ClinicalTrials.gg
CompletedNCT00165854Updated Jun 27, 2014

Study of E7070 Combined With Capecitabine to Determine Efficacy and Recommended Dose of Combination in Patients With Metastatic Colorectal Cancer

A Phase 2 interventional study of E7070 in Colorectal Cancer (CRC), sponsored by Eisai Limited. Completed at 4 sites in 3 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-06-27.

Sponsored by Eisai Limited · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
46
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

Part 1: The primary purpose is to determine the recommended dose of E7070 in combination with capecitabine by dose adjustment. Part 2: The primary purpose is to determine the safety and efficacy of the combination in patients with metastatic CRC resistant to 5-fluorouracil and irinotecan.

02

Conditions studied

  • Colorectal Cancer (CRC)
03

In context

Colorectal Neoplasms

5,734 studies on the registry are indexed under Colorectal Neoplasms; 1,481 are open to participants now.

This study's enrollment of 46 is below the median of 77 across 4,222 interventional studies indexed under Colorectal Neoplasms.

Browse Colorectal Neoplasms studies →

Lead sponsor

Eisai Limited is the lead sponsor of 48 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Part 1 Inclusion Criteria:

  • Histologically or cytologically confirmed solid tumour refractory to standard therapy or for whom no established therapy exists
  • Age >= 18 years
  • Karnofsky performance status of >= 70%
  • Life expectancy of >= 3 months
  • Absolute neutrophil count of >= 1.5 × 109/l, platelet count of ³ 100 × 109/l, haemoglobin level of ³ 10 g/dl (>= 6.2 mmol/l) (prior transfusion is permitted)
  • Normal hepatic and renal function as defined by serum bilirubin £ 1.5 times the upper limit of normal, ALT and AST £ 2.5 times the upper limit of normal (£ 5 times the upper limit of normal in the presence of hepatic metastases), creatinine clearance ³ 50 ml/min (by Cockroft-Gault formula)
  • Male and female patients
  • Written informed consent to participate in the study

Part 1 Exclusion Criteria:

  • More than two previous courses of documented myelosuppresive chemotherapy (epidermal growth factor targeted therapy does not constitute a course of chemotherapy)
  • CNS metastases (a CT or MRI scan should be done if there is a clinical suspicion of CNS metastases)
  • Major surgery, chemotherapy or radiation therapy (except palliative) within 4 weeks of treatment start
  • Previous investigational cytotoxic treatment for malignant disease within 30 days before the start of the study
  • Any treatment with non-oncological investigational drugs within 30 days before the start of the study
  • Pregnancy or breast feeding (all women of childbearing potential must have a pregnancy test before inclusion in the study; post-menopausal women must be amenorrhoeic for at least 12 months). Female patients must use adequate contraceptive protection.
  • Fertile males not willing to use contraception or whose female partners are not using adequate contraceptive protection
  • Uncontrolled infections
  • Clinically significant cardiac impairment or unstable ischaemic heart disease including a myocardial infarction within three months of study entry
  • History of alcoholism, drug addiction, or any psychiatric or psychological condition which in the opinion of the investigator would impair study compliance
  • History of hypersensitivity to sulphonamides
  • Prior severe or unexpected reaction to fluoropyrimidine therapy (which may be explained by dihydropyrimidine dehydrogenase deficiency or hypersensitivity to 5-FU)
  • Malabsorption syndrome or other condition which may affect absorption of drug
  • Concurrent or previous malignancy of a different tumour type within five years of starting the study except for adequately treated non-melanoma skin cancer or cervical intraepithelial neoplasia
  • Treatment within two weeks before the start of the study with any of the following: coumarin anti-coagulants, terfenadine, cisapride, cyclosporin, tacrolimus, theophylline, diazepam, sulphonylurea hypoglycaemics, phenytoin, or carbamazepine
  • Legal incapacity

Part 2 Inclusion Criteria:

