Uno studio sulla monoterapia con belantamab mafodotin in partecipanti con mieloma multiplo con grado normale e variabile di compromissione della funzionalità renale (DREAMM12)
Uno studio di fase I per valutare la farmacocinetica e la sicurezza di Belantamab Mafodotin in monoterapia in partecipanti con mieloma multiplo recidivato e/o refrattario (RRMM) che hanno gradi normali e variabili di compromissione della funzionalità renale (DREAMM 12)
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Tipo di studio
Tipo di studio
Iscrizione (Effettivo)
Iscrizione
Fase
Fase
- Fase 1
Accesso esteso
Accesso esteso
A disposizione
- Disponibile: l'accesso esteso è attualmente disponibile per questo trattamento sperimentale e i pazienti che non partecipano allo studio clinico potrebbero essere in grado di accedere al farmaco, al biologico o al dispositivo medico in fase di studio.
- Non più disponibile: l'accesso esteso era disponibile per questo intervento in precedenza, ma non è attualmente disponibile e non sarà disponibile in futuro.
- Temporaneamente non disponibile: l'accesso esteso non è attualmente disponibile per questo intervento, ma dovrebbe esserlo in futuro.
- Approvato per il marketing: l'intervento è stato approvato dalla Food and Drug Administration degli Stati Uniti per l'uso da parte del pubblico.
Contatti e Sedi
Contatto 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
Luoghi di studio
-
-
-
Busan, Corea del Sud, 49241
- GSK Investigational Site
-
Seoul, Corea del Sud, 06591
- GSK Investigational Site
-
-
-
-
-
Athens, Grecia, 10676
- GSK Investigational Site
-
Athens, Grecia, 11528
- GSK Investigational Site
-
-
Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Descrizione
Criterio di inclusione:
- I partecipanti sono in grado di fornire il consenso informato firmato che include il rispetto dei requisiti e delle restrizioni elencate nel modulo di consenso informato.
- I partecipanti di sesso maschile e/o femminile devono avere almeno 18 anni di età al momento della firma del consenso informato. Nella Repubblica di Corea, i partecipanti devono avere almeno 19 anni al momento della firma del consenso informato.
- Performance status dell'Eastern Cooperative Oncology Group (ECOG) 0-2.
- - Partecipanti con diagnosi di MM confermata istologicamente o citologicamente, come definito nei criteri dell'International Myeloma Working Group: 1. Ha subito un trapianto autologo di cellule staminali (SCT) o è considerato non idoneo al trapianto; 2. Ha fallito almeno 2 linee precedenti di trattamenti anti-mieloma, incluso un farmaco immunomodulatore (esempio [ad esempio], lenalidomide o pomalidomide) e un inibitore del proteasoma (ad esempio, bortezomib, ixazomib o carfilzomib). Nella Repubblica di Corea, i partecipanti devono anche avere una malattia recidivante o refrattaria dopo il trattamento con un anticorpo anti-CD38, se accessibile ai pazienti, o altro standard di cura locale idoneo.
- I partecipanti hanno una malattia misurabile con almeno uno dei seguenti: Proteina M sierica >=0,5 grammi per decilitro (g/dL) (>=5 grammi per litro [g/L]); Proteina M urinaria >=200 milligrammi (mg) per 24 ore (mg/24 ore); e Analisi delle catene leggere libere (FLC) sieriche: livello di FLC interessato >=10 milligrammi per decilitro (mg/dL) (>=100 milligrammi per litro [mg/L]) e un rapporto FLC sierico anormale (<0,26 o >1,65) .
- I partecipanti con una storia di SCT autologo sono idonei per la partecipazione allo studio a condizione che siano soddisfatti i seguenti criteri di ammissibilità: 1. Il trapianto è stato > 100 giorni prima dell'arruolamento nello studio, 2. Nessuna infezione attiva e 3. Il partecipante soddisfa il resto del criteri di ammissibilità delineati nel presente protocollo.
