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Some preclinical data suggests BPC-157 demonstrates oral bioavailability, but direct comparisons between injectable study protocols and oral supplementation in humans have not been established through clinical research

However, the company says they intend to engage the FDA to explore efficient ways to make this medicine available to patients in need. The National Institute of Allergy and Infectious Diseases (NIAID), a part of the United States NIH, is also testing a treatment for CGD in a phase I/II trial

Periodic reassessment every 6 to 12 weeks by labs and outcome measures enables clinicians to fine-tune the protocol

For systemic effects such as gut healing, systemic anti-inflammation, or neurological support, subcutaneous injection into the abdominal area is typically preferred

The site does not recommend or urge the use of its products on humans or animals.

Lujaine AbuBajeh, for her assistance in data extraction and data entry