Single Ascending Doses of ZP4207 Administered in HV and in T1D to Evaluate Safety, Tolerability PKs and PDs of ZP4207 Compared to a Comparator
Primary Purpose
Hypoglycemia
Status
Completed
Phase
Phase 1
Locations
Germany
Study Type
Interventional
Intervention
ZP4207
Glucagon
Sponsored by
About this trial
This is an interventional treatment trial for Hypoglycemia
Eligibility Criteria
Inclusion Criteria:
- Informed consent obtained before any trial-related activities. (Trial-related activities are any procedure that would not have been performed during normal management of the subject).
- Male subjects which are healthy for part 1; for part 2 male subjects with T1D
- Age between 18 and 50 years, both inclusive.
- Body weight between 70 and 90 kg, both inclusive.
- Subjects must be in good health according to age (medical history, physical examination, vital signs, ECG, lab assessments), as judged by the investigator
A subject who is surgically sterilized or must be willing to refrain from sexual intercourse during the trial and until one month after completion of the trial or if sexually active, using condom and partner practices contraception during the trial and until one month after completion of the trial.
For part 2, in addition:
- Male subjects with T1D for at least one year, as defined by the American Diabetes Association.
- Having been treated with insulin for T1D for at least 1 year.
- Stable disease with HbA1c < 8.5 %.
- Stable insulin treatment during participation in trial and 3 month prior to the screening visit.
Exclusion Criteria:
- Known or suspected allergy to trial product(s) or related products.
- Previous participation (randomization) in this trial.
- Receipt of any investigational drug within 3 months prior to screening.
- A history or presence of cancer, diabetes (part 1 only), or any clinically significant cardiovascular, respiratory, metabolic, renal, hepatic, gastrointestinal, endocrinological, hematological, dermatological, venereal, neurological, psychiatric diseases or other major diseases.
- Clinically significant illness within 4 weeks before screening, as judged by the investigator
- Carrier of Hepatitis B surface antigen (HBsAg) or Hepatitis C antibodies.
- Positive result of test for HIV antibodies.
- Any clinically significant abnormal hematology,biochemistry or urinalysis screening tests, as judged by the Investigator.
- Clinically significant abnormal ECG at screening as evaluated by Investigator.
- Donation of blood or plasma in the past month, or in excess of 500 ml within 12 weeks prior to screening.
- A significant history of alcoholism or drug/chemical abuse, or who has a positive result in the urine drug screen, or who consumes more than 28 units of alcohol per week (one unit of alcohol equals about 250 ml of beer, 1 glass of wine, or 20 ml of spirits).
- Habitual smoking, i.e., daily smoking or more than 7 cigarettes/week within the last 3 months prior to screening. Subjects have to accept refraining from smoking while at the clinical site.
- Subjects with mental incapacity or language barriers which preclude adequate understanding or cooperation, who are unwilling to participate in the trial, or who in the opinion of the Investigator should not participate in the trial.
- Surgery or trauma with significant blood loss within the last 2 months prior to screening.
Any condition interfering with trial participation or evaluation or that may be hazardous to the subject.
For part 2, in addition
- Severe hypoglycemic events within one year prior to screening, as judged by the investigator.
- Significant changes in basal insulin within 3 weeks before screening, as judged by the investigator.
- Clinically relevant diabetic complications (macrovascular disease with symptoms of coronary artery disease or peripheral vascular disease, microvascular disease with symptoms of neuropathy, gastroparesis, retinopathy, nephropathy, or poor blood glucose control with polyuria, polydipsia, or weight loss), as judged by the investigator.
Sites / Locations
- Profil GmbH
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
ZP4207
native glucagon
Arm Description
single dose of ZP4207 in ascending doses (s.c. and i.m.)
