An Open-Label, Randomized, Crossover Study to Assess the Comparative Bioavailability of New TEV-56286 Formulations Compared to a Reference TEV-56286 Capsule Formulation Following Single-Dose Administration in Healthy Participants
Teva Identifier
TV56286-BA-10218
ClinicalTrials.gov Identifier
NCT06911567
Study Status
Recruiting
Trial Condition(s)
Healthy Participants
Interventions
Drug: TEV-56286 Test | Drug: TEV-56286 Reference
Study Description
The primary objective of the study is to assess the relative bioavailability of TEV-56286 test formulations compared to TEV-56286 reference product in healthy adult participants.
The secondary objective is to evaluate the safety and tolerability of TEV-56286.
The planned duration for each participant is approximately 70 days which includes a 45 day screening period.
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