by subject admission, within previous 4 weeks of time of consent.
  17. History of sensitivity to murine proteins or E. coli proteins.
  18. Known history of substance abuse, determined by medical record or subject admission, within 6 months of time of consent.
  19. Patient with systemic reaction to anti-thymocyte globulin or any other equine gamma globulin preparation
  20. Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.
Terms in these criteria, in plain language(20)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Creatinine clearance (CrCl)

How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
8 participants (estimated)

Study arms

  • Experimental
    Autologous Stem Cell Transplantation

    CD34-selected autologous stem cell being performed on CliniMACS depletion device. Conditioning regimen will not start sooner than 3 weeks, and ideally no more than 90 days, after cyclophosphamide dose in the mobilization regimen.

    Drug: Cyclophosphamide · Drug: Mesna · Drug: Rituximab · Drug: Alemtuzumab · Drug: Thiotepa · Drug: GM-CSF · Drug: Intravenous immunoglobulin · Radiation: Total Body Irradiation · Drug: Anti Thymocyte Globulin

Interventions

06

What researchers measure

Primary outcomes

  1. High Dose Immunoablative therapy-Safety

    Safety will be determined by monitoring for death of any cause, regimen-related toxicities, and severe or life-threatening infections.

    Time frame: Up to 36 months post HSCT

  2. Death

    How many, if any, patients die

    Time frame: Post Transplant through study completion, an average of 36 months

  3. Respiratory Failure

    defined by one of the following 3 criteria without explanation for causation other than disease progression: 1. decline in DLCO of ≥30% or FVC≥20% as measured by actual difference in percent predicted units; 2. Resting arterial p02 \< 60 mmHg or pCO2 \> 50 mmHg supplemental oxygen;3. Resting pulse oximetry of 88% or lower measured by forehead probe.

    Time frame: Post Transplant through study completion, an average of 36 months

  4. Renal Failure

    Defined by chronic dialysis for \>6 months or renal transplantation

    Time frame: Post Transplant through study completion, an average of 36 months

  5. The occurrence of cardiomyopathy

    confirmed by clinical congestive heart failure (New York Heart Association) or LVEF (left ventricular ejection fraction) \<30% on echocardiogram

    Time frame: Post Transplant through study completion, an average of 36 months

  6. Treatment-related mortality (TRM)

    defined as death occurring at any time after stem cell mobilization and definitely or probably resulting from treatment given in the study. TRM will be determined yearly with a focus on the first 2 years.

    Time frame: Mobilization through study completion, an average of 36 months

  7. High Dose Immunoablative therapy-Treatment Effect

    Treatment effect will be determined by assessing event-free survival in comparison to a SSc observational cohort control group treated with standard of care medication (mycophenolate mofetil) at 12 and 36 months post hematopoietic stem cell transplant (HSCT).

    Time frame: up to 36 months post HSCT (hematopoietic stem cell transplantation)

Secondary outcomes

  1. An increase of mRSS (modified Rodnan skin score ) by ≥5 points for skin score

    To assess cutaneous response the modified Rodnan skin score (mRSS) will be used.

    Time frame: Disease response will be defined as subject improvement. This will be assessed for both skin and interstitial lung disease at 12 and 24 months post-HSCT.

  2. Increase by ≥25% if the baseline mRSS > 20.

    To assess cutaneous response the modified Rodnan skin score (mRSS) will be used.

    Time frame: Disease response will be defined as subject improvement. This will be assessed for both skin and interstitial lung disease at 12 and 24 months post-HSCT.

  3. Worsening of > 10% of FVC (pulmonary function testing)

    to evaluate interstitial lung disease an increase of ≥15% in DLCO or ≥10% of FVC (actual change in % predicted units from baseline) sustained for ≥3 months on 2 determinations.

    Time frame: 1 year post transplant through study completion, an average of 36 months

  4. Decrease in DLCO sustained for 3 months or longer on pulmonary function tests (PFT)

    to evaluate interstitial lung disease an increase of ≥15% in DLCO or ≥10% of FVC (actual change in % predicted units from baseline) sustained for ≥3 months on 2 determinations.

