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| ID | Type | Description | Link |
|---|---|---|---|
| AT-1501-I203 | Other Identifier | Anelixis |
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This study will evaluate the safety, tolerability and efficacy of AT-1501 in an immunomodulation regimen in adult patients with T1D undergoing an islet cell transplant.
This study will evaluate the safety, tolerability and efficacy of AT-1501 in an immunomodulation regimen in adult patients with T1D undergoing an islet cell transplant. This study will also provide valuable data with respect to its potential additional uses in autoimmunity and solid organ transplant. This is a single arm open-label study and up to 6 participants will be recruited at a single center in Canada.
The objectives include:
The duration of treatment may vary from participant to participant and could be up to 20 months. Participants may receive up to 2 islet cell transplants.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| AT-1501 Single Arm | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AT-1501 | Drug | AT-1501 IV infusion |
|
| Measure | Description | Time Frame |
|---|---|---|
| Safety- Adverse Events (AE) and Adverse Events of Special Interest (AEoSI) | Incidence of adverse events | Accessed from date of transplant through 1 year post transplant for approximately 2 years |
| Efficacy- Insulin independence | Change in the proportion of participants that become insulin independent at Days 75 and 365 post-first, and final transplant | Days 75 , Day 365 post-first transplant, and final transplant and 1 year after discontinuation of AT-1501 |
| Measure | Description | Time Frame |
|---|---|---|
| Efficacy- Graft failure | Proportion of participants with graft failure | Day 365 |
| Efficacy- Durability of insulin independence- long term | Change in the proportion of participants that become insulin independent at year 2 and year 3 |
| Measure | Description | Time Frame |
|---|---|---|
| Exploratory- Hypoglycemia unawareness (using the method of Clarke) | Proportion of participants with hypoglycemia unawareness | Day 75, 365, and 1, 2 and 3 years after discontinuation of AT-1501 |
| Exploratory- Glycemic lability (using CGMS) |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jeff Bornstein, MD | Eledon Pharmaceuticals | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Alberta | Edmonton | Alberta | T6G 2E1 | Canada |
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| ID | Term |
|---|---|
| D003922 | Diabetes Mellitus, Type 1 |
| D004700 | Endocrine System Diseases |
| D008659 | Metabolic Diseases |
| D007154 | Immune System Diseases |
| D001327 | Autoimmune Diseases |
| D007003 | Hypoglycemia |
| D006943 | Hyperglycemia |
| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D009750 | Nutritional and Metabolic Diseases |
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| 2 and 3 years after discontinuation of AT- 1501 |
| Efficacy- HbA1c |
| Day 365 and free of serious hypoglycemic events from Day 28 to 365 post-first transplant |
Change in glycemic lability using CGMS- Continuous Glucose Monitoring System
| Day 75, 365, and 1, 2 and 3 years after discontinuation of AT-1501 |
| Exploratory- Glycemic variability (using CGMS) | Change in glycemic variability using CGMS- Continuous Glucose Monitoring System | Day 75, 365, and 1, 2 and 3 years after discontinuation of AT-1501 |
| Exploratory- Albumin excretion ratio (AER) | Change in albumin excretion ratio (AER) | Day 365 post-first, and final transplant |
| Exploratory- eGRF | Change in eGRF | Day 365 post-first, and final transplant |
| Exploratory- Macroalbuminemia | Change in percent new macroalbuminemia | Day 365 post-first, and final transplant |
| Exploratory- biomarkers of tissue damage and inflammation | Biomarkers | Day -2, 3, 14, 28, 75, 175, 364 |
| Exploratory -Pharmacokinetic Parameters-AUC | Pharmacokinetics (PK) of AT-1501 | T=0 (pre infusion), 1 (end of infusion), 2, 4, 8, 12, 24 and 48 hrs. |
| Exploratory- Pharmacokinetic Parameters-Cmax | Pharmacokinetics (PK) of AT-1501 | T=0 (pre infusion), 1 (end of infusion), 2, 4, 8, 12, 24 and 48 hrs. |
| Exploratory- Pharmacokinetic Parameters-CL | Pharmacokinetics (PK) of AT-1501 | T=0 (pre infusion), 1 (end of infusion), 2, 4, 8, 12, 24 and 48 hrs. |
| Exploratory- Pharmacokinetic Parameters- Vdss | Pharmacokinetics (PK) of AT-1501 | T=0 (pre infusion), 1 (end of infusion), 2, 4, 8, 12, 24 and 48 hrs. |
| Exploratory- Pharmacokinetic Parameters- (t1/2) | Pharmacokinetics (PK) of AT-1501 | T=0 (pre infusion), 1 (end of infusion), 2, 4, 8, 12, 24 and 48 hrs. |