Trial Utilizing Metronidazole to Optimize the Microbiome of Rectal Adenocarcinoma Undergoing Neoadjuvant Therapy

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center

About this trial

To learn if adding metronidazole to standard therapy can decrease populations of Fusobacterium nucleatum (F. nucleatum) and other anaerobes (small organisms that cause infections) in participants with rectal cancer receiving neoadjuvant therapy, compared to neoadjuvant therapy alone.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participants with locally advanced rectal cancers (T3, T4, or N+ disease) with decision to treat with total neoadjuvant therapy.

No previous cycles of cytotoxic chemotherapy in management of the index tumor.

Age ≥18 years. Because of dosing differences between pediatric and adult populations and the introduced variability with these regiments to the study's primary outcomes, participants <18 years of age, children are excluded from this study.

ECOG performance status ≤2 (Karnofsky ≥60%,)

Disqualifiers

Participants who have had chemotherapy or radiotherapy within 1 year prior to entering the study.

Participants who are receiving any other investigational agents.

Participants with brain metastases or other unresectable metastases who would therefore not undergo standard of care proctectomy.

History of allergic reactions attributed to compounds of similar chemical or biologic composition to metronidazole or other agents used in study.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Metronidazole

    Drug

    Given by PO

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Standard of Care Neoadjuvant Therapy + MetronidazoleExperimental treatment 1 intervention
Group B: Standard of Care Neoadjuvant TherapyNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Safety and adverse events (AEs)

Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0

Time frame
Through study completion; an average of 1 year.

Secondary outcomes

Other outcomes

Sponsors and contacts

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