Safety and Efficacy Study of Sapanisertib in Combination With Exemestane or Fulvestrant in Postmenopausal Women With Estrogen Receptor Positive/Human Epidermal Growth Factor Receptor 2 Negative (ER+/HER2-) Metastatic Breast Cancer
A Phase 1b/2 Study of Safety and Efficacy of MLN0128 (Dual TORC1/2 Inhibitor) in Combination With Exemestane or Fulvestrant Therapy in Postmenopausal Women With ER+/HER2- Advanced or Metastatic Breast Cancer That Has Progressed on Treatment With Everolimus in Combination With Exemestane or Fulvestrant
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
The drug being tested in this study is called sapanisertib (MLN0128). Sapanisertib is being tested in women with estrogen receptor positive/human epidermal growth factor receptor 2 negative (ER+/HER2-) advanced or metastatic breast cancer who progressed on treatment with everolimus. This study will look at the safety and efficacy of sapanisertib when given in combination with exemestane or fulvestrant.
The study enrolled 118 patients. This study has two phases: phase 1 and phase 2. Phase 1 has 2 parts. In part 1 of phase 1, unmilled active pharmaceutical ingredient (API) capsules were administered, while in part 2, capsules based on milled API were administered.
- Phase 1 (Part 1): sapanisertib 5 mg (unmilled) + exemestane
- Phase 1 (Part 1): sapanisertib 5 mg (unmilled) + fulvestrant
- Phase 1 (Part 2): sapanisertib 3 mg (milled) + exemestane
- Phase 1 (Part 2): sapanisertib 3 mg (milled) + fulvestrant
- Phase 1 (Part 2): sapanisertib 4 mg (milled) + exemestane
In phase 2, participants were enrolled into one of 2 parallel cohorts, depending on the quality and/or duration of their prior response to everolimus in combination with either exemestane (any country) or fulvestrant (US only).
Everolimus-Resistant Cohort: patients who had progressed on treatment with everolimus in combination with either exemestane (any country) or fulvestrant (US only) without achieving an objective response (CR or PR) or after achieving stable disease for <6 months as their best response.
Everolimus-Sensitive Cohort: participants who had progressed on treatment after achieving a CR or PR of any duration, or stable disease for ≥6 months with prior everolimus treatment in combination with either exemestane (any country) or fulvestrant (US only). Participants were to receive MLN0128 in combination with the same dose of the previously administered treatment (exemestane [any country] or fulvestrant [US only]).
This multi-center trial will be conducted worldwide. The overall time to participate in this study was 52 months. Participants made multiple visits to the clinic and were contacted by telephone every 3 months for a follow-up assessment.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 2
Contatti e Sedi
Luoghi di studio
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Antwerpen, Belgio, 2650
- UZ Antwerpen
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Bruxelles, Belgio, 1000
- Institut Jules Bordet
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Bruxelles, Belgio, 1090
- Universitair Ziekenhuis Brussel
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Charleroi, Belgio, 6000
- GHdC Notre Dame
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Libramont, Belgio, 6800
- Centre Hospitalier de l'Ardenne
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Wilrijk, Belgio, 2610
- GZA Ziekenhuizen - Campus Sint-Augustinus
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Calvados
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Caen Cedex 05, Calvados, Francia, 14076
- Centre François Baclesse
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Loire Atlantique
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Nantes, Loire Atlantique, Francia, 44202
- Centre Catherine de Sienne
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Sarthe
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Le Mans Cedex 02, Sarthe, Francia, 72015
- Clinique Victor Hugo - Centre Jean Bernard
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Vaculuse
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Avignon, Vaculuse, Francia, 84000
- Institut Sainte Catherine
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California
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Los Angeles, California, Stati Uniti, 90017
- Los Angeles Hematology
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San Francisco, California, Stati Uniti, 94143
- University of California at San Francisco (PARENT)
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Santa Barbara, California, Stati Uniti, 93105
- Santa Barbara Hematology Oncology Medical Group, Inc.
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Colorado
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Aurora, Colorado, Stati Uniti, 80045
- University of Colorado Cancer Center
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Lakewood, Colorado, Stati Uniti, 80228
- Rocky Mountain Cancer Centers, LLP
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Florida
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Miami Beach, Florida, Stati Uniti, 33140
- Mount Sinai Medical Center
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Plantation, Florida, Stati Uniti, 33324
- Florida Cancer Research Institute
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Kansas
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Westwood, Kansas, Stati Uniti, 66205
- University of Kansas Medical Center Research Institute, Inc.
