PGEN for HTN: Investigating the Use of Genetics to Guide Pharmacologic Therapy for Hypertension

Sponsor
Geneticure, LLC (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT02988245
Collaborator
Fairview Health Services (Other), University of Minnesota (Other)
1,000
15
2
18
66.7
3.7

Study Details

Study Description

Brief Summary

Hypertension is one of the most important preventable contributors to disease and death in the United States and represents the most common condition seen in the primary care setting. Approximately 78 million adults living in the U.S. have hypertension with more than 5 million new diagnoses made each year. Unfortunately, despite a significant impulse in the medical community to move towards an "individualized medicine" approach to patient centered treatment, the current clinical treatment strategy is based on a set algorithm which does not take into account individual patient differences. As a result hypertension is often sub-optimally treated based on "population averages", rather than a person's genetic make-up, with significant burden on our health care system. In fact, 40% of patients who are adherent to their blood pressure therapy (taking their medicines as prescribed by their clinician) do not have their blood pressure under control. Previous work has demonstrated significant functional polymorphisms within the kidney, vessels, and heart that will likely predict a patient's response to blood pressure pharmacotherapy. Previous work by our group, utilizing a retrospective design, has determined that the addition of genetic knowledge to prescribing can improve therapeutic guidance and decrease the time to blood pressure control significantly. Despite this, to date, there are no prospective trials to guide blood pressure therapy using multiple organ systems that are important in the three most common classes of drugs: diuretics, vasodilators, and beta-blockers. The objective of this clinical trial is to determine the efficacy of genetically guided therapeutic options for pharmacologic treatment of essential hypertension in newly diagnosed patients.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Specific Aim:

To determine the efficacy of genetically guided therapeutic options for pharmacologic treatment of essential hypertension, when compared to conventional standard of care (JNC 8 guideline directed therapy).

Hypothesis A: Patients randomized to genetically guided blood pressure therapy will have significantly reduced time to optimal blood pressure control compared to conventional standard of care.

Hypotheses B: Patients randomized to genetically guided blood pressure therapy will have significantly greater absolute blood pressure reduction compared to conventional standard of care.

Hypothesis C: Patients randomized to genetically guided blood pressure therapy will have to take fewer classes of blood pressure medicines in order to achieve blood pressure control.

Secondary Aim:

To determine if genetically guided blood pressure therapy reduces number of medication changes in patients with hypertension.

Hypotheses: Patients randomized to genetically guided blood pressure therapy will have significantly less medication changes.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1000 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Prospective Randomized Controlled Trial Investigating the Use of Genetic Predisposition to Guide Pharmacologic Therapy for Hypertension
Anticipated Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Genetically-Guided Treatment for HTN

Using a patient's genetic composition to guide BP prescribing for patients with hypertension, post diagnosis.

Drug: Geneticure Panel for HTN therapy
Using either Genetics (Geneticure for HTN multi-gene panel) or JNC-8 guidelines for prescribing for patients with hypertension

Active Comparator: JNC-8-Guided Treatment

Using traditional (JNC-8) guidelines for BP prescribing for patients with hypertension, post diagnosis.

Drug: JNC-8
Using JNC-8 guidelines to guide therapy

Outcome Measures

Primary Outcome Measures

  1. Time to Blood Pressure Control [1 year]

    Time to BP control between genetically-guided prescribing and JNC-8 guided prescribing

  2. Change in Blood Pressure [1 year]

    Change (absolute) in BP (systolic, SBP, diastolic, DBP, and mean arterial, MAP) between genetically-guided prescribing and JNC-8 guided prescribing

  3. Number of Blood Pressure Medicines [1 year]

    Number of blood pressure medicines needed to obtain control of hypertension between genetically-guided prescribing and JNC-8 guided prescribing

Secondary Outcome Measures

  1. Number of Medication Changes [1 year]

    Number of blood pressure medicine changes needed to obtain control of hypertension between genetically-guided prescribing and JNC-8 guided prescribing

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Subject with new diagnosis of hypertension or uncontrolled hypertension and on one medication

  2. Subject is able and willing to provide informed consent

  3. Subject is ≥ 30 and ≤ 80 years of age

  4. Subject with a Body Mass Index (BMI) ≥ 19 and ≤ 50

Exclusion Criteria:
  1. Subject has been diagnosed with chronic kidney disease as determined by serum creatinine levels of >1.3 mg/dl for men and >1.1 for women.

  2. Subject has clinically significant cardiac disease as determined by diagnosed coronary artery disease, diagnosed heart failure, and congenital cardiac disease.

  3. Subject has clinically significant vascular disease as determined by diagnosed peripheral vascular disease and diagnosed pulmonary hypertension.

  4. Liver dysfunction is defined using the normal reference range for lower limit of normal and upper limit of normal used by Fairview labs and as determined by diagnosed liver disease /cirrhosis as listed in the patient's problem list based on ICD-10.

  5. Subject has secondary hypertension.

  6. Subject has prior diagnosis of endocrine disorders except uncomplicated type 2 diabetes and well controlled hypothyroidism.

  7. Subject is pregnant.

  8. Subject is breastfeeding.

  9. Subject becomes pregnant during study

  10. Subjects lacking the capacity to consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fairview Health Clinics - Andover Andover Minnesota United States 55304
2 Fairview Health Clinics - Blaine Blaine Minnesota United States 55449
3 Fairview Health Clinics - Bloomington, Oxboro Bloomington Minnesota United States 55420
4 Fairview Clinics - Brooklyn Park Brooklyn Park Minnesota United States 55443
5 Fairview Clinics- Burnsville Burnsville Minnesota United States 55337
6 Fairview Clinics - Columbia Heights Columbia Heights Minnesota United States 55421
7 Fairview Health Clinics - Edina Edina Minnesota United States 55345
8 Fairview Health Clinics - Elk River Elk River Minnesota United States 55330
9 Fairview Clinics - Fridley Fridley Minnesota United States 55432
10 Fairview Clinics - Lino Lakes Lino Lakes Minnesota United States 55014
11 Fairview Clinics - Hiawatha Minneapolis Minnesota United States 55406
12 Fairview Clinics - North Branch N. Branch Minnesota United States 55056
13 Fairview Clinic - New Brighton New Brighton Minnesota United States 55112
14 Fairview Clinics - Wyoming Wyoming Minnesota United States 55092
15 Fairview Health Services - Zimmerman Zimmerman Minnesota United States 55398

Sponsors and Collaborators

  • Geneticure, LLC
  • Fairview Health Services
  • University of Minnesota

Investigators

  • Principal Investigator: Pamela Phelps, PharmD, Fairview Health Services
  • Study Director: Weihong Tang, MD, PhD, University of Minnesota
  • Principal Investigator: Michael Schulenberg, MD, Fairview Health Services

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Geneticure, LLC
ClinicalTrials.gov Identifier:
NCT02988245
Other Study ID Numbers:
  • Geneticure
First Posted:
Dec 9, 2016
Last Update Posted:
Feb 2, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 2, 2022