MK-677

Tested in people

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It has been tested in people, but it is not an approved medicine. The studies are usually small.

Compiled and reviewed by the PeptideSearch Editorial Team · Status checked 2026-05-14

Also called Ibutamoren / Ibutamoren mesylate / MK-0677 / Nutrobal

A pill, not a peptide. Raises growth hormone and IGF-1. Tested in people but never approved.

Official status: 503A Category 2 – significant safety risk · Checked 2026-05-14

Can a doctor prescribe this?

Small pharmacy (503A)
Category 2 — FDA flagged a safety concern
Large outsourcing facility (503B)
Category 2 — FDA flagged a safety concern

The FDA has "Ibutamoren Mesylate" — the chemical name for MK-677 — in Category 2 of the substances put forward for small-pharmacy (503A) compounding: the group it says raises a real safety concern. Pharmacies are not allowed to make it.

503A is a pharmacy making a single prescription for one patient. 503B is a facility making batches. They are governed by separate lists. Where a category is shown, it is a position on the FDA's list of substances that have been put forward and are still being worked through — not the final list, which is set by rulemaking. Category 1 means the FDA does not plan to act against a pharmacy that makes it while the review runs.

Lab suppliers we list: 9

Doses used in research

Taken word for word from the studies and trials listed on this page. This is not a recommendation and not a dose for anyone to take.

Spot an error? corrections@peptidesearch.org

What has happened so far

  1. 14 May 2026503A

    FDA lists "Ibutamoren Mesylate" — MK-677 — under 503A Category 2: Bulk Drug Substances that Raise Significant Safety Risks. Read from the FDA 503A category document headed "Updated May 14, 2026".

    FDA

  2. 21 March 2025503B

    FDA lists "Ibutamoren Mesylate" — MK-677 — under 503B Category 2: Bulk Drug Substances that Raise Significant Safety Risks. Read from the FDA 503B category document dated March 21, 2025.

    FDA

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