- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01939899
Phase 2 Study of Oral IXAZOMIB in Adult Participants With Relapsed and/or Refractory Follicular Lymphoma
7 ottobre 2019 aggiornato da: Millennium Pharmaceuticals, Inc.
An Open-label, Multicenter, Phase 2 Study of Oral IXAZOMIB (MLN9708) in Adult Patients With Relapsed and/or Refractory Follicular Lymphoma
The primary purpose of this study is to evaluate the anti-tumor activity of oral Ixazomib as measured by overall response rate (ORR) in adult participants with relapsed and/or refractory follicular lymphoma (FL).
Panoramica dello studio
Tipo di studio
Interventistico
Iscrizione (Effettivo)
29
Fase
- Fase 2
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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Gent, Belgio
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Leuven, Belgio
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Wilrijk, Belgio
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Quebec
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Montreal, Quebec, Canada
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London, Regno Unito
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Manchester, Regno Unito
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Newcastle Upon Tyne, Regno Unito
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Plymouth, Regno Unito
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Southampton, Regno Unito
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Sutton, Regno Unito
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Massachusetts
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Boston, Massachusetts, Stati Uniti
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New York
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New York, New York, Stati Uniti
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Tennessee
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Nashville, Tennessee, Stati Uniti
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Texas
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Houston, Texas, Stati Uniti
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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
18 anni e precedenti (Adulto, Adulto più anziano)
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion Criteria:
- Male or female participants 18 years or older.
- Participants must have a pathologically confirmed diagnosis of non-Hodgkin lymphoma (NHL) (for the lead-in dose-finding phase) and FL (for phase 2).
- Participants must have radiographically or clinically measurable disease.
- Participants must be relapsed and/or refractory after at least 1 prior therapy (excluding radiation) with documented progressive disease at the time of enrollment.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
- Female participants who are post menopausal, surgically sterile, or agree to practice 2 effective methods of contraception or agree to practice true abstinence.
- Male participants who agree to practice effective barrier contraception or agree to practice true abstinence.
- Voluntary written consent.
- Suitable venous access.
- Appropriate clinical laboratory values as defined in the protocol.
- Recovered from toxicities of prior anticancer therapy.
- If the trial proceeds to the second step on the basis of the tandem 2-step design, participants must be confirmed PSMB1 positive at the central laboratory before treatment.
Exclusion Criteria
- Peripheral neuropathy that is greater or equal to Grade 2 or Grade 1 with pain.
- Female participants who are lactating and breastfeeding or have a positive serum pregnancy test during the Screening period.
- Autologous stem cell transplant within 6 months before Day 1 of Cycle 1, or prior allogeneic stem cell transplant at any time.
- Major surgery within 14 days before the first dose of study drug.
- Infection requiring systemic antibiotic therapy or other serious infection within 14 days before the first dose of study drug.
- Comorbid systemic illnesses or other severe concurrent disease that, in the judgment of the investigator, would make the participants inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens.
- Evidence of current uncontrolled cardiovascular conditions including uncontrolled hypertension, severe uncontrolled ventricular arrhythmias, unstable angina, New York Heart Association (NYHA) Class III or IV cardiac disease, or myocardial infarction within the past 6 months.
- Diarrhea greater than (>) Grade 1 on the basis of the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) categorization.
- Systemic antineoplastic (including glucocorticoids > the equivalent of 15 mg of prednisone daily), experimental, or radiation therapy within 21 days before the first dose of study drug.
- Prior treatment with rituximab or other unconjugated antibody treatment within 42 days (21 days if clear evidence of progressive disease or immediate treatment is mandated).
- Treatment with radioimmunoconjugates or toxin immunoconjugates within 12 weeks before the first dosing of study treatment.
- Systemic treatment with strong inhibitors of Cytochrome P450 1A2 (CYP1A2) or Cytochrome P450 3A (CYP3A), or strong CYP3A inducers within 14 days before the first dose of IXAZOMIB - Ongoing systemic therapy with corticosteroids.
- Central nervous system (CNS) involvement that is clinically uncontrolled or newly diagnosed in the last 4 months.
- Ongoing or active systemic viral infection, known human immunodeficiency virus (HIV) positive, known active hepatitis B virus or known active hepatitis C virus.
- Diagnosed or treated for another malignancy within 2 years before study enrollment or previously diagnosed with another malignancy and have any evidence of residual disease with the exception of nonmelanoma skin cancer or any completely resected carcinoma in situ.
- Platelet transfusions within 3 days before the 1st dose of study drug.
- Inability to swallow capsules, or inability or unwillingness to avoid taking anything by mouth except for water and prescribed medication for 2 hours before and 1 hour after dose of IXAZOMIB - Known allergy to boron or excipients in the formulation.
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: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: IXAZOMIB
Ixazomib 4, 5.3 and 7 milligram (mg), orally, once on Days 1, 8 and 15 in a 28 day treatment cycle followed by a rest period of 13 days, for up to Cycle 29 or until disease progression or unacceptable toxicity at lead-in phase for participants with NHL.
After completion of lead-in phase, participants will continue into Phase 2. Participants in Phase 2 will receive Ixazomib at RP2D dose, orally, once weekly on Days 1, 8 and 15 in a 28 day treatment cycle followed by a rest period of 13 days , for up to Cycle 29 or until disease progression or unacceptable toxicity in Phase 2 for participants with RRFL.
