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Clinical Trials/NCT04719065
NCT04719065
Unknown
Phase 1

A Multicenter, Randomized, Open-label, Phase Ib Study to Evaluate the Safety, Efficacy and Pharmacokinetic Characteristics of Mitoxantrone Hydrochloride Liposome Injection in Subjects With Advanced Solid Tumor

CSPC ZhongQi Pharmaceutical Technology Co., Ltd.8 sites in 1 country90 target enrollmentJanuary 13, 2021

Overview

Phase
Phase 1
Intervention
Mitoxantrone Hydrochloride Liposome, intravenous injection (IV)
Conditions
Advanced Solid Tumor
Sponsor
CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Enrollment
90
Locations
8
Primary Endpoint
adverse events (AEs)
Last Updated
4 years ago

Overview

Brief Summary

This is a multicenter, randomized, open-label, phase Ib study to evaluate the safety, efficacy and pharmacokinetic characteristics of Mitoxantrone Hydrochloride Liposome in subjects with advanced solid tumor.

Detailed Description

This is a multicenter, randomized, open-label, phase Ib study to evaluate the safety, efficacy and pharmacokinetic characteristics of Mitoxantrone Hydrochloride Liposome in subjects with advanced solid tumor. 90 subjects will be recruited. The first 60 subjects will be randomly assigned into 2 groups, group A and group B. The 30 subjects in group A will receive the Mitoxantrone Hydrochloride Liposome 20 mg/m2 by an intravenous infusion (IV), every 28 days (q4w, 1 cycle). The 30 subjects in group B will receive Mitoxantrone Hydrochloride Liposome 20 mg/m2, IV, every 21 days (q3w, 1 cycle). After this, the last 30 subjects will be assigned into group B. All subjects will receive the treatment until disease progression, intolerable toxic reaction, death, or withdrawal by investigator or subject decision (a maximum of 8 cycles). Delays in drug administration is allowed from cycle 2, however, the delays should be no more than 3 weeks. Dose adjustments after cycle 2 is permitted, and the minimum dose is 12 mg/m2.

Registry
clinicaltrials.gov
Start Date
January 13, 2021
End Date
April 13, 2024
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects fully understand and voluntarily participate in this study and sign informed consent;
  • Age ≥18, without gender limitation;
  • Histologically and/or cytologically confirmed diagnosis of unresectable local or metastasizing advanced solid tumor;
  • Fail to respond to standard therapy or lack of effective treatment, including no standard therapy, intolerance of standard therapy, etc.;
  • At least one measurable lesion according to RECIST v1.1;
  • ECOG performance status of 0 or 1;
  • 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);
  • Adequate organ function;
  • Subjects of childbearing potential must agree to use effective contraceptive measures. Female subjects must have a negative pregnancy test before enrollment;
  • Fully comply with the protocol.

Exclusion Criteria

  • History of allergy to mitoxantrone hydrochloride or any excipients of the study drug;
  • Untreated or symptomatic central nervous system (CNS) metastases;
  • CTCAE Grade 3 or Grade 4 gastrointestinal hemorrhage within 12 weeks prior to the first dose administration;
  • History of allotransplantation;
  • Known hepatitis B virus (HBV), hepatitis C virus (HCV), human immunodeficiency virus (HIV) or other active viral infection;
  • Serious infection or interstitial pneumonia within 1 week prior to the first dose administration;
  • Use of other anticancer treatment within 4 weeks prior to the first dose administration;
  • Enrolled in any other clinical trials within 4 weeks prior to the first dose administration;
  • Major surgery within 3 months prior to the first dose administration, or have a surgical schedule during the study period;
  • Thrombosis or thromboembolism within 6 months prior to screening;

Arms & Interventions

Group A, Mitoxantrone Hydrochloride Liposome Injection, q4w

Subjects with advanced or metastatic solid tumor will receive Mitoxantrone Hydrochloride Liposome every 28 days (a cycle) for a maximum of 8 cycles. The starting dose of Mitoxantrone Hydrochloride Liposome is 20mg/m2.

Intervention: Mitoxantrone Hydrochloride Liposome, intravenous injection (IV)

Group B, Mitoxantrone Hydrochloride Liposome Injection, q3w

Subjects with advanced or metastatic solid tumor will receive Mitoxantrone Hydrochloride Liposome every 21 days (a cycle) for a maximum of 8 cycles. The starting dose of Mitoxantrone Hydrochloride Liposome is 20mg/m2.

Intervention: Mitoxantrone Hydrochloride Liposome, intravenous injection (IV)

Outcomes

Primary Outcomes

adverse events (AEs)

Time Frame: from the first dose injection to 28 days after the last dose injection, assessed up to 36 weeks

The incidence and severity of AEs, abnormalities in physical exams, vital sign assessments, clinical laboratory assessments, ultrasonic cardiograms (UCGs) and electrocardiographs (ECGs).

Secondary Outcomes

  • duration of response (DoR)(From the enrollment to CR,PR, PD, death, lost to follow-up, withdrawal, or study end, whichever occurred first, assessed up to 36 months)
  • duration of complete response (DCR)(From the enrollment to the final documentation of response of the last subject (assessed up to 36 months))
  • overall response rate (ORR)(From the enrollment to the final documentation of response of the last subject (assessed up to 36 months))
  • progression-free survival (PFS)(From the enrollment to CR,PR, PD, death, lost to follow-up, withdrawal, or study end, whichever occurred first, assessed up to 36 months)
  • overall survival (OS)(From the enrollment to CR, PR, PD, death, lost to follow-up, withdrawal, or study end, whichever occurred first, assessed up to 36 months)
  • maximum time (Tmax)(Cycle 1 to cycle 4, approximately 16 weeks)
  • maximum concentration (Cmax)(Cycle 1 to cycle 4, approximately 16 weeks)
  • area under the plasma concentration-time curve from time zero to the time of last observed concentration (AUC0-t)(Cycle 1 to cycle 4, approximately 16 weeks)
  • apparent terminal half-life (t1/2)(Cycle 1 to cycle 4, approximately 16 weeks)

Study Sites (8)

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