ClinicalTrials.gov / global locations / 2026

Retatrutide is not approved. Two trial records are recruiting.

A current registry tracker for retatrutide trial locations, enrollment status, active studies, expanded access, and the difference between an overall Recruiting label and an open local site.

Registry matches34
Recruiting2
Active, closed11
Recruiting-site countries27
Direct answer

Two records are recruiting overall. Neither is a simple open-enrollment route for obesity treatment.

ClinicalTrials.gov returned 34 intervention-search matches in the current snapshot: 20 Completed, 11 Active, not recruiting, 2 Recruiting, and 1 Available expanded-access record.

The two recruiting records have different sponsors, conditions, designs, and countries. SYNERGY-Outcomes is a multiple-agent MASLD master protocol. The separate China study is sponsored by Hudson Biotech and uses the LY3437943 development code. Together they retain 564 listed locations, while 450 individual site observations are currently marked Recruiting.

The Lilly obesity and chronic-low-back-pain study changed to Active, not recruiting before this release. It is therefore shown in the closed-to-new-enrollment table, not as a recruiting route.

Run the live ClinicalTrials.gov search →
Recruiting now

Read the study before the location list.

Overall status can change after this snapshot. Every card links to the live registry record, where the study team controls eligibility and current contact information.

01Recruiting
NCT07165028 / Phase 3

SYNERGY-Outcomes master protocol in adults with metabolic dysfunction-associated steatotic liver disease

A multiple-agent master protocol that lists both retatrutide and tirzepatide interventions. The location ledger is not a retatrutide-arm assignment list and does not mean every site is enrolling every arm.

Sponsor
Eli Lilly and Company
Estimated enrollment
4,500
Listed locations
563
Countries
34
Primary completion
August 2030
Registry updated
2026-07-17
Check status, eligibility, and contacts
02Recruiting
NCT07467447 / Phase 2

LY3437943 versus placebo in participants with obesity or overweight

A China-based study sponsored by Hudson Biotech. Its registry record uses LY3437943, but it is not an Eli Lilly-sponsored TRIUMPH trial.

Sponsor
Hudson Biotech
Estimated enrollment
300
Listed locations
1
Countries
1
Primary completion
March 2027
Registry updated
2026-03-12
Check status, eligibility, and contacts
United States

34 states contain at least one site currently marked Recruiting.

A state name means at least one individual registry location currently carries a Recruiting site status. It does not establish an open appointment, eligibility, or assignment to a retatrutide arm.

Do not apply here

Active does not mean recruiting.

These studies can still be treating participants, collecting outcomes, or completing follow-up. Their overall status explicitly says they are not recruiting.

StudyPhaseEnrollmentLocationsPrimary completionLive record
NCT07035093Retatrutide in participants with obesity or overweight and chronic low back painPhase 358640 across 4 countriesSeptember 2027Verify ↗
NCT05882045Retatrutide in participants with obesity and cardiovascular diseasePhase 31,946169 across 10 countriesApril 2026Verify ↗
NCT05929079TRIUMPH-2 in participants with type 2 diabetes who have obesity or overweightPhase 31,00098 across 8 countriesMay 2026Verify ↗
NCT06260722TRANSCEND-T2D-2, retatrutide compared with semaglutide in type 2 diabetesPhase 31,25077 across 5 countriesAugust 2026Verify ↗
NCT06297603TRANSCEND-T2D-3 in type 2 diabetes with moderate or severe renal impairmentPhase 332076 across 7 countriesOctober 2026Verify ↗
NCT06383390TRIUMPH-Outcomes cardiovascular and kidney outcomes studyPhase 310,000743 across 27 countriesFebruary 2029Verify ↗
NCT06662383TRIUMPH-5, retatrutide compared with tirzepatide in adults with obesityPhase 380065 across 5 countriesNovember 2026Verify ↗
NCT06859268Retatrutide in the maintenance of weight reduction in individuals with obesityPhase 364353 across 3 countriesApril 2028Verify ↗
NCT06982859Retatrutide effects on insulin secretion and insulin sensitivity in type 2 diabetesPhase 1951 across 1 countryDecember 2026Verify ↗
NCT07232719Retatrutide in participants with obesity or overweightPhase 325031 across 2 countriesJuly 2027Verify ↗
NCT07357415Retatrutide in participants without type 2 diabetes who have obesity or overweightPhase 360035 across 3 countriesOctober 2028Verify ↗
Enrollment check

Use four gates, in order.

  1. 01

    Match the exact condition

    Obesity alone does not satisfy a study requiring chronic low back pain, MASLD, diabetes, renal impairment, or another defined condition.

  2. 02

    Check overall status

    Recruiting, Active not recruiting, Completed, and Available expanded access are different categories. Only the live registry record is current.

  3. 03

    Check the specific location

    A study can be Recruiting overall while a particular site is full, paused, not yet open, or assigned to a different arm within a master protocol.

