Clinical Pharmacokinetics of TKIs in Chinese Patients of Hepatitis B (HBV)
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| ClinicalTrials.gov Identifier: NCT03680183 |
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Recruitment Status : Unknown
Verified September 2018 by Tian-Tian Cheng, Affiliated Cancer Hospital & Institute of Guangzhou Medical University.
Recruitment status was: Recruiting
First Posted : September 21, 2018
Last Update Posted : September 28, 2018
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| Condition or disease | Intervention/treatment |
|---|---|
| Non Small Cell Lung Cancer Hepatitis B | Drug: Entecavir 1Mg Oral Tablet |
| Study Type : | Observational [Patient Registry] |
| Estimated Enrollment : | 300 participants |
| Observational Model: | Case-Control |
| Time Perspective: | Prospective |
| Target Follow-Up Duration: | 1 Year |
| Official Title: | Clinical Pharmacokinetics of Tyrosine Kinase Inhibitors in Chinese Patients of Hepatitis B |
| Actual Study Start Date : | May 22, 2018 |
| Estimated Primary Completion Date : | March 1, 2019 |
| Estimated Study Completion Date : | December 31, 2021 |
| Group/Cohort | Intervention/treatment |
|---|---|
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Pre-exposure
Entecavir 1Mg Oral Tablet
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Drug: Entecavir 1Mg Oral Tablet
The anti-HBV treatment includes a anti-HBV antibiotics and a drug of protecting liver cells or decrease alanine aminotransferase (ALT) or aspartate transaminase (AST)
Other Name: Bicyclol Tablets |
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Post-exposure
Entecavir 1Mg Oral Tablet
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Drug: Entecavir 1Mg Oral Tablet
The anti-HBV treatment includes a anti-HBV antibiotics and a drug of protecting liver cells or decrease alanine aminotransferase (ALT) or aspartate transaminase (AST)
Other Name: Bicyclol Tablets |
- Average plasma concentration of the drugs (TKIs) [ Time Frame: one year after recruit ]compare the concentration of TKIs prior to and after anti-HBV treatment
- Incidence of adverse reaction caused by TKIs [ Time Frame: one year after recruit ]the adverse reaction of TKIs before and after anti-HBV treatment
Biospecimen Retention: Samples Without DNA
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years to 70 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- pathological confirmed non-small-cell lung cancer
- with epidermal growth factor receptor (EGFR) or anaplastic lymphoma kinase (ALK) genetic mutation required by different TKIs
- liver function, ALT and/or AST <= 2*upper limit of normal (ULN)
- diagnosed of chronic hepatitis B
- Hepatitis B negative as controlled group
- receiving one type of TKIs
- Age between 18-70
Exclusion Criteria:
- diagnosed of acute/ active hepatitis B
- diagnosed of AIDS
- unable to make decision because of metastasis to central nervous system
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03680183
| Contact: Wenying Shu, PhD | 86-20-66673666 ext 2006 | 790840799@qq.com |
| China, Guangdong | |
| Affiliated Cancer Hospital & Institute of Guangzhou Medical University | Recruiting |
| Guangzhou, Guangdong, China, 510182 | |
| Contact: Wenying Shu, PhD 86-20-66673666 ext 2006 790840799@qq.com | |
| Contact: Tiantian Cheng, MD 86-20-66673677 gyzlgcp@163.com | |
| Study Director: | Shuzhong Cui, MD | Affiliated Cancer Hospital & Institute of Guangzhou Medical University |
| Responsible Party: | Tian-Tian Cheng, Secretary of GCP, Affiliated Cancer Hospital & Institute of Guangzhou Medical University |
| ClinicalTrials.gov Identifier: | NCT03680183 |
| Other Study ID Numbers: |
PTKI-HBV-01 |
| First Posted: | September 21, 2018 Key Record Dates |
| Last Update Posted: | September 28, 2018 |
| Last Verified: | September 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Studies a U.S. FDA-regulated Drug Product: | Yes |
| Studies a U.S. FDA-regulated Device Product: | No |
| Product Manufactured in and Exported from the U.S.: | Yes |
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Tyrosine kinase inhibitors pharmacokinetics Hepatitis B |
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Hepatitis A Hepatitis B Hepatitis Liver Diseases Digestive System Diseases Hepatitis, Viral, Human Virus Diseases Infections Enterovirus Infections |
Picornaviridae Infections RNA Virus Infections Blood-Borne Infections Communicable Diseases Hepadnaviridae Infections DNA Virus Infections Entecavir Antiviral Agents Anti-Infective Agents |

