drugset / Trial / NCT06608641

Efficacy and Safety of Endoxifen in Bipolar I Disorder Patients

NCT06608641

RandomizedParallel-groupQuadruple-blindTreatment

Summary

Bipolar disorder (BPD) is a chronic debilitating illness characterized by drastic swings in mood, energy and functional ability that affects the adult population. Endoxifen is an active metabolite of the marketed drug Tamoxifen and the present study aims to evaluate the efficacy and safety of 8 mg endoxifen in the Bipolar I disorder patient population compared to a placebo arm. Endoxifen will be compared to a placebo to demonstrate that the test product is active and to establish that the study is sufficiently sensitive to detect differences between the investigational products. Thus, Endoxifen will be compared to placebo to demonstrate that the test product is safe and active.

Timeline

Start
2024-03-19
Primary completion
2025-06
Completion
2025-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Endoxifen Small molecule 8 mg Oral

Indications