Partial SeizuresNCT04257604
A Study of Perampanel as Add-on Therapy in Adult and Adolescent Participants With Focal Seizures
An observational study of Partial Seizures, run by Eisai Limited.
Trial summary
The primary objective of the present study will be to assess the effectiveness of add-on perampanel in participants with focal seizures in a real-life clinical setting. Read more about this study
- Who is it for?
- Ages 12 years and older
- Conditions the study is for
- Partial Seizures
- What is being tested?
- Perampanel
- Type of treatment
- Pill or oral medicine
- How many people
- 243 participants
- Where
- No sites listed yet
- Study dates
- 3 Jan 2016to 30 Apr 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 12 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Participants with epilepsy aged 12 years or older.
Who may be able to join
- Prescribe perampanel according to the approved indication
- Participants with focal seizures with or without secondary generalization
- Participants with seizure frequency data available at the baseline visit
- Based on the physician's clinical judgment, the participant seizure activity is not controlled sufficiently with the current treatment with 1-3 AEDs and it is in the participants best interest to be prescribed adjunctive perampanel
- The decision to prescribe perampanel is made by the physician before and independently of his/her decision to include the participant in the study
- Treatment with perampanel is not yet started before baseline
Who cannot join
- Participants contraindicated for perampanel use (according to SmPC)
- Participants with moderate to severe renal impairment
- Participants with severe hepatic impairment
- Pregnant or lactating women
- Participants suffering from clinically significant psychiatric illness, psychological or behavioral problems which could interfere with study participation
About this study
Official title: A Multicenter, Prospective, Real-life Observational Study of Perampanel as Add-on Therapy in Adult and Adolescent Patients With Focal Seizures (A Mirroring Clinical Practice Study of Perampanel in Adults and Adolescents) (The AMPA Study)
The primary objective of the present study will be to assess the effectiveness of add-on perampanel in participants with focal seizures in a real-life clinical setting.
- Conditions
- Partial Seizures
- Being tested
- Perampanel
- Keywords
- Perampanel, Partial seizures, Focal seizures
- Medical subject headings
- Seizures
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PerampanelDrug
Also called Fycompa, E2007
Perampanel tablets.
| Study group | Role | What they receive |
|---|---|---|
| Perampanel | Participants with partial-onset seizures, with or without secondary generalization will receive perampanel tablets as add-on therapy according to the approved summary of product characteristics (SmPC) after the baseline visit as part of the clinical practice and will be observed after 3 months (visit 1), 6 months (visit 2), and 12 months (final visit). Receives: Drug: Perampanel |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage Change From Baseline in all Seizures Frequency at Month 6
Seizure frequency is derived from information (seizure count and type) recorded in participant diary. Seizure frequency is based on the number of seizures per 28 days, calculated as the number of seizures over the entire time interval divided by the number of days in the interval and multiplied by 28.
Measured: Baseline, Month 6
Secondary outcomes (14)
Percentage of Participants Remaining on Perampanel at Months 6 and 12
The retention rate is defined as the percentage of participants remaining on perampanel, starting from the first dose of study drug.
Measured: Months 6 and 12
Percentage of Participants With Adverse Drug Reactions (ADRs) and Serious Adverse Drug Reactions (SADRs)
ADR is a noxious and unintended response to a medicinal product related to any dose. A causal relationship between the medicinal product and the adverse response is at least a reasonable possibility. A SADR is any untoward medical occurrence that at any dose results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization¸ results in persistent or significant disability/incapacity, or is a congenital anomaly/birth defect.
Measured: Up to Month 12
Percentage of Participants Who Withdraw due to ADR
ADR is a noxious and unintended response to a medicinal product related to any dose. A causal relationship between the medicinal product and the adverse response is at least a reasonable possibility.
Measured: Up to Month 12
Percentage of Participants Who Withdraw due to Lack of Efficacy
Lack of efficacy is if the participant had poor seizure control (defined as experiencing a seizure despite being on the maximum dose for equal to 2 weeks). The participant can withdraw at any time due to lack of efficacy.
