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Study of Motesanib (AMG 706) in Combination With Paclitaxel and Carboplatin for Advanced Non-Squamous Non-Small Cell Lung Cancer

10 dicembre 2015 aggiornato da: Takeda

A Global Phase 3, Randomized, Placebo Controlled, Double-Blind Trial of AMG 706 in Combination With Paclitaxel and Carboplatin for Advanced Non-Squamous Non-Small Cell Lung Cancer (Asian Phase 3 Study)

This study will evaluate progression free survival (PFS), overall survival (OS), objective response rate (ORR), duration of response, and safety of motesanib (AMG706) in combination with paclitaxel and carboplatin compared to placebo in combination with paclitaxel and carboplatin.

Panoramica dello studio

Descrizione dettagliata

The drug being tested in this study is called motesanib. Motesanib is being tested in combination with paclitaxel and carboplatin to treat people who have Stage IV or recurrent non-squamous non-small cell lung cancer (NSCLC). This study will look at progression free survival, overall survival, overall response and safety.

The study enrolled 401 patients. Participants were randomly assigned (by chance, like flipping a coin) to one of the two treatment groups-which remained undisclosed to the patient and study doctor during the study (unless there is an urgent medical need):

  • Motesanib 125 mg + Paclitaxel + Carboplatin
  • Placebo (dummy inactive pill) - this is a tablet that looks like the study drug but has no active ingredient + Paclitaxel + Carboplatin

All participants were asked to take 5 X 25 mg motesanib tablets or placebo at the same time each day throughout the study. All participants received treatment with paclitaxel 200 mg/m^2 intravenous (IV) and carboplatin IV on Day 1 of each 3 week Cycle for up to 6 Cycles. After 6 Cycles participants could continue to receive motesanib or placebo alone for up to 36 months.

This multi-centre trial was conducted worldwide. The overall time to participate in this study was up to 36 months. Participants made multiple visits to the clinic, plus a final visit 30 days after receiving their last dose of study drug for a follow-up assessment.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

401

Fase

  • Fase 3

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:

Disease Related:

  1. Histologically or cytologically confirmed, Stage IV or recurrent non-squamous non-small cell lung cancer (NSCLC) (except diagnosis by sputum cytology only). Adenosquamous histology or an unclear histology subtype containing more than 10% squamous cells was not allowed.
  2. No prior chemotherapy, molecularly-targeted therapy, or immunotherapy. Neoadjuvant and post-operative adjuvant therapy except chemotherapy with platinum agent completed 1 year prior to randomization was permitted.
  3. Measurable or non-measurable lesion per Response Evaluation Criteria in Solid Tumor (RECIST) Version 1.1 criteria (except non-measurable lesion with malignant effusion only).
  4. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1.
  5. Life expectancy of ≥ 3 months as documented by the Investigator.

Demographic:

Must have been 18 years of age or older at the time informed consent was obtained.

Laboratory:

  1. Hematological function, as follows:

    • Absolute neutrophil count (ANC) ≥ 1.5 x 10^9/L.
    • Platelet count ≥ 100 x 10^9/L and ≤ 850 x 10^9/L.
    • Hemoglobin ≥ 9 g/dL.
  2. Renal function, as follows:

    • Creatinine clearance (GFR) > 40 mL/min (calculated by Cockcroft-Gault formula).
    • Urinary protein quantitative value of ≤ 30 mg in urinalysis or ≤ 1+ on dipstick unless total quantitative protein was < 500 mg in a 24-hour urine sample.
  3. Hepatic function, as follows:

    • Aspartate aminotransferase (AST) ≤ 2.5 x upper limit of normal (ULN) or AST < 5 x ULN if liver metastases were present.
    • Alanine aminotransferase (ALT) ≤ 2.5 x ULN or ALT < 5 x ULN if liver metastases were present.
    • Alkaline phosphatase (ALP) ≤ 2.0 x ULN or ALP < 5 x ULN if liver or bone metastases were present.
    • Total bilirubin < 1.5 x ULN.
  4. Coagulation function, as follows:

    • Partial thromboplastin time (PTT) or activated partial thromboplastin time (aPTT) ≤ 1 x ULN.
    • International normalized ratio (INR) ≤ 1.5 x ULN.

Ethical:

Ability to give written informed consent.

General:

  1. Able to take oral medications.
  2. Able to start protocol-directed therapy within 7 days from the date of randomization.

Exclusion Criteria:

Disease Related:

  1. Symptomatic central nervous system metastases. Participants with asymptomatic brain metastases were eligible if definitive therapy had been administered (surgery and/or radiation therapy), there was no planned treatment for brain metastasis, and the participant was clinically stable and off corticosteroids for at least 2 weeks prior to randomization. Participants with asymptomatic brain metastases were also eligible if the participant did not need definitive therapy (surgery and/or radiation therapy) or corticosteroids according to the Investigator's judgement.
  2. Palliative radiation therapy:

    • Radiation therapy within 28 days prior to randomization for central (chest).
    • Radiation therapy within 14 days prior to randomization for distant metastatic foci.
  3. History of pulmonary hemorrhage or gross hemoptysis (approximately 3 mL of bright red blood or more) within 6 months prior to randomization.

