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Efficacy/Safety of Imprime PGG® Injection With Bevacizumab and Paclitaxel/Carboplatin in Patients With Untreated Advanced Non-Small Cell Lung Cancer (NSCLC)

1 marzo 2017 aggiornato da: HiberCell, Inc.

A Phase 2, Randomized, Efficacy and Safety Study of Imprime PGG® Injection in Combination With Bevacizumab and Concomitant Paclitaxel and Carboplatin Therapy in Patients With Previously Untreated Advanced (Stage IIIB or IV) Non-Small Cell Lung Cancer

The Phase 2 study described in this protocol will serve to evaluate the antitumor activity, safety and pharmacokinetic profile of Imprime PGG when combined with bevacizumab and concomitant paclitaxel and carboplatin therapy in patients with previously untreated advanced NSCLC. Additionally, this study will provide guidance for the design of more definitive efficacy studies of Imprime PGG in NSCLC patients.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Effettivo)

90

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

      • Halle/Saale, Germania
        • Hospital Marth-Maria Halle Dolau
      • Kassel, Germania
        • Clinical Kassel GmbH
      • Köln, Germania
        • Kliniken der Stadt Koln gGmbH
      • Mainz, Germania
        • University of Mainz
      • Munich, Germania
        • University of Munich
      • Oldenburg, Germania
        • Pius-Hospital Oldenburg
      • Ulm, Germania, 89081
        • Universitatsklinikum Ulm
    • Arkansas
      • Fayetteville, Arkansas, Stati Uniti, 72703
        • Highlands Oncology Group
    • Ohio
      • Canton, Ohio, Stati Uniti, 44718
        • Gabrail Cancer Center
    • Texas
      • San Antonio, Texas, Stati Uniti, 78229
        • University of Texas Health Science Center, San Antonio

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

Da 18 anni a 75 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. Has read, understood and signed the informed consent form (ICF) approved by the Independent Review Board/Ethics Committee (IRB/EC);
  2. Is between the ages of 18 and 75 years old, inclusive;
  3. Has histologically or cytologically confirmed stage IIIB (malignant pericardial or pleural effusion) or stage IV non-small cell lung cancer;
  4. Has non-squamous, non-small cell lung cancer
  5. Has measurable disease, defined as at least one tumor that fulfills the criteria for a target lesion according to RECIST;
  6. Has an ECOG performance status of 0 or 1;
  7. Has a life expectancy of > 3 months;
  8. Has adequate hematologic function as evidenced by:

    1. ANC ≥ 1,500/μL
    2. PLT ≥ 100,000/μL
    3. HGB ≥ 9 g/dL obtained within 1 week prior to the first dose of study medication;
  9. Has adequate renal function as evidenced by:

    1. Serum creatinine ≤ 1.5 X the upper limit of normal (ULN) for the reference lab
    2. Urine dipstick for proteinuria of < 1+ (i.e., either 0 or trace) within 2 weeks of Day 1 If urine dipstick is ≥ 1+, then urine protein excretion must be ≤ 500 mg over a 24 hour collection obtained within 1 week prior to the first dose of study medication;
  10. Has adequate hepatic function as evidenced by:

    1. Serum total bilirubin ≤ 1.0 mg/dL
    2. AST ≤ 2.5X ULN for the reference lab (≤ 5X ULN for subjects with known hepatic metastases)
    3. ALT ≤ 2.5X ULN for the reference lab (≤ 5X ULN for subjects with known hepatic metastases) obtained within 1 week prior to the first dose of study medication;
  11. Has adequate coagulation function as evidenced by:

    1. INR ≤ 1.5
    2. PTT ≤ ULN for the reference lab obtained within 1 week prior to the first dose of study medication;
  12. If a woman of childbearing potential or a fertile man (and his partners), must agree to use an effective form of contraception (hormonal contraceptive, double-barrier method or abstinence) during the study.

Exclusion Criteria:

  1. Has received prior systemic chemotherapy at any time for lung cancer;
  2. Has received previous radiation therapy to >30% of active bone marrow or any radiation therapy within 3 weeks of Day 1;
  3. Has a known hypersensitivity to baker's yeast, or has an active yeast infection;
  4. Has had previous exposure to Betafectin® or Imprime PGG;
  5. Has an active infection;
  6. Presents with any of the following medical diagnoses/conditions at the time of screening:

    1. Central nervous system (CNS) metastases
    2. Uncontrolled hypertension (>150/100 mmHg) or hypertension that requires > two agents for adequate control
    3. Peripheral neuropathy ≥ grade 2 from any cause
    4. Fever of >38.5° C within 3 days prior to screening or Day 1, initial dosing
    5. Known HIV/AIDs, Hepatitis B, Hepatitis C, connective tissue or autoimmune disease, or other clinical diagnosis, ongoing or intercurrent illness that in the physician's opinion could interfere with participation
  7. Has a history of any of the following medical diagnoses/conditions:

