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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
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

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Anaheim Clinical Trials
Coordinator of this site? Confirm its status
AnaheimUnited StatesUnknown status
ProSciento, Inc.
Coordinator of this site? Confirm its status
Chula VistaUnited StatesUnknown status
QPS Miami Research Associates
Coordinator of this site? Confirm its status
MiamiUnited StatesUnknown status
Progressive Medical Research
Coordinator of this site? Confirm its status
Port OrangeUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.