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- Sperimentazione clinica NCT01962532
A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of JNJ-42756493 in Patients With Advanced or Refractory Solid Tumors or Lymphoma
13 maggio 2019 aggiornato da: Janssen Research & Development, LLC
A Phase 1 Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of JNJ-42756493, a Pan-Fibroblast Growth Factor Receptor (FGFR) Tyrosine Kinase Inhibitor, in Subjects With Advanced or Refractory Solid Tumors or Lymphoma
The purpose of this study is to determine a dose for future development and to evaluate the safety, pharmacokinetics, pharmacodynamics, and efficacy profiles of JNJ-42756493 in Japanese and other Asian patients with advanced or refractory solid tumors or lymphoma.
Panoramica dello studio
Stato
Completato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
This is an open-label (identity of assigned study drug will be known), multicenter, 2-part, Phase 1 dose escalation/expansion to evaluate the safety, pharmacokinetics (study of what the body does to a drug), pharmacodynamics (study of what a drug does to the body) and clinical activity of JNJ-42756493 administered orally once daily in 21-day cycles or 28 days cycles of intermittent dosing regimen (7 days on/7 days off) to Japanese and Asian participants >=20 years of age with advanced or refractory solid tumors or lymphoma who are not candidates for approved or available therapies.
Approximately 40 participants will be enrolled.
In Part 1 Participants will be required to be hospitalized after the first dose on Day 1 of Cycle 1 until Day 2 of Cycle 2 (for daily continuous dosing) or until Day 14 of Cycle 1 (for intermittent dosing), however extension of hospitalization will be allowed until Day 2 of Cycle 2 according to investigators clinical judgment.
The Part 1 dose-escalation phase is designed to determine the recommended Phase 2 dose (RP2D) based on safety, pharmacokinetic, and pharmacodynamic data of JNJ-42756493.
Participants will be enrolled in sequential cohorts based on the 3+3 dose-escalation scheme; the first cohort will receive the starting dose and subsequent cohorts will receive increased doses of JNJ-42756493.
After the last participants in each cohort completes Cycle 1, the Safety Evaluation Team (SET) will evaluate the safety and pharmacokinetic data according to protocol-defined criteria and make the decision whether to escalate the dose in a new cohort.
To determine the recommended Phase 2 dose, the SET will review all safety, pharmacokinetic, and pharmacodynamic data from Part 1 before initiation of Part 2. The total number of participants enrolled in Part 1 will depend on the dose level at which the recommended Phase 2 dose is established.
After the recommended Phase 2 dose is established, the Part 2 dose-expansion phase will be opened.
Part 2 study will be done in a molecularly-defined subset of Participants with gastric adenocarcinoma including gastroesophageal junctions at the RP2D.
In Part2, Participants can be hospitalized until Day 8 of Cycle 1 as needed.
In addition, extension of hospitalization will be allowed until Day 15 of Cycle 1 according to investigator's clinical judgment.
In Part 2, approximately 25 participants will be treated at the recommended Phase 2 dose as 28 days cycles of intermittent dosing regimen in order to evaluate fibroblast growth factor receptor target modulation in tumor, to further elaborate safety, pharmacokinetics, and pharmacodynamics of JNJ-42756493, as well as to evaluate preliminary clinical responses.
Participants who are tolerating study drug treatment and achieve clinical responses or stable disease will continue to receive study drug at the same dose until disease progression, unacceptable toxicity, or withdrawal of consent.
Serial pharmacokinetic and pharmacodynamic samples will be collected, and safety and efficacy will be monitored throughout the study.
