ClinicalTrials.gov registry snapshot / 2026-07-24

Peptide trials,
without the maze.

Search every official registry record matched to 13 tracked peptide and next-generation weight-loss programs. Find current status, phase, enrollment, countries, US states, recruiting cities, postal areas, completion timing, and the direct NCT source.

268unique NCT records
13named programs
53countries represented
1,840recruiting cities
11registry result modules
Recruiting footprint by program

Study status is not drug rank.

Bar length shows registry-listed sites individually marked Recruiting. Larger programs can create larger counts. This does not compare efficacy, safety, approval odds, sponsor quality, or enrollment availability.

Official registry finder

Filter the exact records.

Search names, former codes, NCT IDs, sponsors, interventions, conditions, cities, and postal codes. Filtered URLs are shareable but intentionally excluded from search indexing so this page remains the canonical source.

Reset
14matching registry records
Snapshot timestampJuly 24, 2026 at 9:00 AM UTC
Program and recordStatusPhase and enrollmentLocationsPrimary completionRegistry updateSource
A Study to Evaluate the Effect of Maridebart Cafraglutide on Insulin Sensitivity and β-cell Function in Participants With Type 2 Diabetes MellitusNCT07160257 / AmgenActive, not recruitingVerified 2026-06Phase 156 actual0 recruiting1 listed / 1 countriesNov 15, 2026estimatedJun 12, 2026ClinicalTrials.govOpen NCT07160257
Effect of Maridebart Cafraglutide on the Heart's Electrical ActivityNCT07229157 / AmgenActive, not recruitingVerified 2026-01Phase 181 actual0 recruiting2 listed / 1 countriesAug 26, 2026estimatedJan 23, 2026ClinicalTrials.govOpen NCT07229157
Effect of Maridebart Cafraglutide on How Oral Contraceptives Are Absorbed and Processed in the Body in Postmenopausal Female Participants Living With Overweight or ObesityNCT07523711 / AmgenActive, not recruitingVerified 2026-07Phase 149 actual0 recruiting2 listed / 1 countriesNov 18, 2026estimatedJul 20, 2026ClinicalTrials.govOpen NCT07523711
Single and Multiple Ascending Dose Study of AMG 133 in Participants With ObesityNCT04478708 / AmgenCompletedVerified 2025-11Registry results postedPhase 1110 actual0 recruiting3 listed / 1 countriesNov 18, 2022actualDec 10, 2025ClinicalTrials.govOpen NCT04478708
Study of AMG 133 Administered Subcutaneously in Healthy Japanese and Caucasian ParticipantsNCT05056246 / AmgenCompletedVerified 2025-01Registry results postedPhase 134 actual0 recruiting1 listed / 1 countriesApr 8, 2022actualFeb 25, 2025ClinicalTrials.govOpen NCT05056246
A Study to Evaluate AMG 133 in Chinese Participants With Obesity or OverweightNCT06352892 / AmgenCompletedVerified 2026-01Phase 120 actual0 recruiting1 listed / 1 countriesAug 27, 2024actualJan 8, 2026ClinicalTrials.govOpen NCT06352892
A Study to Evaluate AMG 133 Administered Subcutaneously in Participants With Overweight or ObesityNCT06976372 / AmgenCompletedVerified 2025-10Phase 1120 actual0 recruiting3 listed / 1 countriesDec 27, 2024actualOct 8, 2025ClinicalTrials.govOpen NCT06976372
Comparing the Extent to Which Maridebart Cafraglutide (AMG 133) is Made Available in the Body When Administered Using Two Subcutaneous (SC) PresentationsNCT07226778 / AmgenCompletedVerified 2026-06Phase 1348 actual0 recruiting4 listed / 1 countriesMay 28, 2026actualJun 17, 2026ClinicalTrials.govOpen NCT07226778
A Trial to Evaluate Interactions Between Antiemetic Medication and AMG 133 in Participants Living With Overweight or ObesityNCT07310563 / AmgenCompletedVerified 2025-12Phase 159 actual0 recruiting1 listed / 1 countriesMay 9, 2025actualDec 30, 2025ClinicalTrials.govOpen NCT07310563
A Trial to Compare the Extent to Which Maridebart Cafraglutide (AMG 133) is Made Available in the Body When Administered Using Two Subcutaneous PresentationsNCT07313761 / AmgenCompletedVerified 2026-07Phase 1349 actual0 recruiting4 listed / 1 countriesJun 26, 2026actualJul 16, 2026ClinicalTrials.govOpen NCT07313761
A Study to Evaluate AMG 133 in Participants With Varying Degrees of Hepatic Impairment or Normal Hepatic FunctionNCT07428525 / AmgenCompletedVerified 2026-03Phase 136 actual0 recruiting5 listed / 1 countriesFeb 26, 2026actualMar 11, 2026ClinicalTrials.govOpen NCT07428525
The Effect of AMG 133 on Gastric EmptyingNCT07429032 / AmgenCompletedVerified 2025-12Phase 157 actual0 recruiting1 listed / 1 countriesNov 26, 2025actualFeb 24, 2026ClinicalTrials.govOpen NCT07429032
A Trial to Assess the Effect of Kidney Impairment on How AMG 133 is Absorbed, Broken Down, and Eliminated by the BodyNCT07429045 / AmgenCompletedVerified 2025-12Phase 144 actual0 recruiting5 listed / 1 countriesNov 21, 2025actualFeb 24, 2026ClinicalTrials.govOpen NCT07429045
A Trial to Assess Bioavailability of AMG 133 in Participants With Overweight or ObesityNCT07717814 / AmgenCompletedVerified 2026-07Phase 1154 actual0 recruiting4 listed / 1 countriesMay 22, 2025actualJul 21, 2026ClinicalTrials.govOpen NCT07717814
Clinical trial finder FAQ

