Blood Collection for Various Cancers
Collection of Blood From Patients With Cancer
Recruiting
Observational Study
Prostate Cancer
Breast Cancer
Colon Cancer
Lung Cancer
Liver Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 1,750 (estimated)
- Sponsor
- National Cancer Institute (NCI) · NIH
Who this trial is looking for
This trial is looking for patients aged 18 and older with cancer to take part in a study that collects blood samples. The collected blood will help researchers understand immune response changes before and after chemotherapy.
Are You a Good Fit for This Trial?
You may be able to join if
- I am 18 years of age or older
- I have a known or suspected cancer
- I can understand and sign a consent form
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your Eligibility
About This Trial
This study will collect blood from patients with cancer to study the level of cells which decrease the immune response (suppressor cells) before and after chemotherapy. Patients 18 years of age and older with cancer may participate. This study does not involve treatment.
Participants will have about 50 ml (3 tablespoonfuls) of blood drawn. Depending on their condition, patients may be invited to …
Trial Locations
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Eligibility Criteria
* INCLUSION CRITERIA:
Patients with a known or suspected malignancy and healthy volunteers 18 years of age and older are eligible.
Performance status of ECOG 0, 1, 2, or 3 for admission to this protocol.
Ability to understand and the willingness to sign a written informed consent document.
INCLU…
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