Status:
COMPLETED
Pharmacokinetics Study of Azelaprag (BGE-105) in Older Adult Healthy Volunteers
Lead Sponsor:
BioAge Labs, Inc.
Conditions:
Healthy Volunteer Study
Eligibility:
All Genders
60+ years
Phase:
PHASE1
Brief Summary
This study is a single-dose, open-label, randomized crossover and multiple-dose, open-label study to evaluate the PK of azelaprag in older adult healthy volunteers.
Detailed Description
This study is a single-dose, open-label, randomized crossover and multiple-dose, open-label study to evaluate the PK of azelaprag in older adult healthy volunteers. The study will enroll approximately...
Eligibility Criteria
Inclusion
- Key
- Patients who meet ALL the following inclusion criteria will be eligible to participate in the study:
- Healthy male or female volunteers ≥ 60 years of age
- No history or evidence of clinically relevant medical disorders
- Body mass index (BMI) between 18 and 40 kg/m2
- Acceptable physical examination findings, including vital signs, and electrocardiogram (ECG)
- Acceptable clinical laboratory values
- Female participants of non-childbearing potential
- Key
Exclusion
- Currently receiving treatment with another investigational drug or investigational device within 30 days (or 5 half-lives, whichever is longer)
- Current or previous malignancy within 5 years, with the exception of non-melanoma skin cancers, cervical or breast ductal carcinoma in situ, or adenocarcinoma of the prostate
- Positive test result for COVID (rapid test), human immunodeficiency virus (HIV) antibodies, hepatitis B surface antigen (HBsAg), or hepatitis C (HCV) antibodies
- Use of any medications that might affect the metabolism of the study drug as assessed by the Investigator and Sponsor and use of any herbal supplements, vitamins, or nutritional supplements within the 14 days prior to the dose day of each dosing period or during study participation.
- Planned elective surgery within 30 days prior to Screening, during the study period or before the participant's red blood cell (RBC) have returned to normal levels
- Systolic blood pressure \> 150 mm Hg or \< 90 mm Hg or diastolic blood pressure \> 95 mm Hg or \< 60 mm Hg
- Unwilling or unable to abstain from the use of nicotine or tobacco containing products (including but not limited to snuff, chewing tobacco, cigars, cigarettes, pipes, or nicotine patches) or the use of cannabis or marijuana
- Positive urine drug screen or alcohol breath test at screening and/or known history of drug or alcohol abuse within 1 year prior to screening
- History or evidence of any other clinically significant disorder, condition, or disease, that, in the opinion of the investigator or Sponsor medical monitor, if consulted, would pose a risk to participant safety, or interfere with the study evaluation, procedures, or completion
- Concurrent or previous use of aspirin within 14 days and NSAIDs within 3 days before the dose day of each dosing period.
Key Trial Info
Start Date :
November 17 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 2 2024
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT06141889
Start Date
November 17 2023
End Date
February 2 2024
Last Update
February 23 2024
Active Locations (1)
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1
New Zealand Clinical Research
Auckland, New Zealand