BPC 157 Safety and Medical Use
BPC 157 should not be used for medical treatment without supervision as it lacks FDA approval and sufficient clinical evidence supporting its safety and efficacy in humans.
Current Regulatory Status
- BPC 157 (Body Protection Compound 157) is a pentadecapeptide isolated from human gastric juice 1
- Not approved by the FDA or other global regulatory authorities for medical use 1, 2
- Was temporarily banned by the World Anti-Doping Agency (WADA) in 2022 1
- Currently used by some clinicians and athletes despite lack of regulatory approval 2
Available Evidence on BPC 157
Preclinical Evidence
- Demonstrated pleiotropic effects in various preclinical models including:
Clinical Evidence
- Extremely limited human data available
- One retrospective study showed 7 of 12 patients reported relief for >6 months after intraarticular injection for chronic knee pain 2
- A small pilot study (n=2) of intravenous BPC 157 (10-20mg) reported no adverse effects in healthy adults who had previously received the compound 5
Safety Concerns
- Lack of comprehensive clinical trials evaluating safety in humans
- No standardized dosing protocols established
- Potential risks include:
- Unregulated manufacturing processes
- Possible contamination
- Unknown drug interactions
- Unpredictable adverse effects 2
Pharmacokinetics
- Metabolized in the liver
- Half-life less than 30 minutes
- Cleared by the kidneys 2
Expert Recommendation
For individuals interested in BPC 157:
- Consult with a healthcare provider before considering use
- Understand the experimental nature of this compound
- Be aware of potential regulatory issues with sports organizations
- Consider FDA-approved alternatives with established safety profiles
Conclusion
While preclinical studies suggest potential benefits of BPC 157 for various conditions, particularly musculoskeletal injuries, the lack of robust clinical trials, standardized formulations, and regulatory approval makes unsupervised use inadvisable. The single small human safety study 5 is insufficient to establish safety across broader populations or for various administration routes. Patients should work with healthcare providers to explore evidence-based, approved treatment options for their conditions.