NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000000591

Registered date:15/02/2007

Study of pharmacokinetics and the best way of administration of gefitinib for treated lung adenocarcinoma

Basic Information

Recruitment status
Health condition(s) or Problem(s) studiedLung adenocarcinoma
Date of first enrollment2006/10/01
Target sample size15
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)250mg of gefitinib, every other day. 250mg of gefitinib everyday, every other week.

Outcome(s)

Primary OutcomeTolerance
Secondary OutcomePharmacokinetics of gefitinib Response rate

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximum80years-old
GenderMale and Female
Include criteria
Exclude criteriasevere complication pregnant diarrhea current smoker

Related Information

Contact

public contact
Name
Address Japan
Telephone
E-mail shirano@imcj.hosp.go.jp
Affiliation International madical center of Japan Respiratory medicine
scientific contact
Name Satoshi Hirano
Address 1-21-1, Toyama, Shinjuku-ku, Tokyo, Japan, 162-8655 Japan
Telephone
E-mail
Affiliation International madical center of Japan Respiratory medicine