Healthy Volunteers Needed for an Upcoming Clinical Trial!

  • STATUS
    Recruiting
  • days left to enroll
    7
Updated on 21 October 2022
Accepts healthy volunteers

Summary

Altasciences LA, formerly WCCT Global (a clinical research organization located in Cypress, CA), is looking for healthy volunteers to participate in an upcoming clinical research trial of investigational medicine for Alzheimer’s disease.

Description

Qualifications (All must apply):
  • Generally healthy males and females
  • Must be fully vaccinated against COVID-1
  • Age 18 to 55
  • Have a Body Mass Index (BMI) between 18.5 and 30 kg/m² *Check your BMI here
  • Non-smokers for the last 3 month
  • Non-marijuana user
  • Available for one of the following trial schedule:
    o1 screening visit, a 19-night stay, and 1 outpatient visit
    o1 screening visit, a 13-night stay, and 1 outpatient visit
    o1 screening visit, a 5-night stay, and 1 outpatient visit
     
    You May Receive:
  • Compensation up to $11,250
  • COVID-19 test at no cost

Details
Condition Healthy Volunteers
Clinical Study IdentifierTX304151
Last Modified on21 October 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Qualifications (All must apply)
Generally healthy males and females
Must be fully vaccinated against COVID-1
Age 18 to 55
Have a Body Mass Index (BMI) between 18.5 and 30 kg/m²
Non-smokers for the last 3 month
Non-marijuana user
Available for one of the following trial schedule
o1 screening visit, a 19-night stay, and 1 outpatient visit
o1 screening visit, a 13-night stay, and 1 outpatient visit
o1 screening visit, a 5-night stay, and 1 outpatient visit
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

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