Flexible Study Visits
You may complete some study
visits from home.
Could More Seizure-Free Days Be in Your Future?
Participate in POWER2, an epilepsy study that offers the convenience of completing some visits from home.
Could More Seizure-Free Days Be in Your Future?
Participate in POWER2, an epilepsy study that offers the convenience of completing some visits from home.
About the POWER2 study
The POWER2 study is a research study evaluating a new investigational
medicine,
in accordance with FDA requirements, as a potential treatment for focal
onset seizures
in adults.
No Cost
Any travel expenses and other costs
associated with the study will be paid by
the sponsor. Insurance is not required.
Duration
Up to 6 weeks of screening, followed by a 12 week study treatment period with an option to receive vormatrigine for up to 2 years, in an open-label extension.
If you are considering joining this study, the first step is to answer a questionnaire about your health and medical history. If you qualify, you can schedule time with one of our trial navigators to hear more about the study.
Why take part?
If you qualify and decide to participate, you will receive
All study-related care at no cost, including travel expenses
Close monitoring by an experienced doctor and study staff who understand epilepsy
The opportunity to advance medical knowledge and potentially help others with epilepsy
Option to enroll in an extension study and receive vormatrigine treatment for up to 2 years, after completing participation in the initial study
If you ever have questions or concerns, you will have a direct contact
who you can engage for support at any time.
Your participation is voluntary. You are free to withdraw
at any time and for any reason. Your privacy will be maintained throughout
the study.
Participation requirements
are as followsa:
18 to 85 years old
Take 1 to 3 anti-seizure medications
Currently experience seizures
aAdditional criteria to be assessed at screening.
What to expect if I participate
If you qualify and decide to participate, you will receive
Complete the short health questionnaire to see if you prequalify.
Schedule a call with a clinical trial navigator to hear more about the trial and to discuss your health history.
After reviewing your medical information, if you're eligible, we'll connect you with a clinical trial site.
If you decide to enroll in the study, you'll receive clear instructions on participation and next steps.
Your safety is the highest priority. If you ever have questions or concerns, you can reach out to our team at any time.
About Praxis
Precision Medicines
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating insights from genetic epilepsies into the development of therapies for central nervous system, or CNS, disorders characterized by neuronal excitation-inhibition imbalance.
Frequently asked questions
About POWER2
The main purpose of this research is to see how well vormatrigine works for treating focal onset seizures compared with placebo, as well as its safety and side effects compared with placebo.
Vormatrigine is a new investigational medicine that is taken once a day and is currently being studied to see if it can help people with focal onset seizures. This study drug could potentially offer better seizure control with fewer side effects.
A placebo is an inactive material that looks like vormatrigine but does not contain any active study drug. Researchers use a placebo to see if the vormatrigine works better or is safer than taking nothing.
The study staff will provide you with more information about whether you will be able to continue your other medications. Please do not make any changes to your medications without first talking to your doctor and the study staff.
Yes, you will be able to continue taking your current epilepsy medications. Please do not make any changes to your medications without first talking to your doctor and the study staff.
You can expect to be in the study for about 20 weeks.
Your participation in the research study is entirely voluntary and you may withdraw from the study at any time. You may decide to stop taking part in the study by notifying the study doctor of your decision.
Privacy, Costs, and Permissions
The study staff respects and protects your privacy and will not share your information, except as required by law, and will store your personal information with codes that protect your medical information. The Informed Consent Form will provide more information about how your privacy will be maintained.
There is no charge for taking part. All assessments and investigational medicines related to the research study are provided at no charge.
Your doctor does not have to give permission for you to participate; however, either you or the study doctor, with your permission, may contact your regular doctor to discuss your participation before you begin and keep your doctor updated about your participation. You will continue to see your regular doctors for routine office visits and checkups that you would normally have.
Clinical Trials
Clinical trials are central to our mission of delivering innovative medicines to individuals with specific diseases or conditions. A clinical trial is a research study that is conducted to determine whether an investigational medicine can improve an individual's health. They depend entirely on the participation of patients and healthy volunteers.
Participants who meet all required eligibility criteria and are willing to participate in all study-related assessments, as described in the Informed Consent Form, may take part in a clinical trial.
To ensure that a research study is ethical, and that participants' rights are protected, Institutional Review Boards review and approve study protocols that detail all aspects of how the study is conducted. In addition, study monitors, also known as clinical research associates, confirm that the study protocol procedures and research study requirements and regulations are being followed throughout the study.
An investigational medicine is a medication that has not been approved by regulatory or health authorities (eg, the US Food and Drug Administration) for prescription use that is utilized to conduct clinical research studies. An investigational medicine can also be called an experimental medicine and is being studied to see if your disease or medical condition improves while taking it.