Tipo di studio
Interventistico
Iscrizione (Effettivo)
19
Fase
- Fase 1
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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Kashiwa, Giappone
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Matsuyama, Giappone
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Tokyo, Giappone
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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
20 anni e precedenti (Adulto, Adulto più anziano)
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion Criteria:
- Part 1: Histologically or cytologically confirmed solid malignancy or lymphoma that is metastatic or unresectable, and for which standard curative treatment is no longer effective
- Part 2: Histologically or cytologically confirmed gastric adenocarcinoma including gastroesophageal junctions that is metastatic, locally advanced or unresectable, and for which standard treatment is no longer effective or tolerable
- Eastern Cooperative Oncology Group performance status score 0 or 1
- Adequate bone marrow, liver, and renal function according to protocol-defined criteria within the 7 days prior to Day 1 of Cycle 1
- Laboratory values within protocol -defined parameters
- Agrees to protocol-defined use of effective contraception
- Negative urine pregnancy test (urine or serum beta human chorionic gonadotropin [beta-HCG]) at screening for women of child bearing potential
Exclusion Criteria:
- Has had chemotherapy, radiotherapy, immunotherapy, or treatment with an investigational anticancer agent within 3 weeks (nitrosoureas and mitomycin C within 6 weeks) before the first administration of study drug (localized radiation therapy for palliative purposes and ongoing luteinizing hormone-releasing hormone agonists and antagonists for patients with prostate cancer, bisphosphonates and denosumab are permitted
- History or current condition of uncontrolled cardiovascular disease as defined in the protocol
- Taking medications known to have a risk of causing QTc prolongation and Torsades de Pointes or known as strong CYP3A inhibitors or inducers
- Left ventricular ejection fraction less than (<) 50 percent (%) as assessed by echocardiography (or multi-gated acquisition [MUGA]) performed at screening
- Uncontrolled intercurrent illness including, but not limited to, poorly controlled hypertension or diabetes, ongoing active infection, psychiatric illness, or a risk of gastrointestinal perforation
Woman who is pregnant, breast-feeding, or planning to become pregnant or is a man who plans to father a child, while the participant is enrolled in this study and is within 3 or 5 months, respectively, after the last dose of the study drug
- Not recovered from reversible, clinically significant toxicity of prior anticancer therapy
- Presence of any medical condition that requires intact wound healing capacity and is expected to endanger participant safety if wound healing capacity would be severely reduced during administration of the investigational agent
- Major surgery within 4 weeks before enrollment
- Known human immunodeficiency virus infection
- Known hepatitis B or C (except hepatocellular carcinoma)
- Active, symptomatic, or untreated brain metastasis
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 |
|---|---|
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Sperimentale: Part 1: Dose Escalation (Daily Dosing)
Dose escalation of JNJ-42756493 is to occur until a dose at which <33 percent of participants experience a dose-limiting toxicity, the maximum concentration of JNJ-42756493 is less than the protocol-defined cardiovascular threshold, and JNJ-42756493 is biologically active.
Participants will receive study drug once day on Day 1 of Cycle 1 followed by a 2-day drug-free period (Days 2 and 3 of Cycle 1) and continues throughout the 21 day cycle.
For all subsequent cycles once a day for 21 days.
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JNJ-42756493 dose escalation starting at dose of 2 mg orally daily for 21-day cycles and 28 day cycles Intermitting dosing regimen (7 days on and 7 days off) up to the maximum tolerated dose in order to determine the recommended Phase 2 dose.
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Sperimentale: Part 1: Dose Escalation (Intermittent Dosing)
Intermitting dosing regimen will be 28 days (7 days on and 7 days off).
Participants will receive JNJ-42756493 on Days 1 to 7 and Days 15 to 21 of each cycle; JNJ-42756493 will not be administered on Days 8 to 14 and Days 22 to 28 of each cycle.
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JNJ-42756493 dose escalation starting at dose of 2 mg orally daily for 21-day cycles and 28 day cycles Intermitting dosing regimen (7 days on and 7 days off) up to the maximum tolerated dose in order to determine the recommended Phase 2 dose.
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Sperimentale: Part 2: Dose Expansion
Participants will receive the recommended Phase 2 JNJ-42756493 dose determined in Part 1 as Intermitting dosing regimen (28 days, 7 days on and 7 days off).
Participants who are tolerating study drug treatment and achieve clinical responses or stable disease will continue to receive study drug at the same dose until disease progression, unacceptable toxicity, or withdrawal of consent.
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Recommended Phase 2 JNJ-42756493 dose determined in Part 1 administered orally for 28-days cycles (Intermitting dosing regimen).
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
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Numero di partecipanti affetti da eventi avversi secondo la classificazione per sistemi e organi MedDRA (SOC) e termine preferito (PT)
Lasso di tempo: Fino a 30 giorni dopo l'ultima dose del farmaco in studio
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Fino a 30 giorni dopo l'ultima dose del farmaco in studio
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Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
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Maximum observed plasma concentration of JNJ-42756493
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Minimum observed plasma concentration of JNJ-42756493
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Time correspondent to the maximum observed plasma concentration of JNJ-42756493
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Area under the plasma concentration-time curve from time 0 to 24 hours of JNJ-42756493
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Half-life of JNJ-42756493
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Apparent volume of distribution of JNJ-42756493
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Total clearance of drug of JNJ-42756493
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Accumulation index of JNJ-42756493
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 1
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Number of participants with complete response
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Number of participants with partial response
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Number of participants with stable disease
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Number of participants with progressive disease
Lasso di tempo: Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Up to Part 2 Cycle 4 (each cycle is 28 days) Day 28
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Pubblicazioni e link utili
La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.
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)
21 agosto 2013
Completamento primario (Effettivo)
28 gennaio 2016
Completamento dello studio (Effettivo)
28 gennaio 2016
Date di iscrizione allo studio
Primo inviato
26 luglio 2013
Primo inviato che soddisfa i criteri di controllo qualità
10 ottobre 2013
Primo Inserito (Stima)
14 ottobre 2013
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
15 maggio 2019
Ultimo aggiornamento inviato che soddisfa i criteri QC
13 maggio 2019
Ultimo verificato
1 maggio 2019
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- CR102388
- 42756493GAC1001 (Altro identificatore: Janssen Research & Development, LLC)
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 .