Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 11:10 AM
Ignite Modification Date:
2025-12-26 @ 11:10 AM
NCT ID:
NCT00778128
Eligibility Criteria:
Inclusion Criteria:
1. Histologically or cytologically confirmed solid tumour diagnosis
2. Locally advanced or metastatic disease, for which there is no known effective treatment
3. Performance Status 0 - 2 according to ECOG (Eastern Cooperative Oncology Group) Performance Status
4. Age 18 years or more
5. Life expectancy \> 3 months
6. Adequate hematological and biological functions:
7. Signed informed consent
Exclusion Criteria:
1. Symptomatic brain metastases
2. Current peripheral neuropathy of grade \> 1 according to the National Cancer Institute (NCI) - Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0
3. Radiotherapy
* to more than 30 % of bone marrow
* single dose up to 8 Gy
* less than one week prior to the study treatment
* of the upper GI tract
4. Mucositis of the upper digestive tract, including stomatitis
5. Participation in another therapeutic clinical study within 30 days of enrolment or during this clinical study
6. Previous anticancer therapy (chemotherapy, hormone therapy or immunotherapy) within 30 days prior to the first dose of oral CP-4126 \[6 weeks for mitomycin C and BCNU (= carmustine) and CCNU (=lomustine)\]
7. Requirement of concomitant treatment with a non-permitted medication including alternative drugs and high doses of vitamins
8. History of allergic reactions to gemcitabine
9. Presence of any serious concomitant systemic disorders incompatible with the clinical study (e.g. uncontrolled inter-current illness including ongoing or active infection)
10. Presence of any significant central nervous system or psychiatric disorder(s) that would hamper the patient's compliance
11. Pregnant or breast feeding women
12. Absence of adequate contraception for both male and female fertile patients for the duration of the study; and also for six months after last treatment
13. Known positive status for HIV and/or hepatitis B or C
14. Any reason why, in the investigator's opinion, the patient should not participate
15. Condition that impairs ability to swallow pills
16. Coeliac disease or any other lipid malabsorption syndrome
17. Drug and/or alcohol abuse
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00778128
Study Brief:
Protocol Section:
NCT00778128