Status, location, and enrollment are different fields.

These answers prevent the most common registry-search errors before a reader follows an official source.

01

Are any Retatrutide clinical trials recruiting?

Yes. This 2026-07-24 snapshot contains 2 Retatrutide registry records with an overall Recruiting status and 450 listed sites individually marked Recruiting. Overall status does not mean every site is open, and neither status establishes eligibility or enrollment. Open the exact NCT record and verify the individual location before contacting a study team.

02

How do I find a peptide clinical trial near me?

Enter a city or postal code, optionally add a country or US state, and then open the exact ClinicalTrials.gov record. This finder retains location rows individually marked Recruiting but omits facility and personal contact fields. Confirm current recruitment, eligibility, official contact route, and travel requirements on the registry. Peptide Local does not enroll participants.

03

Does Recruiting mean I can join the trial?

No. Recruiting is a registry status, not an eligibility decision or appointment. A study can be recruiting overall while some listed locations are not yet recruiting, active but closed, completed, suspended, or missing a current site status. The study team applies the protocol's eligibility and consent process.

04

Are the drugs in this clinical trial finder FDA approved?

A ClinicalTrials.gov record is not FDA approval. The finder covers investigational programs and can also include studies involving components or comparators with separate regulatory histories. Approval must be verified on the exact FDA label or regulator record, not inferred from a phase, sponsor, trial result, or recruiting status.

05

Why do only some registry records show posted results?

11 of 268 records in this snapshot expose a ClinicalTrials.gov results module. A record without posted registry results can still have a publication or sponsor announcement elsewhere, while a posted module still requires careful interpretation. Results availability is not a quality rank.

06

How current is the peptide clinical trial data?

The registry data timestamp is July 24, 2026 at 9:00 AM UTC. The refresh workflow searches exact intervention names and aliases, deduplicates by NCT ID, preserves multi-program studies, and stores overall and individual-site status separately. Registry fields can change after that timestamp, so the direct source remains authoritative for enrollment decisions.

Evidence boundary

A registry finder, not an enrollment service.

A dated transformation of ClinicalTrials.gov intervention-search records for thirteen named Peptide Local pipeline programs. Study sponsors or investigators submit and maintain registry records. Overall status, individual-site status, enrollment, locations, completion dates, and results availability can change. Recruiting status does not establish eligibility, enrollment, treatment access, regulatory approval, routine availability, or a favorable benefit-risk conclusion.

Peptide Local omits personal contact details and does not screen participants, recommend a protocol, interpret eligibility, arrange treatment, or authenticate commercial products that reuse an investigational program's name.

Read the official API documentation ↗Understand evidence categories →