- Partecipanti con adeguate funzioni del sistema di organi come definito di seguito: Conta assoluta dei neutrofili >=1,0 x 10^9 per litro (/L); Emoglobina >=7,0 g/dL o 4,9 millimoli per litro (mmol/L); Piastrine >= 50 x 10^9/L; Bilirubina totale <=1,5 x Limite superiore della norma (ULN) (la bilirubina isolata >=1,5 x ULN è accettabile se la bilirubina è frazionata e la bilirubina diretta <35% [%]); Alanina aminotransferasi <=2,5 x ULN; iGFR, Gruppo 1: normale/lievemente compromesso >=60 millilitri al minuto (mL/min); Gruppo 2: grave 15-29 ml/min; Gruppo 3: ESRD (non in dialisi) <15 ml/min; Gruppo 4: ESRD (in dialisi) <15 ml/min; e frazione di eiezione ventricolare sinistra mediante ecocardiogrammi >=40%.
- Principali criteri di inclusione aggiuntivi nel Gruppo 1 (partecipanti di controllo corrispondenti): abbinati ad almeno un partecipante con insufficienza renale grave in base al peso corporeo al basale (+/-20%) e ai livelli di albumina al basale (+/-10%).
- Partecipanti di sesso femminile: l'uso di contraccettivi da parte delle donne deve essere coerente con le normative locali relative ai metodi di contraccezione per coloro che partecipano a studi clinici. Una partecipante di sesso femminile è idonea a partecipare se non è incinta o in allattamento e si applica almeno una delle seguenti condizioni: Non è una donna in età fertile (WOCBP) OPPURE è una WOCBP e utilizza un metodo contraccettivo altamente efficace (con un tasso di fallimento <1% all'anno), preferibilmente con bassa dipendenza dell'utente, durante il periodo di intervento e per almeno 4 mesi dopo l'ultima dose dell'intervento dello studio e si impegna a non donare ovuli (ovuli, ovociti) a scopo di riproduzione durante questo periodo. Lo sperimentatore deve valutare l'efficacia del metodo contraccettivo in relazione alla prima dose dell'intervento in studio. Un WOCBP deve avere un test di gravidanza su siero altamente sensibile negativo entro 72 ore dalla somministrazione del Ciclo 1 Giorno 1 e accettare di utilizzare una contraccezione altamente efficace durante lo studio e per 4 mesi dopo l'ultima dose del farmaco in studio. Lo sperimentatore è responsabile della revisione della storia medica, della storia mestruale e dell'attività sessuale recente per ridurre il rischio di inclusione di una donna con una gravidanza precoce non rilevata.
- Partecipanti di sesso maschile: l'uso di contraccettivi da parte di uomini deve essere coerente con le normative locali relative ai metodi di contraccezione per coloro che partecipano a studi clinici. I partecipanti di sesso maschile sono idonei a partecipare se accettano quanto segue dal momento della prima dose di studio fino a 6 mesi dopo l'ultima dose del trattamento in studio per consentire l'eliminazione di qualsiasi sperma alterato: astenersi dal donare sperma e entrambi; Essere astinenti dai rapporti eterosessuali come stile di vita preferito e abituale (astinenza a lungo termine e persistente) e accettare di rimanere astinenti; OPPURE devono accettare di utilizzare un preservativo maschile anche se hanno subito una vasectomia riuscita e la partner femminile deve utilizzare un metodo contraccettivo aggiuntivo altamente efficace con un tasso di fallimento <1% all'anno come quando ha rapporti sessuali con un WOCBP (comprese le donne incinte) .
Criteri di esclusione:
- - Partecipanti con leucemia plasmacellulare attiva al momento dello screening. Amiloidosi sintomatica, sindrome POEMS attiva (polineuropatia, organomegalia, endocrinopatia, alterazioni delle proteine del mieloma e della pelle), macroglobulinemia di Waldenstroem
- I partecipanti avevano un precedente trapianto di cellule staminali allogeniche. . I partecipanti che hanno subito un trapianto di midollo osseo singenico saranno ammessi solo se non vi è alcuna storia o nessuna malattia del trapianto contro l'ospite (GvHD) attualmente attiva.
