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Only clinical study designs (S)randomised controlled trials (RCTs), non-RCTs, cohort, or case-control studieswere included

During this initial phase, its important to monitor for any adverse reactions and assess individual tolerance

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Regulatory and safety status: Emideltide is not approved for use in humans and is currently pending FDA review

Figure 2 While depletion of B cells and loss of antibodies is a reported side-effect of Daratumumab treatment, we also observed strong depletion of CD38+ CD8+ T cell subsets that was previously unreported ( Figure 2B ) ( Figure 2B )