Impact of Pharmacogenetic-Guided Treatment on Type 2 Diabetes.
NCT06851962 · Active, not recruiting
Last updated 2026-05-28This clinical trial compares whether using genetic testing to guide diabetes treatment helps more people with type 2 diabetes reach their blood sugar target within 24 weeks compared to standard treatment.
What this study is testing ClinicalTrials.gov NCT06851962 ↗
Description as written by the study sponsor.
The goal of this clinical trial is to assess the efficacy of a pharmacogenetics-guided treatment, compared to standard optimized treatment, in patients with inadequately controlled type 2 diabetes. The main questions it aims to answer are: * Is the disease better controlled when the treatment prescribed is based on the participant's pharmacogenetic profile? * What medical problems do participants experience while taking the treatment? Participants will: * Take the treatment described according to the Summary of Product Characteristics (SmPC). * Visit the clinic once every 12 weeks for checkups and tests. * Keep a diary of their symptoms to inform the Investigator.
Treatments tested
- Metformin Drug
Metformin maximum daily dose 2000 mg
- Dulaglutide Drug
Dulaglutide
- Semaglutide 1.0 mg Drug
Semaglutide
- Empagliflozin (BI 10773) Drug
Empagliflozin
- Canagliflozin Drug
Canagliflozin
- Dapagliflozin Drug
Dapagliflozin
- pioglitazone Drug
Pioglitazone
- Sitagliptin Drug
Sitagliptin
- Vildagliptin (Galvus) Drug
vildagliptin
- linagliptin Drug
linagliptin
| Main thing measured | Comparison of HbA1c ≤7% goal at Week 24 between Pharmacogenetic-Guided and Standard Treatment in Type 2 Diabetes |
|---|---|
| Sponsor | Fundación para la Investigación del Hospital Clínico de Valencia |
| Conditions studied | Diabetes Mellitus Type 2 |
| GLP-1 drugs | — |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT06851962 ↗