Growth factor fragments
Mechano growth factor
MGF; IGF-1Ec
- US status
- No lawful route
- Class
- Growth factor fragments
- Approved product
- None
- Route
- None lawful; sold as research-use-only material
Regulatory record
- May 2026
- The section 503A bulks list FDA published May 14, 2026 lists mechano growth factor (MGF) in Category 3, the file for substances nominated without adequate support to evaluate. The pegylated form appears in no category of the same document; that separate disposition is recorded on the PEG-MGF row.
- September 2026
- Drugs@FDA holds no approved product with mechano growth factor as an active ingredient, and neither form was among the seven peptides the advisory committee reviewed in July 2026. Two forms of one molecule therefore hold two different dispositions and the same absence of a lawful route.
- FDA final action
- None as of September 2026.
Every entry above is dated; the record is current as of the review date.
Definition
Mechano growth factor is a splice variant of insulin-like growth factor 1, produced in skeletal muscle in response to mechanical loading and damage. It is also written IGF-1Ec, which is the name the physiology literature mostly uses, and the two names describe one thing: a locally expressed peptide whose job is to signal that a muscle has been worked.
It reaches buyers as synthetic research-use-only material, in two forms. The unpegylated peptide is what this page tracks. The pegylated form, PEG-MGF, is a separate substance in the federal record with a separate and different disposition, and the distinction is invisible on the products themselves.
Evidence
Across five name variants PubMed returns 236 indexed records, of which 134 carry the Humans subject heading, 12 the clinical-trial publication type, and 11 the randomized-controlled-trial type [1]. The publication-type filter was proved live in the same run against a control term returning 8,906 records under the clinical-trial type and 6,115 under the randomized type, the invalid tag returned zero for that control term, and a deliberately invalid record identifier errored in the same run [1].
All twelve trial-type records were opened, and not one of them administers the peptide. Every one measures how much mechano growth factor a person's own muscle expresses after an intervention: resistance training with or without recombinant growth hormone [2], therapeutic ultrasound applied to skeletal muscle [3], testosterone therapy alongside resistance exercise in older men [4], neuromuscular electrical stimulation, high-intensity interval training, and comparable designs [1]. The count is a count of exercise physiology, and the exercise is the intervention.
That distinction decides what the literature can support. A study showing that heavy loading raises expression of a locally acting splice variant establishes something about how muscle responds to loading; it establishes nothing about what happens when a synthetic version of that variant is injected, because no indexed trial has done that. The gap is not that the evidence is weak. The gap is that the evidence is about a different experiment.
Lawful access
There is no lawful United States supply route. Drugs@FDA holds no approved product with mechano growth factor as an active ingredient; the same query form in the same session returned one application for bremelanotide and fourteen for liraglutide, and returned nothing for a deliberately invented ingredient name [5].
The section 503A bulks list FDA published May 14, 2026 lists mechano growth factor (MGF) in Category 3 — the file for substances nominated without adequate support to evaluate [6]. Category 3 is not a safety finding and it is not a permission; it records that the submission behind the nomination was too thin to review. The substance appears in neither Category 1 nor Category 2 of the same document.
The pegylated form is in a different position again. PEG-MGF appears in no category of that list, because its nomination was withdrawn by its nominators; FDA's Category 2 safety-risk page still carries the concern it recorded while the nomination stood, which is that the agency identified no human exposure data for the substance by any route [7]. Neither form has a route, and the reasons differ. That is the whole of what separates them.
Neither form was among the seven peptides the advisory committee reviewed in July 2026 [6]. Both are sold as research-use-only material.
Elsewhere in this index
Filed under
- Research-onlyNo lawful route
- Growth factor fragments3 molecules in this class
- The molecule indexEvery molecule, filterable by status and class
Evidence reviews
- Category 3: Nominated, Not ReviewedWhat does Category 3 of the FDA 503A bulks list actually mean?
Reference tables
- The 2026 recordWhat happened to United States peptide compounding law in 2026, in order?
- The nomination trackerWhat became of each peptide's nomination to the 503A bulks list?
- The human trial recordHow many human clinical trials exist for each peptide in this index?
- The WADA Prohibited ListWhich peptides in this index are prohibited in sport, and under which class?
References
- PubMed, National Library of Medicine. Census run 2026-09-01 across five name variants — "mechano growth factor" OR "mechano-growth factor" OR "IGF-1Ec" OR "IGF-1 Ec" OR "MGF peptide" — returning 236 indexed records, 134 carrying the Humans MeSH term, 12 under "clinical trial"[Publication Type] and 11 under "randomized controlled trial"[Publication Type]. All 12 trial-type records were retrieved through esummary and read individually; every one measures endogenous expression after an exercise or hormonal intervention and none administers the peptide. In the same run the control term aspirin returned 8,906 records under the clinical-trial filter and 6,115 under the randomized filter; the invalid tag clinicaltrial[pt] returned 0 for that same control term; and esummary on the invalid record identifier 99999999 errored. Source
- Hameed M, Lange KH, Andersen JL, Schjerling P, Kjaer M, Harridge SD, et al. The effect of recombinant human growth hormone and resistance training on IGF-I mRNA expression in the muscles of elderly men. J Physiol. 2004 Feb 15;555(Pt 1):231-40. PMID 14565994
- Delgado-Diaz DC, Gordon BS, Dompier T, Burgess S, Dumke C, Mazoué C, et al. Therapeutic ultrasound affects IGF-1 splice variant expression in human skeletal muscle. Am J Sports Med. 2011 Oct;39(10):2233-41. PMID 21785002
- Gharahdaghi N, Rudrappa S, Brook MS, Idris I, Crossland H, Hamrock C, et al. Testosterone therapy induces molecular programming augmenting physiological adaptations to resistance exercise in older men. J Cachexia Sarcopenia Muscle. 2019 Dec;10(6):1276-1294. PMID 31568675
- US Food and Drug Administration, openFDA Drugs@FDA endpoint. Absence probe run 2026-09-01: a search by active-ingredient name returned no records for mechano growth factor. In the same run and the same query form, bremelanotide returned one application and liraglutide returned fourteen, and a deliberately invented ingredient name returned none — a positive and a negative control beside the zero. Source
- US Food and Drug Administration. Bulk Drug Substances Nominated for Use in Compounding Under Section 503A of the Federal Food, Drug, and Cosmetic Act, updated May 14, 2026. Fetched and read in full 2026-09-01: Mechano growth factor (MGF) appears in Category 3; the pegylated form appears in no category. Source
- US Food and Drug Administration. Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks, content current as of April 22, 2026. Read 2026-09-01: Mechano growth factor pegylated (PEG-MGF) appears on the list of substances previously in category 2 whose nominations were withdrawn. Source