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Dose Escalating Study of BPI-3016 in Healthy Subjects

Phase 1
Conditions
Healthy Subject
Interventions
Drug: Placebo
Registration Number
NCT03188848
Lead Sponsor
Betta Pharmaceuticals Co., Ltd.
Brief Summary

This is a randomized, double-blind, placebo-controlled, dose finding study evaluating the safety, pharmacokinetics and pharmacodynamics of subcutaneously injected BPI-3016 in Chinese healthy subjects.

Detailed Description

BPI-3016 is a novel analogue of glucagon-like peptide-1 (GLP-1) that developed for the treatment of type 2 diabetes mellitus. This is a randomized, double-blind, placebo-controlled, dose finding study evaluating the safety, pharmacokinetics and pharmacodynamics of subcutaneously injected BPI-3016 in Chinese healthy subjects.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
63
Inclusion Criteria
  • Healthy
  • Subject's body mass index (BMI) is >=19 kilogram (kg)/meter(m)^2 and <=25 kg/m^2
  • Male or female: if she is not pregnant (as confirmed by a test at screening and at other timepoints), not lactating, and at least one of the following conditions applies: a) cannot bear children OR b) agrees to follow contraception requirements defined in the protocol
  • Capable of giving signed informed consent
Exclusion Criteria
  • Family history of multiple endocrine neoplasia, medullary carcinoma of the thyroid, or diabetes mellitus
  • History of thymus disease, acute or chronic pancreatitis, or thyroid dysfunction
  • History of gallstones, biliary motility dysfunction, cholecystitis or other gallbladder disease
  • History of weight loss over 5% within 3 months of the study
  • Abnormal blood pressure
  • Abnormal blood routine, blood chemistry or test at screening
  • Personal or family history of long QT syndrome, QT interval > 450 milliseconds (msec), or heart rate is >100 beats/min at Screening
  • History of sensitivity or contraindication to any of the study medications or components thereof or a history of drug or other allergy
  • A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result, or a positive test for Human immunodeficiency virus (HIV) antibody
  • A positive pre-study drug/alcohol screen
  • The subject participated in a clinical trial and received an investigational product within 90 days
  • History of drug or other allergy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlaceboSingle-dose subcutaneous injection of placebo to match BPI-3016
BPI-3016BPI-3016Single-dose subcutaneous injection of BPI-3016 with escalating dose from 0.6 mg
Primary Outcome Measures
NameTimeMethod
Number of subjects with adverse events and serious adverse events1 month

An AE is any untoward medical occurrence in a subject, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a medicinal product. Any untoward event resulting in death, life threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, congenital anomaly/birth defect or any other situation according to medical or scientific judgement will be categorized as SAE

Plasma Concentrations of single-dose BPI-301615 days

The concentration of BPI-3016 following single-dose administration was estimated

Tmax of single-dose BPI-301615 days

Time of the maximum observed plasma concentration (tmax) following single-dose administration of BPI-3016 was estimated

AUC15 days

The area under the concentration-time (AUC) curve from time zero to the last quantifiable concentration (0-last) and AUC (0-inf) of BPI-3016 were measured

T1/215 days

The half-life (t1/2) of single-dose BPI-3016 was measured

Secondary Outcome Measures
NameTimeMethod
Change From Baseline in Fasting Plasma Glucose8 days

Fasting Plasma Glucose was measured pre-dose at baseline, day 2, day 3, day 4, day 5, and day 8

Change From Baseline in 2 hours postprandial blood glucose8 days

Fasting Plasma Glucose was measured pre-dose at baseline, day 2, day 3, day 4, day 5, and day 8

Trial Locations

Locations (1)

Beijing Hospital

🇨🇳

Beijing, Beijing, China

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