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Study details
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A Study of NALIRIFOX in Combination With Radiation Therapy in People With Pancreatic Ductal Adenocarcinoma (PDAC)

Memorial Sloan Kettering Cancer Center
NCT IDNCT05851924ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

60

Study length

about 3.1 years

Ages

18+

Locations

7 sites in NJ, NY

What this study is about

This trial is testing whether using the chemotherapy regimen NALIRIFOX in combination with ablative dose radiation therapy (AD-XRT) and the standard chemotherapy drug capecitabine is an effective treatment approach for people with locally advanced or borderline resectable pancreatic ductal adenocarcinoma (PDAC) before surgery. The researchers will also look at whether the sequence of the treatment approach (NALIRIFOX + ADXRT and capecitabine followed by surgery, when it is possible) is effective and causes few or mild side effects in participants. An important purpose of it is to see how it treatment (NALIRIFOX + AD-XRT and capecitabine) affects participants' quality of life.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take AD-XRT and Capecitabine
  • 2.Take NALIRIFOX

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

capecitabine

Drug routes

oral (Oral Tablet)

Endpoints

Primary: event-free survival (EFS)

Secondary: overall survival (OS) rate