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NCT04362826RECRUITINGanonymous

A Randomized, Double-blind, Placebo Controlled, Parallel Study to Investigate Efficacy of a Novel Probiotic on the Bacteriome and Mycobiome of Breast Cancer Patients

Sponsor

Source record

Case Comprehensive Cancer Center

Phase

Source record

Not Applicable

Modality

AI-normalized

protein therapy

Target

AI-normalized

Bacteriome and Mycobiome modulation in breast cancer patients

Indication / condition

AI-normalized

Breast Cancer

Intervention

Source record

Novel probiotic, Placebo

Source & freshness

Source record

NCT ID

NCT04362826

Original source

ClinicalTrials.gov

Source last updated

Apr 09, 2026

Ingested at

Jun 12, 2026

Internal sync

Jun 12, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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View original source fields

NCT ID

NCT04362826

Title

A Randomized, Double-blind, Placebo Controlled, Parallel Study to Investigate Efficacy of a Novel Probiotic on the Bacteriome and Mycobiome of Breast Cancer Patients

Sponsor

Case Comprehensive Cancer Center

Status

RECRUITING

Phase

Not Applicable

Condition raw

Breast Cancer

Condition normalized

Breast Cancer

Modality raw

protein therapy

Modality normalized

protein therapy

Target raw

Bacteriome and Mycobiome modulation in breast cancer patients

Target normalized

Bacteriome and Mycobiome modulation in breast cancer patients

Interventions

Novel probiotic, Placebo

Public preview

Source record

The study, sponsored by Case Comprehensive Cancer Center, aims to evaluate the efficacy of BIOHM, a novel probiotic, in altering the microbiome profiles of breast cancer patients. Given the increasing interest in the role of the microbiome in cancer treatment and prevention, successful outcomes could position BIOHM as a complementary therapy in breast cancer management. The market for probiotics is growing, with a focus on personalized medicine and microbiome research. If proven effective, this could lead to significant commercial opportunities for BIOHM Health LLC, particularly in oncology. The competitive landscape includes other microbiome-focused therapies, necessitating a robust differentiation strategy. Due diligence should consider regulatory pathways, potential market access challenges, and the need for further studies to establish clinical utility.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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