- - Il partecipante ha ricevuto un farmaco sperimentale entro 14 giorni o 5 emivite, a seconda di quale sia più breve, prima della prima dose del farmaco oggetto dello studio. Ciò include il trattamento precedente con un anticorpo monoclonale. L'unica eccezione è l'uso di emergenza di un breve ciclo di corticosteroidi sistemici (equivalente o inferiore a: desametasone 40 milligrammi al giorno [mg/giorno] per un massimo di 4 giorni) prima del trattamento.
- Precedente terapia con belantamab mafodotin.
- - Il partecipante ha ricevuto un forte inibitore del polipeptide di trasporto di anioni organici entro 14 giorni o 5 emivite, a seconda di quale sia più breve, prima della prima dose del farmaco in studio.
- Infezione sistemica attiva che richiede trattamento.
- Qualsiasi tossicità irrisolta >=Grado 2 dal trattamento precedente ad eccezione di alopecia o neuropatia periferica fino al Grado 2.
- Plasmaferesi entro 7 giorni prima della prima dose del farmaco in studio. Lo screening dei valori di laboratorio deve essere eseguito dopo l'ultima plasmaferesi.
- Qualsiasi intervento chirurgico importante nelle ultime 4 settimane prima del giorno 1 dello screening.
- Qualsiasi disturbo medico, psichiatrico preesistente grave e/o instabile o altre condizioni (incluse anomalie di laboratorio ad eccezione dell'insufficienza renale) che potrebbero interferire con la sicurezza del partecipante, l'ottenimento del consenso informato o la conformità alle procedure dello studio.
- Evidenza di mucosa attiva o sanguinamento interno.
- Attuale malattia epatica o biliare instabile secondo la valutazione dello sperimentatore definita dalla presenza di ascite, encefalopatia, coagulopatia, ipoalbuminemia, varici esofagee o gastriche, ittero persistente o cirrosi. (La malattia epatica cronica stabile [(inclusa la sindrome di Gilbert o i calcoli biliari asintomatici]) o il coinvolgimento epatobiliare della neoplasia è accettabile se il partecipante soddisfa i criteri di ammissione)
- Sono esclusi i partecipanti con tumori maligni precedenti o concomitanti diversi da MM, a meno che il tumore maligno precedente non sia stato considerato clinicamente stabile per almeno 2 anni. Il partecipante non deve ricevere una terapia attiva, diversa dalla terapia ormonale per questa malattia. (I partecipanti con cancro della pelle non melanoma trattato in modo curativo sono ammessi senza una restrizione di 2 anni)
- Evidenza di rischio cardiovascolare, inclusa una delle seguenti: Evidenza di aritmie non trattate clinicamente significative in corso, comprese anomalie dell'elettrocardiogramma clinicamente significative come blocco atrioventricolare di secondo grado (Mobitz tipo II) o di terzo grado; Storia di infarto miocardico (nei 18 mesi precedenti), sindromi coronariche acute (inclusa angina instabile), angioplastica coronarica o impianto di stent o bypass entro 3 mesi dallo screening; Insufficienza cardiaca di classe III o IV come definita dal sistema di classificazione funzionale della New York Heart Association e ipertensione incontrollata.
- Reazione nota di ipersensibilità immediata o ritardata o reazione idiosincratica a farmaci chimicamente correlati a belantamab mafodotin o a uno qualsiasi dei componenti del trattamento in studio.
