Follistatin isoform FST-344 (recombinant human follistatin, 344 amino acids)
Human data is very limited. Most evidence comes from case reports or observational studies.
A naturally occurring protein that blocks signals limiting muscle growth. A gene therapy version showed promise for Becker muscular dystrophy in a small clinical trial. The injectable form available through unregulated sources has no controlled human evidence and quality cannot be guaranteed.
This entry is a cited research summary, not an established treatment reference. Dosing language is included as source context, not as medical instruction.
Follistatin 344 has limited human evidence; signal requires confirmation.
Human data is very limited. Most evidence comes from case reports or observational studies.
Safety data is extremely limited for injectable recombinant follistatin. No consistent side-effect profile for direct FS344 peptide use has been established. The most controlled data comes from AAV gene therapy trials: the Phase 1/2a BMD trial (6 patients) reported no adverse effects (PMC5240576; PMC4426808), and the sIBM trial (3 patients at low dose) reported no adverse events PMC5240576. Minicircle's gene therapy program (500+ patients) reported the most common side effect as a slight LDL increase (~8 mg/dl) in roughly one-third of patients, which they describe as not clinically significant (minicircle.io). Community reports of injectable use include flu-like symptoms from a single online communities user, and weakened ligaments/tendons from bodybuilding community reports (SelfHacked). These effects may be attributable to product impurities rather than follistatin itself, given that only 9/17 tested products contained actual follistatin PMID 31758732. Myostatin is expressed in cardiac tissue, and chronic inhibition raises theoretical cardiovascular concerns, but no long-term human data addresses this (peptidesunleashed.com). Black-market adulteration remains a separate and substantial safety concern PMID 31758732.
If real-world use or exposure is being considered, review potential interactions, contraindications, and monitoring needs with a licensed clinician rather than relying on summary copy alone.
Every claim on this page links to one of the 10 sources below. Identifiers are PubMed (PMID), ClinicalTrials.gov (NCT), or DOI; click through to the source of record before acting on a claim.