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and evaluating LPA inhibitor combinations with AR blockade, immunotherapy, and metabolic interventions in preclinical models, followed by rapid clinical translation through micro-dose or umbrella trials

4c, d), suggesting an improvement in anti-inflammatory capacity

To begin to evaluate the potential clinical utility of dihexa Adult male Sprague- Dawley rats were administered 10 mg/kg dihexa intravenously and in~vivo pharmacokinetics determined

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