- Infezione da virus dell'immunodeficienza umana nota, a meno che il partecipante non soddisfi tutti i seguenti criteri: Terapia antiretrovirale (ART) stabilita per almeno 4 settimane e carica virale dell'HIV <400 copie/mL prima della prima dose; Conta delle cellule T CD4+ (CD4+) ≥350 cellule/L e nessuna storia di infezioni opportunistiche che definiscono l'AIDS negli ultimi 12 mesi
- I partecipanti con epatite B saranno esclusi a meno che non possano essere soddisfatti i seguenti criteri: Se il partecipante è positivo agli anticorpi core dell'epatite B (HbcAb) o negativo all'antigene di superficie dell'epatite B (HbsAg), allora l'acido deossiribonucleico (DNA) del virus dell'epatite B (HBV) dovrebbe non essere rilevabile al momento dello screening; Se HbsAg+ allo screening o <= 3 mesi prima della prima dose del trattamento in studio, allora il DNA dell'HBV non dovrebbe essere rilevabile, il trattamento antivirale altamente efficace dovrebbe essere iniziato ≥4 settimane prima della prima dose del trattamento in studio. I partecipanti con cirrosi sono esclusi.
- Risultato positivo del test degli anticorpi dell'epatite C o risultato positivo del test dell'acido ribonucleico dell'epatite C allo screening o entro 3 mesi prima della prima dose del trattamento in studio, a meno che il partecipante non soddisfi i seguenti criteri: test dell'RNA negativo e trattamento antivirale riuscito (di solito durata 8 settimane) ), seguito da un test HCV RNA negativo dopo un periodo di washout di almeno 4 settimane prima della prima dose.
- Partecipanti con compromissione renale dovuta a malattia epatica (sindrome epatorenale).
- Malattia epiteliale corneale in corso, ad eccezione della lieve cheratopatia punteggiata.
- Il partecipante è una donna incinta o che allatta.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
|
Sperimentale: Parte 1: Partecipanti con funzionalità renale normale / lievemente compromessa
Partecipanti con funzionalità renale normale o lievemente compromessa (Normale: velocità di filtrazione glomerulare individuale [iGFR]: >=90 millilitri al minuto; Lieve compromissione: iGFR: 60-89 mL/min verrà somministrato con belantamab mafodotin 2,5 mg/kg per via endovenosa infusione della durata di 30 minuti Q3W il giorno 1 di ogni ciclo di 21 giorni fino a conferma della progressione della malattia, decesso, tossicità inaccettabile, revoca del consenso o fine dello studio, a seconda di quale evento si verifichi per primo.
|
Belantamab mafodotin sarà fornito come polvere liofilizzata che sarà disponibile come 100 milligrammi per flaconcino (mg/flaconcino) in flaconcino monouso per la ricostituzione.
Il belantamab mafodotin liofilizzato verrà ricostituito utilizzando acqua per preparazioni iniettabili, diluito con normale soluzione fisiologica allo 0,9% prima dell'uso.
Altri nomi:
|
|
Sperimentale: Parte 1: Partecipanti con grave compromissione renale
Ai partecipanti con funzionalità renale gravemente compromessa (iGFR: 15-29 mL/min) verrà somministrato belantamab mafodotin 2,5 mg/kg come infusione endovenosa nell'arco di 30 minuti ogni 3 settimane il giorno 1 di ogni ciclo di 21 giorni fino a conferma della progressione della malattia, morte, tossicità inaccettabile, ritiro del consenso o fine dello studio, a seconda di quale evento si verifichi per primo.
|
Belantamab mafodotin sarà fornito come polvere liofilizzata che sarà disponibile come 100 milligrammi per flaconcino (mg/flaconcino) in flaconcino monouso per la ricostituzione.
Il belantamab mafodotin liofilizzato verrà ricostituito utilizzando acqua per preparazioni iniettabili, diluito con normale soluzione fisiologica allo 0,9% prima dell'uso.
Altri nomi:
|
|
Sperimentale: Parte 2: Partecipanti con ESRD (non in dialisi)
Ai partecipanti con ESRD (iGFR: <15 mL/min) non in dialisi verrà somministrato belantamab mafodotin 2,5 mg/kg o 1,9 mg/kg (o altra dose aggiustata) come infusione endovenosa della durata di 30 minuti Q3W il giorno 1 di ogni Ciclo di 21 giorni fino a conferma della progressione della malattia, decesso, tossicità inaccettabile, revoca del consenso o fine dello studio, a seconda di quale evento si verifichi per primo.
