A phase III multicenter, randomized, double-blind, double-dummy, active-controlled, parallel group study of the efficacy and safety of oral netupitant administered in combination with palonosetron and dexamethasone compared to oral palonosetron and dexamethasone for the prevention of nausea and vomiting in cancer patients receiving moderately emetogenic chemotherapy
- Conditions
- ausea and vomiting in cancer patients receiving moderately emetogenic theraphyMedDRA version: 14.1Level: PTClassification code 10054133Term: Prophylaxis of nausea and vomitingSystem Organ Class: 10042613 - Surgical and medical procedures
- Registration Number
- EUCTR2009-016775-30-PL
- Lead Sponsor
- Helsinn Healthcare SA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 1460
1. Signed written informed consent. 2. Male or female patient greater or equal than 18 years of age. 3. Naïve to cytotoxic chemotherapy. Previous biological or hormonal therapy will be permitted. 4. Scheduled to receive first course of an anthracycline and cyclophosphamide containing moderately emetogenic chemotherapy (MEC) regimen for the treatment of a solid malignant tumor: cyclophosphamide I.V. (500 to 1500 mg/m2) and I.V. doxorubicin (greater or equal than 40 mg/m2) or cyclophosphamide I.V. (500 to 1500 mg/m2) and I.V. epirubicin (greater or equal than 60 mg/m2). 5. If scheduled to receive chemotherapy agents of minimal to low emetogenic potential they could be given on any day. 6. ECOG Performance Status of 0, 1, or 2. 7. Female patients of either: a. non-childbearing potential (i.e., physiologically incapable of becoming pregnant, including any female who is postmenopausal. For purposes of this study, postmenopausal is defined as 12 consecutive months of amenorrhea. In addition, postmenopausal definition has to be confirmed by consistent age and/or Follicle-Stimulating Hormone (FSH) levels). b. child-bearing potential with a negative urine dipstick pregnancy test within 24 hours prior to the first dose of investigational product of Day 1 and with a commitment to consistent and correct use throughout the clinical trial of one of the following contraceptive methods: - whose male partner is sterile prior to the female patient’s entry into the study and is the sole sexual partner, - using double-barrier method of contraception consisting of spermicide with either condom or diaphragm, also if taking any oral contraceptive, for a period after the trial to account for a potential drug interaction (minimum four weeks), - with intrauterine device (IUD), - with complete abstinence from intercourse for two weeks before exposure to the investigational product and throughout the clinical trial, and for a period after the trial to account for elimination of the drug (minimum of twenty one days); should patients become sexually active during the period described above, they must agree to follow an acceptable method of birth control, as described above. 8.Hematologic and metabolic status adequate for receiving a moderately emetogenic regimen and fulfilment of the following criteria: a. Total Neutrophils greater or equal than 1500/mm3 (Standard units: greater or equal than 1.5 x 10^9/L); b. Platelets greater or equal than 100,000/mm3 (Standard units: greater or equal than 100.0 x 10^9/L); c. Bilirubin less or equal than 1.5 x Upper Limit of Normal (ULN); d. Liver enzymes: - without known liver metastases, Aspartate aminotransferase (AST) and/or Alanine aminotransferase (ALT) less or equal than 2.5 x ULN; - with known liver metastases, AST and/or ALT less or equal than 5.0 x ULN; e. Serum Creatinine less or equal than 1.5 mg/dL (Standard units: less or equal than 132.6 µMOL/L) or Creatinine Clearance greater or equal than 60 mL/min. 9. Able to read, understand, follow the study procedure and complete patient diary.
Inclusion Criteria (Multiple-Cycle Extension):
The following inclusion criteria must be checked prior inclusion at each cycle of the Multiple-Cycle Extension: 1. Participation in the study during the next cycle of chemotherapy is considered appropriate by the investigator and does not pose unwarranted risk to the patient. 2. Satisfactory study compliance in the preceding cycle of chemotherapy and related study procedures. 3. Sched
1. If female, pregnant or lactating. 2. Current use of illicit drugs or current evidence of alcohol abuse. 3. Scheduled to receive any highly emetogenic chemotherapy (HEC) from Day 1 to Day 5 or moderately emetogenic chemotherapy (MEC) from Day 2 to Day 5 following the allowed MEC regimen. 4. Received or is scheduled to receive radiation therapy to the abdomen or the pelvis within 1 week prior to Day 1 or between Days 1 to 5 in cycle 1. 5.Any vomiting, retching, or mild nausea (grade greater or equal than I as defined by National Cancer Institute) within 24 hours prior to Day 1. 6. Symptomatic primary or metastatic CNS malignancy. 7. Active peptic ulcer disease, gastrointestinal obstruction, increased intracranial pressure, hypercalcemia, an active infection or any uncontrolled medical condition (other than malignancy) that, in the opinion of the investigator, may confound the results of the study, represent another potential etiology for emesis and nausea (other than chemotherapy-induced nausea and vomiting, CINV) or pose unwarranted risks in administering the study drugs to the patient. 8. Known hypersensitivity or contraindication to 5-HT3 receptor antagonists (e.g., palonosetron, ondansetron, granisetron, dolasetron, tropisetron, ramosetron) or dexamethasone. 9. Previously received an NK1 receptor antagonist (e.g., aprepitant, casopitant). 10.Participation in a clinical trial involving oral netupitant administered in combination with palonosetron. 11. Any investigational drugs taken within 4 weeks prior to Day 1 of cycle 1, and/or is scheduled to receive any investigational drug during the study.
12. Systemic corticosteroid therapy at any dose within 72 hours prior to Day 1 of cycle 1. However topical and inhaled corticosteroids with a steroid dose of less or equal than 10 mg of prednisone daily or its equivalent are permitted. 13. Scheduled to receive bone marrow transplantation and/or stem cell rescue therapy. 14. Any medication with known or potential antiemetic activity within 24 hours prior to Day 1 of cycle 1, including: - 5 HT3 receptor antagonists (e.g. ondansetron, granisetron, dolasetron, tropisetron, ramosetron, palonosetron); - benzamides (e.g., metoclopramide, alizapride); - phenothiazines (e.g., prochlorperazine, promethazine, fluphenazine, perphenazine, thiethylperazine, chlorpromazine); - benzodiazepines (except if the subject is receiving such medication for sleep or anxiety and has been on a stable dose for at least seven days prior to Day 1); - butyrophenones (e.g., haloperidol, droperidol); - anticholinergics (e.g., scopolamine, with the exception of inhaled anticholinergics for respiratory disorders e.g., ipratropium bromide); - antihistamines (e.g., cyclizine, hydroxyzine, diphenhydramine, chlorphenhyramine), except for prophylactic use for taxane therapy; - domperidone; - mirtazapine; - oolanzapine; - prescribed cannabinoides (e.g. tetrahydrocannabinol or nabilone). 15. Scheduled to receive any strong or moderate inhibitor of CYP3A4 or its intake within 1 week prior to Day 1. 16. Scheduled to receive any of the following CYP3A4 substrates: terfenadine, cisapride, astemizole, pimozide. 17.Scheduled to receive any CYP3A4 inducer or its intake within 4 weeks prior to Day 1. 18. History or predisposition to cardiac conduction abnormalities, except for incomplete right bundle branch block. 19. History of risk factors for Torsade de Point (heart failure, hypokalemia, family history of Long QT Syndrome). 20. Sev
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method