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Study identifier: NCT06548789 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Neoadjuvant Immune Checkpoint Blockade + a Prebiotic Food-enriched Dietary Intervention to Optimize Immune Response in Melanoma: NEO-PreFED

Condition: Melanoma  ·  Sponsor: M.D. Anderson Cancer Center

PhasePhase 2
Planned participants35
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

To Determine the feasibility, compliance and adherence to PreFED intervention in resectable melanoma patients initiating neoadjuvant Ipi/Nivo.

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

Talk to the study team

Erez Baruch, MD,PHD  ·  713-745-5530  ·  ENBaruch@mdanderson.org,

Always discuss trial participation with your own doctor first.

Locations (1)

MD Anderson Cancer CenterHouston, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06548789