Our portfolio company Juvabis AG announces the completion and positive results from its first-in-human single intravenous dose Phase 1 study in healthy volunteers. EBL-1003 (apramycin) was safe and well-tolerated in all dose groups. The results support further clinical development of EBL-1003 in patients.
Juvabis AG is a clinical-stage biopharmaceutical company focused on discovering and developing treatments in high unmet medical needs involving multidrug-resistant bacterial infections. The randomized, double-blind, placebo-controlled study was designed to assess the safety, tolerability, and pharmacokinetics of single intravenous doses in healthy volunteers. Read their press release here:JUV_PR_EBL-1003_Phase1a_20201117_juv_clean
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