Nella Parte 2, la dose sarà decisa dopo la valutazione dei dati di farmacocinetica e sicurezza della Parte 1.
|
Belantamab mafodotin sarà fornito come polvere liofilizzata che sarà disponibile come 100 milligrammi per flaconcino (mg/flaconcino) in flaconcino monouso per la ricostituzione.
Il belantamab mafodotin liofilizzato verrà ricostituito utilizzando acqua per preparazioni iniettabili, diluito con normale soluzione fisiologica allo 0,9% prima dell'uso.
Altri nomi:
|
|
Sperimentale: Parte 2: Partecipanti con ESRD (in emodialisi)
Ai partecipanti con ESRD (iGFR: <15 mL/min) in emodialisi verrà somministrato belantamab mafodotin 2,5 mg/kg o 1,9 mg/kg (o altra dose aggiustata) come infusione endovenosa della durata di 30 minuti Q3W il giorno 1 di ogni 21 ciclo di un giorno fino alla progressione confermata della malattia, morte, tossicità inaccettabile, revoca del consenso o fine dello studio, a seconda di quale evento si verifichi per primo.
Nella Parte 2, la dose sarà decisa dopo la valutazione dei dati di farmacocinetica e sicurezza della Parte 1.
|
Belantamab mafodotin sarà fornito come polvere liofilizzata che sarà disponibile come 100 milligrammi per flaconcino (mg/flaconcino) in flaconcino monouso per la ricostituzione.
Il belantamab mafodotin liofilizzato verrà ricostituito utilizzando acqua per preparazioni iniettabili, diluito con normale soluzione fisiologica allo 0,9% prima dell'uso.
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Part 1: Area Under the Concentration-time Curve to Last Quantifiable Timepoint (AUC(0-tlast)) Following Administration of Belantamab Mafodotin (Antibody-drug Conjugate (ADC))
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
Only those participants who were measured and analyzed (i.e., contributed to data reported in the table) were included in the Overall Number of Participants Analyzed field.
'Number Analyzed' signifies participants evaluable for the specified timepoints.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Area Under the Concentration-time Curve During the Dosing Interval (AUC(0-tau)) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Observed Plasma Concentration at the End of Infusion (C-EOI) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: End of infusion on C1D1 and C3D1
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
|
End of infusion on C1D1 and C3D1
|
|
Part 1: Maximum Observed Concentration (Cmax) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Time to Reach Cmax (Tmax) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Trough Concentration Prior to the Next Dose for Each Cycle (Ctrough) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Time of Last Observed Quantifiable Concentration (Tlast) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1 (up to Day 30 in C1 and C3)
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
For some participants, dosing in Cycle 2 or Cycle 4 was delayed, resulting in the pre-dose samples in these cycles (C2D1 or C4D1) being collected later than the protocol-defined planned days after dosing in C1D1 or C3D1.
Consequently, the last PK samples for these participants were collected outside the pre-defined protocol time points, and certain Tlast values in the data table extend beyond the original protocol-defined Time Frame.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1 (up to Day 30 in C1 and C3)
|
|
Part 1: Area Under the Concentration-time Curve to Last Quantifiable Timepoint (AUC(0-tlast)) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Area Under the Concentration-time Curve During the Dosing Interval (AUC(0-tau)) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin total Antibody.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Observed Plasma Concentration at the End of Infusion (C-EOI) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: End of infusion on C1D1 and C3D1
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
|
End of infusion on C1D1 and C3D1
|
|
Part 1: Maximum Observed Concentration (Cmax) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Time to Reach Cmax (Tmax) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin total antibody.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Trough Concentration Prior to the Next Dose for Each Cycle (Ctrough) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Time of Last Observed Quantifiable Concentration (Tlast) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1 (up to Day 30 in C1 and C3)
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
For some participants, dosing in Cycle 2 or Cycle 4 was delayed, resulting in the pre-dose samples in these cycles (C2D1 or C4D1) being collected later than the protocol-defined planned days after dosing in C1D1 or C3D1.
