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Study 1 (NCT 00123253) This study re-randomized 207 HIV-infected patients with lipodystrophy who completed a 2 mg dose of EGRIFTA (1 mg/vial formulation) treatment in the Main Phase to receive either EGRIFTA (N=154) or placebo (N=50) for an additional 26-week duration (3:1 randomization ratio)

Canadian Regulatory Context BPC-157 is not approved by Health Canada for human therapeutic use

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Part of the PlexusDx Education Hub, this article sits alongside our wider coverage of longevity protocols and the genetics that shape metabolic decisions

The primary difference between BPC-157 sellers is not availability, but transparency and verification