FAQ

  • Q.
    What is the difference between "Phase I studies" and "Bioequivalence studies?"
    A.
    Phase I studies are studies conducted in healthy adults to determine the safety (presence or absence of side effects) and pharmacokinetics (how the drug is absorbed and excreted by the body) of a drug under development. Bioequivalence studies are studies to determine whether a drug already approved as a pharmaceutical product is bioequivalent to a drug under development with the same ingredients.
    Bioequivalence means that the drug enters circulating bloodstream of the body at the same rate and in the same amount.
  • Q.
    What are generic drugs?
    A.
    A generic drug is a drug manufactured and sold after the patent for a new drug has expired, made with the same active ingredients as the new drug, and approved by the government as being equivalent to the new drug in terms of efficacy and safety.
  • Q.
    What is a drug withdrawal period?
    A.
    It is the time that must elapse before you can participate in a clinical trial.
    Clinical trials involve many elements (e.g., medications, blood draws, various tests, etc.) that can be physically demanding. The time required for the body to fully recover from the effects of these factors is called the drug withdrawal period. (The withdrawal period is calculated from the date of the last dose of the previous study to the date of the first dose of the next study.)
    The withdrawal period depends on the type of clinical trial but is usually 3 to 4 months. (If you have previously participated in a clinical trial at another site, please allow 4 months.)
  • Q.
    Is there a cost to participate?
    A.
    We do not charge any fees to the participants (subjects) in the clinical trials.
    We are a facility specializing in clinical trials and contracts and fees are exchanged directly with major pharmaceutical companies. Therefore, we do not charge any fees from the time of enrollment to the time of withdrawal. We are not affiliated with any sites that charge information fees for participation, such as high-cost medical part-time jobs, new drug part-time jobs, and high-cost short-term jobs.
  • Q.
    How do you know if someone has quit smoking for a trial with a set period of abstinence?
    A.
    For the dates indicated as "no smoking" in the eligibility criteria, nicotine levels may be measured by urine test at the time of pre-test or admission. Although nicotine metabolism varies from person to person, our site uses 200 ng/mg as the standard for determination. Please note that regardless of whether you smoke or not, nicotine levels are also increased by secondhand smoke.
  • Q.
    Are there any clinical trials for women?
    A.
    Although not many, we also have clinical trials for women, and we will contact enrollees when they are conducted.
  • Q.
    It's hard to participate.
    A.
    At our site, priority is given as follows
    1) Those with previous pre-test dates that they have attended (those with previous pre-test applications for the same dates will be given priority).
    2) Those with better test results.
  • Q.
    How will I spend my time in the hospital?
    A.
    For each clinical trial, the time and number of blood draws, medical exams, etc., will be determined, as will the time you wake up, go to bed, and eat.
    During the rest of the day, you are free to study, use the computer, read manga, or do whatever you like as long as it does not disturb others. However, you are not allowed to go out.
  • Q.
    Can I see my lab test results?
    A.
    Since the clinical examination at our site is not for medical checkups, we do not accept requests for copies or review of the results.
  • Q.
    Can you provide me with a certificate of hospitalization for my hospital stay?
    A.
    We do not provide hospitalization certificates or any other certificates.
  • Q.
    Can I ask a financial institution to perform procedures on my behalf while I am in the hospital?
    A.
    We do not perform any procedures with financial institutions such as utility bills on your behalf to avoid unnecessary problems. Please all necessary procedures are completed prior to admission.
  • Q.
    I forgot my password.
    A.
    Enter the necessary information on the "Forgot your password?" link on the login page. We will issue a temporary password to your registered e-mail address. Login and change your password as soon as you receive the email with the temporary password.
  • Q.
    Can you make it easier to enter My Page?
    A.
    We are a member of the "Japan Association of Contract Institutes for Clinical Pharmacology" and automatically check that there are no errors in the information registered with the association at the time of login. Therefore, security is strictly controlled and we cannot reduce the number of input items.
  • Q.
    I have not received any emails.
    A.
    Make sure that your registered address is correct and that you have not set your spam filtering settings. If you wish to change your address, login to "My Page" → "Change Registered Contents". If you have set your spam filtering settings to reject unsolicited e-mail, please set your e-mail address to allow receipt of "support@seri.co.jp".
  • Q.
    Can I post information about "Sekino Clinical Pharmacology Clinic" on my website or SNS?
    A.
    We have seen many websites that post incorrect recruitment information about our site without our permission. If you wish to post information about our site, please be sure to contact us at "Contact Us".
  • Q.
    I want to withdraw from the membership.
    A.
    Login to "My Page", click "Withdrawal Procedures," confirm that you have completed the withdrawal process correctly, and then click "Withdrawal" to withdraw from membership. You may cancel your membership at any time. Note that once you have withdrawn your membership, you will not be able to register again for 4 months.
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