Fluoxetine for the Modification of Colorectal Tumor Immune Cells Before Surgery in Patients With Colorectal Cancer
Recruiting now · Phase 1
Conditions studied: Colorectal Adenocarcinoma
In brief
This phase I trial tests whether fluoxetine (prozac) works to modify the tumor immune cells before surgery in patients with colorectal cancer. Fluoxetine is a commonly used selective serotonin reuptake inhibitor (SSRI) prescribed for major depressive disorder and generalized anxiety. Giving fluoxetine may modify the immune cell composition in the tumor and its microenvironment and may induce changes in body's immune system and may interfere with the ability of tumor cells to grow and spread in patients with colorectal cancer.
Key facts
- Study ID
- NCT06225011
- Run by
- Jonsson Comprehensive Cancer Center
- People needed
- 10
- Starts
- 2025-03-20
- Expected to finish
- 2027-07-01
- Last updated by the study team
- 2026-05-11
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female ≥ 18 years of age at visit 1
- Previously untreated cytologically or histologically confirmed colorectal adenocarcinoma that will not need neoadjuvant therapy
- Written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study
- World Health Organization (WHO) Eastern Cooperative Oncology Group (ECOG) performance status 0-2
- Absolute neutrophil count (ANC) ≥ 1.5x10\^9/L
- Platelets ≥ 100x10\^9/L
- Hemoglobin ≥ 9 g/dL
- Serum creatinine (sCr) ≤ 1.5 x upper limit of normal (ULN)
- Creatinine clearance (Ccr) ≥ 40 mL/min (as calculated by Modified Cockcroft-Gault formula)
- Serum total bilirubin ≤ 1.5 x ULN
- Aspartate aminotransferase (AST)(serum glutamic-oxaloacetic transaminase [SGOT]) / alanine aminotransferase (ALT)(serum glutamate pyruvate transaminase [SGPT]) ≤ 2.5 x ULN
- Baseline corrected QT (QTc) within normal limits per the Bazett formula. Any electrocardiogram (EKG) done prior to consent is acceptable for baseline QTc monitoring.
- Normal QTc ranges from 350-450 ms for adult men and from 360-460 ms for adult women
You may not qualify if…
- Presence of a condition or abnormality that in the opinion of the investigator would compromise the safety of the participant or the quality of the data
- A diagnosis of metastatic colorectal adenocarcinoma
- Individuals who have received neoadjuvant chemotherapy prior to the planned colon cancer resection
- Individuals with absolute or relative contraindications to fluoxetine
- Baseline prolonged QTc
- Concurrently taking tamoxifen, pimozide, or thioridazine
- Individuals using other SSRIs, serotonin and norepinephrine reuptake inhibitors (SNRIs), monoamine oxidase inhibitors (MAOIs), lithium or other antidepressants at time of initial biopsy
- Currently active second primary malignancy or history of malignancy less than 5 years prior to the time of study eligibility (Patients with history of skin cancers excluding melanoma will be eligible for participation)
Where it is running
- UCLA / Jonsson Comprehensive Cancer Center — Los Angeles, California, United States (enrolling)
Full record on ClinicalTrials.gov
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