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Mitoxantrone Hydrochloride Liposome Injection, Bortezomib and Dexamethasone in the Treatment of R/R MM

A Phase Ⅰ Clinical Study of Mitoxantrone Hydrochloride Liposome Injection in Combination With Bortezomib and Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma

The purpose of this study is to evaluate the safety and efficacy of mitoxantrone hydrochloride liposome injection in combination with bortezomib and dexamethasone in patients with relapsed or refractory multiple myeloma.

Studieoversikt

Detaljert beskrivelse

This is a multicenter, open-label, phase I study aimed to evaluate the safety and efficacy of mitoxantrone hydrochloride liposome injection in combination with bortezomib and dexamethasone in patients with relapsed or refractory multiple myeloma. In the study, 60 patients will be recruited into three dose groups. All patients will receive the treatment for the planned 8 cycles(28 days per cycle)until disease progression or unacceptable drug-related adverse events

Studietype

Intervensjonell

Registrering (Forventet)

60

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Beijing
      • Beijing, Beijing, Kina
        • Rekruttering
        • Beijing Chaoyang Hospital, Capital Medical University
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 75 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  1. Patients fully understand and voluntarily participate in this study and sign informed consent;
  2. Aged 18-75 years, without gender limitation;
  3. Patients with relapsed or refractory multiple myeloma(confirmed by histologically or cytologically) who had received at least one prior line regular treatment;
  4. Patients have at least one of the following conditions:(1)Serum M protein≥10g/L;(2)Urine M protein≥200 mg/24h; (3)Serum free light chain(sFLC): κ/λ FLC ratio is abnormal and affected FLC ≥100mg /L
  5. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2;
  6. Laboratory tests meet the following conditions:

    • Absolute neutrophil count (ANC) ≥1.5x10^9/L (No G-CSF treatment within 1 week prior to the laboratory test);
    • Platelet count ≥ 75x10^9/L (No platelet transfusion within 1 week prior to the laboratory test);
    • Total bilirubin ≤1.5upper limit of normal (ULN);
    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 ULN;
    • Creatinine clearance(Ccr) ≥30mL/min.
  7. Females of childbearing potential must have a negative serum beta human chorionic gonadotrophin (β-hCG) pregnancy test result prior to enrollment and must agree to use an effective contraception method for the duration of the study treatment and 7 months after the last dose of study therapy.
  8. Males patients and their partners must agree to use an effective contraceptive method for the duration of the study treatment and 4 months after the last dose of study therapy.

    -

Exclusion Criteria:

  1. Patients with amyloidosis or central nervous system invasion or on dialysis treatment.
  2. Life expectancy < 3 months.
  3. History of allergy to mitoxantrone hydrochloride or liposomes;or previous treatment with adriamycin or other anthracyclines, with the total cumulative dose (doxorubicin equivalent) ≥350 mg/m^2.
  4. History of allergy (except local injection reaction) or intolerance to bortezomib;or one of the following conditions occurred with prior bortezomib regimens: no treatment response (not reach MR),disease progression within 6 months after the end of last dose.
  5. History of contraindications or intolerance to dexamethasone.
  6. Any anti-myeloma drug treatment or radiotherapy within 4 weeks prior to the first dose; or enrolled in any other clinical trials of anti-myeloma drug within 3 months prior to the first dose.
  7. History of autologous hematopoietic stem cell transplantation within 6 months prior to screening.
  8. History of allogeneic hematopoietic stem cell transplantation or solid organ transplantation.
  9. Adverse events from the previous treatment have not resolved to ≤ Grade 1 (except for alopecia, hyperpigmentation).
  10. Patients with persistent Grade≥2 peripheral neuropathy or Grade 1 peripheral neuropathy with pain.
  11. Patients with impaired cardiac function or significant cardiac disease.
  12. HBsAg/HBcAb positive with HBV-DNA titer higher than the lower limit of the test value of the research center, or HCV antibody positive with HCV-RNA titer higher than the lower limit of the test value of the research center,or human immunodeficiency virus (HIV) antibody positive.
  13. Patients with obvious digestive system dysfunction, which may affect intake, transport and absorption of the study drug.
  14. Active bacterial, fungal or viral infections that require systemic treatment within 1 week prior to the first dose
  15. Patients underwent major surgery within 6 weeks prior to the first dose, or had a surgical schedule during the study period;
  16. History of additional malignant tumor within 5 years, except for locally curable cancer that has been cured.
  17. Other medical conditions that, in the judgment of the investigator, may affect the patient's participation in this study.
  18. Pregnant or breastfeeding women;
  19. Not suitable for this study as decided by the investigator due to other reasons.