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Maryland
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Silver Spring, Maryland, Stati Uniti, 20910
- Holy Cross Hospital
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Michigan
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Novi, Michigan, Stati Uniti, 48322
- Henry Ford Medical Center
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Minnesota
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Minneapolis, Minnesota, Stati Uniti, 55455
- University of Minnesota
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Rochester, Minnesota, Stati Uniti, 55905
- Mayo Clinic
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New York
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Bronx, New York, Stati Uniti, 10469
- Eastchester Center for Cancer Care / BRANY
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Buffalo, New York, Stati Uniti, 14263-0001
- Roswell Park Cancer Institute
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New York, New York, Stati Uniti, 10032
- Herbert Irving Comprehensive Cancer Center
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New York, New York, Stati Uniti, 10065
- Weill Cornell Medical College New York Presbyterian Hospital
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Ohio
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Cincinnati, Ohio, Stati Uniti, 45267-0502
- University of Cincinnati Physicians Company, LLC
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Cleveland, Ohio, Stati Uniti, 44106
- University Hospitals of Cleveland
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Tennessee
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Chattanooga, Tennessee, Stati Uniti, 37403
- Erlanger Medical Center
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Texas
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Beaumont, Texas, Stati Uniti, 77702-1449
- Texas Oncology, P.A. - Beaumont
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Dallas, Texas, Stati Uniti, 75246
- Texas Oncology, P.A.
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Dallas, Texas, Stati Uniti, 75390-9085
- UT Southwestern Medical Center
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Houston, Texas, Stati Uniti, 77030
- The University of Texas MD Anderson Cancer Center
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Houston, Texas, Stati Uniti, 77090
- Millennium Oncology
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Plano, Texas, Stati Uniti, 75093
- Texas Health Physicians Group
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San Antonio, Texas, Stati Uniti, 78217
- Cancer Care Network of South Texas - SAT&BC
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Tyler, Texas, Stati Uniti, 75702
- Texas Oncology, P.A. - Tyler
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Virginia
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Chesapeake, Virginia, Stati Uniti, 23320
- Virginia Oncology Associates - Hampton
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Salem, Virginia, Stati Uniti, 24153
- Oncology and Hematology Assoc. of SW VA, Inc.
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West Virginia
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Morgantown, West Virginia, Stati Uniti, 26506
- West Virginia University
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria
Each patient must meet all of the following inclusion criteria to be enrolled in the study:
Phase 1b and Phase 2
- Advanced or metastatic breast cancer.
- Histological or cytological confirmation of ER+ status (defined as > 1% positive tumor cells), and histological or cytological confirmation of HER2-negative (HER2-) status by local laboratory testing using criteria in the American Society of Oncology (ASCO)/College of American Pathologists (CAP) Clinical Practice Guideline update.
Female patients 18 years of age or older who are postmenopausal for at least 1 year before the Screening visit, where menopause is defined by: Age ≥ 55 years and 1 year or more of amenorrhea. Surgical menopause with bilateral oophorectomy
Age < 55 years and 1 year or more of amenorrhea, with an estradiol assay < 20 pg/mL
Note: Ovarian radiation or treatment with a luteinizing hormone-releasing hormone agonist (goserelin acetate or leuprolide acetate) is not permitted for induction of ovarian suppression.
Have a history of brain metastasis are eligible for the study provided that all the following criteria are met:
Brain metastases which have been treated
- No evidence of disease progression for ≥ 3 months or hemorrhage after treatment
- Off-treatment with dexamethasone for 4 weeks before administration of the first dose of MLN0128
- No ongoing requirement for dexamethasone or anti-epileptic drugs
- Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2.
Clinical laboratory values as specified below within 4 weeks before the first dose of MLN0128:
- Bone marrow reserve consistent with absolute neutrophil count (ANC) ≥ 1.5 x 10^9/L; platelet count ≥ 100 x 10^9/L; hemoglobin ≥ 9 g/dL
- Total bilirubin ≤ 1.5 x the upper limit of the normal range (ULN), aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x ULN (≤ 5 x ULN if liver metastases are present)
- Creatinine clearance ≥ 50 mL/min based either on Cockcroft-Gault estimate or based on a 12- or 24-hour urine collection
- Fasting serum glucose ≤ 130 mg/dL and fasting triglycerides ≤ 300 mg/dL
- Left ventricular ejection fraction (LVEF) within 5 absolute percentage points of institutional standard of normal as measured by echocardiogram (ECHO) or multiple gated acquisition scan (MUGA) within 4 weeks before the first dose of MLN0128 (ie, if the institutional standard of normal is 50%, LVEF may be as low as 45% to be eligible for the study).
- Able to provide paraffin blocks or a minimum of 10 unstained slides of available archival tumor tissues (paraffin blocks are preferred). If archival tumor tissue is not available, a tumor biopsy may be performed before the patient begins treatment with MLN0128. If fewer than 10 slides are available or the tumor content/area requirements are not met, study eligibility will be determined upon discussion with the sponsor.
- Ability to swallow oral medications, willingness to perform mucositis prophylaxis, and suitable venous access for the study-required blood sampling.
Voluntary written consent must be given before the performance of any study related procedure not part of standard medical care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to future medical care.
Phase 1b Only: In addition to the previously mentioned inclusion criteria, each patient must meet the following inclusion criterion to be enrolled in the phase 1b portion of the study:
Patients may have SD or disease progression during their most recent treatment with exemestane or fulvestrant, or everolimus in combination with either exemestane (any country) or fulvestrant (US only). Exemestane or fulvestrant in combination with MLN0128 can also be initiated as a new line of therapy.
