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TerminatedNCT03867851Updated May 16, 2024

Study to Evaluate Safety and Efficacy of IBsolvMIR in Islet Transplantation

A Phase 2 interventional study of IBsolvMIR and Heparin in Diabetes Mellitus, Type 1, sponsored by TikoMed AB. Terminated at 5 sites in 3 countries. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2024-05-16.

Sponsored by TikoMed AB · Phase 2, Interventional, and Treatment

Why this study was terminated
Slow patient recruitment
Phase
Phase 2
Study type
Interventional
Enrollment
7
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

This is a Phase II open, randomized, active comparator-controlled multi center study in patients with severe type-1 diabetes. This is a two-armed study where patients are randomized in a 2:1 ratio between IBsolvMIR and heparin. Eighteen patients are planned to be included.

The study consists of up to 8 visits; screening, transplantation surgery with bolus administration of study drug or active comparator, IBsolvMIR doses on day 1, 3 and 6 after surgery, follow up visits on day 7 and 14, and follow-up phone call on day 44.

The primary endpoint is to study AEs up to 44 days following study drug administration. The secondary endpoints are to evaluate changes in TAT, C-peptide, C3a and HGF at baseline and during the first 24 hours after study drug administration, as well as evaluate a change in levels of C-peptide-glucose-creatinine ratio on day 14 compared to baseline.

02

Conditions studied

  • Diabetes Mellitus, Type 1
03

In context

Diabetes Mellitus, Type 1

3,614 studies on the registry are indexed under Diabetes Mellitus, Type 1; 586 are open to participants now.

This study's enrollment of 7 is below the median of 40 across 2,718 interventional studies indexed under Diabetes Mellitus, Type 1.

Browse Diabetes Mellitus, Type 1 studies →

Lead sponsor

TikoMed 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 60 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

  1. Patient on a waiting list for islet transplantation
  2. Male and female patients age 18 to 60 years of age.
  3. Ability to understand and provide written informed consent.
  4. Mentally stable and able to comply with the procedures of the study protocol.
  5. 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.
  6. Documented C-peptide \<0.1 nmol/L before first islet transplantation (stimulated in response to a MMTT or other confirmatory method).
  7. 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;
  8. At least one episode of severe hypoglycemia in the past 1 year defined as an event with at least one of the following symptoms; memory loss, confusion, uncontrollable behavior, 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
  9. Reduced awareness of hypoglycemia as defined by a Clarke score of 4 or more.

Exclusion criteria

Exclusion Criteria:

  1. Patients with prior organ transplants other than a kidney graft and/or islets. A previous pancreas transplant can be accepted if it failed within the first week due to thrombosis and the graft was removed.
  2. Patients with body mass index (BMI) > 30.
  3. Insulin requirement > 0.7 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;

    • unstable coronary artery disease requiring hospitalization or revascularization within 6 months prior to baseline visit
    • 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. Patients of childbearing potential not willing to use adequate double contraception with \< 1% failure rate after the screening visit until the last visit.
  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 > IFCC 100 mmol/mol, at screening.
  18. Patients with any condition or any circumstance that in the opinion of the investigator would make it unsafe to undergo treatment with IBsolvMIR.
  19. Patients participating in or having participated in any other clinical drug studies in the past four weeks.
  20. History of bleeding disorders
  21. History of severe hypersensitivity
  22. Previous known heparin-induced thrombocytopenia (HIT)
  23. Patients with severe hepatic or renal impairment
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
7 participants (actual)

Study arms

  • Experimental
    IBsolvMIR

    Study drug IBsolvMIR administered intravenously at 18 mg/kg on day of transplantation and 3 mg/kg on post-operative days 1, 3, 6.

    Drug: IBsolvMIR

  • Active comparator
    Heparin

    Heparin treatment according to clinical praxis.

    Drug: Heparin

Interventions

  • DrugIBsolvMIR

    Study drug IBsolvMIR

  • Clinical praxis

06

What researchers measure

Primary outcomes

  1. Bleeding events

    Bleeding events after islet transplantation with total dose of 27 mg/kg BW IBsolvMIR in comparison to active comparator Heparin

    Time frame: Up to 44 days.

  2. Other AEs/SAEs after islet transplantation

    Other AEs/SAEs after islet transplantation with total dose of 27 mg/kg BW IBsolvMIR in comparison to active comparator Heparin

    Time frame: Up to 44 days.

Secondary outcomes

  1. Difference between groups in levels of biomarkers

    Difference between groups in levels of biomarkers after transplantation

    Time frame: Within 7 days.

  2. Change in C-peptide / (glucose x creatinine) ratio (CPGCR)

    Change in CPGCR at day 14 compared to baseline. CPGCR is calculated by: C-peptide (ng/mL) / ( glucose (mg/dL) x creatinine ratio (mg/dL) )

    Time frame: Within 14 days.

07

Study locations

5 sites
  • Leiden University Medical Center
    Leiden, South Holland 2300 RC, Netherlands
  • Oslo Universitetssykehus HF
    Oslo, Norway
  • Sahlgrenska sjukhuset
    Gothenburg, Sweden
  • Karolinska Universitetssjukhuset Huddinge
    Stockholm, Sweden
  • Akademiska sjukhuset
    Uppsala, Sweden
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Feb 2021 to primary completion in May 2024, 39 months.

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

Registered
Mar 5, 2019
First posted
Mar 8, 2019
StartActual
Feb 8, 2021
Primary completionActual
May 13, 2024
CompletionActual
May 13, 2024
Last update
May 16, 2024
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 May 16, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03867851
Lead sponsor
TikoMed AB
Responsible party
Sponsor
First posted
Mar 8, 2019
Start date
Feb 8, 2021
Primary completion
May 13, 2024
Completion
May 13, 2024
Last update
May 16, 2024

Oversight

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

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