TB-500 and Thymosin Beta-4 are also prohibited by WADA/USADA under S2 (Peptide Hormones, Growth Factors, Related Substances and Mimetics), applicable at all times both in-competition and out-of-competition TB-500 / Thymosin Beta-4 Clinical Trials: The RGN-352 and RGN-259 Programs RegeneRx Biopharmaceuticals has pursued two clinical development programs for Thymosin Beta-4, providing the most substantial human clinical data available for any TB-500-related compound: RGN-352 (Injectable Thymosin Beta-4 for Cardiac Repair): Phase 1 trial (completed): A double-blind, placebo-controlled study enrolled 40 healthy volunteers across four cohorts of 10 subjects each, testing escalating dose levels of intravenous Thymosin Beta-4 administered daily over 14 days
TB-500 is a 43-amino acid polypeptide that functions as the primary G-actin sequestering molecule in eukaryotic cells
Research Classification Storage Information BPC-157 Purity & COA Verification Read the BPC-157 research Research-only pharmacokinetic profile of BPC-157: serum half-life, Tmax, route comparisons, clearance and bioavailability curated from published preclinical and clinical PK literature
Units to draw = Desired dose (mg) x 100 / Concentration (mg/mL) At 10 mg/mL, this simplifies to: Units = Desired dose (mg) x 10 That is it
Approximately 5 peptides are expected to remain restricted