Medications:

  1. Prior targeted therapies, including but not limited to:

    • AMG 706, inhibitors of vascular endothelial growth factor (VEGF) (eg, SU5416, SU6668, ZD6474, SU11248, PTK787, AZD2171, AEE-788, sorafenib, bevacizumab), or epidermal growth factor receptor (EGFR) (eg, panitumumab, cetuximab, gefitinib, erlotinib).

  2. Any anticoagulation therapy within 7 days prior to randomization. The use of low-dose warfarin (≤ 2 mg daily) or low molecular weight heparin or heparin flushes for prophylaxis against central venous catheter thrombosis was allowed.
  3. Known history of allergy or hypersensitivity reaction to paclitaxel or carboplatin.

General:

  1. History of arterial or venous thrombosis within 12 months prior to randomization.
  2. History of bleeding diathesis or bleeding within 14 days prior to randomization.
  3. Peripheral neuropathy ≥ Grade 2 per Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0.
  4. Clinically significant cardiovascular disease within 12 months of randomization, including myocardial infarction, unstable angina, ≥ Grade 2 peripheral vascular disease, cerebrovascular accident, transient ischemic attack, percutaneous transluminal coronary angioplasty/stent, congestive heart failure or ongoing arrhythmias requiring medication.
  5. Any kind of disorder that compromised the ability of the participant to comply with the study procedures.
  6. Open wound, ulcer or fracture.
  7. Active or any uncontrolled, infection or inflammatory disease requiring systemic treatment ≤ 14 days prior to randomization.
  8. Diagnosed interstitial lung disease and/or significant interstitial shadow on the computerized tomography (CT) image.
  9. Uncontrolled hypertension as defined by resting blood pressure > 150/90 mmHg despite the use of an antihypertensive.
  10. History (past/current) of other primary cancer unless:

    • Curatively resected non-melanomatous skin cancer.
    • Curatively treated cervical carcinoma in situ.
    • Other primary solid tumor curatively treated with no known active disease present and no curative treatment administered for the last 3 years.
  11. Surgery:

    • Major surgical procedures within 28 days prior to randomization.
    • Minor surgical procedures within 14 days prior to randomization.
    • Failure to recover from prior surgery.
    • Placement of a central venous access device (including ports and tunneled or non-tunneled catheters) within 3 days in principle prior to randomization.
    • Core needle biopsy within 7 days prior to randomization.
  12. Planned elective surgery while on the study treatment.
  13. Not recovered from all previous therapies (ie, radiation, surgery and medications). AEs related to previous therapies must have been CTCAE Grade ≤ 1 at Screening or must have resolved to the participant's Baseline level prior to the most recent previous therapy (except alopecia).
  14. Participation in therapeutic clinical trials or currently receiving other investigational treatment(s) within 30 days prior to randomization.
  15. Pregnant (eg, positive human chorionic gonadotropin [HCG] test-urine or serum) or breast-feeding woman.
  16. Any participant not consenting to use adequate contraceptive precautions, from informed consent until 6 months after the last treatment.
  17. Known to be human immunodeficiency virus (HIV), hepatitis B surface (HBs) antigen or hepatitis C positive. Participants may have been HBs antigen (-) and HB core antibody (+) and /or HBs antibody (+) with hepatitis B virus (HBV) deoxyribonucleic acid (DNA) (-). If HBs antigen (-) but HBV DNA (+), participant could be enrolled with concomitant antiviral treatment (entecavir or tenofovir). In case of hepatitis C virus (HCV) antibody (+) with HCV ribonucleic acid (-) and/or HCV core antigen (-), participants could be enrolled.

    Participant with HBs antigen (+) could be enrolled if AST and ALT were within ULN, and HBV DNA level was less than 3.0 Log. The participant must have received concomitant antiviral treatment (entecavir or tenofovir). Participants who were already on antiviral treatment at Screening were not eligible.

  18. Known chronic hepatitis.
  19. History of any medical or psychiatric condition or laboratory abnormality that, in the opinion of the Investigator, may have increased the risks associated with participation in the study or administration of investigational products (IPs) administration, or may have interfered with the interpretation of the results.
  20. Previously randomized to this study.
  21. Not available for follow-up assessments or unable to comply with study requirements.

