- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02391727
Safety, Immunogenicity and Pharmacokinetics of SYN004 in Patients With Solid Tumors (SYN004_Ph_1)
A Phase 1, Multi-center, Open-Label Dose Escalation Study of SYN004 in Patients With Solid Tumors to Evaluate the Safety, Immunogenicity and Pharmacokinetics of SYN004 Following Administration of Eight Intravenous Doses
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
Study Design:
In this open-label, dose escalation study, subjects will receive a single IV loading dose of SYN004 on Day 1 of the first treatment week, followed by up to 7 fixed weekly doses of SYN004. Subjects will be assigned to loading and fixed doses by dose group.
Each dose group will comprise 3 subjects and may be expanded to 6 subjects. Subjects will enter dose groups in the order in which they are enrolled. There will be no intra-subject dose adjustments.
Only 1 subject in a cohort may receive the loading dose of SYN004 on any given day; at least 1 day must elapse before the next subject in the cohort receives the loading dose.
Study SYN004-001 Dose Matrix. Three initial subjects will be enrolled followed by an additional three if specified by protocol. Dose levels are specified below.
Group 1: Loading dose: 100 mg/m2; Weekly Dose: 62.5 mg/m2. Group 2: Loading dose: 200 mg/m2; Weekly Dose: 125 mg/m2. Group 3: Loading dose: 400 mg/m2; Weekly Dose: 250 mg/m2.
After each dose of IV SYN004, subjects will be observed in the clinic for 12 hours. After the loading dose, subjects will undergo safety evaluations on Days 2, 3 and 5. Safety evaluation will also be performed on Day 1 (pre-treatment) and Day 3 of each fixed dose treatment week.
Dose-limiting toxicities (DLTs) are defined as any Grade ≥3 AE assessed by the investigator or Medical Monitor, with agreement of the Safety Review Board (SRB), as related to SYN004. Subjects with DLTs will be withdrawn from treatment. If 2 or more subjects in a dose group experience DLTs, or one subject in a dose group experiences a Grade ≥3 infusion reaction, all subjects in that dose group will be withdrawn from treatment.
Subjects in the dose groups are considered evaluable for dose escalation decisions if they receive at least 4 doses of SYN004, or discontinue SYN004 because of a DLT.
Subjects who withdraw or are terminated per protocol before receiving 4 doses of SYN004 will be replaced.
For subjects who receive at least 4 doses of SYN004, End of Study CT scans for RECIST (version 1.1) evaluation will be performed six (6) days following the final SYN004 treatment.
There will be a 28-day safety monitoring period following the final dose of SYN004 for all subjects in the study. All subjects will attend an End-of-Study Visit 28 days after the final dose of SYN004.
Subjects who complete Cycles 1 and 2, who have evidence of improvement per RECIST 1.1 (i.e., findings of complete or partial response per RECIST 1.1) and meet the other eligibility criteria will be offered up to 3 additional treatment cycles (i.e., up to 12 additional weekly doses) of SYN004 in the SYN004-001 Extension Study. During the Extension Study, subjects will receive the same fixed dose of SYN004 they received in Cycles 1 and 2.
Dose escalation will proceed according to a standard 3+3 study design.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 1
Contatti e Sedi
Luoghi di studio
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Louisiana
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New Orleans, Louisiana, Stati Uniti, 70121
- Ochsner Medical Center
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Missouri
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Saint Louis, Missouri, Stati Uniti, 63110
- Washington University Medical Center
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
Note: No waivers of the study inclusion or exclusion criteria will be granted.
- Diagnosis of a solid tumor for which the accepted standard of care includesa licensed anti-EGFR therapy;
Tumor progression in patients with RAS wild type metastatic colorectal cancer irrespective of their exposure to licensed anti-EGFR therapy including anti-EGFR antibodies; OR Tumor progression in patients with metastatic colorectal cancer refractory to cetuximab or panitumumab or other anti-EGFR antibodies OR Tumor progression in patients with EGFR-mutated non-small cell lung cancer (NSCLC) who have refused therapy.
OR Tumor progression or recurrence in patients with squamous cell carcinoma of the head and neck irrespective of their exposure to licensed anti-EGFR therapy including anti-EGFR antibodies.
OR Patients with locally advanced or metastatic colorectal carcinoma who have
- relapsed after standard of care treatment,
- proved refractory to standard of care treatment
- refused standard of care treatment
- been found to be medically unsuitable for standard of care treatment
- Completion of written informed consent procedure;
- Male or female subjects over 17 years of age
- Life expectancy of at least 3 months;
- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 2;
- At least one measureable non-irradiated site of disease according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1;
- Adequate bone marrow function, with absolute neutrophil count (ANC) >1,500/mm3, platelet count >100,000/mm3, and hemoglobin > 10 g/mm3;
- Adequate liver function, with bilirubin <1.5 x the upper limit of the normal range (ULN), aspartate aminotransferase (AST) and alanine aminotransferase (ALT) <2.5 x the ULN;
- Adequate renal function, with serum creatinine <1.5 mg/dL;
- Adequate cardiac function, with left ventricular ejection fraction (LVEF) ≥50%, normal electrocardiogram, and absence of significant cardiac disease;
- In women of childbearing potential (defined as women of reproductive capacity who are pre-menopausal or within 12 months of cessation of menses): negative serum pregnancy test and use of an acceptable non-hormonal method of contraception;
- Ability to communicate with the investigator, and understand and comply with the requirements of the protocol;
- Agrees to notify the investigator when deviating from the protocol requirements with regard to concomitant medications;
- Agrees to stay in contact with the study site for the duration of the study and to provide updated contact information as necessary, and has no current plans to move from the study area for the duration of the study.
