That is a good question. I’m a Paramedic, so the
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Information if de-identified in these trials. A researcher may be able to determine that a patient received leronlimab, but know who that patient is.
I believe that clinical tests run do not require specific authorization. My wife has been through a bit medically, and I/we have never had to consent for specific tests (including those that ended with egregious costs as out of network immuno assays).
I hope this is helpful.
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