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Patients With Mouse Tyrp2 DNA: A Phase I Trial to Assess Safety and Immune Response

25 mars 2011 uppdaterad av: Memorial Sloan Kettering Cancer Center

Injection of AJCC Stage IIB, IIC, III and IV Melanoma Patients With Mouse Tyrp2 DNA: A Phase I Trial to Assess Safety and Immune Response

The goal of this study is to find out about the safety of injecting the gene (DNA) for mouse TYRP2 in patients with melanoma. DNA is a material that contains the information needed to produce many substances in the body. TYRP2 is a substance found in melanoma cells that helps to produce their black color. The DNA used in this study is the gene for mouse TYRP2.

The gene is introduced into bacteria, which are grown in large quantities. The DNA vaccine is then made from bacteria that is inactive.

We would like to see if we can immunize patients against TYRP2 by injecting mouse TYRP2 DNA. We will also follow the patients closely to see if there are any side effects. Mouse TYRP2 DNA is very similar to human TYRP2 DNA. We believe, based on lab experiments, that injection of mouse TYRP2 DNA could result in the production of immune substances (antibodies and T cells) that recognize melanoma cells. Antibodies are substances produced by your immune system to defend your body against bacteria and viruses. T cells are a type of white blood cell that can also fight infections. The small differences between mouse and human TYRP2 may allow your immune system to make the antibodies and T cells against melanoma. There is no evidence yet that injection of TYRP2 DNA results in any clinical benefit in patients.

Studieöversikt

Status

Avslutad

Betingelser

Studietyp

Interventionell

Inskrivning (Förväntat)

12

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • New York
      • New York, New York, Förenta staterna, 10065
        • Memorial Sloan-Kettering Cancer Center

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

7 år och äldre (Barn, Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • For all patients, pathology slides must be reviewed by the Memorial Hospital Department of Pathology for confirmation of melanoma diagnosis.
  • Patients must be HLA-A*0201 positive.
  • Patients must have a Karnofsky performance status of at least 80.
  • Patients must be free of detectable brain metastases.
  • Patients must have adequate organ and marrow function as defined below:
  • WBC ≥ than or = to 3,000/μL
  • Absolute neutrophil count ≥ than or = to 1,500/μL
  • Platelets ≥ than or = to 100,000/μL
  • Total bilirubin ≤ than or = to 1.5X upper normal institutional limits
  • LDH ≤ than or = to 2 X institutional upper limit of normal
  • Albumin ≥ than or = to 3.5 mg/dl
  • Creatinine ≤ than or = to 2.0 mg/dl
  • Hemoglobin ≥ than or = to 10 Gm/dl
  • Liver AST, ALT ≤ than or = to 2.5 x ULN
  • Patients must have no known HIV positivity
  • Pediatric patients are eligible if weight is > 25 kg and parent/guardian completes informed assent process.
  • Patients must understand and sign an informed consent and have specifically declined all standard or approved therapies for which they would be considered eligible. Parent or legal guardians of patients who are minors will sign the informed consent form.
  • As part of the consent process, patients must agree to use contraception while on study.

Exclusion Criteria:

  • Patients who have had chemotherapy, immunotherapy or radiotherapy within 4 weeks prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier. For nitrosoureas, at last six weeks must have elapsed.
  • Patients with Grade I fever, active infection, or antibiotics within 72 hours prior to study.
  • Patients who have previously been immunized with any class of vaccine containing TYRP2, including whole cell, shed antigen or cell lysate vaccine.
  • Patients with a history of collagen vascular, rheumatological, or other autoimmune disorders.
  • Any medical condition or use of medication (e.g., corticosteroids) which might make it difficult for the patient to complete the full course of treatments or to respond immunologically to vaccines is grounds for exclusion, at the discretion of the Principal Investigator or co-Principal Investigators.
  • Patients who have preexisting retinal or choroidal eye disease.
  • Patients with serious underlying medical conditions that could be exacerbated by participation, active infections requiring antimicrobial drugs or active bleeding.
  • Pregnant women or women who are nursing are not eligible. Women of child-bearing potential and sexually active men must be using appropriate contraception during the course of this study. Women of child-bearing potential must not be pregnant (negative βHCG within 2 weeks of immunization) nor be nursing during treatment.
  • Patients receiving other investigational agents.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 1
Injection of mouse TYRP2 DNA in patients with highrisk melanoma.
Cohorts of three patients will receive injections with mouse TYRP2 DNA delivered intramuscularly at four different dose levels (500, 2000, 4000 or 8000 μg) every three weeks for six injections.

Vad mäter studien?

Primära resultatmått

Resultatmått
Tidsram
To evaluate the safety and feasibility of intra-muscular DNA injection with mouse TYRP2 DNA. Doses will be escalated by groups to determine the maximal tolerated dose.
Tidsram: conclusion of study
conclusion of study

Sekundära resultatmått

Resultatmått
Tidsram
A secondary endpoint is to observe the patients for evidence of any antitumor response generated after immunizations.
Tidsram: conclusion of study
conclusion of study

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 juli 2006

Primärt slutförande (Faktisk)

1 mars 2011

Avslutad studie (Faktisk)

1 mars 2011

Studieregistreringsdatum

Först inskickad

15 maj 2008

Först inskickad som uppfyllde QC-kriterierna

15 maj 2008

Första postat (Uppskatta)

20 maj 2008

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

28 mars 2011

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

25 mars 2011

Senast verifierad

1 mars 2011

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Kliniska prövningar på Melanom

Kliniska prövningar på injection of mouse TYRP2 DNA

3
Prenumerera