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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.

Aperçu de l'étude

Description détaillée

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

Type d'étude

Interventionnel

Inscription (Anticipé)

60

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Beijing
      • Beijing, Beijing, Chine
        • Recrutement
        • Beijing Chaoyang Hospital, Capital Medical University
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 75 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

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.

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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.

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Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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
Autres noms:
  • Liposome de chlorhydrate de mitoxantrone
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
Autres noms:
  • Bortézomib
Dexamethasone (20 mg/d) will be taken orally on day 1,2,4,5,8,9,11,12 of each 28-day cycle
Autres noms:
  • Dexaméthasone
Expérimental: 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
Autres noms:
  • Liposome de chlorhydrate de mitoxantrone
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
Autres noms:
  • Bortézomib
Dexamethasone (20 mg/d) will be taken orally on day 1,2,4,5,8,9,11,12 of each 28-day cycle
Autres noms:
  • Dexaméthasone
Expérimental: 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
Autres noms:
  • Liposome de chlorhydrate de mitoxantrone
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
Autres noms:
  • Bortézomib
Dexamethasone (20 mg/d) will be taken orally on day 1,2,4,5,8,9,11,12 of each 28-day cycle
Autres noms:
  • Dexaméthasone

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Treatment-emergent adverse events (TEAEs)
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Objective response rate (ORR)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

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

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

20 octobre 2021

Achèvement primaire (Anticipé)

20 avril 2023

Achèvement de l'étude (Anticipé)

20 juin 2024

Dates d'inscription aux études

Première soumission

13 septembre 2021

Première soumission répondant aux critères de contrôle qualité

13 septembre 2021

Première publication (Réel)

22 septembre 2021

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

1 février 2022

Dernière mise à jour soumise répondant aux critères de contrôle qualité

16 janvier 2022

Dernière vérification

1 janvier 2022

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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