    -

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 12 mg/m ^ 2 dose group (ArmA)
Patients with relapsed or refractory multiple myeloma will receive mitoxantrone hydrochloride liposome in combination with bortezomib and dexamethasone for 8 cycles (planned) (28 days per cycle). The dose of mitoxantrone hydrochloride liposome is 12 mg/m^2
Mitoxantrone Hydrochloride Liposome injection will be administered by an intravenous infusion on day 1 of each 28-day cycle
Andre navn:
  • Mitoxantrone Hydrochloride Liposome
Bortezomib (1.3 mg/m^2) will be administered by an intravenous injection or subcutaneously on day 1,4,8,11of each 28-day cycle
Andre navn:
  • Bortezomib
Dexamethasone (20 mg/d) will be taken orally on day 1,2,4,5,8,9,11,12 of each 28-day cycle
Andre navn:
  • Deksametason
Eksperimentell: 16 mg/m ^ 2 dose group (ArmB)
Patients with relapsed or refractory multiple myeloma will receive mitoxantrone hydrochloride liposome in combination with bortezomib and dexamethasone for 8 cycles (planned) (28 days per cycle). The dose of mitoxantrone hydrochloride liposome is 16 mg/m^2
Mitoxantrone Hydrochloride Liposome injection will be administered by an intravenous infusion on day 1 of each 28-day cycle
Andre navn:
  • Mitoxantrone Hydrochloride Liposome
Bortezomib (1.3 mg/m^2) will be administered by an intravenous injection or subcutaneously on day 1,4,8,11of each 28-day cycle
Andre navn:
  • Bortezomib
Dexamethasone (20 mg/d) will be taken orally on day 1,2,4,5,8,9,11,12 of each 28-day cycle
Andre navn:
  • Deksametason
Eksperimentell: 20 mg/m ^ 2 dose group (ArmC)
Patients with relapsed or refractory multiple myeloma will receive mitoxantrone hydrochloride liposome in combination with bortezomib and dexamethasone for 8 cycles (planned) (28 days per cycle). The dose of mitoxantrone hydrochloride liposome is 20 mg/m^2
Mitoxantrone Hydrochloride Liposome injection will be administered by an intravenous infusion on day 1 of each 28-day cycle
Andre navn:
  • Mitoxantrone Hydrochloride Liposome
Bortezomib (1.3 mg/m^2) will be administered by an intravenous injection or subcutaneously on day 1,4,8,11of each 28-day cycle
Andre navn:
  • Bortezomib
Dexamethasone (20 mg/d) will be taken orally on day 1,2,4,5,8,9,11,12 of each 28-day cycle
Andre navn:
  • Deksametason

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Treatment-emergent adverse events (TEAEs)
Tidsramme: From the initiation of the first dose to 28 days after the last dose
To indentify the incidence of TEAEs
From the initiation of the first dose to 28 days after the last dose

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Objective response rate (ORR)
Tidsramme: Throughout the study treatment(Up to 32 weeks)
ORR is defined as the proportion of patients who have a best overall response of partial response (PR),very good partial response(VGPR), complete response (CR) or stringent complete response (sCR) as per International Myeloma Working Group (IMWG)
Throughout the study treatment(Up to 32 weeks)
Clinical Benefit Rate(CBR)
Tidsramme: Throughout the study treatment(Up to 32 weeks)
CBR is defined as the proportion of patients who have a best overall response of minimal response(MR),PR,VGPR,CR or sCR as per IMWG
Throughout the study treatment(Up to 32 weeks)
Disease control rate(DCR)
Tidsramme: Throughout the study treatment(Up to 32 weeks)
DCR is defined as the proportion of patients who have a best overall response of stable disease (SD),MR,PR,VGPR,CR or sCR as per IMWG
Throughout the study treatment(Up to 32 weeks)
Duration of response (DoR)
Tidsramme: Throughout the study completion.(An average of 12 months)
DoR is defined as the time from the first assessment of PR,VGPR,CR orsCR until the date of first occurrence of progressive disease (PD) as per IMWG
Throughout the study completion.(An average of 12 months)
Progression-free survival (PFS)
Tidsramme: Throughout the study completion.(An average of 12 months)
PFS is defined as the time from the date of first dose until the date of first documented PD as per IMWG or death from any cause, whichever occurs first
Throughout the study completion.(An average of 12 months)
Overall survival (OS)
Tidsramme: Throughout the study completion.(An average of 36 months)
OS is defined as the time from the date of first dose until the date of death from any cause
Throughout the study completion.(An average of 36 months)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Wenming Chen, Beijing Chaoyang Hospital Affiliated to Capital Medical University

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

20. oktober 2021

Primær fullføring (Forventet)

20. april 2023

Studiet fullført (Forventet)

20. juni 2024

Datoer for studieregistrering

Først innsendt

13. september 2021

Først innsendt som oppfylte QC-kriteriene

13. september 2021

Først lagt ut (Faktiske)

22. september 2021

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

1. februar 2022

Siste oppdatering sendt inn som oppfylte QC-kriteriene

16. januar 2022

Sist bekreftet

1. januar 2022

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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