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A Study of MBS314 for Injection in Participants With Relapsed/Refractory Multiple Myeloma.

2 novembre 2026 mis à jour par: Beijing Mabworks Biotech Co., Ltd.

A Phase Ⅰ/Ⅱ Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of MBS314 for Injection in Patients With Relapsed/Refractory Multiple Myeloma

This is a Phase I/II, multicenter, open-label, dose-escalation and dose-expansion study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and efficacy of MBS314, a novel asymmetric trivalent trispecific humanized antibody targeting GPRC5D, BCMA and CD3, administered by subcutaneous (SC) injection in participants with relapsed or refractory multiple myeloma. The investigational drug is MBS314 for Injection (high-concentration lyophilized formulation, 90 mg/vial, reconstituted to 90 mg/mL); this study is the first-in-human (FIH) study of this formulation. The study is divided into 2 parts: a dose escalation part (Phase I) and a dose expansion part (Phase II). In Phase I, eligible participants will be sequentially assigned to 1 of the 3 planned dose cohorts and receive MBS314 by SC injection using a step-up dosing (SUD) strategy, and dose escalation follows the Bayesian Optimal Interval (BOIN) design with a target toxicity rate of 33%. In Phase II, 1 to 3 dose groups will be selected based on Phase I results to further evaluate the efficacy of MBS314 at the recommended dose(s).

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Intervention / Traitement

Type d'étude

Interventionnel

Inscription (Estimé)

78

Phase

  • Phase 2
  • 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

  • Nom: Juan Du, Doctor
  • Numéro de téléphone: 86+021-58752345
  • E-mail: Juan_du@live.com

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 et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Able and willing to provide written informed consent and to comply with the study protocol;
  2. Phase I: 18-70 years of age (inclusive) at the time of signing ICF; Phase II: ≥18 years of age;
  3. Documented diagnosis of active or symptomatic multiple myeloma according to the 2014 IMWG diagnostic criteria; Phase I: at least 3 prior lines of systemic anti-myeloma therapy including at least one proteasome inhibitor (PI), one immunomodulatory drug (IMiD) and one anti-CD38 antibody, or no available standard treatment per investigator judgment, and relapsed or refractory to the last line of therapy or intolerant to prior treatment; Phase II: at least 2 prior lines including at least one PI, one IMiD and one anti-CD38 antibody, and relapsed or refractory to the last line of therapy or intolerant to prior treatment;
  4. At least one measurable disease at screening: Serum monoclonal paraprotein (M-protein) ≥5 g/L or Urine M-protein ≥200 mg/24 hours or Serum immunoglobulin free-light chains (FLCs) ≥100 mg/L and abnormal kappa/lambda FLC ratio (<0.26 or >1.65)
  5. Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1.
  6. Life expectancy ≥3 months.
  7. Toxicity from prior anti-myeloma therapy recovered to Grade ≤1 per NCI CTCAE v6.0 (except alopecia, fatigue and Grade 2 peripheral neuropathy);
  8. Left ventricular ejection fraction (LVEF) ≥50%;
  9. Adequate hematologic, hepatic, renal and coagulation function: platelet count ≥75×10^9/L (or ≥50×10^9/L if ≥50% of bone marrow nucleated cells are plasma cells); absolute neutrophil count (NEUT) ≥1.5×10^9/L; hemoglobin ≥75 g/L; AST and ALT ≤2.5×ULN; total bilirubin ≤1.5×ULN (≤3×ULN for participants with Gilbert syndrome); serum creatinine ≤1.5×ULN or creatinine clearance ≥40 mL/min; INR or PT ≤1.5×ULN; APTT ≤1.5×ULN; corrected serum calcium ≤14 mg/dL (≤3.5 mmol/L).

Exclusion Criteria:

