A Phase 2 Multicenter Study Evaluating the Efficacy and Safety of IPI-504 in Combination With Trastuzumab in Patients With Pretreated, Locally Advanced or Metastatic Human Epidermal Growth Factor Receptor 2 (HER2) Positive Breast Cancer
IPI-504
+ Trastuzumab
Maladies du sein+3
+ Néoplasmes du sein
+ Néoplasmes par site
Étude thérapeutique
Résumé
Date de début de l'étude : 1 mars 2009
Date à laquelle le premier participant a commencé l'étude.Recent clinical data has demonstrated that even in heavily pretreated patients with trastuzumab-refractory HER-2 positive breast cancer, targeting HER2 is efficacious. IPI-504 is an HSP90 inhibitor and is chemically related to 17-AAG and it has been studied in a clinical trial in combination with trastuzamab and a response rate of 26% (7/27) was demonstrated in patients with pretreated, HER2-positive breast cancer. These data provide a strong scientific rationale for clinical testing of IPI-504 plus trastuzumab in patients with pretreated, locally advanced or metastatic HER2-positive breast cancer
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.29 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Traitement
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.À partir de 18 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
Inclusion Criteria: * Locally advanced/metastatic breast cancer. * HER2-expressing primary or metastatic tumor * Two prior regimens with HER2. Trastuzumab must have been given. No limit to prior therapies * Measurable disease with RECIST 1.1 * Clinical progression * LVEF WNL * ECOG 0 or 1 * Last dose of chemotherapy, radiotherapy, surgery, ablative therapy, tyrosine kinase inhibitor, ≥2 weeks * Administration of biological therapy ≥4 weeks * Last dose of trastuzumab must be ≥1, or ≥3 weeks prior to start, if previously administered on an every 3 week schedule. * Resolution of toxic effects to baseline or Grade 1, except alopecia (NCI CTCAE Version 3.0 * Organ and marrow function: * Hemoglobin ≥8.0 g/dL * ANC ≥1200/µL * Platelets ≥75,000 /µL * ALT and AST ≤ 1.5 x ULN * Alkaline phosphatase ≤2.5 x ULN, or ≤3.0 x ULN if secondary to liver metastases. * Serum bilirubin WNL * Serum albumin ≥3.0 g/dL * PT, PTT ≤1.5 x ULN * Serum creatinine ≤1.5 x ULN * Negative pregnancy test Exclusion Criteria: * Prior treatment with Hsp90 inhibitor. * Grade 4 AE secondary to trastuzumab. Grade 3/4 infusion reactions or Grade 3/4 symptomatic heart failure * Medication/food that is a CYP3A inhibitor or inducer. * Hx 6 months: cardiac disease - acute coronary syndrome or unstable angina, symptomatic congestive heart failure, uncontrolled hypertension, cirrhotic liver disease, cerebrovascular accident or significant co-morbid condition * Grade 3 or 4 hemorrhagic event within 6 months. * HIV positivity * Baseline QT corrected, QTcF \>470 ms * Sinus bradycardia \<50 bpm Secondary to pharmacologic therapy may enroll if stopping therapy normalizes heart rate. * Malignancies within 3 years other than non-melanomatous skin cancers, non-muscle-invasive bladder cancer and carcinoma in situ of cervix. * Active keratitis or keratoconjunctivitis * Active brain metastasis (e.g., requiring therapy with steroids or radiation therapy; or with intracranial progression 4 weeks after the completion of radiation therapy) uncontrolled seizure disorder, ongoing spinal cord compression, or carcinomatous meningitis. If clinically stable brain metastasis (previously treated or untreated)are present pt is eligible.
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.Un seul groupe d'intervention est désigné dans cette étude
Cette étude ne comporte pas de groupe placebo.
Groupes de traitement
Groupe I
ExpérimentalObjectifs de l'étude
Objectifs principaux
Objectifs secondaires
Centres d'étude
Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.Cette étude comporte 11 sites
Comprehensive Cancer Center at Desert Regional Medical Center
Palm Springs, United StatesOuvrir Comprehensive Cancer Center at Desert Regional Medical Center dans Google MapsBoca Raton Comphrensive Cancer Care
Boca Raton, United StatesFlorida Cancer Research Institute
Davie, United StatesPeachtree Hematology-Oncology Consultants, P.C.
Atlanta, United States