- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07609706
A Study of the Combination of Belantamab Mafodotin, Bortezomib, and Dexamethasone (BVd) in Participants With Multiple Myeloma and Moderate Hepatic Impairment
20 maggio 2026 aggiornato da: GlaxoSmithKline
A Phase 1 Study to Evaluate the Pharmacokinetics and Safety of the Combination of Belantamab Mafodotin, Bortezomib, and Dexamethasone (BVd) in Participants With Multiple Myeloma and Moderate Hepatic Impairment
The goal of the clinical trial is to collect safety data and information on how the body processes BVd in people with multiple myeloma (MM) who have moderate liver problems, compared with similar participants who have normal liver function.
It also compares how liver problems affect the body's handling of belantamab mafodotin and uses the results to help set safe and appropriate dosing guidance for MM participants with moderate liver problems.
Panoramica dello studio
Stato
Non ancora reclutamento
Condizioni
Intervento / Trattamento
Tipo di studio
Interventistico
Iscrizione (Stimato)
20
Fase
- Fase 1
Accesso esteso
A disposizione al di fuori della sperimentazione clinica.
Vedi record di accesso esteso.
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: US GSK Clinical Trials Call Center
- Numero di telefono: 877-379-3718
- Email: GSKClinicalSupportHD@gsk.com
Backup dei contatti dello studio
- Nome: EU GSK Clinical Trials Call Center
- Numero di telefono: +44 (0) 20 89904466
- Email: GSKClinicalSupportHD@gsk.com
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
Inclusion Criteria:
- Is at least 18 years of age or the legal age of consent in the jurisdiction in which the study is taking place at the time of signing the informed consent form (ICF).
- Has histologically or cytologically confirmed diagnosis of MM, as defined by the International Myeloma Working Group (IMWG).
- Previously treated with at least 1 prior line of MM therapy and must have documented disease progression during or after their most recent therapy.
Has at least 1 aspect of measurable disease, defined as at least 1 of the following:
- Urine M-protein excretion ≥200 milligram (mg)/24 hours (≥0.2 gram [g]/24 hours)
- Serum M-protein concentration ≥0.5 g/ deciliter (dL) (≥5.0 g/L)
- Serum Free light chain (FLC) assay: involved FLC level ≥10 mg/dL (≥100 mg/L) and an abnormal serum FLC ratio (<0.26 or >1.65).
- Plasmacytoma measurable as per IMWG criteria
- Bone Marrow infiltration by plasma cells >30%
- For those participants with a history of autologous stem cell transplant, they are eligible for study participation provided the following eligibility criteria are met: transplant was >100 days prior to study enrollment; no active infection(s); participant meets the remainder of the eligibility criteria
- All prior treatment-related toxicities (defined by National Cancer Institute Common terminology criteria for adverse events [NCI-CTCAE] v5.0) must be Grade ≤1 at the time of treatment assignment, except for alopecia (any grade), neuropathy (Grade ≤2), or endocrinopathy managed with replacement therapy (any grade).
- Is willing to use adequate contraception male and female participants.
- Female participants are eligible to participate if they are not pregnant or breastfeeding and meet additional requirements.
- Is capable of giving signed informed consent including compliance with the requirements and restrictions listed in the ICF and protocol.
- Has adequate organ function for hematological and renal function tests.
- Has specific hepatic function ranges for serum bilirubin and AST for Group 1 and Group 2.
- Participants in Group 1 (normal hepatic function) will only be enrolled if they match a participant in Group 2 (moderate hepatic impairment). Each Group 1/Group 2 pair will be matched based on the Group 2 participant's baseline body weight (±20%).
- Participants with a history of Hepatitis B virus (HBV) and/or Hepatitis C virus (HCV) and Human immunodeficiency virus (HIV) exposure are eligible under specific conditions
Exclusion Criteria:
- Has an active plasma cell leukemia at the time of screening, symptomatic amyloidosis, active POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes), or Waldenström macroglobulinemia.
- Has a previous or concurrent invasive malignancy other than MM, except for any other disease from which the participant must be considered medically stable for at least 1 year; or the participant must not be receiving active therapy, other than hormonal therapy for this disease.
- Known immediate or delayed hypersensitivity reaction or idiosyncratic reaction to drugs chemically related to belantamab mafodotin, or any of the components of the study treatment.
- Has evidence of active mucosal or internal bleeding.
