BPC-157 Dosage Guide: Injection & Oral Protocols
Comprehensive BPC-157 dosage guide covering subcutaneous, intramuscular, and oral administration protocols. Includes reconstitution instructions, cycle guidance, stacking considerations, and references to published preclinical research on this gastric pentadecapeptide.
Medical Disclaimer
This guide is for educational and informational purposes only. It is not medical advice. Dosages described reflect ranges discussed in published research and clinical practice literature — they are not recommendations. Always consult a licensed healthcare provider before using any peptide. Legality and availability vary by jurisdiction.
Overview
BPC-157 (Body Protection Compound-157) is a synthetic pentadecapeptide derived from a partial sequence of human gastric juice protein. It consists of 15 amino acids and has been the subject of extensive preclinical research since the 1990s, with published studies investigating its effects on wound healing, tendon and ligament repair, gastrointestinal mucosal protection, and various organ injuries in animal models. The peptide has demonstrated cytoprotective properties in over 100 published animal studies, with proposed mechanisms involving modulation of the nitric oxide system, growth factor upregulation (including VEGF and EGF), and interaction with the dopaminergic system. Despite this substantial preclinical evidence base, no completed human clinical trials have been published as of the current date, and BPC-157 is not FDA approved for any indication. Dosage protocols in circulation are extrapolated from animal study data and anecdotal practitioner experience.
Dosing Protocols
Subcutaneous Injection — Standard
Subcutaneous injection near the site of injury is the most commonly discussed administration route. A dose of 250–500 mcg once or twice daily is the most frequently referenced protocol in practitioner communities. The rationale for local injection is based on animal studies suggesting local tissue effects, though systemic activity has also been reported in preclinical research.
Subcutaneous Injection — Lower Dose
A lower dose approach is sometimes discussed for general systemic support or for individuals new to the peptide. Some practitioners suggest starting at a lower dose to assess tolerability before escalating to the standard 250–500 mcg range.
Oral Administration — Gut Health
Oral BPC-157 is discussed primarily for gastrointestinal applications (gut lining support, mucosal protection). BPC-157 has shown stability in gastric juice in preclinical studies, which is unusual for peptides. Oral dosing is often higher than injection dosing because oral bioavailability is lower. Some sources suggest holding the solution sublingually for 60–90 seconds before swallowing.
Intramuscular Injection
Intramuscular injection is sometimes discussed for muscle injury or deep tissue concerns. The dose is similar to subcutaneous protocols. Injection into the belly of the affected muscle is the commonly described approach, though evidence for superiority over subcutaneous administration is anecdotal.
Reconstitution & Storage
| Vial sizes | 5 mg lyophilized vials (most common); 2 mg and 10 mg vials also available from some suppliers |
| Recommended water volume | 2 mL bacteriostatic water (BAC water) per 5 mg vial yields a concentration of 2.5 mg/mL (2,500 mcg/mL). At this concentration: 0.1 mL = 250 mcg, 0.2 mL = 500 mcg. Some users prefer 1 mL BAC water for a 5 mg/mL concentration to minimize injection volume. |
| Storage | Store unreconstituted vials at room temperature or refrigerated. After reconstitution, refrigerate at 36–46 °F (2–8 °C). Keep away from direct sunlight. |
| Stability once reconstituted | Reconstituted BPC-157 is generally considered stable for up to 30 days when refrigerated. Some sources suggest peptide degradation may begin after 2–3 weeks. Discard if solution becomes cloudy or discolored. |
Use our reconstitution calculator to determine exact syringe units for your dose.
Cycle Guidance
BPC-157 is most commonly discussed in cycles of 4–8 weeks, followed by an off-cycle period of equal duration before repeating if needed. The rationale for cycling is primarily precautionary — there is limited data on long-term continuous use. Some practitioners suggest that BPC-157 produces its primary effects within the first 4–6 weeks for acute injury applications, making extended use unnecessary for specific healing goals. For chronic conditions such as ongoing gut health support, some practitioners have discussed longer protocols of 8–12 weeks. There is no published human data establishing optimal cycle duration, and recommendations are derived from practitioner experience and extrapolation from animal study timelines.
Stacking Considerations
- BPC-157 is frequently discussed in combination with TB-500 (Thymosin Beta-4 fragment) for injury recovery — the proposed rationale is complementary healing mechanisms (BPC-157 for local tissue repair and angiogenesis, TB-500 for systemic anti-inflammatory and cell migration effects).
- Some practitioners combine BPC-157 with GHK-Cu for skin and wound healing applications, citing complementary mechanisms involving collagen synthesis and tissue remodeling.
- BPC-157 has been discussed alongside growth hormone secretagogues (e.g., Ipamorelin, CJC-1295) in the context of recovery optimization, though no published data evaluate these specific combinations.
- Preclinical research has investigated BPC-157 in the context of NSAID-induced gastrointestinal damage, suggesting potential protective effects — some practitioners discuss this as a rationale for concurrent use during NSAID therapy, though human data are lacking.
- BPC-157 has shown interactions with the dopaminergic system in animal studies, which is relevant when considering concurrent use with dopamine-affecting medications or supplements.
Potential Side Effects
- No significant adverse effects have been reported in the published preclinical literature at the doses studied
- Mild injection site discomfort (redness, swelling) — reported anecdotally and generally transient
- Mild nausea when taken orally (reported anecdotally, typically at higher doses)
- Lightheadedness or dizziness (reported infrequently in anecdotal accounts)
- Headache (reported infrequently in anecdotal accounts)
- Theoretical concern regarding angiogenesis promotion in individuals with existing tumors — BPC-157 upregulates VEGF in preclinical studies, which is relevant for individuals with active malignancies
- Long-term safety in humans is unknown due to the absence of completed human clinical trials
Contraindications & Cautions
- Active cancer or history of cancer — due to BPC-157's pro-angiogenic properties (VEGF upregulation) observed in preclinical studies, there is a theoretical risk of promoting tumor vascularization
- Pregnancy and breastfeeding — no safety data available
- Children and adolescents — no safety data available
- Known hypersensitivity to any component of the formulation
- Individuals on anticoagulant therapy should exercise caution, as some preclinical data suggest BPC-157 may influence platelet function (evidence is limited and conflicting)
- Note: Because no human clinical trials have been completed, the full contraindication profile is not established and all use carries inherent uncertainty
Related
References
- Stable Gastric Pentadecapeptide BPC 157: Novel Therapy in Gastrointestinal Tract (2011) — PubMed
- Pentadecapeptide BPC 157 — a Review of Pharmacological Effects and Mechanisms of Action (2020) — PubMed
- Pentadecapeptide BPC 157 Enhances the Growth Hormone Receptor Expression in Tendon Fibroblasts (2011) — PubMed
- BPC 157 and Its Role in Accelerating Wound Healing (2020) — PubMed
- Stable Gastric Pentadecapeptide BPC 157 in Trials for Inflammatory Bowel Disease (2022) — PubMed