Could More Seizure-Free Days Be in Your Future?
Participate in POWER2, an epilepsy study that offers the convenience of completing some visits from home.
Could More Seizure-Free Days Be in Your Future?
Participate in POWER2, an epilepsy study that offers the convenience of completing some visits from home.
About the POWER2 study
The POWER2 study is a research study evaluating a new investigational medicine, in accordance with FDA requirements, as a potential treatment for focal onset seizures in adults.
Flexible Study Visits
You may complete some study
visits from home.
No Cost
Any travel expenses and other costs
associated with the study will be paid by
the sponsor. Insurance is not required.
Duration
Up to 6 weeks of screening, followed by a 12 week study treatment period with an option to receive vormatrigine for up to 2 years, in an open-label extension.
If you are considering joining this study, the first step is to answer a questionnaire about your health and medical history. If you qualify, you can schedule time with one of our trial navigators to hear more about the study.
Why take part?
If you qualify and decide to participate, you will receive
All study-related care at no cost, including travel expenses
Close monitoring by an experienced doctor and study staff who understand epilepsy
The opportunity to advance medical knowledge and potentially help others with epilepsy
Option to enroll in an extension study and receive vormatrigine treatment for up to 2 years, after completing participation in the initial study
If you ever have questions or concerns, you will have a direct contact who you can engage for support at any time.
Your participation is voluntary. You are free to withdraw at any time and for any reason. Your privacy will be maintained throughout the study.
Participation requirements are as followsa:
18 to 85 years old
Take 1 to 3 anti-seizure medications
Currently experience seizures
aAdditional criteria to be assessed at screening.
What to expect if I participate
If you qualify and decide to participate, you will receive
Complete the short health questionnaire to see if you prequalify.
Schedule a call with a clinical trial navigator to hear more about the trial and to discuss your health history.
After reviewing your medical information, if you're eligible, we'll connect you with a clinical trial site.
If you decide to enroll in the study, you'll receive clear instructions on participation and next steps.
Your safety is the highest priority. If you ever have questions or concerns, you can reach out to our team at any time.
About Praxis Precision Medicines
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating insights from genetic epilepsies into the development of therapies for central nervous system, or CNS, disorders characterized by neuronal excitation-inhibition imbalance.
Frequently asked questions
About POWER2
The main purpose of this research is to see how well vormatrigine works for treating focal onset seizures compared with placebo, as well as its safety and side effects compared with placebo.
Vormatrigine is a new investigational medicine that is taken once a day and is currently being studied to see if it can help people with focal onset seizures. This study drug could potentially offer better seizure control with fewer side effects.
A placebo is an inactive material that looks like vormatrigine but does not contain any active study drug. Researchers use a placebo to see if the vormatrigine works better or is safer than taking nothing.
The study staff will provide you with more information about whether you will be able to continue your other medications. Please do not make any changes to your medications without first talking to your doctor and the study staff.
Yes, you will be able to continue taking your current epilepsy medications. Please do not make any changes to your medications without first talking to your doctor and the study staff.
You can expect to be in the study for about 20 weeks.
Your participation in the research study is entirely voluntary and you may withdraw from the study at any time. You may decide to stop taking part in the study by notifying the study doctor of your decision.
Privacy, Costs, and Permissions
The study staff respects and protects your privacy and will not share your information, except as required by law, and will store your personal information with codes that protect your medical information. The Informed Consent Form will provide more information about how your privacy will be maintained.
There is no charge for taking part. All assessments and investigational medicines related to the research study are provided at no charge.
Your doctor does not have to give permission for you to participate; however, either you or the study doctor, with your permission, may contact your regular doctor to discuss your participation before you begin and keep your doctor updated about your participation. You will continue to see your regular doctors for routine office visits and checkups that you would normally have.
Clinical Trials
Clinical trials are central to our mission of delivering innovative medicines to individuals with specific diseases or conditions. A clinical trial is a research study that is conducted to determine whether an investigational medicine can improve an individual's health. They depend entirely on the participation of patients and healthy volunteers.
Participants who meet all required eligibility criteria and are willing to participate in all study-related assessments, as described in the Informed Consent Form, may take part in a clinical trial.
To ensure that a research study is ethical, and that participants' rights are protected, Institutional Review Boards review and approve study protocols that detail all aspects of how the study is conducted. In addition, study monitors, also known as clinical research associates, confirm that the study protocol procedures and research study requirements and regulations are being followed throughout the study.
An investigational medicine is a medication that has not been approved by regulatory or health authorities (eg, the US Food and Drug Administration) for prescription use that is utilized to conduct clinical research studies. An investigational medicine can also be called an experimental medicine and is being studied to see if your disease or medical condition improves while taking it.