    1. Arterial or venous thromboembolic or hemorrhagic disorders including stroke, transient ischemic attack or cerebral infarction
    2. Deep vein thrombosis within 1 year prior to screening
    3. Myocardial infarction or an unstable or uncontrolled disease or condition related to or impacting cardiac function (e.g., unstable angina, congestive heart failure) within the previous 6 months
    4. Second malignancy within the previous 5 years, other than basal cell carcinoma, cervical intra-epithelial neoplasia or curatively treated prostate cancer with a PSA of <2.0 ng/mL
  8. Has a known hypersensitivity to bevacizumab, murine proteins, or any component of bevacizumab;
  9. Has a know sensitivity to polyethoxylated castor oil;
  10. Has previously received treatment with bevacizumab;
  11. Has had surgery within 4 weeks of Day 1 or needle or open biopsy within 1 week of Day 1;
  12. Has a non-healing wound or gastric ulcer;
  13. Has a non-healed bone fracture;
  14. Is receiving systemic anti-coagulation therapy (e.g., dipyridalmole (Persantine®), ticlopidine (Ticlid®), clopidogrel (Plavix®) and /or cilostazol (Pletal®);
  15. Is receiving chronic daily treatment with aspirin (>100 mg/day) or other nonsteroidal anti-inflammatory agents known to inhibit platelet function within 1 week of Day 1;
  16. Presents with any of the following medical diagnoses/conditions at the time of screening:

    a. Predominant squamous cell histology

  17. Has a history of any of the following medical diagnoses/conditions:

    1. Hemoptysis (≥ ½ tsp red blood)
    2. Bleeding diathesis or coagulopathy
  18. If female, is pregnant or breast-feeding;
  19. Is receiving concurrent investigational therapy or has received investigational therapy within a period of 30 days prior to the first scheduled day of dosing (investigational therapy is defined as treatment for which there is currently no regulatory-authority-approved indication);
  20. Has previously received an organ or progenitor/stem cell transplant.

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: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 1
Imprime PGG + bevacizumab + paclitaxel/carboplatin
4 mg/kg, i.v. over 2 hr, weekly until progression or discontinuation
15 mg/kg, i.v., over 90 minutes, on Day 1 only of each 3-week treatment cycle
200 mg/m2, i.v. over 3 hr, on Day 2 of each 3-week treatment cycle for the first 4 to 6 treatment cycles.
AUC of 6 mg./mL · min based on the Calvert formula; i.v. over 30 min, on Day 2 of each 3-week treatment cycle for the first 4 to 6 treatment cycles
Altro: 2
bevacizumab + paclitaxel/carboplatin
15 mg/kg, i.v., over 90 minutes, on Day 1 only of each 3-week treatment cycle
200 mg/m2, i.v. over 3 hr, on Day 2 of each 3-week treatment cycle for the first 4 to 6 treatment cycles.
AUC of 6 mg./mL · min based on the Calvert formula; i.v. over 30 min, on Day 2 of each 3-week treatment cycle for the first 4 to 6 treatment cycles

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
To determine the objective response rate (ORR) in each study arm
Lasso di tempo: Approximately 1.5 years
Approximately 1.5 years

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
To determine the disease control rate (DCR) in each study arm
Lasso di tempo: Approximately 1.5 years
Approximately 1.5 years
To determine the complete response (CR), partial response (PR), and stable disease (SD) rates in each study arm
Lasso di tempo: Approximately 1.5 years
Approximately 1.5 years
To determine the duration of objective tumor response in each study arm
Lasso di tempo: Approximately 1.5 years
Approximately 1.5 years
To determine the duration of stable disease in each study arm
Lasso di tempo: Approximately 1.5 years
Approximately 1.5 years
To determine the duration of time to progression (TTP) in each study arm
Lasso di tempo: Approximately 1.5 years
Approximately 1.5 years
To assess the safety of the dosing regimen within each study arm
Lasso di tempo: Approximately 1.5 years
Approximately 1.5 years
To determine the pharmacokinetic (PK) profile of Imprime PGG (in active treatment arm only)
Lasso di tempo: Approximately 1.5 years
Approximately 1.5 years

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Investigatore principale: Folker Schneller, MD, Klinikum rechts der Isar der Technischen Universitaet Muenchen

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

1 giugno 2009

Completamento primario (Effettivo)

1 aprile 2016

Completamento dello studio (Effettivo)

1 maggio 2016

Date di iscrizione allo studio

Primo inviato

1 aprile 2009

Primo inviato che soddisfa i criteri di controllo qualità

1 aprile 2009

Primo Inserito (Stima)

2 aprile 2009

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

3 marzo 2017

Ultimo aggiornamento inviato che soddisfa i criteri QC

1 marzo 2017

Ultimo verificato

1 marzo 2017

Maggiori informazioni

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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