Exclusion Criteria:
- Participation in a study of an investigational agent or use of an investigational device at the time of screening or within 4 weeks of enrollment;
- Receipt of treatment with a monoclonal antibody (mAb) within 4 weeks of enrollment or not recovered from an adverse event (i.e., event is >Grade 1 or subject has not returned to baseline) due to treatment with a mAb administered >4 weeks before enrollment;
- Receipt of chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to enrollment, or not recovered from an adverse event (i.e., event is >Grade 1 or subject has not returned to baseline) due to a previously-administered agent;
- Major surgical procedure or significant traumatic injury within 4 weeks prior to screening;
- Diagnosis of an additional malignancy that is progressing and requires treatment; exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin, and in situ cervical cancer that has undergone potentially curative therapy;
- Active autoimmune disease requiring systemic treatment within the past 3 months, or a documented history of severe autoimmune disease, or a syndrome that requires systemic steroids or immunosuppressive agents (subjects with vitiligo or resolved childhood asthma/atopy are allowed);
- Diagnosis of an immune deficiency;
Receipt of systemic steroids or any form of immunosuppressive therapy within 7 days prior to enrollment, with the following exceptions:
- Stable doses of topical, ocular, intranasal or inhaled corticosteroids
- Doses of systemic steroids that, in the opinion of the investigator, are pysiologic replacement doses
- Systemic steroids as prophylactic treatment for subjects with allergy to contrast media
- Non-absorbed intra-articular steroid injections
- Systemic corticosteroids required for control of infusion reactions or AEs if doses have been tapered to <10 mg prednisone or equivalent for 2 weeks prior to the first study treatment
- Evidence of interstitial lung disease or active, non-infectious pneumonitis;
- Active infection requiring systemic therapy;
- History of cerebrovascular accident, transient ischemic attack, or subarachnoid hemorrhage within 6 months prior to screening;
- Active hepatitis B (i.e., hepatitis B surface antigen [HBsAg] positive) or hepatitis C (i.e., hepatitis C virus [HCV] ribonucleic acid [RNA; qualitative] is detected);
- Serious non-healing wound, ulcer, or bone fracture;
- Any severe or uncontrolled medical condition or other condition that could affect participation in the study;
- Any current medical, psychiatric, occupational, or substance abuse problems that, in the opinion of the investigator, will make it unlikely that the subject will comply with the protocol.
Piano di studio
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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Altro: SYN004
open label study
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subjects who have received effective treatment for their cancers are eligible
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Number of patients with adverse events
Lasso di tempo: 28 days of last SYN004 Administration
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cutaneous toxicity, hypersensitivity
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28 days of last SYN004 Administration
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
maximum plasma concentration (Cmax)
Lasso di tempo: 84 days
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Cmax will be determined using noncompartmental methods for SYN004
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84 days
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time to Cmax (Tmax)
Lasso di tempo: 84 days
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Tmax will be determined using noncompartmental methods for SYN004
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84 days
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elimination rate constant (λz)
Lasso di tempo: 84 days
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λz will be determined using noncompartmental methods for SYN004
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84 days
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elimination half-life (t½)
Lasso di tempo: 84 days
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t½ will be determined using noncompartmental methods for SYN004
|
84 days
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mean residence time (MRT)
Lasso di tempo: 84 days
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MRT will be determined using noncompartmental methods for SYN004
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84 days
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area under the plasma concentration vs. time curve from 0 (initiation of infusion) to the time of the last detectable concentration (AUC0-t), AUC from time 0 extrapolated to infinity (AUC0-∞)
Lasso di tempo: 84 days
|
AUC0-t and AUC0-∞ will be determined using noncompartmental methods for SYN004
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84 days
|
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systemic clearance (CL)
Lasso di tempo: 84 days
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CL will be determined using noncompartmental methods for SYN004
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84 days
|
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volume of distribution in the terminal phase (Vdβ), and estimated steady-state volume of distribution (VSS)
Lasso di tempo: 84 days
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Vdβ and VSS will be determined using noncompartmental methods for SYN004
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84 days
|
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anti-cancer activity
Lasso di tempo: 84 days
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Measurement of objective response (OR), durability of objective response (DOR), and progression-free survival (PFS).
The number and proportion of subjects who achieve objective tumor response (complete response [CR], partial response [PR], and CR+PR) or stable disease (SD) using Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, according to local radiological assessments from date of first administration of the investigational product to the end of the study treatment.
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84 days
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Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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To assess biomarkers of relevance to SYN004 mechanism of action and activity
Lasso di tempo: 84 days
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Blood samples will be collected for the evaluation of IgE antibodies to Galα1,3Gal
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84 days
|
Collaboratori e investigatori
Sponsor
Investigatori
- Direttore dello studio: John McClain, MD, Synermore Biologics Co., Ltd.
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- SYN004-001
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
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 .
Prove cliniche su Colon Cancer, Breast Cancer, Cancer of the Head and Neck
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University of California, DavisNational Cancer Institute (NCI)ReclutamentoCancro al seno in stadio anatomico III AJCC v8 | Neoplasia solida maligna avanzata | Cancro al polmone in stadio III AJCC v8 | Cancro al polmone in stadio IV AJCC v8 | Cancro a cellule renali in stadio III AJCC v8 | Cancro a cellule renali in stadio IV AJCC v8 | Melanoma cutaneo in stadio clinico... e altre condizioniStati Uniti
Prove cliniche su SYN004
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Synermore Biologics Co., Ltd.Synermore Biologics USA LimitedAttivo, non reclutanteTumore solido | Carcinoma epitelialeStati Uniti