Personalized Models for Cancer Research

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNew York Stem Cell Foundation Research Institute

About this trial

The New York Stem Cell Foundation (NYSCF) Research Institute is performing this research to accelerate cancer research ranging from disease mechanisms to personalized medicine approaches that will help to realize the promise of precision medicine for oncology.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adults ages 18 and older with a solid tumor cancer diagnosis.

Adults ages 18 and older serving as healthy controls.

Disqualifiers

Human fetuses.

Neonates.

Children.

Wards of the state.

Trial population

Adults with a solid tumor cancer diagnosis or adults without a medical condition to serve as healthy controls (a comparison group for those with a solid tumor cancer diagnosis).

Trial design

Design model

Other

Time perspective

Other

Treatments tested in this trial

  • Biological Sample Collection

    Other intervention

    Excess/leftover biospecimens that were (or will be) collected for other purposes (e.g., medical procedure).

Treatment groups

500 Participants
are divided into 2 treatment groups
Group A: Affected Subjects1 intervention
Group B: Healthy Control1 intervention

Trial outcomes

Primary outcomes

1

Implement organoid culture technologies.

NYSCF will establish patient specific tumor models known as organoids. Organoids are three dimensional cell culture laboratory models with self-organizing capabilities and long-term expansion potential that recapitulate the tissue they are derived from at the histological, molecular, and phenotypic level. We will create organoids from each subject sample collected. Primary outcome measure is successful growth of organoids from individual tumor samples.

Time frame
Baseline
2

Validate genotypic and phenotypic relevance of tumor-derived organoids for biobanking.

To ensure the validity of outcome 1, NYSCF will perform a series of molecular and histological evaluations in primary tissues versus the derived organoid model.

Time frame
Baseline
3

Establish functional testing using organoid cultures alone or in combination with additional cell types.

To validate the clinical utility of the organoid models and the discovery of novel therapeutic strategies, NYSCF will establish methodologies to evaluate organoid responses (i.e., genetic, phenotypic, morphological changes) to small molecules and/or additional treatment modalities such as immunotherapies, antibody-based therapeutics, and others.

Time frame
Baseline
4

Perform drug testing and screens to identify new targets and/or new therapeutic strategies to effectively treat cancer.

As with outcome 3, to validate the clinical utility of the organoid models and the discovery of novel therapeutic strategies, NYSCF will establish methodologies to evaluate organoid responses (i.e., genetic, phenotypic, morphological changes) to small molecules and/or additional treatment modalities such as immunotherapies, antibody-based therapeutics, and others.

Time frame
Baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

New York Stem Cell Foundation Research Institute

Lead sponsor

Stevens Institute of Technology

Collaborator