← Trials/Trial dossier/NCT05766358

EXPEND-FU

Completed

Role Of Metabolic Adaptation In Weight Regain

Role Of Metabolic Adaptation In Weight Regain: Expend Follow-Up

Asset

Tirzepatide

Subcutaneous · GLP-1 / GIP dual

Listed sites

1

Recruiting sites

Enrollment

27

actual

Study population

Obesity / overweight

Key I/E criterion

Primary endpoint

Body weight

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT05766358
Org study IDPBRC 2022-027

Timeline

Milestones

Study start2022-10-06actual
Study first posted2023-03-13actual
Primary completion2024-05-24actual
Study completion2024-05-24actual
Last update posted2024-06-10actual

Assets

Investigational agents

Study populations

Who this study enrolls

Obesity / overweight

Eligibility

Who can enroll

Minimum age18 Years
SexAll
Healthy volunteersNot accepted
Sampling methodNon probability sample

Study population text

Participants having completed the NCT04081337 study.

Inclusion criteria

Having participated in the study NCT04081337.

Exclusion criteria

Being pregnant.

Endpoints (9)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Weight & body composition

9 endpoints
Primary/protocol endpoint/low confidence

Body weight

Time frame:24 months

descriptive, improvement

Secondary/protocol endpoint

Body weight

Time frame:12 months

descriptive, improvement

Secondary/protocol endpoint

Body weight

Time frame:18 months

descriptive, improvement

Secondary/protocol endpoint

Body fat mass (DXA)

Time frame:12 months

Total fat mass

change from baseline, improvement

Secondary/protocol endpoint

Body fat mass (DXA)

Time frame:18 months

Total fat mass

change from baseline, improvement

Secondary/protocol endpoint

Body fat mass (DXA)

Time frame:24 months

Total fat mass

change from baseline, improvement

Secondary/protocol endpoint

Body fat free mass (DXA)

Time frame:12 months

Lean mass

change from baseline, improvement

Secondary/protocol endpoint

Body fat free mass (DXA)

Time frame:18 months

Lean mass

change from baseline, improvement

Secondary/protocol endpoint

Body fat free mass (DXA)

Time frame:24 months

Lean mass

change from baseline, improvement

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.