single fixed dose of glucagon
Outcomes
Primary Outcome Measures
Safety and Tolerability: Number of participants with adverse events
Safety and Tolerability: Changes or findings from baseline in clinical safety laboratory assessments
Safety and Tolerability: Changes or findings from baseline in physical examination
Safety and Tolerability: Changes or findings from baseline in vital signs
Safety and Tolerability: Changes or findings from baseline in ECG
Safety and Tolerability: Findings in local tolerability
Secondary Outcome Measures
Pharmacokinetics (PK): Area under the curve (AUC) from time-point 0 until 300min
Pharmacokinetics: maximum observed concentration of ZP4207 (Cmax)
Pharmacokinetics: time to maximum observed concentration of ZP4207 (tmax)
Pharmacokinetics: terminal elimination rate constant estimated during the terminal phase of ZP4207 (λz)
Pharmacokinetics: the terminal plasma elimination half-life of ZP4207 (t½),
Pharmacokinetics: apparent volume of distribution of ZP4207 based on plasma concentration values (Vz), estimated during the terminal Phase (f): (Vz/f)
Pharmacokinetics: apparent plasma clearance rate of ZP4207(CL) estimated during the terminal Phase (f)
Pharmacokinetics: mean residence time for plasma ZP4207 (MRT)
Pharmacodynamics (PD): Area under the Plasma glucose curve from time-point 0 until 300 min (AUCgluc 0-300)
Pharmacodynamics: maximum observed concentration (Cmax)
Pharmacodynamics: time to maximum observed concentration (tmax)TPG≥70mg/dL
Pharmacodynamics: Time to plasma glucose equal or above (70 mg/dL)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02367053
Brief Title
Single Ascending Doses of ZP4207 Administered in HV and in T1D to Evaluate Safety, Tolerability PKs and PDs of ZP4207 Compared to a Comparator
Official Title
A Randomized, Double-blinded Trial of Single Ascending Doses of ZP4207 Administered s.c. or i.m. to HV and a SD of ZP4207 Administered s.c. to Hypoglycemic T1D to Evaluate the Safety, Tolerability, PKs and PDs of ZP4207 as Compared to an Active Comparator
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
December 2014 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
April 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zealand Pharma
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The trial is a randomized, double-blind First in Human trial to evaluate the safety and tolerability of ZP4207 in healthy volunteers (HV) and in insulin-induced hypoglycemic T1D (type 1 diabetes) subjects as compared to native glucagon. The trial includes two parts.
Part 1 includes dose escalation of ZP4207 in cohorts of 8 subjects. In each cohort, subjects will be randomized 3:1 to receive either a single ascending dose of ZP4207 (6 subjects) or a single fixed dose (SD) of native glucagon (2 subjects). The doses will be administered s.c. in 4-5 cohorts and i.m. in 3 cohorts.
Part 2 includes two sequence groups of 10 hypoglycemic T1D subjects. The subjects will be treated with fixed single doses of ZP4207 and native glucagon s.c. in a sequential cross-over design in a randomized treatment order.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoglycemia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
111 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ZP4207
Arm Type
Experimental
Arm Description
single dose of ZP4207 in ascending doses (s.c. and i.m.)
Arm Title
native glucagon
Arm Type
Active Comparator
Arm Description
single fixed dose of glucagon
Intervention Type
Drug
Intervention Name(s)
ZP4207
Intervention Type
Drug
Intervention Name(s)
Glucagon
Primary Outcome Measure Information:
Title
Safety and Tolerability: Number of participants with adverse events
Time Frame
28 days
Title
Safety and Tolerability: Changes or findings from baseline in clinical safety laboratory assessments
Time Frame
28 days
Title
Safety and Tolerability: Changes or findings from baseline in physical examination
Time Frame
28 days
Title
Safety and Tolerability: Changes or findings from baseline in vital signs
Time Frame
28 days
Title
Safety and Tolerability: Changes or findings from baseline in ECG
Time Frame
28 days
Title
Safety and Tolerability: Findings in local tolerability
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Pharmacokinetics (PK): Area under the curve (AUC) from time-point 0 until 300min
Time Frame
5 hours
Title
Pharmacokinetics: maximum observed concentration of ZP4207 (Cmax)
Time Frame
5 hours
Title
Pharmacokinetics: time to maximum observed concentration of ZP4207 (tmax)
Time Frame
5 hours
Title
Pharmacokinetics: terminal elimination rate constant estimated during the terminal phase of ZP4207 (λz)
Time Frame
5 hours
Title
Pharmacokinetics: the terminal plasma elimination half-life of ZP4207 (t½),
Time Frame
5 hours
Title
Pharmacokinetics: apparent volume of distribution of ZP4207 based on plasma concentration values (Vz), estimated during the terminal Phase (f): (Vz/f)
Time Frame
5 hours
Title
Pharmacokinetics: apparent plasma clearance rate of ZP4207(CL) estimated during the terminal Phase (f)
Time Frame
5 hours
Title
Pharmacokinetics: mean residence time for plasma ZP4207 (MRT)
Time Frame
5 hours
Title
Pharmacodynamics (PD): Area under the Plasma glucose curve from time-point 0 until 300 min (AUCgluc 0-300)
Time Frame
5 hours
Title
Pharmacodynamics: maximum observed concentration (Cmax)
Time Frame
5 hours
Title
Pharmacodynamics: time to maximum observed concentration (tmax)TPG≥70mg/dL
Time Frame
5 hours
Title
Pharmacodynamics: Time to plasma glucose equal or above (70 mg/dL)
Time Frame
5 hours
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Informed consent obtained before any trial-related activities. (Trial-related activities are any procedure that would not have been performed during normal management of the subject).
