Current partner codePEPTIDESDE
NCT07728812·Not applicable·INTERVENTIONAL

Pragmatic Trial to Study the Cost-Effectiveness of MyPhenome-RX Test to Guide Anti-Obesity Pharmacotherapy

Status

Not yet recruiting

Phase

Not applicable

Enrollment

424

Locations

0

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

A pragmatic, randomized, parallel-arm, controlled study of weight loss outcomes using AOMs guided by MyPhenome test.

Interventions

Treatment arms and agents.

GENETIC

Genetic Test

The MyPhenome test is a genetic and clinical assessment that classifies individuals into biologically defined obesity phenotypes to guide personalized treatment. Using a saliva DNA sample combined with brief clinical inputs, the test predicts whether a patient has abnormalities in high CTSGRS ("Hungry Brain"), low CTSGRS ("Hungry Gut"), or hedonic eating ("Emotional Hunger").

DRUG

Anti-Obesity Medication (AOM) treatment

Available AOMs will be: GLP-1 Receptor Agonists (semaglutide or tirzepatide), Phentermine-Topiramate ER, and naltrexone-bupropion SR

Timeline

From registration to results.

  1. First posted

    Jul 27, 2026

  2. Study start

    Sep 1, 2026

  3. Primary completion

    Jul 1, 2028

  4. Study completion

    Jan 1, 2029

  5. Results posted

    Not reported

  6. Registry updated

    Jul 27, 2026

Outcomes

What the study measures.

Primary outcomes

Total Body Weight Loss (TBWL) at 6 Months %

Time frame · 6-Months

TWBL% at 6 months

Secondary outcomes

TBWL% at 3 Months

Time frame · 3-months

TBWL% at 3 Months

TBWL% at 9 Months

Time frame · 9-Months

TBWL% at 9 Months

TBWL% at 12 Months

Time frame · 12-Months

TBWL% at 12 Months

TBWL% at 18 Months

Time frame · 18-Months

TBWL% at 18 Months

TBWL% at 24 Months

Time frame · 24-Months

TBWL% at 24 Months

Degree of Treatment Response

Time frame · 6-Months

6-Months: non-responsive (\<3% TBWL), partial responsive (3%-15% TBWL), successful (\>15%-20% TBWL) and highly successful (\>20% TBWL)

Cost of Treatment

Time frame · 3, 6, 9, 12, 18, 24 Months

Cost of Treatment

Cost-Effectiveness

Time frame · 3, 6, 9, 12, 18, 24 Months

Cost-Effectiveness Pharmacy resource utilization data will be collected during the study. Pharmacotherapy costs will be directly compared between control and intervention groups and compared to weight loss outcomes.

Patient Satisfaction

Time frame · 3, 6, 9, 12, 18, 24 Months

Client Satisfaction Questionnaire (CSQ-8): Given the design of the study, we will measure and evaluate patient satisfaction with a program of care rather than satisfaction with a specific medication. The satisfaction with the program will be evaluated with the adapted Client Satisfaction Questionnaire (CSQ-8). This is an 8-item measure that captures overall satisfaction with the care received, including perceived quality, whether care met patient needs, and willingness to recommend the program (each item score 1-4). The items will be lightly adapted to refer to weight management care with a total score ranging from 8 to 32 .

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Adults - age 18 or older * obesity (BMI ≥ 30 kg/m2) without obesity related diseases (ORDs). Or obesity (BMI ≥ 27 kg/m2) with obesity related diseases (ORDs). * Mayo Clinic employee or dependent * Referred to Community Internal Medicine Weight Management Program Exclusion Criteria: * Pregnancy or currently breast feeding. * No contraindications to the weight loss medications: Phentermine-Topiramate Extended Release (Qsymia®); Oral naltrexone extended-release/bupropion extended-release (NBSR; Contrave®, Mysimba™); Liraglutide (Saxenda®), Semaglutide (Wegovy®), and Tirzepatide (Zepbound®).

Study locations

0 registered sites.

No country data reported. Showing up to 24 locations stored in the fast local snapshot.

No study locations reported.

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Tirzepatide.

Related PeptideStat pages

Put the record in context.

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