    Time frame: 1 year post transplant through study completion, an average of 36 months

  5. Worsening of cardiac involvement

    With use of Imaging, EKG, Echocardiogram, Cardiac MRI, right heart cauterization, implanted loop recorder and 2 week cardiac event monitor. Defined as new or worsening arrhythmias that require medical treatment of 3 months or longer, or require ablative therapy, pacemaker or defibrillator insertion or defined as a decline in ejection fraction of ≥10 EF units, determined by echocardiogram.

    Time frame: Post Transplant through study completion, an average of 36 months

  6. Development of scleroderma renal crisis (hypertensive or non-hypertensive)

    Hypertensive renal crisis can be defined as a rise in SBP ≥ 30 points or DBP ≥ 20 points from baseline and one of the following: 1) Increase in baseline serum creatinine of ≥ 50%, 2) thrombocytopenia \< 100,000 plts/mm3 or 3. hemolysis by blood smear or increased reticulocyte count.

    Time frame: Post Transplant through study completion, an average of 36 months

07

Study locations

3 of 3 sites recruiting
  • Children's Hospital of Pittsburgh of UPMC
    Pittsburgh, Pennsylvania 15213, United States
    Recruiting
    • Shawna McIntyre, RN · Contactmcintyresm@upmc.edu · 412-692-5552
    • Paul Szabolcs, MD · Principal investigator
    • Robyn Domsic, MD, MPH · Sub investigator
    • Annie Im, MD · Sub investigator
    • Daniel Kass, MD · Sub investigator
    • Geoffrey Kurland, MD · Sub investigator
    • Robert Lafyatis, MD · Sub investigator
    • Adam Olson, MD · Sub investigator
    • Kathryn Torok, MD · Sub investigator
    • Allison Morris, MD, MS · Sub investigator
    • Kirsten Rose-Felker, MD · Sub investigator
    • Franziska Rosser, MD, MPH · Sub investigator
    • Paulina Horvei, MD · Sub investigator
    • Joshua Levenson, MD · Sub investigator
    • Archana Ramgopal, DO · Sub investigator
  • University of Pittsburgh Medical Center
    Pittsburgh, Pennsylvania 15261, United States
    Recruiting
  • University of Pittsburgh Medical Center
    Pittsburgh, Pennsylvania 15261, United States
    Recruiting
08

References and documents

Publications

  • Torok KS, Horvei P, Li J, Rosser F, Alexander JL, Rose-Felker K, Sood V, Olson A, Hogue N, Vandergrift V, Stanczak H, Miglioretti M, Farver L, Koster W, Mcguire D, Havrilla H, McIntyre S, Domsic RT, Lafyatis RA, Szabolcs P. Autologous stem cell transplantation (ASCT) for Refractory juvenile-onset systemic sclerosis (JSSc). Ann Rheum Dis. 2026 Jun 17:S0003-4967(26)00299-2. doi: 10.1016/j.ard.2026.05.022. Online ahead of print. PubMed 42309868 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2018 (actual). Primary completion is estimated for Aug 2028, 120 months after the start.

Of 48 phase 2 interventional studies under Scleroderma, Systemic, half reached primary completion within 37 months of starting (the median), counting those still running; a quarter within 24 and three quarters within 83. This study's planned 120 months is above that.

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

Registered
Aug 7, 2018
First posted
Aug 14, 2018
StartActual
Jul 31, 2018
Primary completionEst.
Aug 1, 2028
CompletionEst.
Aug 1, 2028
Last update
Aug 14, 2026
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 Aug 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03630211
Lead sponsor
Paul Szabolcs
Responsible party
Paul Szabolcs (Chief, Division of Blood and Marrow Transplantation and Cellular Therapy, University of Pittsburgh) — Sponsor-investigator
First posted
Aug 14, 2018
Start date
Jul 31, 2018
Primary completion
Aug 1, 2028 (estimated)
Completion
Aug 1, 2028 (estimated)
Last update
Aug 14, 2026

Study contacts

Paul Szabolcs, MD
Contact
paul.szabolcs@chp.edu
412-692-6225
Shawna McIntyre, RN
Contact
mcintyresm@upmc.edu
412-692-5552
Paul Szabolcs, MD
principal investigator · University of Pittsburgh

Oversight

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

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Studies of the drugs tested here: Cyclophosphamide · Mesna · Rituximab · Alemtuzumab · Thiotepa · Granulocyte-Macrophage Colony-Stimulating Factor · Immunoglobulins, Intravenous · Antilymphocyte Serum

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