Reviewed & approved by Dr. Nova Reyes · Last checked 2026-10-25. ← Back to Evidence Library

Efinopegdutide: what the evidence says

At a glance

What it is: an experimental long-acting injected peptide that activates two receptors, GLP-1 (the target of semaglutide) and glucagon. It was first developed by Hanmi, tested by Johnson & Johnson under the code JNJ-64565111, and is now developed by Merck as MK-6024. R1, R2, R3

What the evidence says: in one open-label phase 2 trial in fatty liver disease, it cut liver fat more than semaglutide. In two older phase 2 trials, it caused weight loss vs placebo (a dummy treatment), but in people with type 2 diabetes blood sugar did not improve. R1, R2, R3

Biggest risks: nausea and vomiting were more common than with placebo, liraglutide or semaglutide. Many people stopped early in the older trials. Long-term safety is unknown. Gray-market vials add unknown identity, strength and purity. R1, R2, R3

Human Human evidence (fatty liver, liver fat) Limited: one open-label phase 2a RCT (randomized controlled trial; 145 people) vs semaglutide, measuring liver fat on scans, not liver scarring; a larger phase 2b trial finished without published results R1, R4
Human Human evidence (weight) Limited: two phase 2 RCTs (474 and 195 people) vs placebo, plus weight data from the liver trial; high dropout; no phase 3 R1, R2, R3
Human Human evidence (type 2 diabetes, blood sugar) Very limited (mixed results): one short phase 2 RCT produced weight loss but found no HbA1c improvement and a slight rise in fasting glucose and fasting insulin R3
Animal Animal evidence Not rated here
Regulatory Not FDA-approved (no Drugs@FDA record) · EU, Japan, China: UNVERIFIED not checked against EMA, PMDA or NMPA · WADA: not named; S0 (unapproved substances) likely applies R5
Established human dose None. There is no label. Trial study arms are listed only in Study details

Evidence verdict: Human (liver fat): Limited · Human (weight): Limited · Human (type 2 diabetes): Very limited (mixed results) · Animal: not rated here Card verdict: Limited (liver fat and weight) · Type 2 diabetes: Very limited (mixed results) Card note: Varies by use, see page

This page reports what studies used. It is not dosing advice.

Legend: HUMAN data · ANIMAL / LAB data · UNKNOWN · UNVERIFIED: not yet confirmed against a primary source


What is it?

Efinopegdutide is a lab-made peptide that activates both the GLP-1 receptor and the glucagon receptor. R1 GLP-1 action lowers appetite. Glucagon action raises energy use and may push the liver to burn fat directly, which is why it is being studied for fatty liver disease. R1 Glucagon also raises blood sugar, which may explain the diabetes result below. R3 Unknown

Does it help fatty liver disease?

Does it help weight loss?

Does it help type 2 diabetes?

Is it safe?

What the trials reported:

Compounded and gray-market Efinopegdutide: extra risks

What we don't know

Is it legal?

Not FDA-approved; no Drugs@FDA record was found (openFDA search, Oct 24, 2026). We found no registered phase 3 trial and no announced filing for approval. R4 EU, Japan, China: UNVERIFIED not checked against EMA, PMDA or NMPA. WADA: not named on the 2026 Prohibited List; S0 bans at all times any unapproved substance in development that no other section covers, which describes Efinopegdutide R5. WADA has not ruled on Efinopegdutide by name. As of Oct 24, 2026.

What's in the vial?

Real efinopegdutide is only available inside clinical trials. We have not found published lab tests of gray-market Efinopegdutide. Under the Open Peptide Standard, a GLP-1 vial overfilled by more than 20% is a critical fail (draft threshold). See results at /tests/. A passing test covers one batch, tested on one date. It does not mean the compound itself is safe.

What do users report?

Self-report, not evidence.

Unknown TBD. We'll only list this once we can cite a public source.

Study details

These are doses researchers used, not recommendations. All injections subcutaneous.

R1 Human: Fatty liver (Merck)

Study People Route Dose used Follow-up Reported Side effects / dropouts Citation
Phase 2a, open-label (Romero-Gómez 2023), NCT04944992 145 (72 vs 73) Subcutaneous Efinopegdutide 10 mg once weekly vs semaglutide 1 mg once weekly, titrated over 8 weeks 24 wk Liver fat −72.7% vs −42.3% (p<0.001); weight −8.5% vs −7.1% (p=0.085) Slightly more AEs, mainly GI PMID 37355043

R2, R3 Human: Weight and diabetes (Janssen, as JNJ-64565111)

Study People Route Dose used Follow-up Reported Side effects / dropouts Citation
Phase 2, obesity BMI 35–50, no T2D (Alba 2021) 474 Subcutaneous 5.0, 7.4 or 10.0 mg, no escalation, vs placebo; open-label liraglutide 3.0 mg 26 wk Placebo-subtracted −6.8%, −8.1%, −10.0%; liraglutide −5.8% More nausea and vomiting; 72.4% completed PMID 33475255
Phase 2, T2D with BMI 35–50 (Di Prospero 2021) 195 Subcutaneous 5.0, 7.4 or 10.0 mg vs placebo 12 wk Placebo-subtracted −4.6%, −5.9%, −7.2%; no HbA1c change; fasting glucose rose (5.0, 7.4 mg) More nausea and vomiting; 73.8% completed PMID 33475251

R4 Ongoing trials (as of Oct 24, 2026)

ClinicalTrials.gov: phase 2b in MASH NCT05877547, 381 enrolled, completed Dec 2025, no results posted. No phase 3 found. FDA: no Drugs@FDA record (openFDA query, Oct 24, 2026). EMA, PMDA, NMPA: UNVERIFIED not checked.

Full reference list (all PMIDs verified on PubMed, Oct 24, 2026)

  1. Romero-Gómez M, et al. J Hepatol. 2023;79(4):888-897. doi:10.1016/j.jhep.2023.05.013. PMID 37355043
  2. Alba M, et al. Clin Obes. 2021;11(2):e12432. doi:10.1111/cob.12432. PMID 33475255
  3. Di Prospero NA, et al. Clin Obes. 2021;11(2):e12433. doi:10.1111/cob.12433. PMID 33475251
  4. ClinicalTrials.gov. NCT05877547.
  5. WADA. World Anti-Doping Code International Standard: Prohibited List 2026 (in force Jan 1, 2026). https://www.wada-ama.org/sites/default/files/2025-09/2026list_en_final_clean_september_2025.pdf (text read Oct 24, 2026)

Disclaimer

This page is for education and harm reduction. It is not medical advice and not a recommendation to use Efinopegdutide. Please talk to a clinician you trust before making medical decisions, seek care right away for severe stomach pain or repeated vomiting, and report problems to FDA MedWatch (https://www.fda.gov/safety/medwatch).

Approved for Adam Greene by Dr. Nova Reyes, 2026-10-25.