NCT05762471CompletedPhase 1/2
Phase 1b/2a Study of GSBR-1290 in Adult Overweight or Obese Healthy Subjects and Subjects With Type 2 Diabetes Mellitus
A Phase 1b/2a, Randomized, Double-blind, Placebo-controlled, Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Doses of GSBR-1290 in Adult Overweight or Obese Healthy Subjects and in Subjects With Type 2 Diabetes Mellitus on Metformin
Source: ClinicalTrials.gov · Last updated 25 Apr 2024
Brief summary (registry, in English)
This study will evaluate safety, tolerability, pharmacokinetic (PK) profile, and pharmacodynamic (PD) effects on GSBR-1290 in healthy overweight/obese volunteers (HOV) and Type 2 Diabetes Mellitus on Metformin (T2DM) This study includes 5 planned cohorts. Participants will receive multiple-ascending doses of GSBR-1290 or Placebo from Day 1 to Day 84
- Status (registry)
- Completed
- Phase (registry)
- Phase 1/2
- Study type
- Interventional
- Enrollment
- 142 (actual)
- First submitted
- 25 Jan 2023
- Start date
- 9 Jan 2023
- Primary completion date
- 11 Apr 2024
- Lead sponsor
- Gasherbrum Bio, Inc., a wholly owned subsidiary of Structure Therapeutics
- Diseases
- Obesity, Type 2 diabetes
- NCT number
- NCT05762471
What you commit to
- Study type: Interventional · Phase 1/2
- Participants enrolled: 142
- From 9 Jan 2023 to the primary completion date, 11 Apr 2024
- 4 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Any other condition or prior therapy that would make the participant unsuitable for this study
Other illness
- History or presence of significant cardiovascular, pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, dermatologic or neurological disease, including any acute illness or major surgery within the major 3 months
- Evidence of abnormality on the screening visit ECG, or a history of known arrhythmia or prolonged QTcF pr prolonged QRS interval
- Known hypersensitivity to any of the study drug ingredients
Lab values
- Liver function test results elevated \> 2.0-fold above the ULN for gamma glutamyl transferase, alkaline phosphatase, aspartate aminotransferase or alanine aminotransferase. Bilirubin above the ULN
Other
- A sitting BP after resting for 5 minutes \> 160mm Hg systolic or \> 100 mm Hg diastolic or an apical pulse rate \<50 or \>100 beats per minute.
- Estimated glomerular filtration rate \< 60mL/min/1.73 m2 body surface area
Who the study is looking for
- Provided evidence of a signed consent
- Age ≥ 18 and ≤ 75 years
- Healthy overweight/obese adult men and women with body mass index ≥ 27 and ≤ 40 kg/m2
- No nicotine use
- Have a suitable venous access for blood sampling
- Men and women with T2DM of ≥6 months duration
- Age ≥ 18 and ≤ 75 years
- BMI ≥ 27 and ≤ 40 kg/m2
- Treated with stable doses of ≥500 mg of metformin with a duration ≥6 months and at stable doses for ≥2 months with a screening HbA1c ≥7.0% and ≤10.5%.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Anaheim Clinical Trials Coordinator of this site? Confirm its status | Anaheim | United States | Unknown status |
| ProSciento, Inc. Coordinator of this site? Confirm its status | Chula Vista | United States | Unknown status |
| QPS Miami Research Associates Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Progressive Medical Research Coordinator of this site? Confirm its status | Port Orange | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.