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. 2017 Nov 22;18(1):51–54. doi: 10.1007/s40268-017-0218-4
The bioavailability of orally administered des-aspartate-angiotensin I (DAA-I) was investigated in human subjects.
Prostaglandin E2 metabolite (PGEM), a stable metabolite derivative of PGE2 was measured as a biomarker of DAA-I in plasma samples obtained from 15 subjects in a single-dose phase I trial on DAA-I.
Plasma of two of the three subjects who were administered a preclinical efficacious dose of DAA-I (0.7 mg/kg) showed a significant PGEM peak concentration at 5–6 h postdose. No similar significant PGEM peak was present in the plasma of the other subjects who were administered a subefficacious and a two-time efficacious dose. This observation was in concordance with the known in vivo actions of DAA-I.