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Each 28-day treatment cycle will include oral administration of IXAZOMIB on Days 1, 8, and 15 followed by a rest period of 13 days.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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Number of Participants With Overall Response Rate (ORR)
Lasso di tempo: Baseline up to Day 15 Cycle 29 (approximately up to Day 802) or until PD or the start of alternate therapies
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ORR is defined as the percentage of participants with complete response (CR) or partial response (PR) as assessed by the investigator using the international Working Group criteria for participants CR: disappearance of all target lesions, non-target lesions, no new lesions, and normalization of tumor marker level.
PR: At least a 30 percent (%) decrease in the sum of diameters of target lesions, no progression in non-target lesion, and no new lesions.
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Baseline up to Day 15 Cycle 29 (approximately up to Day 802) or until PD or the start of alternate therapies
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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Lead-in Dose Finding Phase: Recommended Phase 2 Dose (RP2D)
Lasso di tempo: Baseline up to Cycle 1 Day 28
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Baseline up to Cycle 1 Day 28
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Progression Free Survival (PFS)
Lasso di tempo: Time from the date of first dose of study treatment to the date of first documented PD or death (approximately up to Day 802)
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PFS is defined as the time from the date of first dose of study treatment to the date of first documented PD or death.
Participants without documentation of PD will be censored at the date of last response assessment that is SD or better.
Participants without response assessment will be censored at the date of first dose.
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Time from the date of first dose of study treatment to the date of first documented PD or death (approximately up to Day 802)
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Phase 2: Rate of Disease Control
Lasso di tempo: Baseline or until occurrence of disease progression, unacceptable toxicities, or discontinuation of study due to any other reasons (approximately up to Day 805)
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Rate of disease control is defined as percentage of participants who achieved a SD or better for greater than or equal to (>=) 6 months.
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Baseline or until occurrence of disease progression, unacceptable toxicities, or discontinuation of study due to any other reasons (approximately up to Day 805)
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Time to Response (TTR)
Lasso di tempo: Time from the date of first dose of study treatment to the date of first documented PR or better response or death (approximately up to Day 802)
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TTR is defined as the time from the date of first dose of study treatment to the date of the first documentation of a PR or better response in a participant who responded.
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Time from the date of first dose of study treatment to the date of first documented PR or better response or death (approximately up to Day 802)
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Duration of Response (DOR)
Lasso di tempo: Time from the date of first documentation of a response to the date of first documented PD (approximately up to Day 802)
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The DOR is defined as the time from the date of first documentation of a response to the date of first documented PD.
Responders without documentation of PD will be censored at the date of last response assessment.
DOR was categorized as CR+PR and CR.
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Time from the date of first documentation of a response to the date of first documented PD (approximately up to Day 802)
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Phase 2: Number of Participants With Response Rates in PSMB1 Positive and PSMB1 Negative
Lasso di tempo: Baseline up to occurrence of disease progression, unacceptable toxicities, or discontinuation of study due to any other reasons (approximately up to Day 802)
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Baseline up to occurrence of disease progression, unacceptable toxicities, or discontinuation of study due to any other reasons (approximately up to Day 802)
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Number of Participants Experiencing 1 or More Treatment-Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
Lasso di tempo: Baseline up to 30 days after last dose of study drug (approximately up to Day 832)
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Baseline up to 30 days after last dose of study drug (approximately up to Day 832)
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Lead-in Dose Finding Phase: Cmax: Maximum Observed Plasma Concentration for Ixazomib
Lasso di tempo: Cycle 1, Days 1 and 15 pre-dose and at multiple time points (up to 168 hours) post-dose
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Cycle 1, Days 1 and 15 pre-dose and at multiple time points (up to 168 hours) post-dose
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Lead-in Dose Finding Phase: Tmax: Time to Reach the Maximum Plasma Concentration (Cmax) for Ixazomib
Lasso di tempo: Cycle 1, Days 1 and 15 pre-dose and at multiple time points (up to 168 hours) post-dose
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Cycle 1, Days 1 and 15 pre-dose and at multiple time points (up to 168 hours) post-dose
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Lead-in Dose Finding Phase: AUC(0-168): Area Under the Plasma Concentration-time Curve From Time 0 to 168 Hours Postdose for Ixazomib
Lasso di tempo: Cycle 1, Days 1 and 15 pre-dose and at multiple time points (up to 168 hours) post-dose
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Cycle 1, Days 1 and 15 pre-dose and at multiple time points (up to 168 hours) post-dose
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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 (Effettivo)
31 ottobre 2013
Completamento primario (Effettivo)
1 giugno 2016
Completamento dello studio (Effettivo)
23 marzo 2017
Date di iscrizione allo studio
Primo inviato
28 agosto 2013
Primo inviato che soddisfa i criteri di controllo qualità
6 settembre 2013
Primo Inserito (Stima)
11 settembre 2013
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
29 ottobre 2019
Ultimo aggiornamento inviato che soddisfa i criteri QC
7 ottobre 2019
Ultimo verificato
1 ottobre 2019
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Neoplasie
- Malattie linfoproliferative
- Malattie linfatiche
- Disturbi immunoproliferativi
- Linfoma non Hodgkin
- Linfoma
- Linfoma, follicolare
- Meccanismi molecolari dell'azione farmacologica
- Inibitori enzimatici
- Agenti antineoplastici
- Inibitori della proteasi
- Ixazomib
Altri numeri di identificazione dello studio
- C16017
- 2013-002302-32 (Numero EudraCT)
- U1111-1164-7551 (Altro identificatore: WHO)
- 166547 (Identificatore di registro: HC-CTD)
- REec-2016-2137 (Identificatore di registro: REec)
- 13/EM/0373 (Identificatore di registro: NRES)
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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University Hospital, CaenTerminato
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Memorial Sloan Kettering Cancer CenterVanderbilt University Medical Center; Tufts Medical CenterAttivo, non reclutante