← Back to Search

K-757 and K-833 combination for Obesity

Phase 1
Waitlist Available
Research Sponsored by Kallyope Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up days 14 and 28

Summary

This trial is testing two new medications, K-757 and K-833, in overweight or obese patients with Type 2 diabetes. The goal is to see if these medications are safe, how they move through the body, and what effects they have.

Eligible Conditions
  • Diabetes
  • Obesity

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~days 14 and 28
This trial's timeline: 3 weeks for screening, Varies for treatment, and days 14 and 28 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Proportion of participants who discontinued study medication due to an AE
Proportion of participants who experienced 1 or more treatment-emergent AEs
Secondary study objectives
AUC of plasma K-833
Area under the concentration-time curve [AUC] of plasma K-757
Cl of plasma K-833
+9 more

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: K-757 and K-833 combinationExperimental Treatment1 Intervention
Group II: PlaceboPlacebo Group1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
K-757 and K-833
2023
Completed Phase 2
~240

Find a Location

Who is running the clinical trial?

Kallyope Inc.Lead Sponsor
3 Previous Clinical Trials
242 Total Patients Enrolled
3 Trials studying Obesity
242 Patients Enrolled for Obesity
~9 spots leftby Nov 2025