Bioequivalence Study of Irinotecan Liposome Injection in Chinese Advanced Pancreatic Cancer.

NCT ID: NCT04482257

Last Updated: 2020-07-22

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-07-07
• Study Completion Date: 2021-03-31

Brief Summary

Randomized, Open-label, Single-dose, Two-sequence, Two-period, Crossover Bioequivalence Trial of Irinotecan Liposome Injection in Patients With Advanced Pancreatic Cancer.

Detailed Description

The purpose of this study was to determine the bioequivalence of two formulations of Irinotecan Liposome Injection (70mg/m2) in Chinese patients with Advanced Pancreatic Cancer, under fasting condition. These data were to be evaluated statistically to determine if the products meet bioequivalence criteria.

Conditions

Advanced Pancreatic Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

T-R

Subjects will receive Irinotecan Liposome Injection (CSPC) 70mg/m2 plus 5-FU/LV, followed by Irinotecan Liposome Injection (Ipsen) 70mg/m2 plus 5-FU/LV

Group Type: EXPERIMENTAL

Irinotecan Liposome Injection combined with 5-FU/LV

Intervention Type: DRUG

Drug: Irinotecan Liposome Injection 70mg/m2 (CSPC) combined with 5-FU/LV; Drug: Irinotecan Liposome Injection 70mg/m2 (Ipsen, ONIVYDETM) combined with 5-FU/LV;

R-T

Subjects will receive Irinotecan Liposome Injection (Ipsen) 70mg/m2 plus 5-FU/LV, followed by Irinotecan Liposome Injection (CSPC) 70mg/m2 plus 5-FU/LV

Group Type: EXPERIMENTAL

Irinotecan Liposome Injection combined with 5-FU/LV

Intervention Type: DRUG

Drug: Irinotecan Liposome Injection 70mg/m2 (CSPC) combined with 5-FU/LV; Drug: Irinotecan Liposome Injection 70mg/m2 (Ipsen, ONIVYDETM) combined with 5-FU/LV;

Interventions

Irinotecan Liposome Injection combined with 5-FU/LV

Drug: Irinotecan Liposome Injection 70mg/m2 (CSPC) combined with 5-FU/LV; Drug: Irinotecan Liposome Injection 70mg/m2 (Ipsen, ONIVYDETM) combined with 5-FU/LV;

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Signed written informed consent for participation in the trial.

2. Advanced pancreatic cancer diagnosed by histopathology and / or cytology.

3. Age ≥ 18 years, men or women. BMI is above 17.

4. ECOG score 0 to 2.

5. Life expectancy ≥ 3 months.

6. Adequate bone marrow function.

7. Adequate hepatic function.

8. Adequate renal function.

9. Patient with reproductive potential must agree to use adequate contraception from the signing of informed consent to at least 6 months after the trial

Exclusion Criteria

1. Patients who have a severe allergy or a significant history of hypersensitivity or an idiopathic reaction attributed to irinotecan or compounds of similar chemical composition to irinotecan ;

2. Patients who have previously used irinotecan liposomes and experienced treatment failure or serious adverse reactions;

3. Patients with severe cardiovascular, lung, liver, kidney, gastrointestinal, endocrine, immune system, skin, musculoskeletal, neurological or psychiatric diseases that occurred within 3 months of the first dose of the study drug, and not suitable for this study as determined by the researchers;

4. Patients who have undergone major surgery within 4 weeks of screening or have a schedule for major surgery during the study period;

5. Patients who have received any radiotherapy or chemotherapy and other anti-tumor treatment within 4 weeks of the first dose of the study drug, traditional Chinese medicine with anti-tumor indications within 4 weeks of the first dose of the study drug, or small molecule targeted drugs within 2 weeks (or 5 half-lives whichever is longer) of the first dose of the study drug;

6. Patients who currently enrolled in any other clinical study, or received other investigational agents within 4 weeks of the first dose of the study drug；

7. Blood donation or massive blood loss (>400mL) within 90 days of screening;

8. Concomitant use of strong CYP3A4 inhibitors or inducers, or UGT1A1 inhibitors within 4 weeks of the first dose of the study drug;

9. Patients who received certain diet (such as grapefruit) which may interfere with the evaluation of PK results;

10. LVEF≤50%;

11. Patients with extended QT/QTc interval (QTcF>480ms);

12. History of alcohol or drugs abuse;

13. Pregnant or lactating women;

14. Patients with known Hepatitis B Virus (HBV DNA≥104), Hepatitis C Virus (anti-HCV positive, HCV RNA positive), Human immunodeficiency virus antibody (anti-HIV positive), or active Treponema Pallidum viral infection;

15. Patients with homozygous UGT1A1*28 genotype or UGT1A1*6 genotype;

16. Patients who are not suitable for this study as determined by the researchers.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

CSPC Ouyi Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jihui Hao, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Tianjin Cancer Hospital

Locations

Tianjin Cancer Hospital

Tianjin, Tianjin Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

xuekun Yao

Role: CONTACT

yaoxuekun@mail.ecspc.com

0311-67808678

Facility Contacts

Tianqiang Song

Role: primary

ec_tjcih@126.com

022-23340123 ext. 6012

Other Identifiers

HE072-BE-002

Identifier Type: -

Identifier Source: org_study_id