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The report was uncontrolled, unblinded, not randomized, had no comparator arm, used patient-reported outcomes rather than validated pain instruments, and did not publish dose, effect size, confidence intervals, p-values, or systematically collected adverse events limitations that severely constrain any clinical inference

The posterior predictive distributions were used to estimate various statistics on the readout responses (median, 95% credible range etc.), PoDs, Concentration Dependency Scores (CDS) and two Effect Scores (increase and decrease)

Expression of immunoglobulin-T-cell receptor chimeric molecules as functional receptors with antibody-type specificity

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