Consequently, the last PK samples for these participants were collected outside the pre-defined protocol time points, and certain Tlast values in the data table extend beyond the original protocol-defined Time Frame.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1 (up to Day 30 in C1 and C3)
|
|
Part 1: Area Under the Concentration-time Curve to Last Quantifiable Timepoint (AUC(0-tlast)) Following Administration of Belantamab Mafodotin (Cysteine Maleimidocaproyl Monomethyl Auristatin F (Cys-mcMMAF))
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Area Under the Concentration-time Curve During the Dosing Interval up to 168 Hours (AUC (0-168h)) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, and D15; Anytime on C3 D4, D8, and D15
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
In cases where the nominal Day 8 sample was collected prior to 168 hours and earlier time points did not permit reliable extrapolation to 168 hours, a later sample (e.g., Day 15) with a measurable concentration was used to support estimation of the concentration at 168 hours.
Outcome data are reported only for AUC over 0-168 hours.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, and D15; Anytime on C3 D4, D8, and D15
|
|
Part 1: Observed Plasma Concentration at the End of Infusion (C-EOI) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: End of infusion on C1D1 and C3D1
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
|
End of infusion on C1D1 and C3D1
|
|
Part 1: Maximum Observed Concentration (Cmax) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Time to Reach Cmax (Tmax) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 1: Time of Last Observed Quantifiable Concentration (Tlast) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As pre-specified in protocol, only specified treatment arms were planned to be analyzed for this outcome measure.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Area Under the Concentration-time Curve to Last Quantifiable Timepoint (AUC(0-tlast)) Following Administration of Belantamab Mafodotin (Antibody-drug Conjugate (ADC))
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Area Under the Concentration-time Curve During the Dosing Interval (AUC(0-tau)) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Observed Plasma Concentration at the End of Infusion (C-EOI) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: End of infusion on C1D1 and C3D1
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
|
End of infusion on C1D1 and C3D1
|
|
Part 2: Maximum Observed Concentration (Cmax) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Time to Reach Cmax (Tmax) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Trough Concentration Prior to the Next Dose for Each Cycle (Ctrough) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Time of Last Observed Quantifiable Concentration (Tlast) Following Administration of Belantamab Mafodotin (ADC)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1 (up to Day 30 in C1 and C3)
|
Blood samples were collected for PK analysis of belantamab mafodotin ADC.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
For some participants, dosing in Cycle 2 or Cycle 4 was delayed, resulting in the pre-dose samples in these cycles (C2D1 or C4D1) being collected later than the protocol-defined planned days after dosing in C1D1 or C3D1.
Consequently, the last PK samples for these participants were collected outside the pre-defined protocol time points, and certain Tlast values in the data table extend beyond the original protocol-defined Time Frame.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1 (up to Day 30 in C1 and C3)
|
|
Part 2: Area Under the Concentration-time Curve to Last Quantifiable Timepoint (AUC(0-tlast)) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Area Under the Concentration-time Curve During the Dosing Interval (AUC(0-tau)) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Observed Plasma Concentration at the End of Infusion (C-EOI) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: End of infusion on C1D1 and C3D1
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
|
End of infusion on C1D1 and C3D1
|
|
Part 2: Maximum Observed Concentration (Cmax) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Time to Reach Cmax (Tmax) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Trough Concentration Prior to the Next Dose for Each Cycle (Ctrough) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Time of Last Observed Quantifiable Concentration (Tlast) Following Administration of Belantamab Mafodotin (Total Antibody)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1 (up to Day 30 in C1 and C3)
|
Blood samples were collected for PK analysis of belantamab mafodotin Total Antibody.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
For some participants, dosing in Cycle 2 or Cycle 4 was delayed, resulting in the pre-dose samples in these cycles (C2D1 or C4D1) being collected later than the protocol-defined planned days after dosing in C1D1 or C3D1.
