ClinicalTrials.gg
CompletedNCT01586455HPDSCUpdated Oct 25, 2022

Human Placental-Derived Stem Cell Transplantation

A Phase 1 interventional study of Human Placental Derived Stem Cell in Mucopolysaccharidosis I, Mucopolysaccharidosis VI and Adrenoleukodystrophy, sponsored by New York Medical College. Completed at 3 sites in United States. Open to participants aged 0 Years to 55 Years. Per ClinicalTrials.gov, last updated 2022-10-25.

Sponsored by New York Medical College · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
43
Allocation
Non-randomized
Ages
0 Years to 55 Years
Sex
All
01

Study summary

The purpose of this clinical trial is to investigate the safety of human placental-derived stem cells (HPDSC) given in conjunction with umbilical cord blood (UCB) stem cells in patients with various malignant or nonmalignant disorders who require a stem cell transplant. Patients will get either full dose (high-intensity) or lower dose (low intensity) chemo- and immunotherapy followed by a stem cell transplantation with UCB and HPDSC.

02

Conditions studied

  • Mucopolysaccharidosis I
  • Mucopolysaccharidosis VI
  • Adrenoleukodystrophy
  • Niemann-Pick Disease
  • Metachromatic Leukodystrophy
  • Wolman Disease
  • Krabbe's Disease
  • Gaucher's Disease
  • Fucosidosis
  • Batten Disease
  • Severe Aplastic Anemia
  • Diamond-Blackfan Anemia
  • Amegakaryocytic Thrombocytopenia
  • Myelodysplastic Syndrome
  • Acute Myelogenous Leukemia
  • Acute Lymphocytic Leukemia

Keywords

  • umbilical cord blood
  • stem cell transplantation
  • placental stem cell
  • inborn errors of metabolism
  • marrow failure
  • Severe Combined Immunodeficiency Disease
  • AML
  • ALL
  • MDS
03

In context

Mucopolysaccharidosis I

74 studies on the registry are indexed under Mucopolysaccharidosis I; 7 are open to participants now.

This study's enrollment of 43 is above the median of 14 across 47 interventional studies indexed under Mucopolysaccharidosis I.

Browse Mucopolysaccharidosis I studies →

Lead sponsor

New York Medical College is the lead sponsor of 71 studies on the registry; 24 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
0 Years to 55 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

  • \< 55 years of age
  • greater than 3 months
  • Lansky performance status ≥ 50% (children) or performance status ≥ 70% (adults) or performance status 0-2 (adults)
  • DLCO > 50 percent predicted
  • > 40% estimated
  • or estimated . 60 mL/min/1.73m2
  • Serum \< 1.5x
  • Transaminases \< 3x upper limit of normal
  • Absence of uncontrolled infection
  • negative

Exclusion criteria

Exclusion Criteria:

  • Fanconi Anemia
  • Myocardial infarction within 6 months prior to enrollment or has (NYHA) Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities
  • Uncontrolled infection
  • Pregnant or breast-feeding females
  • Received other agents within 30 days prior to the start of the conditioning regimen
Terms in these criteria, in plain language(11)

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.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

Karnofsky performance status (KPS)

A 0–100 scale of how well someone can carry out everyday activities. 100 is no complaints and no signs of illness; 70 is able to look after yourself but not to work or keep up normal activity; 50 is needing considerable help and frequent medical care.

Studies often ask for 60 or 70 and above. Your doctor gives the score.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

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.

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.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

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.

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.

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.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
43 participants (actual)

Study arms

  • Experimental
    Group A

    related cord blood with ≥3/6 HLA match to the patient and related HPDSC

    Drug: Human Placental Derived Stem Cell

  • Experimental
    Group B

    unrelated cord blood with ≥ 4/6 HLA match to the patient and unrelated HPDSC

    Drug: Human Placental Derived Stem Cell

  • Experimental
    Group C

    unrelated cord blood with ≥4/6 HLA match to the patient but related to HPDSC

    Drug: Human Placental Derived Stem Cell

  • Experimental
    Group D

    double unrelated cord blood units with ≥4/6 HLA match to patient and each other and unrelated HPDSC

    Drug: Human Placental Derived Stem Cell

Interventions

  • DrugHuman Placental Derived Stem Cell

    Infusions of thawed HPDSC to be given following UCB infusion.

    Also known as: HPDSC

06

What researchers measure

Primary outcomes

  1. Safety

    to evaluate the safety of human placental-derived stem cells (HPDSC) administered in conjunction with umbilical cord blood (UCB) stem cells in patients with malignant and non-malignant diseases.

    Time frame: 100 days

Secondary outcomes

  1. donor chimerism

    donor chimerism will be assessed at set timepoints

    Time frame: 1 year

  2. engraftment

    Time frame: 1 year

  3. Survival

    Time frame: 100 days and 180 days

  4. Relapse

    Time frame: 100 days and 180 days

  5. Mortality

    Time frame: 1 year

07

Study locations

3 sites
  • Children's Hospital Colorado
    Denver, Colorado, United States
  • New York Medical College
    Valhalla, New York 10595, United States
  • University of Utah
    Salt Lake City, Utah, United States
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Apr 2013 to primary completion in Jun 2020, 86 months.

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

Registered
Apr 25, 2012
First posted
Apr 26, 2012
StartActual
Apr 2013
Primary completionActual
Jun 2020
CompletionActual
Sep 2022
Last update
Oct 25, 2022
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 Oct 25, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01586455
Lead sponsor
New York Medical College
Responsible party
Sponsor
First posted
Apr 26, 2012
Start date
Apr 2013
Primary completion
Jun 2020
Completion
Sep 2022
Last update
Oct 25, 2022

Study contacts

Mitchell S Cairo, MD
principal investigator · New York Medical College

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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

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