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Actively Recruiting

Age: 2Months +
All Genders
ID02474160

Patient-Derived Models Tissue Procurement Protocol for the National Cancer Institute NCI

Led by National Cancer Institute LAO · Updated on 2026-03-05

5000

Participants Needed

140

Research Sites

N/A

Total Duration

On this page

Sponsors

N

National Cancer Institute LAO

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are collecting and storing tissue and blood samples from patients with various types of cancer to help create better models for studying cancer and testing new cancer drugs. This observational study focuses on patients with hematopoietic and lymphatic system neoplasms, malignant solid tumors, metastatic malignant solid tumors, and recurrent malignant solid tumors. The goal is to procure biological tissues and materials to develop preclinical cancer models for future laboratory analysis. During the study, tumor tissue and blood samples are collected during medical procedures required for the patients cancer treatment. These samples are then preserved using methods such as xenograft models, where tissues are transplanted to another species, or in vitro cell cultures. This process allows for future scientific study without additional invasive procedures beyond routine clinical care. Participants will be involved in routine clinical procedures during which tissue and blood samples are collected. Researchers will store these specimens and monitor their use in creating cancer models over a period of up to five years. The main outcome measured is the successful procurement and storage of tissue and blood specimens for research purposes. Participation will continue as long as samples can be collected during clinical management, with no additional treatment or interventions required specifically for this study.

CONDITIONS

Brief Title

Collection and Storage of Tissue and Blood Samples From Patients With Cancer

Who Can Participate

Age: 2Months +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients older than 2 months who are being evaluated, treated, or enrolled in a cancer clinical trial at participating sites
  • Patients with a histologically or cytologically confirmed diagnosis of cancer
  • Patients without confirmed cancer diagnosis but approved by the coordinating site study coordinator based on clinical and diagnostic indications
  • Patients with newly diagnosed primary or metastatic solid tumors or hematologic malignancies not yet treated
  • Patients with recurrent, newly metastasized, or progressing solid tumors or hematologic malignancies
  • Patients currently undergoing treatment, with specimen collection timed away from recent drug doses
  • Patients with ongoing partial response or stable disease, confirmed by pathology or flow cytometry
  • Ability to understand and sign informed consent (or assent with parental permission for pediatric patients)
Not Eligible

You will not qualify if you...

  • Patients with cancer-like syndromes or blood disorders such as systemic mastocytosis or monoclonal gammopathy of undetermined significance
  • Patients with invasive fungal infections
  • Patients with active, uncontrolled, or recently treated infections without at least one week symptom-free post-treatment
  • Patients with HIV, active or chronic hepatitis B or C, or history of these infections unless testing is clinically indicated
  • Patients with hepatitis A infection indicated by IgM reactivity
  • Patients with benign tumors or complete disease response

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