Consequently, the last PK samples for these participants were collected outside the pre-defined protocol time points, and certain Tlast values in the data table extend beyond the original protocol-defined Time Frame.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1 (up to Day 30 in C1 and C3)
|
|
Part 2: Area Under the Concentration-time Curve to Last Quantifiable Timepoint (AUC(0-tlast)) Following Administration of Belantamab Mafodotin (Cysteine Maleimidocaproyl Monomethyl Auristatin F (Cys-mcMMAF))
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Area Under the Concentration-time Curve During the Dosing Interval up to 168 Hours (AUC (0-168h)) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, and D15; Anytime on C3 D4, D8, and D15
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
In cases where the nominal Day 8 sample was collected prior to 168 hours and earlier time points did not permit reliable extrapolation to 168 hours, a later sample (e.g., Day 15) with a measurable concentration was used to support estimation of the concentration at 168 hours.
Outcome data are reported only for AUC over 0-168 hours.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, and D15; Anytime on C3 D4, D8, and D15
|
|
Part 2: Observed Plasma Concentration at the End of Infusion (C-EOI) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: End of infusion on C1D1 and C3D1
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
|
End of infusion on C1D1 and C3D1
|
|
Part 2: Maximum Observed Concentration (Cmax) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Time to Reach Cmax (Tmax) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
|
Part 2: Time of Last Observed Quantifiable Concentration (Tlast) Following Administration of Belantamab Mafodotin (Cys-mcMMAF)
Lasso di tempo: Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Blood samples were collected for PK analysis of belantamab mafodotin Cys-mcMMAF.
As first dose of belantamab mafodotin was administered on Day 1, cycle length correlates to Day 1 plus 21 days i.e., Day 22 in timeframe.
|
Pre-dose, end of infusion (EOI), start of infusion (SOI)+2hour (h), SOI+4h, SOI+8h and SOI+24h on Cycle(C) 1 Day(D) 1 and C3D1; Anytime on C1 D4, D8, D15, D22; Anytime on C3 D4, D8, D15, D22; Pre-dose on C2D1 and C4D1.
|
Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Part 1 and Part 2: Change From Baseline (CFB) in Vital Signs: Diastolic Blood Pressure (DBP) and Systolic Blood Pressure (SBP)
Lasso di tempo: Baseline (Day 1) and up to approx. 236 weeks
|
Blood pressures (DBP and SBP) were measured after resting for at least 5 minutes in a supine or semi-recumbent position.
Baseline (Day 1) was defined as latest pre-dose assessment with a non-missing value, including unscheduled visits.
Change from Baseline was calculated as post-dose visit value minus Baseline value.
The "0" participants analyzed represents that data was not collected or available for analysis at that particular time point for the respective Arms/Groups.
|
Baseline (Day 1) and up to approx. 236 weeks
|
|
Part 1 and Part 2: Change From Baseline (CFB) in Vital Signs: Heart Rate
Lasso di tempo: Baseline (Day 1) and up to approx. 236 weeks
|
Heart rate was measured after resting for at least 5 minutes in a supine or semi-recumbent position.
Baseline (Day 1) was defined as latest pre-dose assessment with a non-missing value, including unscheduled visits.
Change from Baseline was calculated as post-dose visit value minus Baseline value.
|
Baseline (Day 1) and up to approx. 236 weeks
|
|
Part 1 and Part 2: Number of Participants With Adverse Events (AEs)
Lasso di tempo: Up to approximately 236 weeks
|
An AE is defined as any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study intervention, whether or not considered related to the study intervention.
AEs were coded using the Medical Dictionary for Regulatory Activities (MedDRA) coding system.
|
Up to approximately 236 weeks
|
|
Part 1 and Part 2: Number of Participants With Worst Case Hematology Results by Maximum Grade Increase Post-Baseline Relative to Baseline
Lasso di tempo: Baseline (Day 1) and up to approx. 236 weeks
|
Blood samples were collected for the analysis of hematology parameters and are categorized in alignment with Common Terminology Criteria for Adverse Events (CTCAE) version 5 as Grade 1: mild; Grade 2: moderate; Grade 3: severe or medically significant; and Grade 4: life-threatening consequences.