  • Ambulant patients with progressive metastatic CRC who have received prior treatment with 5 FU and irinotecan and/or oxaliplatin either as single agents or in combination. Either 5 FU and/or irinotecan and/or oxaliplatin may have been administered in the adjuvant setting or for the treatment of metastatic disease. Patients who have received both 5-FU and irinotecan or oxaliplatin in the adjuvant setting only must have experienced disease recurrence within one year of starting chemotherapy.
  • At least one unidimensionally measurable lesion according to the RECIST criteria
  • Age ³ 18 years
  • Karnofsky performance status of ³ 70%
  • Life expectancy of ³ 3 months
  • Absolute neutrophil count of ³ 1.5 × 109/l, platelet count of ³ 100 × 109/l, haemoglobin level of ³ 10 g/dl (³ 6.2 mmol/l) (prior transfusion is permitted)
  • Normal hepatic and renal function as defined by serum bilirubin £ 1.5 times the upper limit of normal, ALT and AST £ 2.5 times the upper limit of normal (£ 5 times the upper limit of normal in the presence of hepatic metastases), creatinine clearance ³ 50 ml/min (by Cockroft-Gault formula)
  • Male and female patients
  • Written informed consent to participate in the study

Part 2 Exclusion Criteria:

  • Prior chemotherapy other than 5-FU, irinotecan and/or oxaliplatin
  • CNS metastases (a CT or MRI scan should be done if there is a clinical suspicion of CNS metastases)
  • Major surgery, chemotherapy or radiation therapy (except palliative) within 4 weeks of treatment start
  • Previous investigational cytotoxic treatment for malignant disease within 30 days before the start of the study
  • Any treatment with non-oncological investigational drugs within 30 days before the start of the study
  • Pregnancy or breast feeding (all women of childbearing potential must have a negative pregnancy test before inclusion in the study; post-menopausal women must be amenorrhoeic for at least 12 months). Female patients must use adequate contraceptive protection.
  • Fertile males not willing to use contraception or whose female partners are not using adequate contraceptive protection
  • Uncontrolled infections
  • Clinically significant cardiac impairment or unstable ischaemic heart disease including a myocardial infarction within three months of study start
  • History of alcoholism, drug addiction, or any psychiatric or psychological condition which in the opinion of the investigator would impair study compliance
  • History of hypersensitivity to sulphonamides
  • Prior severe or unexpected reaction to fluoropyrimidine therapy (which may be explained by dihydropyrimidine dehydrogenase deficiency or hypersensitivity to 5-FU)
  • Malabsorption syndrome or other condition which may affect absorption of drug
  • Concurrent or previous malignancy of a different tumour type within five years of starting the study except for adequately treated non-melanoma skin cancer or cervical intraepithelial neoplasia
  • Treatment within two weeks before the start of the study with any of the following: coumarin anti-coagulants, terfenadine, cisapride, cyclosporin, tacrolimus, theophylline, diazepam, sulphonylurea hypoglycaemics, phenytoin, or carbamazepine
  • Legal incapacity
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
46 participants

Interventions

06

What researchers measure

Primary outcomes

  1. To determine the recommended dose of E7070 in combination with capecitabine by dose adjustment;

  2. to determine the safety, tolerability and efficacy (in terms of response rate and progression-free survival) of the combination in patients with metastatic CRC.

Secondary outcomes

  1. Determine the pharmacokinetic profile of capecitabine and E7070 when administered in combination;

  2. measure duration of response and stable disease; to measure median and one year survival.

07

Study locations

4 sites
  • Centre Léon Bérard
    Lyon, F-69373, France
  • Institut Curie
    Paris, F-75005, France
  • Universitätsklinikum der GHS-Essen
    Essen, D-45122, Germany
  • Netherlands Cancer Institute
    Amsterdam, 1066 CX, Netherlands
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 27, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00165854
Lead sponsor
Eisai Limited
Responsible party
Sponsor
First posted
Sep 14, 2005
Start date
Mar 2003
Last update
Jun 27, 2014

Study contacts

Jantien Wanders
study director · Eisai Limited
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2006. You cannot join it, but the record below documents what was studied.

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