Measured: Up to Month 12
Mean Change From Baseline in the Number of Concomitant Anti-epileptic Drugs (AEDs)
Change from baseline in the number of concomitant AEDs along with the Perampanel will be reported.
Measured: Baseline up to Month 12
Percentage of Participants With at Least 50 Percent (%) and 75% Reduction From Baseline in All Seizure Frequency at Months 3, 6 and 12
A 50% or 75% responder rate is percentage of participants who experience at least 50% or 75% reduction in all seizure frequency during the study.
Measured: Baseline, Months 3, 6, and 12
Percentage of Participants With at Least 50% and 75% Reduction From Baseline in Secondarily Generalized Tonic-clonic Seizures (SGTCS) Frequency at Months 3, 6 and 12
A 50% or 75% responder rate for SGTCS is percentage of participants who experience at least 50% or 75% reduction of SGTCS frequency during the study. Focal to bilateral toni-clonic seizures (FBTCS) replaces older term SGTCS. FBTCS is a seizure type with focal onset, with awareness or impaired awareness, either motor or nonmotor, progressing to bilateral tonic-clonic activity.
Measured: Baseline, Months 3, 6, and 12
Percentage of Participants Who Were Seizure-free
Participants will be considered seizure-free if participants will not experience any partial-onset seizure during the study.
Measured: Up to Month 12
Median Percentage Change From Baseline in All Seizure Frequency at Months 3 and 12
Seizure frequency is based on the number of seizures per 28 days, calculated as the number of seizures over the entire time interval divided by the number of days in the interval and multiplied by 28.
Measured: Baseline, Months 3 and 12
Median Percentage Change From Baseline in SGTCS Frequency at Months 3, 6 and 12
SGTCS frequency is based on the number of SGTC seizures per 28 days, calculated as the number of SGTC seizures over the entire time interval divided by the number of days in the interval and multiplied by 28. FBTCS replaces older term SGTCS. FBTCS is a seizure type with focal onset, with awareness or impaired awareness, either motor or nonmotor, progressing to bilateral tonic-clonic activity.
Measured: Baseline, Months 3, 6, and 12
Mean Change From Baseline in 31-item Quality of Life in Epilepsy (QOLIE-31) Questionnaire Score in Adult Participants at Month 6 and 12
The Italian version of the QOLIE-31 will be used in this study. The QOLIE-31 inventory is a 31-item self-administered questionnaire evaluating Quality of Life (QOL) perception in adults 18 years or older with epilepsy in 7 domains: seizure worry, emotional wellbeing, energy/fatigue, cognitive functioning, medication effects, social functioning, overall QOL. The overall score is derived by weighing and then summing the 7 domain scores. Pre-coded numeric values for some domains are such that a higher number reflects a more favorable health state; others are such that a higher number reflects a less favorable state. Pre-coded values are converted to 0 to 100 point scores; a higher converted score indicates a higher self-reported QOL.
Measured: Baseline, Months 6 and 12
Mean Change From Baseline in Epworth Sleepiness Scale (ESS) Score in Adult Participants at Months 3, 6, and 12
The ESS is a self-administered questionnaire with 8 questions. It provides a measure of a participant's general level of daytime sleepiness, or average sleep propensity in daily life. The ESS asks the participant to rate, on a 4-point scale (0 [low] to 3 [high]) his or her usual chances of dozing off or falling asleep in 8 different situations or activities that most people engage in as part of their daily lives. The total ESS score provides an estimate of a general characteristic of each person's average level of sleepiness in daily life (0= no chance of dozing/no daytime sleepiness to 24=high chance of dozing/lots of daytime sleepiness).