  1. Known active central nervous system (CNS) involvement or exhibits clinical signs of meningeal involvement of multiple myeloma.
  2. Active infection within 14 days prior to the first MBS314 administration requiring anti-infective treatment or hospitalization (including infections requiring IV antibiotics and/or hospitalization within 4 weeks, or oral antibiotics within 2 weeks prior to first dose); participants with a positive SARS-CoV-2 test result, with or without symptoms or suspected infection, are excluded;
  3. HBsAg and/or HBcAb positive with HBV DNA above the upper limit of normal; HCV antibody positive with HCV RNA above the upper limit of normal; HIV seropositive; Treponema pallidum antibody (TP-Ab) positive;
  4. Received the following anti-myeloma treatments within the specified time frame prior to the first administration: targeted therapy, immunotherapy, antibody drugs, cytotoxic drugs, antibody-drug conjugates, radiotherapy, tumor embolization, epigenetic therapy or investigational drugs (or invasive investigational medical devices) within 21 days or 5 half-lives (whichever is shorter); PIs within 14 days; IMiDs within 14 days; anti-tumor Chinese herbal medicines within 14 days; cell therapy (including but not limited to CAR-T, NK cells, neoantigen vaccines, etc.) or autologous hematopoietic stem cell transplantation within 3 months; prior allogeneic hematopoietic stem cell transplantation;
  5. Live, attenuated vaccines within 28 days prior to the first administration of MBS314, or expected to receive live, attenuated vaccines during the study period;
  6. Major surgery within 28 days prior to the first administration of MBS314, or expected to undergo major surgery during the study treatment, or with serious unhealed wounds, trauma or ulcers (except diagnostic biopsy and central venous catheterization);
  7. History of autoimmune diseases (except participants with autoimmune-related hypothyroidism on a stable dose of thyroid replacement therapy, and participants with well-controlled type 1 diabetes);
  8. History of severe allergic reactions (≥Grade 3 per NCI CTCAE v6.0) to other antibody drugs, or known allergies or hypersensitivity to any components of MBS314;
  9. Smoldering multiple myeloma, plasma cell leukemia (plasma cells >2.0×10^9/L), Waldenström macroglobulinemia, POEMS syndrome, or concurrent primary or secondary amyloidosis;
  10. Prior treatment with agents targeting both BCMA and GPRC5D, including but not limited to BCMA/GPRC5D-targeted trispecific antibodies, chimeric antigen receptor T-cell (CAR-T) therapy, or simultaneous or sequential treatment with BCMA- and GPRC5D-targeted drugs; participants previously treated with only one of the BCMA or GPRC5D targets may enroll;
  11. Other severe, poorly controlled comorbidities that may affect protocol compliance or interpretation of results, including but not limited to: clinically significant valvular heart disease; history of congestive heart failure; angina requiring medication or unstable angina; NYHA Class III or higher cardiac dysfunction; QTcF ≥470 ms (female) or ≥450 ms (male) or history of congenital long QT syndrome; myocardial infarction or acute coronary syndrome within 6 months prior to screening; thromboembolic or vascular events within 6 months prior to screening; clinically significant arrhythmias; poorly controlled hypertension (SBP >160 mmHg or DBP >100 mmHg); poorly controlled diabetes (fasting glucose ≥10 mmol/L); clinically significant pulmonary disease; uncontrolled pleural, pericardial or peritoneal effusions requiring repeated drainage or medical intervention;
  12. Any other invasive malignancy within the past 3 years (except radically treated basal or squamous cell skin cancer, carcinoma in situ of the cervix, breast or bladder, or other malignancy with low metastasis or death risk [5-year survival >90%]); progressive multifocal leukoencephalopathy; severe bleeding disorders such as hemophilia A, hemophilia B, von Willebrand disease, or spontaneous bleeding requiring transfusion or other medical intervention;
  13. Pregnant or lactating women; women of childbearing potential who do not agree to use appropriate contraception (e.g., oral contraceptives, intrauterine device, barrier contraception or spermicide) during the treatment period and for at least 6 months after the last dose of study drug;
  14. Men who do not agree to use barrier contraception during the treatment period and for at least 6 months after the last dose of study drug, and do not agree to have their partners use appropriate contraception;
  15. Any other condition that, in the judgment of the investigator, makes the participant unsuitable for participation in this study.

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: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: MBS314

Phase I: Eligible participants will be sequentially assigned to one of three dose groups under BOIN design (Dose Group 1: 3-step SUD [0.5/3.0/15.0 mg], target dose 90.0 mg; Dose Group 2 [tentative]: 3-step SUD [1.5/9.0/45.0 mg], target dose 135.0 mg; Dose Group 3 [tentative]: 3-step SUD [2.5/15.0/90.0 mg], target dose 180.0 mg). MBS314 is given subcutaneously (single injection volume ≤2.0 mL; injection sites ≥2 cm apart). Step-up dosing is used in Cycle 1: priming doses on C1D1, C1D4, C1D7 and target dose on C1D10. From Cycle 2 onwards, target dose is administered Q4W.

Phase II: Based on Phase I findings, 1-3 dose groups will be selected for dose expansion (10-20 participants per group, total 10-60).

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Phase I :Percentage of Participants with Adverse Events (AEs)
Délai: From Baseline up to 28 (+7) days after the last dose of MBS314]

Percentage of Participants with AEs and SAEs Assessed by NCI CTCAE v6.0.

From Baseline up to 28 (+7) days after the last dose of MBS314]
Phase I:Incidence of Dose Limiting Toxicities (DLTs)
Délai: From Baseline up to 4 weeks
From Baseline up to 4 weeks
Phase I:Maximum Tolerated Dose (MTD) (if any) or Optimal Biological Dose (OBD) of MBS314
Délai: Up to approximately 7 months
Up to approximately 7 months
Phase I:Recommended Phase Ⅱ Dose (RP2D) of MBS314
Délai: Up to approximately 7 months
Up to approximately 7 months
Phase II:Efficacy: Overall Response Rate (ORR) as Assessed by the Investigator
Délai: Up to approximately 15 months

ORR is defined as the proportion of participants who achieve sCR, CR, VGPR or PR according to the 2016 IMWG response criteria, as assessed by the investigator.

Up to approximately 15 months

Collaborateurs et enquêteurs

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

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 (Estimé)

1 novembre 2026

Achèvement primaire (Estimé)

1 décembre 2027

Achèvement de l'étude (Estimé)

1 novembre 2028

Dates d'inscription aux études

Première soumission

28 octobre 2026

Première soumission répondant aux critères de contrôle qualité

28 octobre 2026

Première publication (Réel)

3 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

4 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

2 novembre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

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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