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Bioequivalence test of gefitinib tablets in Chinese healthy subjects under fed conditions

An open, randomized, tuo periods, double cross bioequivalence test of gefitinib tablets in Chinese healthy subjects under fed conditions

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008903
Enrollment
Unknown
Registered
2016-07-25
Start date
2016-07-20
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

non-small cell carcinoma

Interventions

1:T-R
2:R-T

Sponsors

The first hospital of Jilin university
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) To be able to understand and provide written informed consent and voluntary consent to participate in the study; 2) To be able to complete the study in compliance with the protocol; 3) No birth plan during the study and within 6 months after the study; 4) Healthy male Chinese volunteers aged from 18 to 65 (including 18 and 65); 5) BW more than 50 kg, BMI between 18 to 28 (including the criticals); 6) Healthy status: no heart, liver, kidney, digestive system, nervous system, mental disorders and metabolic disorders and other medical history; 7) Physical examination is normal or determined by no clinically significant.

Exclusion criteria

Exclusion criteria: 1) Consume more than 5 cigarettes per day or the equivalent within three months before the test; 2) Have known allergies to compounds related to gefitinib; 3) The subjects have a history of drug and /or alcohol abbuse (alcohol in take 14 units weekly:1 unit=285ml beer,or 25ml liquor,or 1 cup of wine); 4) Have a blood donation or blood loss (450 ml)within three months before taking research drugs; 5) if the subjects taking any drugs of changing the liver enzyme activity or not within 28 days before taking medicine ; 6) have taken any prescription,non-prescriiption drugs ,any vitamin products or herbs within 14 days prior to the study; 7) take over special diet (including pitava,mango,pomelo,and/or xanthine diet)or taking strenous exercise, or the other factors that affect drug absorption,distribution, metabolism and excretion within 2 weeks before the test; 8) Use any inhibitors or inducers associated with CYP3A4 Bcrp or P-gp, such as itraconazoleketoconazole, or dornedarone, ect.; 9) If there were any major changes or not on a diet or exercise habits recently; 10) Whether to take study drug or participated in drug clinical trials within three months before the study; 11) Have a history of gastrointestinal diseases about difficulty swallowing or any effects of drug absorption; 12) Suffering from any increased bleeding risk of diseasas such as hemorrhoids,acute gastritis or gastric and duodenal ulcers ect; 13) Abnormal ECG have clinical significance; 14) Clinical laboratory examination were abnormal clinical significancce or other clinical findings show that there are cllinical significance of the following diseases (including but nnot limited to the gastrointestinal tractkidney liver neural blood endocrine tumor lung immune mental or cardiovascular disease; 15) Have hepatitis (including hepatitis B and C) and tested positive for HIV/AIDS screening; 16) Acute illness happened before the screening stage prior to the study or before taking study drugs; 17) The subjects intake of chocolate,any caffeinated,or xanthine-containing food or drinks within 48 hours before taking study drugs; 18) Use any alcoholic products within 24 hours before taking study medication; 19) The subjects Screened positive for drug and alcohol or had has a history of substance abuse in the past five years or used drugs 3 months before the study.

Design outcomes

Primary

MeasureTime frame
Cmax;AUC;

Secondary

MeasureTime frame
safety indicator;

Countries

China

Contacts

Public ContactYanhua Ding

The First Hospital of Jilin University

dingyanhua2003@126.com+86 0431-88782168

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026