Continued Access Program for Tumor Treating Fields (TTFields) Used With Chemotherapy (Gemcitabine and Nab-Paclitaxel) in Adults With Locally Advanced Pancreatic Cancer (PANOVA-3CA)
PANOVA-3CA
Tumor Treating Fields (TTFields, 150kHz) Concomitant With Gemcitabine and Nab-paclitaxel for Front-line Treatment of Locally Advanced Pancreatic Adenocarcinoma: EF-54/PANOVA-3CA
1 other identifier
expanded_access
N/A
0 countries
N/A
Brief Summary
The EF-54 program (PANOVA-3CA) is a continued access program for adults with locally advanced pancreatic cancer to access TTFields therapy in combination with gemcitabine and nab-paclitaxel. The purpose of the program is to allow eligible patients to have access to TTFields while the NovoTTF-200T system is under FDA review. Safety and device performance will be monitored during routine clinical care.
Trial Health
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 18, 2025
CompletedFirst Posted
Study publicly available on registry
January 6, 2026
CompletedJanuary 6, 2026
December 1, 2025
December 18, 2025
December 18, 2025
Conditions
Interventions
per standard of care
TTFields is a non-invasive locoregional therapy that uses alternating electric fields. TTFields are delivered to the abdomen though adhesive transducer arrays connected to the NovoTTF-200T system.
per standard of care
Eligibility Criteria
You may qualify if:
- Age ≥ 22 years
- Histologically or cytologically confirmed de novo pancreatic adenocarcinoma
- Locally advanced, non-metastatic disease
- ECOG performance status of 0-2
- Candidate for treatment with gemcitabine and nab-paclitaxel
- Able to operate the NovoTTF-200T system independently or with caregiver support
You may not qualify if:
- Prior palliative treatment to the pancreatic tumor
- Other active malignancies within the past 5 years (except certain early-stage cancers)
- Significant uncontrolled medical conditions or infections that would interfere with therapy
- Implantable electronic devices in the torso
- Known severe hypersensitivity to adhesives, hydrogel, or chemotherapy agents
- Pregnancy or breastfeeding
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- NovoCure GmbHlead
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- expanded access
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 18, 2025
First Posted
January 6, 2026
Last Updated
January 6, 2026
Record last verified: 2025-12