Altamonte Springs, FLNCT06401421Now EnrollingIRB Ready

Breast Cancer Clinical Trial in Altamonte Springs, FL

Access cutting-edge breast cancer treatment through this clinical trial at a research site in Altamonte Springs. Study-provided care at no cost to qualified participants.

Sponsored by Exact Sciences Corporation

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Expert Care in Altamonte Springs

Access breast cancer specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related breast cancer treatment provided free

Apply for This Altamonte Springs Location

Check if you qualify for this breast cancer clinical trial in Altamonte Springs, FL

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Altamonte Springs

    Convenient for FL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Altamonte Springs site if eligible
  4. 4Begin participation

About This Breast Cancer Study in Altamonte Springs

The EXActDNA-003 study will prospectively enroll participants who are planning to undergo chemotherapy for high-risk, early breast cancer, who are willing to provide tissue and blood specimens for circulating tumor DNA (ctDNA) analysis. Participants will be followed for up to 5.5 years.

Sponsor: Exact Sciences Corporation

Who Can Participate

Inclusion Criteria

The participant or a legally authorized representative must provide study-specific informed consent prior to study entry.
The participant must be ≥ 18 years of age.
ECOG performance status 0 or 1.
Histologically confirmed invasive carcinoma of the breast.
Planned neoadjuvant therapy which includes cytotoxic chemotherapy.
Tumor size ≥ 2.1 cm in greatest diameter.
Unifocal or multifocal cancer documented to be the same histologic clinical subtype.
Clinically node positive or if node negative, any one of the following:
TNBC or HER2+ subtype
HR+/HER2-negative with at least one of the following: i. High tumor grade (G3) ii. Ki67 index of 20% or higher iii. High genomic risk (Oncotype DX® (ODX) Breast Recurrence Score of \> 25, MammaPrint® High, etc.)
Willing and able to comply with the study requirements, which includes the collection of a total of 34 cc (2.5 Tablespoons) of blood for each research blood draw.
Available residual tissue from diagnostic biopsy from the breast or an involved ipsilateral lymph node for submission to create a bespoke ctDNA assay.

Exclusion Criteria

Definitive clinical or radiologic evidence of metastatic disease.
Initiated neoadjuvant therapy for current breast cancer diagnosis.
Synchronous diagnosis of another invasive cancer, other than this breast cancer, except for non-melanoma skin cancers.
Completed all therapy (including endocrine therapy) \<5 years ago for any previous invasive solid organ malignancy (with exception of non-melanoma skin cancers) including prior breast cancer. Individuals with a prior history of noninvasive (in situ) carcinomas may participate if they have received definitive treatment.
Completed all therapy for any previous hematologic malignancy \< 5 years ago.
Multicentric or contralateral invasive breast cancers.
Known pregnancy at time of enrollment.
Prior solid organ transplant.
Prior allogeneic hematopoietic stem cell transplant.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Altamonte Springs?

Yes, this clinical trial (NCT06401421) has an active research site in Altamonte Springs, FL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Breast Cancer Treatment Options in Altamonte Springs, FL

If you're searching for breast cancer treatment options in Altamonte Springs, FL, this clinical trial (NCT06401421) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Altamonte Springs research site is actively enrolling participants for this clinical trial. You'll receive care from experienced breast cancer specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all breast cancer clinical trials near you to find additional studies recruiting in your area.

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