Saniona Files FDA IND for SAN2465 in Major Depressive Disorder
Saniona submitted an IND to the FDA for SAN2465. A Phase 1 study in healthy volunteers is expected to begin by the end of 2026, contingent on FDA clearance.
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Saniona submitted an IND to the FDA for SAN2465. A Phase 1 study in healthy volunteers is expected to begin by the end of 2026, contingent on FDA clearance.