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Phase II randomized trial evaluating modified FOLFIRINOX and FOLFOX in the treatment of locally advanced or metastatic small bowel adenocarcinoma [FIRE-12]

Status
Not yet recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-524131-39-00
Enrollment
112
Registered
2026-08-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

locally advanced or metastatic small bowel adenocarcinoma

Brief summary

Progression-free survival, defined as the time from the date of randomization to the date of first radiological disease progression according to RECIST 1.1 or the date of death from any cause. Date of the last contact known alive respectively date of the last tumor assessment known progression-free.

Detailed description

Overall survival (OS), is defined as the time from the date of randomisation to the date of death (from any cause). The date of the last contact known alive respectively date of the last tumor assessment known progression-free will be censored at the date of last data entry., Objective respone rate (ORR), defined as rate of complete (CR) and partial responses (PR) during study treatment compared to baseline according to RECIST 1.1., Depth of response (DpR), defined as change in percent from baseline to smallest tumor diameter (measurements according to RECIST 1.1 definition)., Type, incidence, severity, and causal relationship to study treatment of non-serious adverse events and serious adverse events (severity evaluated according to CTCAE version 6.0)., Quality of life (QoL) as assessed with the QoL questionnaire EQ-5D-5L

Interventions

Sponsors

Charite Universitaetsmedizin Berlin KöR
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Progression-free survival, defined as the time from the date of randomization to the date of first radiological disease progression according to RECIST 1.1 or the date of death from any cause. Date of the last contact known alive respectively date of the last tumor assessment known progression-free.

Secondary

MeasureTime frame
Overall survival (OS), is defined as the time from the date of randomisation to the date of death (from any cause). The date of the last contact known alive respectively date of the last tumor assessment known progression-free will be censored at the date of last data entry., Objective respone rate (ORR), defined as rate of complete (CR) and partial responses (PR) during study treatment compared to baseline according to RECIST 1.1., Depth of response (DpR), defined as change in percent from baseline to smallest tumor diameter (measurements according to RECIST 1.1 definition)., Type, incidence, severity, and causal relationship to study treatment of non-serious adverse events and serious adverse events (severity evaluated according to CTCAE version 6.0)., Quality of life (QoL) as assessed with the QoL questionnaire EQ-5D-5L

Outcome results

None listed

Source: EU CTIS · Data processed: Aug 14, 2026