GSBR-1290
DrugPatients will receive GSBR-1290 or matching Placebo
NCT Number: NCT05762471
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
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Notify Me18 year–75 year
All sexes
Interventional
Phase 1 / Phase 2
Anaheim Clinical Trials, Anaheim, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
cohorts 1-4:
Inclusion criteria
cohort 5:
Exclusion criteria
Patients will receive GSBR-1290 or matching Placebo
Patients will receive GSBR-1290 or matching Placebo
Time frame: 42 days
Time frame: 31 days
Time frame: 31 days
Time frame: 31 days
Time frame: 31 days
Gasherbrum Bio, Inc., a wholly owned subsidiary of Structure Therapeutics
Industry
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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