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[5] In this multinational, non-randomized, open-label trial, investigators first gave a single 0.3-mg subcutaneous dose to people with Child-Pugh class A, B, or C cirrhosis and to matched healthy individuals, measuring pharmacokinetics
Bisher wurde keine klinische Phase-III-Studie am Menschen in indexierten Fachzeitschriften verffentlicht
Combining the contents of two separate, opened vials dramatically increases the risk of cross-contamination