Infinimmune OnSite Program
HELP MAKE A DIFFERENCE
Playground Global AGM: Infinimmune Healthy Donor Recruitment Program
Study Name:
Infinimmune Healthy Donor Program
Location: Palo Alto, CA
Length: 10-20 minutes
The main purpose of this research study is to collect fresh blood samples from healthy volunteers to be used in various research studies across Infinimmune. Your samples will help researchers advance science and may be used for efforts such as, but not limited to, blood biomarker analysis, genotyping, and the development of new treatment options for patients. All blood draws will be performed on-site at Infinimmune.
You can participate if you:
- Are 18 to 100 years of age
- Are in general good health
- Are attendees of the annual Infinimmune investor meeting at the designated location in Palo Alto, CA
You cannot participate if you:
- Are pregnant
- Have an infectious disease, such as active HIV, hepatitis, or other infectious diseases
- Experienced excess blood loss including blood donation defined as 250 mL in the last month or 500 mL in the last two months
- Have active HIV, hepatitis, MRSA, or tuberculosis (TB)
- Are currently engaging in recreational drug use, such as cocaine and methamphetamine. Use of nicotine, tobacco, cannabis, and alcohol are not excluded unless otherwise specified.
- Have received a blood product within 30 days before the study blood draw
- Have donated 250ml within 1 month of the study blood draw
- Have a history of fainting or other adverse events when donating blood
- Have received an investigational (unapproved) drug within 30 days before the study blood draw
How the Donation Process Works
Screening
Once you have signed up to participate in the Infinimmune Onsite Healthy Donor Program, one of our research coordinators will reach out to conduct an over-the-phone screening that takes about 10-15 minutes.
During the screen, you will be asked questions about your health and demographic information.
Informed Consent and Documentation
Once you are deemed eligible to participate in a study, you will be emailed an Informed Consent Form (ICF).
Informed Consent is the most important aspect of any research study as it outlines and confirms research participants' rights. The ICF may be signed electronically.
Appointment
After all proper documentation is on file, we will schedule your blood collection with one of our trained, licensed phlebotomists at the Playground Annual General Meeting on March 25th from 2 to 6 p.m.
On the day of your appointment, please make sure to be hydrated and follow all instructions provided by your research coordinator.
About Sanguine
We are the missing link in clinical trials, connecting patients and researchers seamlessly and conveniently using a mobile health platform to advance medical research from home. Our goal is to develop innovative solutions that empower patients to participate in research for conditions that matter most to them, regardless of their location or ability to travel.
We work directly with patients and advocacy groups to accelerate research through convenience and transparency while guiding each patient every step of the way.
Have a question?
You can withdraw from the study or decline participation at any time without providing a reason.
Your safety and privacy are our primary concerns. All private health information (PHI) provided to Sanguine is kept confidential and coded, so no one can identify you or connect you with your medical information. No samples we share with researchers contain any information that can directly identify you. We implement policies and procedures to protect your PHI in compliance with the law. If you want to learn more about your privacy rights, please see our privacy policy.
All of our mobile health staff undergo an extensive background check and screening process, ensuring that only the most experienced and trusted mobile health staff are a part of the Sanguine team.
