Impact of Pharmacogenetic-Guided Treatment on Type 2 Diabetes.
NCT06851962 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 504
Last updated 2026-02-23
Summary
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.
Conditions
- Diabetes Mellitus Type 2
Interventions
- DRUG
-
Metformin maximum daily dose 2000 mg
- DRUG
-
Dulaglutide
- DRUG
-
Semaglutide 1.0 mg
Semaglutide
- DRUG
-
Empagliflozin (BI 10773)
Empagliflozin
- DRUG
-
Canagliflozin
Canagliflozin
- DRUG
-
Dapagliflozin
- DRUG
-
pioglitazone
Pioglitazone
- DRUG
-
Sitagliptin
Sitagliptin
- DRUG
-
Vildagliptin (Galvus)
vildagliptin
- DRUG
-
linagliptin
linagliptin
Sponsors & Collaborators
-
Instituto de Salud Carlos III
collaborator OTHER_GOV -
European Union Next Generation
collaborator UNKNOWN -
Fundación para la Investigación del Hospital Clínico de Valencia
lead OTHER
Principal Investigators
-
Sergio Martínez Hervás, Doctor · Hospital Clínico Universitario de Valencia
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 40 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-05-26
- Primary Completion
- 2026-06-30
- Completion
- 2026-06-30
Countries
- Spain
Study Locations
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