Follistatin 344
Myostatin Inhibitor Peptide
aka FS-344 · FST · follistatin · activin binding protein
A glycoprotein that binds and neutralises myostatin, the protein that naturally limits muscle growth.
Sequence
MVRARHQPGGLCLLLLLLCQFMEDRSAQAGNCWLRQAKNGRCQVLYKTELSKEECCSTGRLSTSWTEEDVNDNTLFKWMIFNGGAPNCIPCKETCENVDCGPGKKCRMNKKNKPRCVCAPDCSNITWKGPVCGLDGKTYRNECALLKARCKEQPELEVQYQGRCKKTCRDVFCPGSSTCVVDQTNNAYCVTCNRICPEPASSEQYLCGNDGVTYSSACHLRKATCLLGRSIGLAYEGKCIKAKSCEDIQCTGGKKCLWDFKVGRGRCSLCDELCPDSKSDEPVCASDNATYASECAMKEAACSSGVLLEVKHSGSCNSISEDTEEEEEDEDQDYSFPISSILEW
Mechanism of action
Follistatin 344 works by binding to and inhibiting myostatin, a protein that limits muscle growth. This inhibition allows for increased muscle cell proliferation and differentiation. Additionally, follistatin can bind to other members of the TGF-beta superfamily, potentially influencing various cellular processes. The result is enhanced muscle growth and regeneration.
What the evidence actually shows
There are currently no robust human clinical trials specifically investigating Follistatin 344. Most evidence comes from animal studies and in vitro experiments, which suggest potential for muscle growth. Human data is limited and primarily anecdotal, highlighting a significant gap in clinical research.
Regulatory status
In the UK, Follistatin 344 is considered a research compound and is not approved for medical use. It is primarily used in laboratory settings.
Source ↗Pharmacokinetics
Dosing — what backs each figure
The only human follistatin-344 studies are gene therapy, not peptide injection: AAV1.CMV.FS344 delivered once by direct bilateral intramuscular quadriceps injection at 3 x 10^11 vg/kg/leg (cohort 1) or 6 x 10^11 vg/kg/leg (cohort 2) in Becker muscular dystrophy (PMID 25322757), and 6 x 10^11 vg/kg in sporadic inclusion body myositis (PMID 28279643), plus a 43-participant phase 1 FST344 plasmid study by Minicircle (NCT06411366) that publishes no dose. There is no established - or even published - human dose for injected follistatin-344 protein.
AAV-delivered follistatin (FS344) to muscle increased muscle size and strength; translational dose-ranging preceding the human trials
mouse and non-human primate (macaque) · intramuscular AAV gene transfer · PMID 19208403
Animal doses do not convert to human doses by body weight alone. Route matters too — a compound dosed intraperitoneally in mice tells you little about subcutaneous use.
- Dose
- 100-300 mcg/day
- Frequency
- Daily for 10-30 days
- Cycle
- 10-30 day cycles· unsourced
Why this isn't evidence
No human (or animal) study has ever injected follistatin-344 protein at a microgram-per-day dose: every human trial delivered the FS344 GENE - AAV1.CMV.FS344 at 3-6 x 10^11 vg/kg/leg as a one-off intramuscular gene transfer - which is a completely different modality that cannot be converted into a daily microgram peptide dose.
This figure is shown because it is what circulates and what people search for — not because it is supported. Cycle lengths in particular tend to be convention copied between compounds rather than anything derived from a compound's own pharmacokinetics.
Handling and storage
Safety
- ·Injection site reactions
- ·Muscle pain
- ·Potential for abnormal muscle growth
- ·Unknown long-term effects
- ·Pregnancy
- ·Breastfeeding
- ·"Known hypersensitivity to follistatin"
- ·None well-documented due to limited human research
Reported combinations
- ·Creatine
- ·"Branched-chain amino acids (BCAAs)"
- ·Myostatin inhibitors (may lead to excessive muscle growth)
Combination claims in this dataset are largely unsourced and should be treated as folk knowledge until a citation appears beside them.
References (4)
- Mendell JR, Sahenk Z, Malik V, Gomez AM, Flanigan KM, Lowes LP, et al. (2015) A phase 1/2a follistatin gene therapy trial for becker muscular dystrophy ↗Mol TherPMID 25322757DOI
First-in-human phase 1/2a trial of intramuscular AAV1-FS344 gene transfer in Becker muscular dystrophy - i.e. follistatin delivered as a gene therapy vector, not as an injected protein.
- Mendell JR, Sahenk Z, Al-Zaidy S, Rodino-Klapac LR, Lowes LP, Alfano LN, et al. (2017) Follistatin Gene Therapy for Sporadic Inclusion Body Myositis Improves Functional Outcomes ↗Mol TherPMID 28279643DOI
AAV1-FS344 gene therapy trial in sporadic inclusion body myositis reporting improved functional outcomes. NOTE: this paper drew a published critique - Greenberg SA, 'Unfounded Claims of Improved Functional Outcomes Attributed to Follistatin Gene Therapy in Inclusion Body Myositis', Mol Ther 2017, PMID 28927986, doi 10.1016/j.ymthe.2017.09.002.
- Reichel C, Gmeiner G, Thevis M (2019) Detection of black market follistatin 344 ↗Drug Test AnalPMID 31758732DOI
Analysed 17 black-market products labelled 'follistatin 344' or 'follistatin 315'; only nine actually contained follistatin, and growth-promoting substances were found in some others. Confirms follistatin is prohibited under WADA chapter S4.
- Sugino H, Sugino K, Hashimoto O, et al. (1997) Follistatin and its role as an activin-binding protein ↗J Med InvestPMID 9395712
Review of follistatin's biology as an activin-binding protein, the basis for its myostatin/activin-antagonist activity.
Data provenance
Chemistry and citations on this page were checked against primary sources on 2026-08-14. Values that could not be verified were left blank rather than filled with a plausible guess.
Could not verify
molecularFormula, casNumber, pubchemCid, storage, reconstitution