- Has a systemic active infection requiring treatment.
- Has had any major surgery (other than bone-stabilizing surgery) within 28 days prior to the first dose of study treatment.
- Has current corneal epithelial disease except for mild superficial keratopathy.
- Has any serious and/or unstable medical or psychiatric disorder or other condition(s) (including laboratory assessment abnormalities) that could interfere with the participant's safety, obtainment of informed consent, or compliance to the study procedures.
- Has any history of prior allogenic stem cell transplant. Participants who have undergone syngeneic transplant will be allowed only if no history of or no currently active graft versus host disease.
- Has received prior belantamab mafodotin therapy if given within the last 90 days.
- Has received treatment with an investigational agent within 14 days or 5 half-lives, whichever is shorter, preceding the first dose of study drug. This includes prior treatment with a monoclonal antibody and any other B-cell maturation antigen (BCMA) targeting therapy. The only exception is emergency use of a short course of systemic corticosteroids (equivalent to, or less than: dexamethasone 40 mg/day for a maximum of 4 days) before treatment.
- Has received treatment with an inhibitor of Organic anion transporting polypeptide (OATP)1B1 or OATP1B3 within 14 days, preceding the first dose of study drug.
- Has received plasmapheresis within 7 days prior to the first dose of study treatment. Screening laboratory values must be performed after last plasmapheresis.
- Has received any live vaccine within 30 days of enrollment. Vaccination against COVID-19 using vaccines that are authorized via the appropriate regulatory mechanisms (e.g., Conditional Marketing Authorization, or Marketing Authorization Application) are not exclusionary.
Has a known HIV infection, unless the participant meets all of the following criteria:
- Established Anti-retroviral therapy (ART) for at least 4 weeks and HIV viral load <400 copies/milliliter (mL) prior to first dose.
- Has CD4+ T-cell count values ≥350 cells/L
- No history of acquired immunodeficiency syndrome (AIDS)-defining opportunistic infections within the last 12 months.
- Is pregnant, plans to become pregnant, or is breastfeeding.
- Has Gilbert's syndrome.
- Has current unstable liver or biliary disease per investigator assessment defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal/gastric varices, or persistent jaundice in the last 14 days prior to the first dose.
- Has documented presence of Hepatitis B surface antigen (HBsAg) and/or Hepatitis B core antibody (HBcAb) at screening or within 3 months prior to the first dose of study intervention. Participants with hepatitis B will be excluded unless the specific protocol criteria are met.
- Has a positive Hepatitis C virus (HCV) antibody test result at screening or within 3 months prior to the first dose of study intervention unless HCV ribonucleic acid (RNA) is negative, indicating past resolved HCV infection, including participants who have undergone curative treatment, unless specific protocol criteria are met
- Has a positive HCV RNA test result at screening or within 3 months prior to the first dose of study intervention.
Evidence of cardiovascular risk including any of the following:
- Evidence of current clinically significant untreated arrhythmias, including clinically significant electrocardiogram (ECG) abnormalities including second degree (Mobitz Type II) or third degree atrioventricular block.
- History of myocardial infarction, acute coronary syndromes (including unstable angina), coronary angioplasty, or stenting or bypass grafting within 3 months of Screening.
- Class III or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system.
- Uncontrolled hypertension.
- Has QT interval corrected (QTc) >450 milliseconds (msec) or QTc >480 msec for participants with bundle branch block
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Funzionalità epatica normale
|
Verrà somministrato belantamab mafodotin.
Verrà somministrato desametasone.
Bortezomib verrà somministrato.
|
|
Sperimentale: Compromissione epatica moderata
|
Verrà somministrato belantamab mafodotin.
Verrà somministrato desametasone.
