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
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.
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 →TikoMed AB is the lead sponsor of 2 studies on the registry; none are open to participants now.
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Exclusion Criteria:
Patients with increased cardiac risk defined as;
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
Heparin treatment according to clinical praxis.
Drug: Heparin
Study drug IBsolvMIR
Clinical praxis
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.
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.
Difference between groups in levels of biomarkers
Difference between groups in levels of biomarkers after transplantation
Time frame: Within 7 days.
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.
Plan to share: No
No publications or documents are linked to this record.
Ran from Feb 2021 to primary completion in May 2024, 39 months.
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This study is terminated, as verified in May 2024. You cannot join it, but the record below documents what was studied.
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TikoMed AB