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Within approved clinical trial settings, the preparation of injectable investigational medicinal products (IMPs) must comply with Good Clinical Practice (GCP), the trial protocol, and local aseptic compounding policies
doi: 10.21037/atm.2020.02.172 98 LiuWJShenTTChenRHWuHLWangYJDengJKet al
Eli Lilly is on track to apply for FDA approval by late 2025, the drugmaker announced
doi: 10.1007/s11255-020-02585-w 35 BernardiSMichelliAZuoloGCandidoRFabrisB
Patients receive medication that reflects their body, lifestyle, and goals
Titration Approach Increasing the dose gradually, typically every four weeks, minimizes side effects while building toward an effective maintenance level
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