Measured: Baseline, Months 3, 6, and 12
Mean Change From Baseline in Irritability With Epilepsy Questionnaire Score (I-Epi) in Adult Participants at Months 3, 6, and 12
I-Epi is a questionnaire specific for the assessment of irritability in adult participants with epilepsy. I-Epi is an 18-item self-administered questionnaire based on four dimensions related to irritability in participants affected by epilepsy (physical functioning, verbal functioning, temperamental functioning, and epilepsy functioning). Participants have to rate their irritability level on a 6-point Likert scale where 1="never," 2="almost never," 3="rarely,"4="sometimes," 5="often," and 6="always". Higher score means more irritability.
Measured: Baseline, Months 3, 6, and 12
Regression Coefficient For Predictive Factors in Response to Perampanel
Predictive factors include age, age greater than or equal to (>=) 60 years, age less than (<) 18 years, gender, body mass index (BMI), age at seizure onset, age at diagnosis of epilepsy, time since diagnosis of epilepsy, baseline 28-day seizure frequency, seizure type, epilepsy familiarity (yes or no), epilepsy surgery (yes or no), focal known etiology (yes or unknown), number of seizures at baseline, number of AEDs at baseline, presence or absence of enzyme-inducing AEDs, eziologia vascolare (yes versus other). Regression coefficient will be determined to characterize the association between predictive factors and response to perampanel.
Measured: Up to Month 12
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Feb 2020
- Study start3 Jan 2016
- Primary completion30 Apr 2019
- Study completion30 Apr 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Partial SeizuresStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 243 participants (actual)
Sponsor and investigators
- Lead sponsor
- Eisai Limited
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04257604
- Sponsor's protocol ID
- E2007-M044-501
- Status last verified
- Jan 2020
- First submitted
- 10 Jan 2020
- Last updated
- 6 Feb 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Yes: Eisai's data sharing commitment and further information on how to request data can be found on our website http://eisaiclinicaltrials.com/.
Publications
Liguori C, Assenza G, Chiacchiaretta M, Patten A, Sainz-Fuertes R, Gentile AL. Effect of adjunctive perampanel on daytime sleepiness and quality of life in adults with focal-onset seizures: Post hoc analyses of the AMPA study. Epilepsy Behav. 2026 May;178:110962. doi: 10.1016/j.yebeh.2026.110962. Epub 2026 Feb 21.
PubMed 41724127
Study at a glance
From the registry record, last updated by the sponsor on 6 Feb 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Multicenter, Prospective, Real-life Observational Study of Perampanel as Add-on Therapy in Adult and Adolescent Patients With Focal Seizures (A Mirroring Clinical Practice Study of Perampanel in Adults and Adolescents) (The AMPA Study)
- ClinicalTrials.gov ID
- NCT04257604
- Acronym / sponsor ID
- E2007-M044-501
- Conditions
- Partial Seizures
- Keywords
- Perampanel, Partial seizures, Focal seizures
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 243 participants (actual)
- Lead sponsor
- Eisai LimitedIndustry (pharma, biotech, devices)
- Study start
- 3 Jan 2016 (actual)
- Primary completion
- 30 Apr 2019 (actual)
- Study completion
- 30 Apr 2019 (actual)
- First posted
- 6 Feb 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The primary objective of the present study will be to assess the effectiveness of add-on perampanel in participants with focal seizures in a real-life clinical setting.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Perampanel | – | Drug: PerampanelParticipants with partial-onset seizures, with or without secondary generalization will receive perampanel tablets as add-on therapy according to the approved summary of product characteristics (SmPC) after the baseline visit as part of the clinical practice and will be observed after 3 months (visit 1), 6 months (visit 2), and 12 months (final visit). |
Who may qualify
- Ages
- 12 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Participants with epilepsy aged 12 years or older.
