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For these individuals, the ultra-low introduction phase (weeks 1 through 4 at 0.125 to 0.5 mg) may need to be extended to 6 or even 8 weeks
Many patients create a simple chart or use their phone's reminder app to track which site they used each week
Adverse side effects or other safety risks associated with azelaprag or any future product candidates we may develop could delay or preclude approval, cause us to suspend or discontinue clinical trials or abandon further development, change the design of our clinical trials, limit the commercial profile of an approved product, or result in significant negative consequences following regulatory approval, if any
BPC-157 is most associated in animal studies with new blood vessel formation and tissue protection at the injury site
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