A Study of Mitoxantrone Hydrochloride Liposome Injection in the Treatment of Advanced Gastric Carcinoma

NCT ID: NCT04718402

Last Updated: 2024-03-07

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 21 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-03-30
• Study Completion Date: 2022-05-30

Brief Summary

This is a multicenter, open-label, single-arm, phase Ib study to evaluate the safety and efficacy of Mitoxantrone Hydrochloride Liposome in subjects with advanced gastric carcinoma.

Detailed Description

This is a multicenter, open-label, single-arm, phase Ib study to evaluate the safety and efficacy of Mitoxantrone Hydrochloride Liposome in subjects with advanced gastric carcinoma. At least 30 subjects will be recruited in this study. The subjects will receive Mitoxantrone Hydrochloride Liposome 20 mg/m2 by an intravenous infusion (IV), every 21 days (q3w, 1 cycle). All patients will receive the treatment until disease progression, intolerable toxic reaction, death, or withdrawal by investigator or patient decision (a maximum of 8 cycles).

Conditions

Advanced Gastric Carcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Mitoxantrone Hydrochloride Liposome Injection

Subjects with advanced gastric carcinoma will receive 20mg/m2Mitoxantrone Hydrochloride Liposome every 21 days (a cycle) for a maximum of 8 cycles.

Group Type: EXPERIMENTAL

Mitoxantrone Hydrochloride Liposome, intravenous injection

Intervention Type: DRUG

All subjects will receive Mitoxantrone Hydrochloride Liposome 20 mg/m2, IV, on day 1 of each 21-day cycle (q3w).

Interventions

Mitoxantrone Hydrochloride Liposome, intravenous injection

All subjects will receive Mitoxantrone Hydrochloride Liposome 20 mg/m2, IV, on day 1 of each 21-day cycle (q3w).

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Subjects fully understand and voluntarily participate in this study and sign informed consent;

2. Age ≥18, without gender limitation;

3. Histologically confirmed diagnosis of unresectable locally advanced or metastatic gastric carcinoma, including gastroesophageal junction carcinoma;

4. Suitable to receive the study drug as decided by the investigator;

5. At least one measurable lesion according to RECIST v1.1;

6. ECOG performance status of 0 to 2;

7. Life expectancy ≥ 12 weeks;

8. AEs from the previous treatment have resolved to ≤ Grade 1 based on CTCAE (except for the toxicity without safety risk judged by the investigator, such as hair loss, hyperpigmentation);

9. Adequate organ function;

10. Subjects of childbearing potential must agree to use effective contraceptive measures. Female subjects must have a negative pregnancy test before enrolment;

11. Fully comply with the protocol.

Exclusion Criteria

1. History of allergy to mitoxantrone hydrochloride or any excipients of the study drug;

2. Untreated or symptomatic central nervous system (CNS) metastases;

3. Amenable to curative surgery ( radical excision);

4. Pleural effusion, pericardial effusion or peritoneal effusion with overt clinical symptoms (except for those have a drainage within 1 month before screening, asymptomatic and the effusion only detectable by imageological examination);

5. Intestinal obstruction with overt clinical symptom and requiring treatment;

6. CTCAE Grade 3 or Grade 4 gastrointestinal hemorrhage within 12 weeks prior to the first dose administration;

7. History of allotransplantation;

8. Known hepatitis B virus (HBV), hepatitis C virus (HCV), human immunodeficiency virus (HIV) or other active viral infection;

9. Serious infection or interstitial pneumonia within 1 week prior to the first dose administration;

10. Use of other anticancer treatment within 4 weeks prior to the first dose administration;

11. Enrolled in any other clinical trails and had recieved treatment within 4 weeks prior to the first dose administration;

12. Major surgery within 3 months prior to the first dose administration, or have a surgical schedule during the study period;

13. Thrombosis or thromboembolism within 6 months prior to screening;

14. History of, or known additional malignant tumor within 3 years, except for tumors have been cured and have not recurred, and carcinoma in situ;

15. Impaired cardiac function or serious cardiac disease;

16. Previous treatment with adriamycin or other anthracyclines, and the total cumulative dose of prior adriamycin or equivalent is >350 mg/m2.

17. Pregnant or lactating female;

18. Serious and/or uncontrolled systemic diseases;

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

Sponsors

CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jieer Ying, Doctor

Role: PRINCIPAL_INVESTIGATOR

Cancer Hospital of The University of Chinese Academy of Science

Locations

Beijing Luhe Hospital Capital Medical University

Beijing, Beijing Municipality, China

Fujian Cancer Hospital

Fuzhou, Fujian, China

Lanzhou University Second Hospital

Lanzhou, Gansu, China

Hebei General Hospital

Shijiazhuang, Hebei, China

The Fourth Hospital of Hebei Medical University and Hebei Cancer Hospital

Shijiazhuang, Hebei, China

Henan Cancer Hospital

Zhengzhou, Henan, China

Zhejiang Provincial People's Hospital

Hangzhou, Zhejiang, China

Cancer Hospital of The University of Chinese Academy of Science

Hangzhou, Zhejiang, China

Taizhou Hospital of Zhejiang Province

Taizhou, Zhejiang, China

Countries

China

Other Identifiers

HE071-CSP-014

Identifier Type: -

Identifier Source: org_study_id