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: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Motesanib + Paclitaxel + Carboplatin
Motesanib 125 mg, (5 x 25 mg) tablets, orally, once daily and paclitaxel 200 mg/m^2, intravenous, once on Day 1 and carboplatin at a dose to achieve a target Area Under the Curve (AUC) of 6.0 mg/mL x minute, once on Day 1 of a 3 week Cycle for up to 6 Cycles. After 6 Cycles, motesanib 125 mg, tablets, orally, once daily alone until disease progression, drug intolerability, study withdrawal or death for up to 36 months.
Paclitaxel IV
Carboplatino IV
Motesanib (AMG 706) 5 x 25 mg tablets
Altri nomi:
  • AMG 706
Comparatore placebo: Placebo + Paclitaxel + Carboplatin
Motesanib placebo-matching tablets, orally, once daily and paclitaxel 200 mg/m^2, intravenous, once on Day 1 and carboplatin at a dose to achieve a target AUC of 6.0 mg/mL x minute, once on Day 1 of a 3 week Cycle for up to 6 Cycles. After 6 Cycles, motesanib placebo-matching, tablets, orally, once daily alone until disease progression, drug intolerability, study withdrawal or death for up to 36 months.
Paclitaxel IV
Carboplatino IV
Motesanib placebo-matching tablets

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Progression Free Survival
Lasso di tempo: Up to 24 Months
PFS was defined as the time from the date of randomization to the date of disease progression per Response Evaluation Criteria in Solid Tumor (RECIST) Version 1.1 or death from any cause, whichever occurred first. Progressive disease was defined as at least a 20% increase in the sum of the longest diameter (LD) of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions; appearance of one or more new lesions and/or unequivocal progression of existing non-target lesions.
Up to 24 Months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Overall Survival (OS)
Lasso di tempo: 6, 12, 18 and 24 months
OS was defined as the time from randomization to death (or, where applicable, the censoring date). Participants who had not died or were lost to follow-up by the analysis data cut-off date were censored at their last contact date. Participants who withdrew full consent to participate in the study were censored on the date consent was withdrawn.
6, 12, 18 and 24 months
Objective Response Rate (ORR)
Lasso di tempo: Up to 30 months
ORR was defined as the percentage of participants achieving either a complete response (CR) or partial response (PR) per RECIST Version 1.1 criteria. CR= disappearance of all target lesions; disappearance of all non-target lesions and normalization of tumor marker level. PR= At least a 30% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the Baseline sum LD.
Up to 30 months
Duration of Response (DOR)
Lasso di tempo: Up to 30 months
DOR was defined as the time from the date of first response (CR or PR) to disease progression (per RECIST Version 1.1) or death. CR= Disappearance of all target lesions; disappearance of all non-target lesions and normalization of tumor marker level. PR= At least a 30% decrease in the sum of the longest diameter (LD ) of target lesions, taking as reference the Baseline sum LD.
Up to 30 months
Percentage of Participants with Treatment Emergent Adverse Events (TEAEs)
Lasso di tempo: Up to 30 months
An Adverse Event (AE) is defined as any untoward medical occurrence in a clinical investigation participant administered a drug; it does not necessarily have to have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (eg, a clinically significant abnormal laboratory finding), symptom, or disease temporally associated with the use of a drug, whether or not it is considered related to the drug. A treatment-emergent adverse event (TEAE) is defined as an adverse event with an onset that occurs after receiving study drug.
Up to 30 months
Percentage of Participants with Abnormal Clinical Laboratory Findings
Lasso di tempo: Up to 30 months
The percentage of participants with any chemistry or hematology abnormal standard safety laboratory values collected throughout study
Up to 30 months
Cmax: Maximum Observed Plasma Concentration for Montesanib and its Metabolite M4
Lasso di tempo: Predose on Day 1 and 1 to 2 hours postdose in Cycles 3 and 5
Maximum Observed Plasma Concentration (Cmax) is the peak plasma concentration of a drug after administration, obtained directly from the plasma concentration- time curve.
Predose on Day 1 and 1 to 2 hours postdose in Cycles 3 and 5
Cmin: Minimum Observed Plasma Concentration for Montesanib and its Metabolite M4
Lasso di tempo: Predose on Day 1 and 1 to 2 hours postdose in Cycles 3 and 5
Minimum observed plasma concentration (Cmin) is the lowest plasma concentration of a drug after administration, obtained directly from the plasma concentration-time curve.
Predose on Day 1 and 1 to 2 hours postdose in Cycles 3 and 5

Collaboratori e investigatori

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

Sponsor

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 luglio 2012

Completamento primario (Effettivo)

1 settembre 2014

Completamento dello studio (Effettivo)

1 marzo 2015

Date di iscrizione allo studio

Primo inviato

10 dicembre 2015

Primo inviato che soddisfa i criteri di controllo qualità

10 dicembre 2015

Primo Inserito (Stima)

14 dicembre 2015

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

14 dicembre 2015

Ultimo aggiornamento inviato che soddisfa i criteri QC

10 dicembre 2015

Ultimo verificato

1 dicembre 2015

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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