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The Finnish National Study to Facilitate Patient Access to Targeted Anti-cancer Drugs to determine the Efficacy in Treatment of Advanced Cancers with a Known Molecular Profile

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-517478-68-01
Acronym
FINPROVE
Enrollment
250
Registered
2024-11-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-06

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

Conditions

Advanced Cancer

Brief summary

Disease control rate at 16 weeks after treatment initiation (defined as patients by CR, PR, SD)

Detailed description

Duration of treatment on study (time on drug), Treatment-related grade ≥3 and serious adverse events, Best overall response (defined as patients by CR, PR, SD), Progression free survival, Overall survival

Interventions

Sponsors

HUS-Yhtymae
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Disease control rate at 16 weeks after treatment initiation (defined as patients by CR, PR, SD)

Secondary

MeasureTime frame
Duration of treatment on study (time on drug), Treatment-related grade ≥3 and serious adverse events, Best overall response (defined as patients by CR, PR, SD), Progression free survival, Overall survival

Countries

Finland

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026