Healthy
Conditions
Keywords
Adrenoleukodystrophy (ALD), Childhood Cerebral Adrenoleukodystrophy (ccALD), OP-101, Dendrimer, N-Acetyl-Cysteine (NAC)
Brief summary
A clinical study to measure the effect of OP-101 after being administered intravenously in healthy volunteers.
Interventions
DRUGOP-101
Intravenous Injection of OP-101 in healthy volunteers.
Sponsors
Orpheris, Inc.
Study design
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes
Inclusion criteria
Key Inclusion Criteria: * Body Mass Index (BMI) between 18 and 32 kg/m\^2. * Is in general good health, based upon the results of a medical history assessment, physical examination, vital signs, laboratory profile, and 12-lead electrocardiogram (ECG), as judged by the investigator. * Female subjects may not be pregnant, lactating, or breastfeeding. * Subjects must have a negative urine test for drugs of abuse, cotinine, and breath alcohol test at screening and Check-in. Key
Exclusion criteria
* Evidence of clinically significant hematologic, renal, endocrine, pulmonary, cardiac, gastrointestinal, hepatic, psychiatric, neurologic, immunologic, allergic disease, 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. * 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 used medications that affect gastrointestinal motility or gastric emptying; such as metoclopramide, proton pump inhibitors, and H2 blockers; within 30 days prior to Day 1. * Has used prescription or over-the-counter medication, vitamins/herbal supplements (with the exception of hormonal contraceptives) within 14 days prior to Day 1.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants with Treatment Emergent Adverse Events Graded as Assessed by CTCAE Version 4.0 | Screening to Day 15. | Evaluate the safety and tolerability of OP-101 after single IV doses in healthy subjects by monitoring and documenting all adverse events, which include laboratory test variables. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pharmacokinetic (PK) Profile Analysis | Days 1, 2, 3, 4, 8, and 15. | Determine the PK profile of OP-101 after single IV doses in healthy subjects as determined by plasma concentrations using the PK Concentration Population. |
Countries
United States
Outcome results
None listed