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Spots Global Cancer Trial Database for A Study to Evaluate the Safety and Tolerability of Intravenous Brivaracetam (BRV) as Replacement for Oral Brivaracetam in Japanese Subjects >=16 Years of Age With Partial Seizures With or Without Secondary Generalization

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Trial Identification

Brief Title: A Study to Evaluate the Safety and Tolerability of Intravenous Brivaracetam (BRV) as Replacement for Oral Brivaracetam in Japanese Subjects >=16 Years of Age With Partial Seizures With or Without Secondary Generalization

Official Title: A Multicenter, Open-Label Study to Evaluate the Safety and Tolerability of Intravenous Brivaracetam as Replacement for Oral Brivaracetam in Japanese Subjects >=16 Years of Age With Partial Seizures With or Without Secondary Generalization

Study ID: NCT03685630

Interventions

Brivaracetam

Study Description

Brief Summary: The purpose of the study is to evaluate the safety and tolerability of intravenous (iv) brivaracetam (BRV) as adjunctive therapy administered as a replacement for oral BRV at doses ranging from BRV 50 mg/day to 200 mg/day in Japanese subjects \>=16 years of age with partial seizures with or without secondary generalization and to evaluate the partial seizure frequency after switching from oral administration to iv BRV.

Detailed Description:

Eligibility

Minimum Age: 16 Years

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Ep0118 116, Asaka, , Japan

Ep0118 126, Bunkyo, , Japan

Ep0118 111, Hamamatsu, , Japan

Ep0118 121, Itami, , Japan

Ep0118 142, Kamakura, , Japan

Ep0118 112, Koshi, , Japan

Ep0118 104, Shizuoka, , Japan

Ep0118 138, Tsukuba, , Japan

Ep0118 109, Yamagata, , Japan

Contact Details

Name: UCB Cares

Affiliation: 001 844 599 2273 (UCB)

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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