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[ 89 Zr]Zr-DFO-daratumumab demonstrated the ability to detect MM with high sensitivity, localise tumor cell infiltration and quantify disease burden

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Matt Lash, an FDA official, in the meeting on Thursday said the compounded products have not been approved by the FDA and added that compounded products are not required to have labels that notify patients of any safety or doses

Consistent Use (Refills): The clinic tracked prescription refill rates as a surrogate for efficacy/satisfaction

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Treatment should be discontinued if patients have not lost at least 5% of their initial body weight after 12 weeks on the maintenance dose of 3.0 mg