- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01760499
Detection of Immune Cell Infiltration Into Melanomas Treated by PV-10, a Feasibility Study
18 aprile 2017 aggiornato da: H. Lee Moffitt Cancer Center and Research Institute
The main purpose of this study is to find out more about how PV-10 works in melanoma tumors.
Researchers also want to find out if there are changes in the body's immune cells (cells that fight infection and illnesses) after PV-10 is given, both inside the melanoma tumors and circulating in the blood.
Panoramica dello studio
Tipo di studio
Interventistico
Iscrizione (Effettivo)
15
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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Florida
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Tampa, Florida, Stati Uniti, 33612
- H. Lee Moffitt Cancer Center and Research Institute
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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:
- Patients who are diagnosed with metastatic melanoma, or who are suspected to have metastatic melanoma and are subsequently proven to have metastatic melanoma by biopsy
- Patients who are planned to undergo surgical resection of at least two foci of palpable cutaneous or subcutaneous metastatic melanoma, for either palliative or therapeutic intent and who consent for preoperative core biopsies of at least two of the resectable lesions prior to surgery
- Patients who have given informed consent to participate in the study
Exclusion Criteria:
- Patients who decline consent for this study
- Patients who have previously received PV-10 therapy
- Patients who were suspected to have metastatic melanoma but are not proven by preoperative biopsy will be replaced and not counted against the accrual goal
- Patients who do not undergo surgical resection of at least two metastatic melanoma lesions including the PV-10 treated lesion will be replaced and not counted against the accrual goal.
- Patients whose melanoma lesions are contiguous with, encompass or infiltrate a major blood vessel
- Patients with an allergy to shellfish due to reported cross-reactivity to PV-10
- Patients with previous sensitivity to iodide
- Patients who do not have a treatable target lesion on a portion of the body other than the head or neck
Concurrent or Intercurrent Illness:
- Patients with a condition of impaired wound healing (such as uncontrolled diabetes mellitus or immunosuppressive steroid dependence) such that in the opinion of the PI it is unsafe for the patient to undergo intralesional PV-10 treatment
- Patients with severe peripheral vascular disease (i.e., claudication occurring after less than 200 meters of walking, rest pain, ischemic ulceration or gangrene)
- Patients with significant concurrent or intercurrent illness, psychiatric disorders, or alcohol or chemical dependence that would, in the opinion of the principal investigator (PI), compromise their safety or compliance or interfere with interpretation of study results
- Patients with uncontrolled thyroid disease, goiter, partial thyroidectomy, previous radioiodine or surgically-treated Graves' hyperthyroidism or cystic fibrosis
- Patients with clinically significant cardiovascular, cerebrovascular, peripheral vascular, renal, gastrointestinal, pulmonary, immunological, endocrine, bone marrow or central nervous system disorders that have required hospitalization within the past 12 months
Pregnancy
- Female patients who have a positive pregnancy test or are lactating.
- Fertile patients who do not agree to use effective contraception (i.e., oral contraceptives, intrauterine devices, double barrier methods such as condoms and diaphragms, abstinence or equivalent measures) beginning at the time of signing consent until after surgery.
- Patients who are dependent upon concomitant medications that predispose to photosensitivity who cannot stop the medication(s) from the period starting 24 hours prior to and ending 24 hours after PV-10 treatment will be excluded.
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: Immunotherapy Followed by Surgery
PV-10 administration, adverse events assessment, surgery to remove melanoma tumors, follow-up visit.
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PV-10 administration: Within one week after completing the screening tests (or the same day as the screening tests), participants will be scheduled to have the study drug (PV-10) administered.
PV-10 is given as an injection with a needle, directly into one of the participant's tumors.
Participants will be given an injection of a numbing medication before the PV-10 is given.
Altri nomi:
Surgery to remove melanoma tumors (Day 7-14): About 7-14 days after the PV-10 is given, participants will have surgery to remove their melanoma tumors.
A piece of the tumor that was injected with PV-10 along with a piece of one other tumor will be sent to the laboratory for testing as part of the study.
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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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Occurrence of Change in Infiltration of Immune Cells
Lasso di tempo: At baseline and 7-14 days after PV-10 treatment
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The pre-treatment blood sample and tumor biopsies will be the control for the post-PV-10 blood samples and resected tumor samples.
