Trial ID: | L3289 |
Source ID: | NCT06694935
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Associated Drug: |
Qx1206
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Title: |
A Phase 1b Study of QX1206 in T2DM Patients With NAFLD
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Acronym: |
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Status: |
RECRUITING
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Study Results: |
NO
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Results: |
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Conditions: |
Type 2 Diabetes Mellitus (T2DM)|Non-Alcoholic Fatty Liver Disease (NAFLD)
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Interventions: |
DRUG: QX1206
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Outcome Measures: |
Primary: Recommended Phase 2 Dose (RP2D), Baseline Day 1 up to Week 12 | Secondary: Hemoglobin A1c (HbA1c), Change in HbA1c percentage from baseline with QX1206, 12 Weeks|Fasting plasma glucose (FPG), Change in FPG mg/dL from baseline with QX1206, 12 Weeks|Homeostasis Model Assessment of Insulin Resistance (HOMA-IR), Change in the HOMA-IR from baseline with QX1206, 12 Weeks|Fasting insulin, Change in fasting insulin pmol/L from baseline with QX1206, 12 Weeks
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Sponsor/Collaborators: |
Sponsor: 1Globe Health Institute
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Gender: |
ALL
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Age: |
ADULT
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Phases: |
PHASE1
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Enrollment: |
52
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Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
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Start Date: |
2025-01-06
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Completion Date: |
2025-12
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Results First Posted: |
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Last Update Posted: |
2025-01-13
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Locations: |
Centricity Research Toronto LMC., Toronto, Canada
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URL: |
https://clinicaltrials.gov/show/NCT06694935
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