Key inclusion criteria (6 listed)
- Prescribe perampanel according to the approved indication
- Participants with focal seizures with or without secondary generalization
- Participants with seizure frequency data available at the baseline visit
- Based on the physician's clinical judgment, the participant seizure activity is not controlled sufficiently with the current treatment with 1-3 AEDs and it is in the participants best interest to be prescribed adjunctive perampanel
- The decision to prescribe perampanel is made by the physician before and independently of his/her decision to include the participant in the study
Key exclusion criteria (5 listed)
- Participants contraindicated for perampanel use (according to SmPC)
- Participants with moderate to severe renal impairment
- Participants with severe hepatic impairment
- Pregnant or lactating women
- Participants suffering from clinically significant psychiatric illness, psychological or behavioral problems which could interfere with study participation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PerampanelAlso: Fycompa, E2007Perampanel tablets. | Drug | Perampanel |
Primary outcome
Percentage Change From Baseline in all Seizures Frequency at Month 6
Time frame: Baseline, Month 6
Seizure frequency is derived from information (seizure count and type) recorded in participant diary. Seizure frequency is based on the number of seizures per 28 days, calculated as the number of seizures over the entire time interval divided by the number of days in the interval and multiplied by 28.
14 secondary outcomes
Percentage of Participants Remaining on Perampanel at Months 6 and 12
Time frame: Months 6 and 12
Percentage of Participants With Adverse Drug Reactions (ADRs) and Serious Adverse Drug Reactions (SADRs)
Time frame: Up to Month 12
Percentage of Participants Who Withdraw due to ADR
Time frame: Up to Month 12
Percentage of Participants Who Withdraw due to Lack of Efficacy
Time frame: Up to Month 12
Mean Change From Baseline in the Number of Concomitant Anti-epileptic Drugs (AEDs)
Time frame: Baseline up to Month 12
Percentage of Participants With at Least 50 Percent (%) and 75% Reduction From Baseline in All Seizure Frequency at Months 3, 6 and 12
Time frame: Baseline, Months 3, 6, and 12
Percentage of Participants With at Least 50% and 75% Reduction From Baseline in Secondarily Generalized Tonic-clonic Seizures (SGTCS) Frequency at Months 3, 6 and 12
Time frame: Baseline, Months 3, 6, and 12
Percentage of Participants Who Were Seizure-free
Time frame: Up to Month 12
Median Percentage Change From Baseline in All Seizure Frequency at Months 3 and 12
Time frame: Baseline, Months 3 and 12
Median Percentage Change From Baseline in SGTCS Frequency at Months 3, 6 and 12
Time frame: Baseline, Months 3, 6, and 12
Mean Change From Baseline in 31-item Quality of Life in Epilepsy (QOLIE-31) Questionnaire Score in Adult Participants at Month 6 and 12
Time frame: Baseline, Months 6 and 12
Mean Change From Baseline in Epworth Sleepiness Scale (ESS) Score in Adult Participants at Months 3, 6, and 12
Time frame: Baseline, Months 3, 6, and 12
Mean Change From Baseline in Irritability With Epilepsy Questionnaire Score (I-Epi) in Adult Participants at Months 3, 6, and 12
Time frame: Baseline, Months 3, 6, and 12
Regression Coefficient For Predictive Factors in Response to Perampanel
Time frame: Up to Month 12
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Feb 2020.
- Derived from this study: PubMed 41724127Liguori C, Assenza G, Chiacchiaretta M, Patten A, Sainz-Fuertes R, Gentile AL. Effect of adjunctive perampanel on daytime sleepiness and quality of life in adults with focal-onset seizures: Post hoc analyses of the AMPA study. Epilepsy Behav. 2026 May;178:110962. doi: 10.1016/j.yebeh.2026.110962. Epub 2026 Feb 21.
- Individual participant dataSharing planned: Yes. Eisai's data sharing commitment and further information on how to request data can be found on our website http://eisaiclinicaltrials.com/.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Partial Seizures, run by Eisai Limited.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 6 Feb 2020. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage Change From Baseline in all Seizures Frequency at Month 6 (time frame: Baseline, Month 6). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04257604, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Feb 2020.