500 Participants Needed

Biological Sample Collection for Cancer

LV
BW
CR
Overseen ByClinical Research Office
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: New York Stem Cell Foundation Research Institute
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to accelerate cancer research by studying disease mechanisms and developing new, personalized treatments for cancer patients. It includes two groups: healthy individuals and those diagnosed with solid tumor cancers. This study suits adults diagnosed with a solid tumor cancer or healthy individuals willing to participate as controls.

As a Phase 2 trial, the research focuses on evaluating the treatment's effectiveness in an initial, smaller group, providing participants an opportunity to contribute to groundbreaking advancements in cancer treatment.

Do I need to stop taking my current medications for the trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

Why are researchers excited about this trial?

Researchers are excited about the Personalized Models for Cancer Research trial because it aims to develop customized approaches to understanding and treating solid tumor cancers. Unlike traditional treatments that apply a one-size-fits-all methodology, this trial explores individualized models, which could lead to more precise and effective treatments tailored to each patient's unique genetic makeup. By focusing on personalizing cancer treatment, this approach has the potential to significantly improve outcomes and reduce side effects compared to conventional therapies.

Who Is on the Research Team?

LA

Laura Andres-Martin, PhD

Principal Investigator

New York Stem Cell Foundation Research Institute

Are You a Good Fit for This Trial?

Inclusion Criteria

I am 18 or older and in good health.
I am 18 or older with a solid tumor cancer diagnosis.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Sample Collection

Collection of tumor/organoid and stem cell samples from participants for biobanking

Baseline

Organoid Development

Development of patient-specific organoid models to study tumor complexity and responses

Baseline

Functional Testing

Perform drug testing and screens to identify new therapeutic strategies using organoid models

Baseline

Follow-up

Participants are monitored for safety and effectiveness after sample collection and testing

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Biological Sample Collection

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: Healthy ControlExperimental Treatment1 Intervention
Group II: Affected SubjectsExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

New York Stem Cell Foundation Research Institute

Lead Sponsor

Trials
6
Recruited
11,900+

Stevens Institute of Technology

Collaborator

Trials
5
Recruited
8,700+

Stevens Institute of Technology

Collaborator

Trials
5
Recruited
8,700+