PF-AtlasClinical Trials › NCT00590538

Phenylbutyrate/Genistein Duotherapy in Delta F508-Heterozygotes

Sodium 4-Phenylbutyrate · Phase 1

Registry ID
NCT00590538
Phase
Phase 1
Status
Terminated
Drug / intervention
Sodium 4-Phenylbutyrate
Sponsor
Children's Hospital of Philadelphia
Start
2003-02
Enrollment
9
Locations
1

About this trial

The purpose of this research study is to test a new combination of medicines, Phenylbutyrate and Genistein, to determine if they could be used to treat cystic fibrosis (CF). The most common genetic mutation found in patients with CF is called Delta F508. Due to this mutation, there is a lack of salt (chloride) movement in your nose, sinuses, lungs, intestines, pancreas and sweat glands. This lack of movement causes the clinical manifestations of the disease. Although Phenylbutyrate has been extensively used to treat patients with rare metabolic diseases, Phenylbutyrate is an investigational drug for the purpose of this study. Genistein is a naturally occurring substance that is found in food products such as soy and tofu, but is also an investigational drug for this study. When used together, both drugs may be able to restore normal chloride and salt (water) movements in body organs and glands in people with CF. We will be studying salt and water movement in the nose by a technique called nasal transepithelial potential difference (NPD).

View NCT00590538 on ClinicalTrials.gov →

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Medical disclaimer. This page summarizes public trial data for NCT00590538 for information only. It is not medical advice, an endorsement, or an offer to enroll. Confirm details on ClinicalTrials.gov and with a qualified physician.