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CompletedNCT00788827Updated Nov 18, 2019Results posted

Autologous Adult Stem Cells to Patients With Type 1 Diabetes and a Successful Renal Transplant

A Phase 1 interventional study of Autologous CD34+ stem cells in Type 1 Diabetes and Type 2 Diabetes, sponsored by Imperial College London. Completed at 1 site in United Kingdom. Open to participants aged 16 Years to 65 Years. Per ClinicalTrials.gov, last updated 2019-11-18.

Sponsored by Imperial College London · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
7
Allocation
Not applicable
Ages
16 Years to 65 Years
Sex
All
01

Study summary

This is a phase I study to assess the safety and tolerability of infusing expanded stem cells into the pancreas of patients with type I diabetes and a successful renal transplant. The stem cells used in this study occur naturally in the body and are collected from each recipient by a procedure called leukapheresis. The cells are then expanded and differentiated into insulin-like cells in a sterile suite before being injected into the body or tail of the pancreas of the recipient.

Read the detailed description

Islet transplantation as a potential treatment for diabetes has been investigated extensively over the past 10 years. Such an approach, however, will always be limited mainly because it is difficult to obtain sufficiently large numbers of purified islets from cadaveric donors. One alternative to organ or tissue transplantation is to use a renewable source of cells. Adult stem cells are clonogenic cells capable of both self-renewal and multilineage differentiation. These cells have the potential to proliferate and differentiate into any type of cell and to be genetically modified in vitro, thus providing cells, which can be isolated and used for transplantation.

Recent studies have given well-defined differentiation protocols, which can be used to guide stem cells into specific cell lineages as neurons, cardiomyocytes and insulin-secreting cells. Moreover, these derived cells have been useful in different animal models. In this regard, insulin-secreting cells derived from R1 mouse embryonic stem cells restore blood glucose concentrations to normal when they are transplanted into streptozotocin-induced diabetic animals. Our group has isolated stem cells (Cluster Designated (CD) 34 positive subset of stem cells) that are capable of differentiating into multiple tissue types ex vivo. In defined conditions, in culture, about 40 percent of the cells produce insulin and reduce blood sugar levels in streptozotocin-induced mice.

Clinically, we have performed a phase I trial of stem cell administration to patients with liver insufficiency. The procedure was well tolerated with no specific side effects and with sustained signs of clinical benefit. These results support this protocol for the application of adult stem cell therapy in the treatment of diabetes.

In order to evaluate potential clinical applications for these recent advances we have designed a prospective Phase I clinical study of the expanded progeny of an adult CD34 positive subset (InsulinCytes) injected directly into the body and tail of the pancreas of the participants via selective catheterisation of the splenic artery. The study group consists of patients with complicated diabetes mellitus type I plus kidney transplantation with the aim of ascertaining whether this confers clinical benefit as a treatment model for diabetes.

Granulocyte colony-stimulating factor (G-CSF) will be administered to suitable patients to mobilise their haematopoietic stem cells (HSCs) from the bone marrow into the peripheral circulation. These blood cells will be collected from each patient by leukapheresis. CD34 positive stem cells will then be isolated by immunoselection and introduced into a Nunc cell factory where the subset of CD34 positive stem cells will be allowed to attach to the plastic trays within the cell factory for 2 hours at 37 degrees C in 5 percent carbon dioxide. After this period the non-attached CD34 positive cells will be washed from the system and the progeny of the attached cells secreted into the supernatant media expanded in the presence of growth medium supplemented with growth factors. At the end of 6 days expansion, the stem cells will be differentiated into insulin and c-peptide protein excreting cells over the next 14 days by the addition of specified reagents/growth factors and continued incubation at 37 degrees C in 5 percent carbon dioxide in accordance with the principles of Good Manufacturing Practice (GMP). As an optional step the cells can be labelled with iron oxide to allow tracking of the cells by Magnetic Resonance Imaging (MRI) scan, before being infused into the patient.

An ongoing institute experience with liver failure patients who have been infused with undifferentiated stem cells has shown that an administered dose of up to 2 x 10 log 9 cells was well tolerated. The proposed study group will consist of 10 Type I or Type 2 diabetic patients who have had a successful previous kidney transplant.

The primary purpose of the study is to assess the safety and tolerance of stem cell infusion into the pancreas and then to assess the impact of this new modality in the treatment of diabetes.

02

Conditions studied

  • Type 1 Diabetes
  • Type 2 Diabetes

Keywords

  • diabetes type I
  • diabetes type 2
  • renal transplant
  • stem cells
  • successful renal transplant
03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 7 is below the median of 80 across 8,367 interventional studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Imperial College London is the lead sponsor of 824 studies on the registry; 178 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 6 (67%) 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

  • Male or female patients aged from 16 to 65 years of age
  • Patient with Type I or Type 2 diabetes mellitus plus:
  • Successful previous kidney transplant.
  • Good kidney allograft function /no episodes of rejection for at least one year post-transplant
  • Not taking steroids as part of standard immuno-suppression
  • Has a WHO performance score of less than 2
  • Has a life expectancy of at least 3 months
  • Ability to give written consent
  • Women of childbearing potential may be included, but must use a reliable and appropriate contraceptive method