Bortezomib verrà somministrato.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Area under the plasma concentration-time curve from time 0 to the end of the dosing interval (AUC 0-tau) of belantamab mafodotin antibody drug conjugate (ADC)
Lasso di tempo: Up to 3 weeks
|
Up to 3 weeks
|
|
Maximum observed plasma concentration (Cmax) of belantamab mafodotin ADC
Lasso di tempo: Up to 3 weeks
|
Up to 3 weeks
|
|
Concentration at end of infusion (C-EOI) of belantamab mafodotin ADC
Lasso di tempo: Up to 104 weeks
|
Up to 104 weeks
|
|
Drug concentration reached prior to next dose (Ctrough) of belantamab mafodotin ADC
Lasso di tempo: Up to 104 weeks
|
Up to 104 weeks
|
|
Time to reach Cmax (Tmax) of belantamab mafodotin ADC
Lasso di tempo: Up to 3 weeks
|
Up to 3 weeks
|
|
Area under the plasma concentration-time curve from time 0 to 168 hours (AUC 0-168h) of microtubule inhibitor released from belantamab mafodotin (cys-mcMMAF)
Lasso di tempo: Up to 168 hours
|
Up to 168 hours
|
|
Area under the plasma concentration-time curve from time 0 to 240 hours (AUC 0-240h) of cys-mcMMAF
Lasso di tempo: Up to 240 hours
|
Up to 240 hours
|
|
Cmax of cys-mcMMAF
Lasso di tempo: Up to 3 weeks
|
Up to 3 weeks
|
|
Tmax of cys-mcMMAF
Lasso di tempo: Up to 3 weeks
|
Up to 3 weeks
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Number of participants with adverse events (AEs) and serious AEs by severity
Lasso di tempo: Up to 252 weeks
|
Up to 252 weeks
|
|
|
Number of participants with AEs leading to dose modifications or study intervention discontinuation
Lasso di tempo: Up to 252 weeks
|
Up to 252 weeks
|
|
|
Number of participants with changes in visual acuity (VA) and corneal findings by severity as assessed by Keratopathy Visual Acuity scale (KVA) scale
Lasso di tempo: Up to 252 weeks
|
The Keratopathy-Visual Acuity (KVA) scale is a 0-4 grading system used to assess the severity of keratopathy and its impact on visual acuity.
Higher grades reflect increasing severity of corneal findings and visual acuity loss.
|
Up to 252 weeks
|
|
Number of participants with ocular AEs by severity as assessed by Common terminology criteria for adverse events (CTCAE)
Lasso di tempo: Up to 252 weeks
|
Up to 252 weeks
|
|
|
Number of participants with thrombocytopenic events by severity
Lasso di tempo: Up to 252 weeks
|
Up to 252 weeks
|
|
|
Change from baseline in clinical laboratory parameter: serum bilirubin (milligrams per decilitre[mg/dl])
Lasso di tempo: Baseline (Day 1) and up to 252 weeks
|
Baseline (Day 1) and up to 252 weeks
|
|
|
Change from baseline in clinical laboratory parameter: AST and ALT (International Units per litre [IU/L])
Lasso di tempo: Baseline (Day 1) and up to 252 weeks
|
Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) will be analysed.
Both parameters have same unit of measure.
|
Baseline (Day 1) and up to 252 weeks
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
23 ottobre 2026
Completamento primario (Stimato)
22 agosto 2031
Completamento dello studio (Stimato)
22 agosto 2031
Date di iscrizione allo studio
Primo inviato
20 maggio 2026
Primo inviato che soddisfa i criteri di controllo qualità
20 maggio 2026
Primo Inserito (Effettivo)
27 maggio 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
27 maggio 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
20 maggio 2026
Ultimo verificato
1 maggio 2026
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie vascolari
- Malattia cardiovascolare
- Neoplasie
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Malattie ematologiche
- Malattie linfoproliferative
- Disturbi immunoproliferativi
- Neoplasie, plasmacellule
- Disturbi emostatici
- Paraproteinemie
- Disturbi delle proteine del sangue
- Disturbi emorragici
- Malattie emiche e linfatiche
- Mieloma multiplo
- Prodotti chimici organici
- Composti eterociclici, 1-anello
- Composti eterociclici
- Composti policiclici
- Prodotti chimici inorganici
- Incinta
- In gravidanza
- Steroidi
- Composti anelli fusi
- Steroidi, fluorurati
- Incintadienetrioli
- Acidi boronic
- Acidi, non carbossilici
- Acidi
- Composti di boro
- Pirazine
- Bortezomib
- Desametasone
- mafodotina di betantamab
Altri numeri di identificazione dello studio
- 308247
- 2026-526725-18-00 (Ctis)
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Descrizione del piano IPD
GSK will assess requests from qualified researchers for anonymized individual patient-level data and related study documents.
Data sharing is subject to certain criteria, conditions, and exceptions.
For further information, refer to https://www.gsk-studyregister.com/gsk-patient-level-data-sharing-july2025.pdf
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Sì
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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-
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