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Background and Summary of Retrospective Studies Homocystinuria caused by congenital CBS and MTHFR defects or by genetic alteration of cobalamin metabolism is characterized by clinical problems including frequent arterial and venous thromboembolism and premature atherosclerosis (McCully, 1983
The clinical limitation is the half-life
BPC-157 demonstrates prolonged stability in both gastric juice (exceeding 24 hours) and at room temperature
If storage is sub-optimal (room temperature, high humidity, light exposure), expect significantly shorter viability (perhaps only several months for powder, or days for solution)
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