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Study identifier: NCT02455011 Synced from ClinicalTrials.gov · July 28, 2026
● Completed

Dose Escalation Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of REMD-477 in Subjects With Type 2 Diabetes Mellitus

Condition: Type 2 Diabetes Mellitus · Diabetes  ·  Sponsor: REMD Biotherapeutics, Inc.

PhasePhase 1/Phase 2
Planned participants75
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

This is a randomized, placebo-controlled, double-blind, dose escalation study to evaluate safety, tolerability, PK and PD of single and repeated SC doses of REMD-477 in Type 2 diabetic subjects. The study will be conducted at multiple sites in the United States and will enroll approximately 102 subjects with Type 2 diabetes who are either treatment-naïve, controlled with diet and exercise or treated with oral antidiabetic medications.

This description comes directly from the study's public registry record.

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Contact details are listed per location below or on the registry record.

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Locations (3)

Study siteMiami, Florida, United States
Study siteSan Antonio, Texas, United States
Study siteRenton, Washington, United States

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Source record: clinicaltrials.gov/study/NCT02455011