Actively Recruiting
A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of ABS-1230 Given Orally Compared With Placebo in Healthy Participants Aged 18 to 55 Years
Led by Actio Biosciences, Inc. · Updated on 2025-11-26
74
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This first in human trial will evaluate the safety, tolerability, and pharmacokinetics of single ascending doses, multiple ascending doses, and fed and fasted doses of ABS-1230 given orally compared with placebo in adult healthy participants.
CONDITIONS
Official Title
A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of ABS-1230 Given Orally Compared With Placebo in Healthy Participants Aged 18 to 55 Years
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 to 55 years, inclusive
- Body mass index between 18 and 32 kg/m2
- Medically healthy with no clinically significant medical history or abnormal physical exam, vital signs, ECG, or laboratory tests at screening
- Male and female participants must use adequate birth control and agree not to donate sperm or eggs for specified periods in the protocol
You will not qualify if you...
- Positive test for HIV, HBV, or HCV
- History of cancer except treated basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ of the cervix
- History of alcoholism or recreational drug use within 2 years or positive alcohol or tobacco test at screening
- For female participants, pregnancy, breastfeeding, or seeking to become pregnant during the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Scientia Clinical Research
Sydney, New South Wales, Australia
Actively Recruiting
Research Team
A
Actio Biosciences, Inc.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
5
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