Tumor core needle biopsies will be collected from the designated injected and uninjected lesions one week prior to intralesional PV-10 therapy.
Biopsy samples will be fixed in formalin and embedded in paraffin for immunohistochemical (IHC) staining.
On day 0, the injected lesion will be treated with up to 5 mL of PV-10.
Seven to 14 days after intralesional PV-10 treatment, the injected and uninjected lesions will be resected.
A portion of each tumor equivalent to a core needle biopsy specimen will be fixed in formalin and embedded in paraffin for IHC staining.
Immune cell infiltration will be compared between untreated baseline lesions and post-treatment lesions (injected or uninjected) by a blinded pathologist at Moffitt Cancer Center.
Measurement is the ordinal level of the T-cell infiltration into tumors with three levels: 0, no brisk, and brisk.
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At baseline and 7-14 days after PV-10 treatment
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Frequency and Phenotype of Circulating Immune Cells in Peripheral Blood Mononuclear Cells (PBMC)
Lasso di tempo: At baseline, 7-14 days after treatment and 21-28 days after treatment
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This secondary endpoint is to enumerate and phenotype patient immune cells in peripheral blood before and after intralesional (IL) PV-10 treatment.
The pre-treatment blood sample and tumor biopsies will be the control for the post-PV-10 blood samples and resected tumor samples.
T cells will be enumerated and phenotyped in patient blood one week prior to and 7-14 days after intralesional PV-10 therapy.
An additional blood draw 14 days post surgery will take place at the end of the study at the time of the surgical follow-up/end of study visit.
These samples will be used for in vitro experiments in order to determine the frequency and phenotype of T cells in the blood by flow cytometry.
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At baseline, 7-14 days after treatment and 21-28 days after treatment
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Titer of Anti-tumor IgG in the Serum
Lasso di tempo: At baseline, 7-14 days after treatment and 21-28 days after treatment
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This secondary endpoint is to enumerate anti-tumor immunoglobulin G (IgG) in peripheral blood before and after IL PV-10 treatment.
Titer of anti-tumor IgG in the serum prior to, 7-14 days after, and 21-28 days after PV-10 treatment.
The pre-treatment blood sample and tumor biopsies will be the control for the post-PV-10 blood samples and resected tumor samples.
Serum will be phenotyped from patients one week prior to, 7-14 days after and 21-28 days after IL PV-10 therapy.
Serum will be isolated from peripheral blood by centrifugation and will be used to stain patient tumor samples obtained from surgical resection.
Bound serum antibodies will be detected by staining with antihuman IgG antibodies and detected by flow cytometry.
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At baseline, 7-14 days after treatment and 21-28 days after treatment
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Occurrence of Adverse Events (AEs)
Lasso di tempo: During PV-10 administration visit, after 7-14 days, at study end (day 28 or early termination)
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Local and systemic toxicity signs and symptoms per the Common Terminology Criteria for Adverse Events v4.0 (CTCAE).
Any adverse experiences associated with participation on the trial will be recorded.
Adverse events will be assessed within 30 minutes following PV-10 administration and 4 hours after PV-10 administration.
Adverse events assessment: Questions about how participants have been feeling and any changes in the way participants feel immediately after the study drug was given and 4 hours later.
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During PV-10 administration visit, after 7-14 days, at study end (day 28 or early termination)
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Collaboratori
Investigatori
- Investigatore principale: Amod A. Sarnaik, M.D., H. Lee Moffitt Cancer Center and Research Institute
Pubblicazioni e link utili
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Collegamenti utili
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
24 gennaio 2013
Completamento primario (Effettivo)
29 dicembre 2015
Completamento dello studio (Effettivo)
1 aprile 2017
Date di iscrizione allo studio
Primo inviato
21 dicembre 2012
Primo inviato che soddisfa i criteri di controllo qualità
2 gennaio 2013
Primo Inserito (Stima)
4 gennaio 2013
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
19 aprile 2017
Ultimo aggiornamento inviato che soddisfa i criteri QC
18 aprile 2017
Ultimo verificato
1 aprile 2017
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- MCC-17183
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 .