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Clinical Trials/NCT00838747
NCT00838747CompletedNot Applicable

Measurement of the Folate Receptor in Blood

Royal Marsden NHS Foundation Trust1 site in 1 country7 target enrollmentStarted: September 2008Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
7
Locations
1
Primary Endpoint
To measure the levels of folate receptor in blood samples obtained from patients with ovarian cancer and from healthy volunteers

Study Overview

Brief Summary

The folate receptor (FR) is a cell marker that is over expressed on the cell surface of certain cancers, this occurs most frequently in ovarian cancers. Some normal tissues also express the FR, however in these normal tissues the FR is usually located on the tissue surface that is inaccessible to circulating drugs. As such, drugs which target the FR may potentially be used to achieve anti-tumour efficacy whilst reducing toxicity to normal tissues. Therefore the ability to measure FR levels from different cancer types may help to select patients who are most likely to benefit from treatment with FR targeted therapies. One such drug BGC 945 is currently being tested in preclinical study at The Institute of Cancer Research

Detailed Description

A method has been developed in the laboratory which has been able to measure FR obtained from cancer cells in culture that has been added into blood. We would like to study if this method can measure FR in plasma and serum obtained from patients with ovarian cancer. We would also like to analyse plasma and serum samples obtained from healthy volunteers to determine if they have any appreciable levels of FR, which can then be compared to the measurements obtained from cancer patients.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Patients with stage III/IV ovarian cancer
  • healthy volunteers who are staff at the ICR and RMH

Exclusion Criteria

  • patients or healthy volunteers who are unable to give informed consent
  • pregnancy

Outcomes

Primary Outcomes

To measure the levels of folate receptor in blood samples obtained from patients with ovarian cancer and from healthy volunteers

Time Frame: 1 year

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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