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Status unknownNCT00678990Updated Dec 10, 2018

Heparinized Islets in Clinical Islet Transplantation

An interventional study of Transplantation of islets with heparin coating in Type 1 Diabetes Mellitus, sponsored by Corline Biomedical AB. Status unknown at 2 sites in Sweden. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2018-12-10.

Sponsored by Corline Biomedical AB · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2018), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

In this study the islets will be surface modified to carry immobilised heparin (Corline Heparin Conjugate) prior to transplantation. The primary objective is to investigate safety and efficacy of allogeneic islet transplantation using islets coated with immobilised heparin. The modification with heparin has been shown to protect the islets from being attacked by the immediate defence systems in blood (coagulation and inflammation), so that a larger portion of the islets will survive the initial phase and engraft. Evaluation will be based on metabolic and blood chemistry parameters.

Read the detailed description

Transplantation of islets of Langerhans isolated from donated organs is a promising therapy for diabetes type 1. The results so far have, however, not met with the expectations due to relatively low efficiency. Even in situations where the patients have become insulin-free, it has been estimated that the transplanted islet mass is less than 25% of the islet mass of a healthy individual, which in many cases has required repeated use of insulin injections. The islets are transferred to the patient by an infusion drop to the liver via the portal vein.

Researches within the Nordic Network for Clinical Islet Transplantation have in a series of publications shown that the islets are subject to a violent immunological reaction that is non-specific with regard to the individual patient (IBMIR) during the initial contact with blood (Moberg et al, Lancet 2002, among several). The IBMIR reaction is in the earliest phase mediated by coagulation and complement reactions.

In this study the islets will be surface modified to carry immobilised heparin (Corline Heparin Conjugate) prior to transplantation. The primary objective is to protect the islets from being attacked by IBMIR so that a larger portion of the islets will survive the initial phase and engraft. In a paper published by the research group (Cabric et. al., Diabetes, May 2007), the beneficial effects of immobilised heparin on the islets to counteract IBMIR were shown by experiments at the lab bench and in experimental animals.

The evaluation of the transplantations in this study will be based on metabolic and blood chemistry parameters, similar to the evaluations of other transplanted patients within the Nordic Network.

02

Conditions studied

  • Type 1 Diabetes Mellitus

Keywords

  • Islets of Langerhans
  • islets
  • heparin
03

In context

Diabetes Mellitus, Type 1

3,522 studies on the registry are indexed under Diabetes Mellitus, Type 1; 577 are open to participants now.

This study's planned enrollment of 10 is below the median of 40 across 2,649 interventional studies indexed under Diabetes Mellitus, Type 1.

Browse Diabetes Mellitus, Type 1 studies →

Lead sponsor

Corline Biomedical AB is the lead sponsor of 2 studies on the registry; none are open to participants now.

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

04

Who can participate

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

Inclusion criteria

  1. Male and female patients age 18 to 65 years of age.
  2. Ability to understand and provide written informed consent.
  3. Mentally stable and able to comply with the procedures of the study protocol.
  4. Clinical history compatible with type 1 diabetes with onset of disease at \< 40 years of age and insulin-dependence for > 5 years at the time of enrolment.
  5. Stimulated C-peptide \< 0.3 ng/mL (0.1 nmol/L) in response to a MMTT, before first islet transplantation.
  6. All subjects must have received medical treatment of their diabetes under the guidance from an experienced endocrinologist.

    If not previously transplanted the patient must also have;

  7. At least one episode of severe hypoglycaemia in the past 1 year defined as an event with at least one of the following symptoms; memory loss, confusion, uncontrollable behaviour, unusual difficulty in awakening, suspected seizure, loss of consciousness, or visual symptoms, in which the subject was unable to treat him/herself and which was associated with either a blood/plasma glucose level \< 54 mg/dl (3.0 mmol/L) or prompt recovery after oral carbohydrate, intravenous glucose, or glucagon administration OR
  8. Reduced awareness of hypoglycaemia as defined by a Clarke score of 4 or more.

Exclusion criteria

Exclusion Criteria

Patients who meet any of these criteria are not eligible for participation in the study:

  1. Patients with prior organ transplants other than a kidney graft and/or islets.
  2. Patients with body mass index (BMI) > 30.
  3. Insulin requirement > 1 Unit/kg/day at screening.
  4. Consistently abnormal liver function tests (> 1.5 x ULN on two consecutive measurements > 2 weeks apart), at screening.
  5. Proliferative untreated diabetic retinopathy
  6. Increased risk for thrombosis (ex. homozygous APC-resistance) or bleeding (INR>1.5)
  7. Any history of malignancy except for completely resected squamous or basal cell carcinoma of the skin
  8. Patients with increased cardiac risk defined as;

    1. unstable coronary artery disease requiring hospitalization or revascularization within 6 months prior to baseline visit
    2. chronic heart failure which required hospitalization 30 days prior to baseline visit
  9. Patients with active infections, unless treatment is not judged necessary by the investigators
  10. Patients with serological evidence of infection with HIV, hepatitis B (patients with serology consistent with previous vaccination and a history of vaccination are acceptable) or hepatitis C.
  11. Patients with active peptic ulcer disease, symptomatic gallstones or portal hypertension.
  12. Patients who are pregnant or breastfeeding, or who intend to become pregnant.
  13. Sexually active females who are not:

    1. post-menopausal,
    2. surgically sterile, or
    3. using a highly effective method of contraception, such as: intra uterine device, oral contraceptives, implants, injectables or barrier devices combined with spermicidal gel
  14. Active alcohol or substance abuse
  15. Patients with evidence of high-level sensitization (PRA> 50% with flow cytometry).
  16. Patients with psychological conditions that make it unsafe to undergo islet transplantation or which preclude compliance with prescribed therapy
  17. HbA1c >11% (International standard) corresponding to IFCC calibration 97 mmol/mol, at screening.
  18. Medical history of egg allergy
  19. Patients with any condition or any circumstance that in the opinion of the investigator would make it unsafe to undergo an islet transplant
  20. Patients participating in or having participated in any other clinical drug studies in the past four weeks.
05

Study design

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

Study arms

  • Experimental
    Open, single arm

    Transplantation of islets with heparin coating.

    Procedure: Transplantation of islets with heparin coating

Interventions

  • ProcedureTransplantation of islets with heparin coating

    Transplantation of islets with heparin coating

06

What researchers measure

Primary outcomes

  1. Safety

    Number of and grade of Serious Adverse events during the first 105 days after transplantation and Adverse events during the first 75 days after transplantation.

    Time frame: 105 days

07

Study locations

2 sites
  • Department of Transplantation Surgery, Karolinska University Hospital
    Stockholm, SE-141 86, Sweden
  • Department of Transplantation and Liver Surgery, Uppsala University Hospital
    Uppsala, SE-751 85, Sweden
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 10, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00678990
Lead sponsor
Corline Biomedical AB
Responsible party
Sponsor
First posted
May 16, 2008
Start date
Jan 2019 (estimated)
Primary completion
Dec 2019 (estimated)
Completion
Dec 2019 (estimated)
Last update
Dec 10, 2018

Study contacts

Tomas Lorant
Contact
tomas.lorant@surgsci.uu.se
+46 18 6110000
Tomas Lorant
principal investigator · Uppsala University Hospital

Oversight

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

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