A Clinical Study to Measure the Effect of OP-101 After Being Administered Subcutaneous in Healthy Volunteers

NCT ID: NCT04321980

Last Updated: 2021-06-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 8 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-03-19
• Study Completion Date: 2020-05-22

Brief Summary

A clinical study to measure the Safety, Tolerability, and Pharmacokinetics of OP-101 After Subcutaneous Administration in Healthy Volunteers

Conditions

Healthy

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cohort 1

Subjects in Cohort 1 will be administered 4 mg/kg OP-101 as a subcutaneous (SC) injection.

Group Type: EXPERIMENTAL

OP-101

Intervention Type: DRUG

Subcutaneous injection of OP-101 in healthy volunteers

Cohort 2

Subjects in Cohort 2 will be administered 8 mg/kg OP-101 as a SC injection.

Group Type: EXPERIMENTAL

OP-101

Intervention Type: DRUG

Subcutaneous injection of OP-101 in healthy volunteers

Interventions

OP-101

Subcutaneous injection of OP-101 in healthy volunteers

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Is a healthy man or woman age 18 to 65 years, inclusive, at the Screening Visit;
• Has the ability to understand and sign the written Informed Consent Form (ICF) and local medical privacy authorization forms, which must be obtained prior to any study related procedures being completed;
• Body mass index (BMI) between 18 and 32 kg/m2, inclusive;
• Is in general good health, based upon the results of a medical history assessment, physical examination, vital signs, and laboratory profile, as judged by the Investigator;
• Female subjects of non-childbearing potential must be either surgically sterile (hysterectomy, bilateral tubal ligation, salpingectomy, and/or bilateral oophorectomy at least 26 weeks before the Screening Visit) or postmenopausal, defined as spontaneous amenorrhea for at least 2 years, with follicle-stimulating hormone (FSH) in the postmenopausal range at screening, based on the central laboratory's ranges;
• Female subjects of childbearing potential (ie, ovulating, premenopausal, and not surgically sterile) and all male subjects must use a medically accepted contraceptive regimen (including hormonal contraceptives) during their participation in the study and for 30 days after the last administration of study drug. Medically accepted contraceptive methods are defined as those with 90% or greater efficacy;
• Acceptable methods of contraception for male subjects enrolled in the study include the following:

• Condoms or surgical sterilization of subject at least 26 weeks before the Screening Visit (vasectomy);
• Acceptable methods of contraception for female subjects enrolled in the study include the following:

• Surgical sterilization of subject at least 26 weeks before the Screening Visit (includes hysterectomy or bilateral tubal ligation, oophorectomy, or salpingectomy);
• Intrauterine device for at least 12 weeks before the Screening Visit;
• Hormonal contraception (oral, implant, injection, ring, or patch) for at least 12 weeks before the Screening Visit; or
• Diaphragm;
• If male, subjects must agree to abstain from sperm donation through 90 days after administration of the last dose of study drug;
• Female subjects may not be pregnant, lactating, or breastfeeding;
• Female subjects of childbearing potential must have negative result for pregnancy test at screening and Check-in;
• Subjects must have a negative test result for hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCVab), and human immunodeficiency virus (HIV) antibody at screening;
• Subjects must have an estimated glomerular filtration rate (eGFR) of ≥90 mL/min/1.73m2 at screening;
• Subjects must have a negative urine test for drugs of abuse (opiates, benzodiazepines, amphetamines, cannabinoids, cocaine, barbiturates, and phencyclidine), cotinine, and breath alcohol test at screening and Check-in; and
• Subjects must be willing and able to abide by all study requirements and restrictions.

Exclusion Criteria

• Evidence of clinically significant hematologic, renal, endocrine, pulmonary, cardiac, gastrointestinal (GI), hepatic, psychiatric, neurologic, immunologic, allergic disease (including multiple or clinically significant drug allergies), or any other condition that, in the opinion of the Investigator, might significantly interfere with the absorption, distribution, metabolism, or excretion of study drug, or place the subject at an unacceptable risk as a participant in this study;
• History of malignancy (other than successfully treated basal cell or squamous cell skin cancer);
• History or presence of an abnormal ECG that, in the opinion of the Investigator, is clinically significant;
• Laboratory results (serum chemistry, hematology, coagulation, and urinalysis) outside the normal range at screening and Check-in and considered clinically significant in the opinion of the Investigator. Any elevation of aspartate transaminase (AST) and alanine transaminase (ALT) above the upper limit of normal at screening and/or Check-in is exclusionary. One retest of an exclusionary laboratory result is allowed at the discretion of the Investigator;
• Has had an acute illness considered clinically significant by the Investigator within 30 days prior to screening;
• History of alcoholism or drug abuse within 2 years prior to screening;
• Has used any product containing nicotine within 90 days prior to screening or intends to use any product containing nicotine during the course of the study;
• Has had any immunizations (live vaccines) in the 4 weeks prior to screening;
• Has used medications that affect GI motility or gastric emptying; such as metoclopramide, proton pump inhibitors, and H2 blockers; within 30 days prior to Day 1;
• Has used any prescription or over-the-counter medication (with exception of acetaminophen), vitamins/herbal supplements (with the exception of hormonal contraceptives) within 14 days prior to Day 1;
• Has used any other study drug within 30 days or 5 half-lives of the drug (whichever is longer) prior to Day 1;
• Has lost or donated >450 mL of whole blood or blood products within 30 days prior to screening;
• Investigator has reason to believe that the subject may be unable to fulfill the protocol visit schedule or requirements;
• Has any finding that, in the view of the Investigator or Medical Monitor, would compromise the subject's safety requirements; or
• Is employed by the Sponsor, the Contract Research Organization (CRO), or the study site (permanent, temporary contract worker, or designee responsible for the conduct of the study), or is a family member (spouse, parent, sibling, or child) of the Sponsor, CRO, or study site employee.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Orpheris, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

CMAX

Adelaide, South Australia, Australia

Countries

Australia

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

OP-101-003

Identifier Type: -

Identifier Source: org_study_id