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Biomarkers for improving the (cost-)effectiveness and safety of pemetrexed

Biomarkers for improving the (cost-)effectiveness and safety of pemetrexed - biomarkers and pemetrexed

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON39476
Enrollment
200
Registered
2012-08-30
Start date
2012-10-24
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

lung cancer non small cell lung carcinoma

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: patients with non-small cell, non-squamous lungcarcinoma or malignant pleural mesothelioma who have an indication for treatment with pemetrexed containing chemotherapy, both in first line treatment as in following treatment lines and as maintenance therapy.

Exclusion criteria

Exclusion criteria: non able to read dutch clinical condition not fit to receive pemetrexed chemotherapy

Design outcomes

Primary

MeasureTime frame
This is an observational study. The primairy outcome is the question whether there is a relation between pharmacogenetics and pharmacokinetics and repons to treatment with pemetrexed

Secondary

MeasureTime frame
relation between pharmacogenetics and pharmacokinetics and quality of life

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)