Efficacy And Safety Study Of Pregabalin (Lyrica) As Monotherapy In Patients With Partial Seizures
A Double-Blind, Randomized, Multicenter Efficacy And Safety Study Of Pregabalin (Lyrica) As Monotherapy In Patients With Partial Seizures
Sponsor: Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Terminated
See termination reason in detailed description.
Other terminated trials from Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
- Pulmonary Arterial Hypertension · Phase PHASE4 · Feb 2021
- Bipolar Disorder · Phase PHASE3 · Jul 2020
- Bipolar Disorder · Phase PHASE3 · May 2020
- Chronic Low Back Pain With a Neuropathic Component · Phase PHASE4 · Jun 2015
- Adenomatous Polyposis Coli · Phase PHASE3 · Oct 2013
More terminations from Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Other Epilepsies, Partial trials with similar outcome
Listed as NCT00524030, this PHASE3 trial focuses on Epilepsies, Partial and remains terminated or withdrawn. Sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris Inc., it has been updated 10 times since 2007, reflecting substantial change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.
Status Flow
Change History
10 versions recorded-
Sep 2025 — Present [monthly]
Terminated PHASE3
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Sep 2024 — Sep 2025 [monthly]
Terminated PHASE3
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Jul 2024 — Sep 2024 [monthly]
Terminated PHASE3
-
Dec 2021 — Jul 2024 [monthly]
Terminated PHASE3
-
Feb 2021 — Dec 2021 [monthly]
Terminated PHASE3
▶ Show 5 earlier versions
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Jan 2021 — Feb 2021 [monthly]
Terminated PHASE3
-
Feb 2019 — Jan 2021 [monthly]
Terminated PHASE3
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Jun 2018 — Feb 2019 [monthly]
Terminated PHASE3
-
Feb 2017 — Jun 2018 [monthly]
Terminated PHASE3
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Jan 2017 — Feb 2017 [monthly]
Terminated PHASE3
First recorded
Sep 2007
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
For direct contact, visit the study record on ClinicalTrials.gov .