Tests a new drug, IBIO-600, in adults with overweight or obesity
Tests IBIO-600 for safety and dosing in adults with overweight or obesity.
Plain-language title generated from the registry record
Registry title: A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of a Single Dose of IBIO-600 in Overweight or Obese Adults
Key facts
- Where
- Bayswater, AustraliaSee the site
- Phase
- Phase 1
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 65 years old?
Source: NCT07487376, who can take part
Where in Australia
- Veritus ResearchBayswater, AustraliaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- iBio, Inc.
- Trial code
- NCT07487376
- Record updated
- 29 May 2026
- Original description
The goal of this clinical trial is to learn which dose of study drug IBIO-600 has the right balance of safety, tolerability and impact on body composition in overweight and obese adult participants.Read full original descriptionShow less
A Phase I, First-in-Human, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of IBIO-600 in Overweight or Obese Adult Participants (IBIO-600-CT001).
The goal of this clinical trial is to learn which dose of study drug IBIO-600 has the right balance of safety, tolerability and impact on body composition in overweight and obese adult participants.
Inclusion: Aged 18 to 65 years of age; In good general health, with no significant medical history; BMI between ≥ 27.0 and ≤ 34.90 kg/m2; History of self-reported stable body weight (defined as change of no more or less than ± 5%) within 90 days of Screening; Willingness to refrain from any reconstructive and/or cosmetic surgery and/or non-invasive cosmetic procedure that may affect body weight during the study; Must be fully ambulatory without any chronic orthopedic diseases or reliance on crutches, walkers, or a wheelchair that may preclude normal activity; Be a nonsmoker/nonvaper and must not have used any nicotine or synthetic type products within 1 month prior to randomization; Must not be pregnant or breastfeeding; Woman of childbearing potential (WOCBP) or fertile man agrees to use an acceptable method of contraception from the start of Screening until study completion, or for a minimum of 9 months following the last dose of IP, whichever period is longer.
Exclusion: An underlying physical or psychological medical conditions that, in the opinion of the PI or medical designee, would make the participant unlikely to comply with the protocol or complete the study per protocol; History or active diagnosis of diabetes (Type 1 or 2); History of insulinoma or recurrent hypoglycemia (≥ 3 episodes in past 3 months); History or presence of clinically significant muscle disease; History of or active cardiovascular disease including clinically significant arrhythmias, Class I-IV heart failure, coronary artery disease, thromboembolic event, or pulmonary hypertension; History or presence of any condition associated with significant immunosuppression; History of substance abuse or dependency, or recreational IV drug use within the past 5 years (self-reported); Clinically significant laboratory abnormalities that would preclude participation in the study; History of malignancy, except for non-melanoma skin cancer excised > 2 years ago or cervical intraepithelial neoplasia successfully treated > 5 years prior to randomization.