Higher grade indicates greater severity.
An increase in grade was defined relative to the Baseline grade.
Participants with missing baseline values are assumed to have baseline value of grade 0. Increase to a maximum grade of 3 and 4 is presented.
Baseline is defined as the latest pre-dose assessment with a non-missing value, including those from unscheduled visits.
Worst Case Post-Baseline includes all scheduled and unscheduled visits post baseline.
|
Baseline (Day 1) and up to approx. 236 weeks
|
|
Part 1 and Part 2: Number of Participants With Worst Case Clinical Chemistry Results by Maximum Grade Increase Post-Baseline Relative to Baseline
Lasso di tempo: Baseline (Day 1) and up to approx. 236 weeks
|
Blood samples were collected for the analysis of clinical chemistry parameters and are categorized in alignment with Common Terminology Criteria for Adverse Events (CTCAE) version 5 as Grade 1: mild; Grade 2: moderate; Grade 3: severe or medically significant; and Grade 4: life-threatening consequences.
Higher grade indicates greater severity.
An increase in grade was defined relative to the Baseline grade.
Participants with missing baseline values are assumed to have baseline value of grade 0. Increase to a maximum grade of 3 and 4 is presented.
Baseline is defined as the latest pre-dose assessment with a non-missing value, including those from unscheduled visits.
Worst Case Post-Baseline includes all scheduled and unscheduled visits post baseline.
|
Baseline (Day 1) and up to approx. 236 weeks
|
|
Part 1 and Part 2: Change From Baseline (CFB) in Weight
Lasso di tempo: Baseline (Day 1) and up to approx. 236 weeks
|
Physical examination parameter weight was assessed.
Baseline is defined as the latest pre-dose assessment with a non-missing value, including those from unscheduled visits.
Worst Case Post-Baseline includes all scheduled and unscheduled visits post baseline
|
Baseline (Day 1) and up to approx. 236 weeks
|
|
Part 1 and Part 2: Number of Participants With Worst Case Urinalysis Results Post-Baseline Relative to Baseline
Lasso di tempo: Baseline (Day 1) and up to approx. 236 weeks
|
Urine samples were collected to assess occult blood and protein in urine by dipstick method.
Data is presented as "No Change/Decreased" and "Any Increase" that includes Increase to TRACE, Increase to 1+, Increase to 2+ and Increase to 3+ indicating proportional concentrations in the urine sample.
Baseline is defined as the latest pre-dose assessment with a non-missing value, including those from unscheduled visits.
Worst Case Post-Baseline includes all scheduled and unscheduled visits post baseline.
|
Baseline (Day 1) and up to approx. 236 weeks
|
Collaboratori e investigatori
Sponsor
Sponsor
Investigatori
Investigatori
- Direttore dello studio: GSK Clinical Trials, GlaxoSmithKline
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Inizio studio
Completamento primario (Effettivo)
Completamento primario
Completamento dello studio (Stimato)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie urogenitali
- Malattie vascolari
- Malattia cardiovascolare
- Processi patologici
- Neoplasie
- Malattie urogenitali maschili
- Malattie renali
- Malattie urologiche
- Malattie urogenitali femminili
- Malattie urogenitali femminili e complicanze della gravidanza
- Malattia cronica
- Attributi della malattia
- 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
- Insufficienza renale cronica
- Condizioni patologiche, segni e sintomi
- Malattie emiche e linfatiche
- Mieloma multiplo
- Insufficienza renale
- Insufficienza renale cronica
- mafodotina di betantamab
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- 209626
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Descrizione del piano IPD
Periodo di condivisione IPD
Criteri di accesso alla condivisione IPD
Tipo di informazioni di supporto alla condivisione IPD
- STUDIO_PROTOCOLLO
- LINFA
- ICF
- RSI
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
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 .