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Study identifier: NCT07104266 Synced from ClinicalTrials.gov · July 29, 2026
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Triple Negative Breast Cancer and Celecoxib. Pilot Study

Condition: Triple-Negative Breast Cancer  ·  Sponsor: Université de Sherbrooke

PhasePhase 2
Planned participants30
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Relapses occur in 20 to 30% of patients with early-stage triple-negative breast cancer (TNBC), which is characterized by the absence of three receptors: the estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor 2 (HER-2). Radiotherapy (RT) can increase or decrease, depending on the patient, the level of cytokines that promote metastasis development. To help prevent the development of metastasis, the cyclooxygenase-2 (COX-2) inhibitor celecoxib will be administered during RT. This treatment aims to prevent RT-induced cytokine increases and, ultimately, improve patient prognosis. The primary objective of this pilot study is to assess the feasibility of recruiting participants and implementing the study steps, with the intention of conducting a large-scale study in the future. The secondary objective is to evaluate celecoxib ability to inhibit the RT-induced stimulation of cytokines associated with metastasis development. This will be assessed by comparing the levels of these cytokines in plasma samples collected before, during, and after RT. In the exploratory objective, TNBC cells will be incubated in vitro with these plasma samples to determine whether administering celecoxib during RT can prevent increased cancer cell invasion and metastasis formation in mice.

This description comes directly from the study's public registry record.

Talk to the study team

Benoit Paquette, Ph.D.  ·  1-819-821-8000  ·  benoit.paquette@usherbrooke.ca

Hélène Therriault, M.Sc.  ·  1-819-821-8000  ·  Helene.Therriault@USherbrooke.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Faculty of medicine and health sciencesSherbrooke, Quebec, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT07104266