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NCT Number: NCT06318507

The Intestinal Microbiome in Triple Negative Breast Cancer Treated with Immunotherapy

This study will determine how the intestinal microbiome differs between patients with obesity and early triple-negative breast cancer who achieve a pathologic complete response from preoperative anti-PD-1 immunotherapy (pembrolizumab) versus patients who do not.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Pennington Biomedical Research Center

Baton Rouge, Louisiana, 70808, United States

Location status: Recruiting

Location contact

Justin Brown, Ph.D.

CONTACT

[email protected]

225-763-2715

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥18 years
  • Female biological sex
  • Newly diagnosed, previously untreated, histologically confirmed early triple-negative breast cancer
  • Plan to initiate preoperative anti-PD-1 immunotherapy using pembrolizumab
  • Overweight or obesity, defined as a body mass index >=25 kg/m2
  • Ability to provide written informed consent
  • Allow the collection and storage of biospecimens and data for future use

Exclusion criteria

  • Active autoimmune disease
  • Concomitant conditions that require the use of antibiotics (e.g., chronic sinusitis)
  • Digestive disease disorders (e.g., irritable bowel syndrome, Crohn's disease)
  • Currently pregnant, breastfeeding, or planning to become pregnant within the next 24 weeks
  • Recent (within 90 days) use of glucocorticoids for more than 10 consecutive days
  • Any other cardiovascular, pulmonary, orthopedic, neurologic, psychiatric, or other condition that, in the investigator's opinion, would preclude participation or successful compliance with the protocol
  • Any other situation that, in the opinion of the investigator, would negatively impact subject safety or successful compliance with the protocol

Treatment and study plan

Fecal microbial diversity

Combination Product

Fecal microbiome diversity via 16S rRNA and metagenomic sequencing

Primary outcomes

  1. Pathologic Complete Response (pCR)

    Time frame: Week 24

    Defined as ypT0/Tis ypN0, ypT0 ypN0, and ypT0/Tis

Study contacts

Contact information is provided by the study sponsor or research team.

Justin Brown, Ph.D.

CONTACT

[email protected]

225-763-3000

Sponsors and collaborators

Lead sponsor

Pennington Biomedical Research Center

Other

Registry information

Acronym: IMPACT

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Mar 19, 2024
Registry last updated
Feb 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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