Study of Perioperative NP137 and FOLFIRINOX in Resectable Pancreatic Cancer
Part of paid clinical trials in Rochester, New York.
- Sponsor
- Aram Hezel
- Study ID
- NCT06203821
- Phase
- PHASE1
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- NP137 — DRUGNP137 for the Treatment of Resectable Pancreatic Cancer
Study Details
The objective of this study is to investigate whether adding the study drug, NP137, to a patient's treatment regimen (before surgery and in combination with chemotherapy afterward) can alter the behavior of pancreatic cancer..
Key Dates
- Start date
- Sep 1, 2026
- Status verified
- Mar 2025
- Primary completion
- May 30, 2027
- Completion
- Sep 30, 2032
Study Design
- Enrollment
- 25 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: TreatmentPatient receive two doses of the study drug, NP137, approximately two weeks apart. This will be followed by surgery. After the surgery if feasible, patients will begin post-surgical treatment with a standard-of-care chemotherapy regimen called FOLFIRINOX, combined with the study drug, NP137, for a total duration of about 6 months. Upon completing this phase, patients will receive an additional 6 months of treatment with only the study drug NP137.
Primary Outcome Measure
Determining if NP137 can shift the primary tumor MAK's Signature Epithelial-to-Mesenchymal Transition (EMT) Mean Score towards a more epithelial phenotype [ Time Frame: 3-5 years ]
Central Contacts
- Aram Hezel585-275-5863
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Rochester | Rochester | New York | 14642 | Aram Hezel (PRINCIPAL_INVESTIGATOR) |
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