Exclusion criteria

Exclusion Criteria:

  • Patients below the age of 16 or above the age of 65 years
  • Patients with chronic pancreatitis and poor exocrine pancreatic function
  • Pregnant or lactating women
  • Patients with recent recurrent GI bleeding or spontaneous bacterial peritonitis
  • Patients with evidence of HIV or other life threatening infection
  • Patients unable to give written consent
  • Patients with a history of hypersensitivity to G-CSF
  • Patients who have been included in any other clinical trial within the previous month
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
    Autologous CD34+ stem cells

    Up to 5 x 10 log 8 of autologous stem cells on a single occasion

    Biological: Autologous CD34+ stem cells

Interventions

  • BiologicalAutologous CD34+ stem cells

    Up to 5 x 10 log 8 of autologous stem cells on a single occasion

06

What researchers measure

Primary outcomes

  1. Number of Participants Who Experienced Adverse Events

    Safety will be evaluated in terms of adverse events graded according to CTCTAE toxicity criteria and laboratory test results. All adverse events will also be graded for relationship to treatment and as expected and unexpected.

    Time frame: 14 days

Secondary outcomes

  1. Hba1C Data of Pre and Post Stem Cell Infusion

    Mean HbA1c laboratory measurements pre and post stem cell infusion

    Time frame: 12 weeks

  2. Insulin Level

    Mean insulin requirement was calculated for each participant pre and post stem cell infusion

    Time frame: 12 weeks

  3. Amylase Level

    Each participant had mean amylase data analysed to give a pre and post mean result

    Time frame: 12 weeks

  4. Serum Creatinine

    Each participant had serum creatinine analysis pre and post stem cell infusion to give mean result

    Time frame: 12 weeks

07

Results

Posted Nov 18, 2019

Participant flow

Participant flow — Overall Study
MilestoneAutologous CD34+ Stem Cells
Started7
Completed5
Not completed2
Withdrew: Lack of efficacy2

Outcome measures

PrimaryNumber of Participants Who Experienced Adverse Events

Safety will be evaluated in terms of adverse events graded according to CTCTAE toxicity criteria and laboratory test results. All adverse events will also be graded for relationship to treatment and as expected and unexpected.

Time frame:
14 days
Reported as:
Number · participants
Number of Participants Who Experienced Adverse Events
participantsAutologous Stem Cells
Haematoma at femoral catheter insertion1
Fatigue7
SecondaryHba1C Data of Pre and Post Stem Cell Infusion

Mean HbA1c laboratory measurements pre and post stem cell infusion

Time frame:
12 weeks
Reported as:
Mean · percentage
Hba1C Data of Pre and Post Stem Cell Infusion
percentagePre Infusion of Stem CellsPost Infusion of Stem Cells
Hba1C Data of Pre and Post Stem Cell Infusion7.2 ± 1.37.24 ± 1.2
Statistical analysis
  • Pre Infusion of Stem Cells vs Post Infusion of Stem Cells · Mixed Models Analysis · p = <0.05
SecondaryInsulin Level

Mean insulin requirement was calculated for each participant pre and post stem cell infusion

Time frame:
12 weeks
Reported as:
Mean · iu/day
Insulin Level
iu/dayPre Infusion of Stem CellsPost Infusion of Stem Cells
Insulin Level59.4 ± 25.754.06 ± 18.2
SecondaryAmylase Level

Each participant had mean amylase data analysed to give a pre and post mean result

Time frame:
12 weeks
Reported as:
Mean · units/L
Amylase Level
units/LPre Infusion of Stem CellsPost Infusion of Stem Cells
Amylase Level48.49 ± 25.275.52 ± 34.2
SecondarySerum Creatinine

Each participant had serum creatinine analysis pre and post stem cell infusion to give mean result

Time frame:
12 weeks
Reported as:
Mean · umol/L
Serum Creatinine
umol/LPre Infusion of Stem CellsPost Infusion of Stem Cells
Serum Creatinine128.22 ± 11.9118.64 ± 15.5

Adverse events

Collected over 12 weeks. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Single Arm0/7 (0%)0/7 (0%)7/7 (100%)
Most frequent other events
Most frequent other events
EventSingle Arm
FatigueNervous system disorders7/7
HaemotomaBlood and lymphatic system disorders1/7

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Single Arm
<=18 years0
Between 18 and 65 years7
>=65 years0
Age, Continuous
Age, Continuous(years)Single Arm
Mean54.6 ± 4.2
Sex: Female, Male
Sex: Female, Male(Participants)Single Arm
Female2
Male5
Race and Ethnicity Not Collected
Race and Ethnicity Not Collected(Participants)Single Arm
Region of Enrollment
Region of Enrollment(participants)Single Arm
United Kingdom7
08

Study locations

1 site
  • Imperial College NHS Healthcare Trust, Hammersmith Hospital
    London, W12 0HS, United Kingdom
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 Nov 18, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT00788827
Lead sponsor
Imperial College London
Responsible party
Sponsor
First posted
Nov 11, 2008
Start date
Nov 2008
Primary completion
May 2013
Completion
May 2013
Results posted
Nov 18, 2019
Last update
Nov 18, 2019

Study contacts

Charles Pusey, MD
principal investigator · Imperial College London

Oversight

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

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