A Four-Part Study to Assess the Safety, Tolerability, PK and PD of ONO-5788 in Healthy Adult Volunteers

Stopped early · Phase 1 · Has a placebo group

Conditions studied: Acromegaly

In brief

This is a first in human study to determine the safety, tolerability, pharmacokinetics and pharmacodynamics of ONO-5788 in healthy adult volunteers. This study will be conducted in 4 parts: a single-ascending dose part, a multiple-ascending dose part, an elderly part and a proof of principle part.

Key facts

Study ID

NCT03571594

Run by

Ono Pharmaceutical Co., Ltd.

People needed

76

Starts

2018-06-07

Expected to finish

2019-05-16

Last updated by the study team

2019-06-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy, adult, male and female (women of non-child bearing potential, surgically sterile) volunteers, 18-55 years of age, inclusive, at screening (Parts A \& B only).
• Healthy, adult, males and female (women of non-child bearing potential), ≥65 years of age at screening (Part C only).
• Healthy, adult, male, 18-40 years of age, inclusive, at screening (Part D only).
• Medically healthy with no clinically significant medical history, physical examination, laboratory profiles, vital signs or ECG abnormalities (All Parts).
• Body mass index (BMI) of ≥18.5 to ≤30 kg/m2 at screening (Parts A, B \& C).
• Body mass index (BMI) of ≥18.5 to <25 kg/m2 at screening (Part D only).

You may not qualify if…

• History of any illness that, in the opinion of the PI or designee, might confound the results of the study or poses an additional risk to the subject by their participation in the study.
• History or presence of alcoholism or drug abuse within the past 2 years prior to the first dosing.
• History or presence of hypersensitivity or idiosyncratic reaction to the study drugs,excipients or related compounds.
• History or presence of:
• Gallstones, cholangitis, and/or cholecystitis or clinically significant findings on gallbladder ultrasound as determined by the Principal Investigator;
• Pancreatitis;
• Hypothyroidism;
• Known diabetes mellitus type 1 or type 2;
• Hypocalcaemia or hypokalemia;
• Hypoglycemia or hyperglycemia or fasting blood glucose outside normal local range;
• Thrombocytopenia or other clinically significant hematologic abnormalities;
• Inflammatory bowel disease, irritable bowel syndrome, or abdominal surgery;
• Known vitamin B12 deficiency.
• Abnormal gallbladder ejection fraction on hepatobiliary iminodiacetic acid (HIDA) scan at screening (Part B only)
• Positive urine drug, alcohol or cotinine results at screening or check in.
• Clinically significant serum electrolyte (sodium, potassium, chloride, bicarbonate) abnormalities at screening or each check-in, in the estimation and clinical judgment of the PI or designee.
• Positive results at screening for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV).
• Seated blood pressure is less than 90/40 millimeter of mercury (mmHg) or greater than 140/90 mmHg (160/95 mmHg for Part C) at screening.
• Has engaged in strenuous physical exercise in the 48 hours prior first dosing or intends to undergo strenuous physical exercise at any time throughout the study.
• Donation of blood or significant blood loss within 56 days prior to the first dosing.
• Plasma donation within 7 days prior to the first dosing.

Where it is running

• Celerion — Tempe, Arizona, United States

Full record on ClinicalTrials.gov

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