Type1 Diabetes Mellitus
Conditions
Brief summary
Single Center, Double Blind, Active Comparator Controlled 2-Way Crossover Multiple Dose Safety, Tolerability and Efficacy Study
Detailed description
This is a single center, double blind, active comparator controlled 2-Way crossover multiple dose safety, tolerability and efficacy study. The study will consist of three periods. Total duration will be approximately nine weeks, including a screening period of up to 14 days, a 7-day run-in period and two 21-day treatment periods. Subjects will be screened and then they will undergo a week of baseline CGM. They will then be randomized to one of two treatment sequences: three weeks of treatment with HDV-lispro followed by three weeks of treatment with insulin lispro diluted with sterile water to match the insulin concentration in HDV-lispro, or the same treatments in the reverse order. A test meal study (standardized liquid test meal) is to be conducted at the beginning of treatment (baseline study) and at the end of each three week treatment period. As noted above, frequent blood samples will be collected for glucose and insulin levels during the first (baseline study) test meal; during the two test meals performed after the two treatment periods the same sampling for glucose and insulin will be performed, with the addition of collecting samples for glucagon levels. Subjects will also perform blinded continuous glucose monitoring throughout the entirety of the study (7 weeks). Throughout study, subjects will be asked to perform frequent self-monitoring of blood glucose (SMBG), at least 6 times per day (before and 60-90 minutes after each meal) during 3 or more days of each week. This will serve as data for therapeutic decision-making as well as for data collection.
Interventions
DRUGHDV insulin lispro 100 UNIT/mL
Hepatic Directed Vesicle (HDV) added to commercial insulin lispro
DRUGInsulin Lispro 100 Units/mL
Sterile Water for Injection added to commercial insulin lispro
Sponsors
Integrium
Diasome Pharmaceuticals
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Intervention model description
This is a single center, double blind, active comparator controlled 2-Way crossover multiple dose safety, tolerability and efficacy study.
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. T1DM ≥12 months 2. C-peptide \<0.6 ng/mL (a single re-test is allowable) 3. Treatment with rapid analog insulin by CSII for the previous 6 months 4. Familiarity with continuous glucose monitoring (CGM) technology; subjects nee d not be currently using CGM but should have used it in the past. Personal (unblinded) CGM will NOT be allowed during the study 5. Willingness to use insulin lispro as the analog insulin during the study period 6. Use of MiniMed Paradigm® pump for the previous 6 months. Pumps that employ low glucose suspend technology will NOT be allowed during the study 7. BMI ≥18.0 kg/m2 and ≤35.0 kg/m2 8. A1C≤9.0% (a single re-test is allowable)
Exclusion criteria
1. Known or suspected allergy to any component of any of the study drugs in this trial. 2. A patient who has unstable proliferative retinopathy or maculopathy, and/or severe neuropathy, in particular autonomic neuropathy, as judged by the Investigator. 3. Use of oral anti-diabetic or non-insulin anti-diabetic injection therapies (e.g. SGLT-2 inhibitors, pramlintide, GLP-1 agonists, etc.) 4. Current smokers; if a former smoker, no tobacco products (inhaled, oral or buccal) for the previous 3 months 5. As judged by the investigator, clinically significant active disease of the gastrointestinal, cardiovascular (including a history of arrhythmia or conduction delays on ECG), hepatic, neurological, renal, genitourinary, or hematological systems, or uncontrolled hypertension (diastolic blood pressure ≥ 100 mmHg and/or systolic blood pressure ≥ 160 mmHg after 5 minutes in the supine position). 6. History of any illness or disease that in the opinion of the Investigator might confound the results of the trial or pose additional risk in administering the study drugs to the patient.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Glucose area under the curve | 21 days | To evaluate glucose response (incremental AUC) to standardized test meal challenge following 21 days of CSII treatment with HDV insulin lispro versus insulin lispro diluted with sterile water |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| total units Insulin | 21 days | To compare insulin doses (basal, bolus and total) during HDV insulin lispro treatment |
Countries
United States
Outcome results
None listed