A Randomized, Double-blind, Placebo-controlled, Doseescalation Trial to Evaluate the Safety and Tolerability of a Single IV Administration of Dasiglucagon and the Bioavailability of Dasiglucagon Following SC Compared to IV Administration in Healthy Subjects
A Randomized, Double-blind, Placebo-controlled, Doseescalation Trial to Evaluate the Safety and Tolerability of a Single IV Administration of Dasiglucagon and the Bioavailability of Dasiglucagon Following SC Compared to IV Administration in Healthy Subjects
The purpose of the trial is to characterize the safety and tolerability of dasiglucagon 4 mg/mL following IV administration at increasing doses in healthy volunteers. One cohort of subjects will receive a SC dose of dasiglucagon to characterize the bioavailability of dasiglucagon following SC administration compared to IV administration. Furthermore, the trial aims to assess the potential effect of dasiglucagon on corrected QT interval (QTc) prolongation via a concentrationresponse analysis.
Hypoglycemia in patients with diabetes is defined as episodes of an abnormally low plasma glucose concentration. Hypoglycemia is a common, unpredictable, and potentially dangerous side effect of treatment of diabetes mellitus, especially with insulin or sulfonylureas.
Dasiglucagon (ZP4207) is a stable peptide analog of human glucagon, available in a ready-to-use liquid formulation. Dasiglucagon is in development for the treatment of severe hypoglycemia in patients with diabetes mellitus. Dasiglucagon is a specific and full glucagon receptor agonist designed to mimic the effects of glucagon, having a fast absorption and elimination (minutes).
Inclusion Criteria:
Informed consent obtained before any trial-related activities (trial-related activities are any procedures that would not have been performed during normal management of the subject).
Healthy female or male subjects aged between 18 and 45 years, both inclusive.
Body weight between 60 and 90 kg, both inclusive.
Subjects in good health according to age (medical history, physical examination, vital signs, and laboratory assessments), as judged by the investigator.
Systolic Blood Pressure (SBP) ≥90 mmHg, ≤140 mmHg and Diastolic Blood Pressure (DBP) ≤90 mmHg measured after at least 5 min rest in supine position.
A pulse rate of ≥50 and ≤90 b/min measured after at least 5 min rest in supine position.
12-lead ECG with QTcF < 450 ms, PR < 220 ms and QRS < 110 ms.
A female subject must meet one of the following criteria:
Participant is of childbearing potential and agrees to use one of the accepted contraceptive regimens throughout the entire duration of the trial from screening until the last follow-up visit. An acceptable method of contraception includes one of the following:
Single method (use only one method):
Double method:
Hormone contraception A) estrogen and / or progesterone oral contraceptives, B) transdermal patch, C) vaginal ring, D) injection in combination with one of the following: a) vaginal cap with spermicide, b) vaginal sponge (only for women who have never given birth), c) condom, d) female condom
Participant is of non-childbearing potential, if she is either surgically sterilized (ie, by tubal ligation or removal of ovaries), has undergone complete hysterectomy, or is in a menopausal state (i.e., at least one year without menses).
Condoms MUST be combined with one of the following methods:
IUD,
hormone rod inserted under the skin,
vaginal cap with spermicide,
vaginal sponge (only for women who have never given birth),
hormone contraception A) estrogen and / or progesterone oral contraceptives, B) transdermal patch, C) vaginal ring or D) injection
Exclusion Criteria:
Previous participation in any trial with dasiglucagon. Participation defined as enrolled into trial.
Known or suspected hypersensitivity to trial product(s) or related products.
History of severe hypersensitivity to medicines or foods or history of severe medicinal/food induced anaphylactic reaction.
Receipt of any investigational product within 3 months prior to screening.
Females who are pregnant according to a positive pregnancy test, are actively attempting to get pregnant, or are lactating.
Any history or presence of cancer, except adequately treated (as judged by investigator) basal or squamous cell skin cancer or cervical carcinoma in situ.
A history or presence of any clinically significant respiratory, metabolic, renal, hepatic, gastrointestinal, endocrinological, hematological, dermatological, venereal, neurological or psychiatric diseases, or other major diseases at the discretion of the investigator.
Known cardiovascular disease, arthrosclerosis, angina pectoris, or a history of myocardial infarction or coronary arterial bypass graft/percutaneous coronary intervention.
Clinically significant illness (eg, systemic infection) within 4 weeks before screening, as judged by the investigator.
Any significant pre-existing medical condition as well as pre-planned procedures or surgeries.
Positive results for Hepatitis B antigens, Hepatitis C antibodies and/or human immunodeficiency virus (HIV) 1 antigen or HIV1/2 antibodies, at screening.
Any clinically significant abnormal hematology, biochemistry, or urinalysis screening tests, as judged by the investigator.
Any of the following abnormal laboratory parameters at screening:
Renal impairment measured as estimated Glomerular Filtration Rate (eGFR) value of eGFR <90 ml/min/1.73 m2 as defined by Kidney Disease: Improving Global Outcomes (KDIGO) 2012 (14).
Clinically significant abnormal standard 12-lead ECG after 5 min resting in supine position at screening, as evaluated by the investigator.
Donation of blood or blood loss of more than 500 mL within 12 weeks prior to screening.
The use of any non-prescribed systemic medication, except routine vitamins and occasional use of acetylsalicylic acid and paracetamol within 14 days prior to randomization.
A positive result in the alcohol and/or urine drug screen at the screening visit.
A history of alcoholism or drug abuse as judged by the investigator
Smokers (defined as a subject who has been smoking within the last 6 month).
Subjects with mental incapacity or language barriers that 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.