Male subjects which are healthy for part 1; for part 2 male subjects with T1D
Age between 18 and 50 years, both inclusive.
Body weight between 70 and 90 kg, both inclusive.
Subjects must be in good health according to age (medical history, physical examination, vital signs, ECG, lab assessments), as judged by the investigator
A subject who is surgically sterilized or must be willing to refrain from sexual intercourse during the trial and until one month after completion of the trial or if sexually active, using condom and partner practices contraception during the trial and until one month after completion of the trial.
For part 2, in addition:
Male subjects with T1D for at least one year, as defined by the American Diabetes Association.
Having been treated with insulin for T1D for at least 1 year.
Stable disease with HbA1c < 8.5 %.
Stable insulin treatment during participation in trial and 3 month prior to the screening visit.
Exclusion Criteria:
Known or suspected allergy to trial product(s) or related products.
Previous participation (randomization) in this trial.
Receipt of any investigational drug within 3 months prior to screening.
A history or presence of cancer, diabetes (part 1 only), or any clinically significant cardiovascular, respiratory, metabolic, renal, hepatic, gastrointestinal, endocrinological, hematological, dermatological, venereal, neurological, psychiatric diseases or other major diseases.
Clinically significant illness within 4 weeks before screening, as judged by the investigator
Carrier of Hepatitis B surface antigen (HBsAg) or Hepatitis C antibodies.
Positive result of test for HIV antibodies.
Any clinically significant abnormal hematology,biochemistry or urinalysis screening tests, as judged by the Investigator.
Clinically significant abnormal ECG at screening as evaluated by Investigator.
Donation of blood or plasma in the past month, or in excess of 500 ml within 12 weeks prior to screening.
A significant history of alcoholism or drug/chemical abuse, or who has a positive result in the urine drug screen, or who consumes more than 28 units of alcohol per week (one unit of alcohol equals about 250 ml of beer, 1 glass of wine, or 20 ml of spirits).
Habitual smoking, i.e., daily smoking or more than 7 cigarettes/week within the last 3 months prior to screening. Subjects have to accept refraining from smoking while at the clinical site.
Subjects with mental incapacity or language barriers which preclude adequate understanding or cooperation, who are unwilling to participate in the trial, or who in the opinion of the Investigator should not participate in the trial.
Surgery or trauma with significant blood loss within the last 2 months prior to screening.
Any condition interfering with trial participation or evaluation or that may be hazardous to the subject.
For part 2, in addition
Severe hypoglycemic events within one year prior to screening, as judged by the investigator.
Significant changes in basal insulin within 3 weeks before screening, as judged by the investigator.
Clinically relevant diabetic complications (macrovascular disease with symptoms of coronary artery disease or peripheral vascular disease, microvascular disease with symptoms of neuropathy, gastroparesis, retinopathy, nephropathy, or poor blood glucose control with polyuria, polydipsia, or weight loss), as judged by the investigator.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Jax, MD/PhD
Organizational Affiliation
Profil GmbH
Official's Role
Principal Investigator
Facility Information:
Facility Name
Profil GmbH
City
Neuss
ZIP/Postal Code
41460
Country
Germany
12. IPD Sharing Statement
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Single Ascending Doses of ZP4207 Administered in HV and in T1D to Evaluate Safety, Tolerability PKs and PDs of ZP4207 Compared to a Comparator
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