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The aim of this study is to assess PE-A5% as a treatment for patients with ACLF in a pivotal study Methods: A phase 3, multicenter, randomized (1:1), controlled, parallel-group, open-label study (APACHE) compares standard medical treatment (SMT) + PE-A5% (treatment arm) to SMT alone (control arm)
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In its composition has 3000mg per ampoule of L-Carnitine base
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In laboratory and pre-clinical settings, the CJC-1295 Without DAC + Ipamorelin combination has been studied as a dual-pathway tool for investigating GH axis biology
