Clinical trial

A Phase 1, Open-label Study in Healthy Male Subjects of the Absorption, Metabolism, Excretion, and Pharmacokinetics of EDG-5506 and an Absolute Bioavailability Study Using Radiolabeled EDG-5506

Name
EDG-5506-103
Description
This is a Phase 1 2-part, single-center, open-label study in healthy male volunteers. Part A will assess the absorption, metabolism, excretion, and pharmacokinetics of one oral dose of radiolabeled EDG-5506. Part B will assess bioavailability of EDG-5506 with a single oral dose of EDG-5506 and a single intravenous dose of radiolabeled EDG-5506.
Trial arms
Trial start
2023-01-12
Estimated PCD
2023-04-06
Trial end
2023-04-06
Status
Completed
Phase
Early phase I
Treatment
EDG-5506 Tablet
Single Oral Dose - Tablet
Arms:
Part B - aBA
Radiolabeled EDG-5506 Suspension
Single Oral Dose
Arms:
Part A - AME
Radiolabeled EDG-5506 Intravenous
Single Intravenous Dose
Arms:
Part B - aBA
Size
15
Primary endpoint
The mass balance of EDG-5506 as measured by the total radioactivity recovered in urine
Up to 37 days
The mass balance of EDG-5506 as measured by the total radioactivity recovered in feces
Up to 37 days
Plasma maximum measured drug concentration (Cmax) measurements for EDG-5506
Up to 37 days
Characterization of EDG-5506 as measured by urinary recovery (fet1-t2)
Up to 37 days
Absolute bioavailability of EDG-5506 as measured by Fabs
Up to 9 days
Eligibility criteria
Inclusion Criteria: 1. For both Part A and Part B, males, of any race, between 18 and 55 years of age, inclusive. 2. For both Part A and Part B, a body mass index between 18.0 and 32.0 kg/m2, inclusive, and a total body weight greater than or equal to 50 kg. 3. In good health, determined by no clinically significant findings from medical history, 12-lead electrocardiogram, vital signs measurements, and clinical laboratory evaluations at screening and check-in. Exclusion Criteria: 1. Significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, respiratory, endocrine, genitourinary, immunological, or psychiatric disorder, as determined by the investigator (or designee). 2. Participation in a clinical study involving administration of an investigational drug in the past 30 days or 5 half-lives (whichever is longer) prior to dosing. 3. Participation in more than 3 radiolabeled drug studies in the last 12 months. 4. Poor peripheral venous access. 5. Subjects with exposure to significant diagnostic or therapeutic radiation (eg, serial x-ray, computed tomography scan, barium meal) or current employment in a job requiring radiation exposure monitoring within 12 months prior to check-in.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 15, 'type': 'ACTUAL'}}
Updated at
2023-04-18

1 organization

2 products

10 indications

Product
EDG-5506
Indication
Atrophic
Indication
Inborn