Community / anecdotal. Community / anecdotal — no regulatory basis. Not medical advice.
Typical — reference only
~2-2.5 mg per injection, weekly (loading then maintenance)
Worked reconstitution example
10 mg vial + 2 mL BAC = 5 mg/mL; 2.5 mg = 50 U, 2 mg = 40 U on U-100. mg-dosed (mcg confusion = 1000x).
Titration
No real titration; some start ~2 mg to gauge tolerance
Units are not milligrams. mg-vs-mcg confusion drives documented 5–1000× overdoses — always recompute for your own vial (use the calculator →).
Removal from Category 2 ≠ legal to compound ≠ FDA-approved. Removal != legal/approved. WADA S0 prohibited at all times.
StatusRemoved from Cat 2 · pending PCAC
503A bulksNot on the bulks list
Category 2 (2026)Removed from Category 2 Apr 2026
PCAC review2026-07-23/24
WADAProhibited (S0)
03Evidence — the honest read
Danimal-only
Animal-only for consumer use. The sold molecule is a 7-aa FRAGMENT distinct from full-length Tbeta4 used in (unrelated, unpublished) human programs. Zero completed efficacy RCTs. Viral '4.8% LVEF' stat is a vendor-blog fabrication.
Contraindications
- Active/recent cancer (angiogenesis; ~5 yr commonly cited)
- Pregnancyhard stop
- WADA athletes/military
- Bleeding disorders (cautious)
Key interactions
- Anticoagulants/antiplatelets (plausible, unvalidated)
- VEGF inhibitors / antiangiogenic chemo (mechanistically opposed - double contraindication)
Serious signals
- Pro-angiogenic/cancer signal (theoretical)
- Fragment PK unknown in humans
- Marketed fragment may be inactive species
Monitoring
No validated cadence; cancer screening (harm-reduction).
01ClinicalTrials.gov NCT07487363
+PepTrack research dossier — iterations 1–4, 584 de-duplicated sources, adversarially verified.
Not medical or legal advice. Educational / harm-reduction reference. Regulatory and dosing claims in this field move monthly — re-verify against primary sources (FDA docket FDA-2025-N-6895, DailyMed, ClinicalTrials.gov) before acting.
Last reviewed — 2026-06-13 · confidence: med-high