  4. 04

    Use the registry contact

    The study team, not Peptide Local or an online seller, determines current site availability, screening, consent, and eligibility.

Separate pathway

Expanded access is not general access.

An expanded-access record, not a clinical trial, pharmacy channel, general access program, or promise of eligibility. FDA, physician, IRB, sponsor, and serious-condition requirements remain separate gates.

FDA describes expanded access as a potential pathway for a patient with a serious or immediately life-threatening disease or condition when no comparable or satisfactory therapy exists. A licensed physician, the sponsor, an institutional review board, and FDA must each participate in the process.

Read FDA's patient guidance →Open the retatrutide expanded-access record →
Direct questions

Trial locations, TRIUMPH status, and access.

Each answer uses the dated registry denominator. Recheck the live record before acting because recruitment and site details can change.

01

Are any retatrutide clinical trials recruiting?

Yes. The current ClinicalTrials.gov intervention-search snapshot contains two records with an overall Recruiting status. They are not interchangeable: one is a multiple-agent MASLD master protocol and one is a China-based Phase 2 study sponsored by Hudson Biotech. The separate chronic low-back-pain study changed to Active, not recruiting in the July 23 snapshot. The exact record and current site status must be checked before contacting a study team.

02

Where are retatrutide trials recruiting?

The two overall-recruiting records retain 564 listed locations across 34 countries. Of those, 450 individual site observations in 27 countries are currently marked Recruiting. Neither count is a count of open retatrutide slots. The largest record is the multiple-agent SYNERGY-Outcomes master protocol, and a listed site may not enroll every study arm.

03

Can I join TRIUMPH-1?

No new enrollment is indicated. TRIUMPH-1, NCT05929066, is Completed. Its locations and results remain useful evidence, but a completed study is not an enrollment route. Current recruiting records must be searched separately.

04

Is TRIUMPH-5 recruiting?

No. TRIUMPH-5, NCT06662383, is Active, not recruiting in the July 20, 2026 registry snapshot. It directly compares retatrutide with tirzepatide in adults with obesity, but the current status does not indicate new enrollment and no result is posted in this release.

05

Does Recruiting mean every listed trial site is open?

No. Overall study status and individual location availability are different fields. Sites can open, pause, fill, or close on different dates. Use the exact ClinicalTrials.gov record, then confirm the site and study contact information directly. Peptide Local does not collect applications or determine eligibility.

06

Is expanded access the same as joining a clinical trial?

No. Expanded access is treatment use outside a clinical trial for certain serious or immediately life-threatening conditions when no comparable or satisfactory option exists. A licensed physician, the sponsor, an institutional review board, and FDA have separate roles. An Available registry record is not a retail channel, general weight-loss program, or guarantee that a request will proceed.

07

Can I get or buy retatrutide outside a trial?

Retatrutide remains investigational and has no FDA-approved pharmacy product, commercial label, or routine prescription channel. Lilly says no one should take anything claiming to be retatrutide outside a Lilly-sponsored clinical trial. A seller page using the development name does not become clinical-trial material and does not inherit the sponsor's identity, quality, dose, or safety record.

Open data

14 open-program records, ready to inspect.

The release includes all Recruiting, Active not recruiting, and Available expanded-access records in the current 34-match snapshot. Completed studies stay in the denominator but are not duplicated as open-program rows.

Investigational boundaryA trial listing is not approval, a prescription, or proof of an online product.

Retatrutide remains investigational. An NCT number, study dose, location, or research-vial listing does not create a commercial pharmacy channel or authorize self-directed use.

Open the complete Retatrutide evidence profile →
Primary referencesClinicalTrials.gov Retatrutide OR LY3437943 intervention searchComplete 34-record two-name intervention-search denominator and current overall study statusesU.S. National Library of MedicineRetatrutide and chronic low back pain studyCurrent Active, not recruiting Phase 3 status, conditions, eligibility, estimated enrollment, countries, and listed locationsClinicalTrials.govSYNERGY-Outcomes master protocolRecruiting Phase 3 status, multiple-agent design, retatrutide intervention, countries, and listed locationsClinicalTrials.govHudson Biotech LY3437943 studyRecruiting Phase 2 status, China location, sponsor, eligibility, and estimated enrollmentClinicalTrials.govRetatrutide expanded-access recordAvailable expanded-access record and sponsor contact route, separate from clinical-trial enrollmentClinicalTrials.govTRIUMPH-5 retatrutide versus tirzepatideActive-not-recruiting status, Phase 3 design, comparator, listed locations, and projected primary completionClinicalTrials.govExpanded access information for patientsSerious-condition, physician, sponsor, IRB, FDA, and no-satisfactory-alternative requirementsU.S. Food and Drug AdministrationWhat to know about retatrutideInvestigational status, clinical-trial-only public access boundary, and warning about products claiming to be retatrutideEli Lilly and Company