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Effect of ZT-01 on Glucagon During Hypoglycemia in Type 1 Diabetes Mellitus

Sponsored by Zucara Therapeutics Inc.

About this trial

Last updated 2 years ago

Study ID

ZT01-CL-1003

Status

Terminated

Type

Interventional

Phase

Phase 1

Placebo

Yes

Accepting

18-75 Years
18 to 65 Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 3 years ago

What is this trial about?

The purpose of this study is to determine whether ZT-01 increases the glucagon response to hypoglycemia in type 1 diabetes (T1D). ZT-01 is a specific somatostatin (SST) type 2 receptor antagonist hypothesized to increase the counterregulatory glucagon release during hypoglycemia, which is impaired in diabetes, and may thus reduce the occurrence of hypoglycemia. Approximately 25 participants with well-controlled type 1 diabetes will be recruited to a crossover study and be randomized to the order in which they receive a single administration of placebo, low dose and high dose ZT-01 during three euglycemic-hypoglycemic clamps 2 to 6 weeks apart, with a follow-up visit approximately 1 week after the final clamp. Participants will stay overnight in the clinic before each clamp, and their plasma glucose (PG) will be kept at euglycemic levels with IV insulin and dextrose as needed. The following morning, the clamp will begin and the subject's PG will be kept at 5.5 mmol/L (euglycemia) with variable IV insulin (and dextrose as needed). Study treatment will be administered during this euglycemic period, and then insulin will be increased so that PG falls to a plateau of mild hypoglycemia, and then increased further to clinically significant hypoglycemia. Release of glucagon and other counterregulatory hormones will be measured, and a symptom score will be completed, during euglycemia before and following study treatment, and during each level of hypoglycemia. Following the clamp, the participant's blood glucose will be returned to normal levels prior to leaving the clinic.

What are the participation requirements?

Yes

Inclusion Criteria

- Type 1 diabetes for at least 5 years and receiving insulin as the only T1D therapy

- HbA1c ≥6.0 and ≤9.0 %

- BMI ≥18 to ≤27 kg/m^2

- Normal thyroid function

No

Exclusion Criteria

- Impaired hypoglycemia awareness

- Severe hypoglycemia or diabetic ketoacidosis (DKA) within 3 months

- Abnormal blood pressure or ECG, clinically significant cardiovascular, cerebrovascular or peripheral vascular disease

- History of pheochromocytoma, insulinoma, glucagonoma, acromegaly, Cushing's disease, glycogen storage disease or adrenal insufficiency; ongoing or previous treatment with octreotide, lanreotide or pasireotide

- Current use of systemic corticosteroids or beta-blockers

Locations

Location

Status