Phase 2 Only: In addition to the previously mentioned inclusion criteria, each patient must meet all of the following inclusion criteria to be enrolled in the phase 2 portion of the study:
Measurable disease defined as follows:
- At least 1 extra-osseous lesion that can be accurately measured in at least 1 dimension. The lesion must measure ≥ 20 mm with conventional imaging techniques or ≥ 10 mm with spiral computed tomography (CT) or magnetic resonance imaging (MRI), or
- Bone lesions (lytic or mixed [lytic plus sclerotic]) in the absence of measurable disease as defined above
- Patients must have had disease progression during treatment with everolimus in combination with either exemestane (any country) or fulvestrant (US only) (duration of treatment ≥ 4 weeks) and must have tolerated everolimus treatment in combination with exemestane (any country) or fulvestrant (US only) adequately according to the treating physician's judgment. Everolimus in combination with exemestane or fulvestrant is not required to be the most recent treatment before enrollment, but progression on the most recent anticancer therapy is required for enrollment.
Exclusion Criteria
Patients meeting any of the following exclusion criteria are not to be enrolled in the study:
Phase 1b and Phase 2
- Prior anticancer therapy or other investigational therapy within 2 weeks before administration of the first dose of MLN0128 (except for exemestane or fulvestrant, which should be continued). Treatment with everolimus must be discontinued 2 weeks before administration of the first dose of MLN0128.
- Chronic concomitant therapy with bisphosphonates or denosumab for the prevention of bone metastases. Concomitant treatment with bisphosphonates or denosumab is permitted for treatment of osteoporosis or management of existing bone metastases if initiated at least 4 weeks before administration of the first dose of MLN0128.
- Initiation of treatment with hematopoietic growth factors, transfusions of blood and blood products, or systemic corticosteroids (either IV or oral steroids, excluding inhalers) within 1 week before administration of the first dose of MLN0128 (patients already receiving erythropoietin on a chronic basis for ≥ 4 weeks are eligible).
- Previous treatment with dual PI3K/mTOR inhibitors or TORC1/2 inhibitors.
- Manifestations of malabsorption due to prior gastrointestinal (GI) surgery, GI disease, or for an unknown reason that may alter the absorption of MLN0128.
- Poorly controlled diabetes mellitus defined as glycosylated hemoglobin (HbA1c) > 7%; patients with a history of transient glucose intolerance due to corticosteroid administration may be enrolled in this study if all other inclusion/exclusion criteria are met.
- Other clinically significant co-morbidities, such as uncontrolled pulmonary disease, active central nervous system disease, active infection, or any other condition that could compromise participation of the patient in the study.
- Known human immunodeficiency virus infection.
History of any of the following within the last 6 months before administration of the first dose of MLN0128:
- Ischemic myocardial event, including angina requiring therapy and artery revascularization procedures
- Ischemic cerebrovascular event, including transient ischemic attack and artery revascularization procedures
- Requirement for inotropic support (excluding digoxin) or serious (uncontrolled) cardiac arrhythmia (including atrial flutter/fibrillation, ventricular fibrillation, or ventricular tachycardia)
- Placement of a pacemaker for control of rhythm
- New York Heart Association Class III or IV heart failure
- Pulmonary embolism
Significant active cardiovascular or pulmonary disease before administration of the first dose of MLN0128, including:
- Uncontrolled hypertension (ie, systolic blood pressure > 180 mm Hg; diastolic blood pressure > 95 mm Hg)
- Pulmonary hypertension
- Uncontrolled asthma or oxygen saturation < 90% by arterial blood gas analysis or pulse oximetry on room air
- Significant valvular disease; severe regurgitation or stenosis by imaging independent of symptom control with medical intervention; or history of valve replacement
- Medically significant (symptomatic) bradycardia
- History of arrhythmia requiring an implantable cardiac defibrillator
- Baseline prolongation of the rate-corrected QT interval (QTc; eg, repeated demonstration of QTc interval > 480 ms, or history of congenital long QT syndrome, or torsades de pointes)
Diagnosed or treated for another malignancy within 2 years before administration of the first dose of MLN0128 or previously diagnosed with another malignancy and have any evidence of residual disease. Patients with nonmelanoma skin cancer or carcinoma in situ of any type are not excluded if they have undergone complete resection.
Phase 1b Only: In addition to the previously mentioned exclusion criteria, patients meeting the following exclusion criterion are not to be enrolled in the phase 1b portion of the study:
More than 3 prior chemotherapy regimens for locally advanced or metastatic disease.
Phase 2 Only: In addition to the previously mentioned exclusion criteria, patients meeting the following exclusion criterion are not to be enrolled in the phase 2 portion of the study:
- More than 1 prior chemotherapy regimen for locally advanced or metastatic disease.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: TRATTAMENTO
- Assegnazione: NON_RANDOMIZZATO
- Modello interventistico: PARALLELO
- Mascheramento: NESSUNO
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
SPERIMENTALE: Phase 1 (Part 1): Sapanisertib 5 mg + Exemestane
Sapanisertib 5 mg, unmilled active pharmaceutical ingredient (API) capsule, once daily in a 28-day cycle plus exemestane 25 mg, tablets, once daily in a 28-day cycle (Up to 12 cycles).
|
Sapnisertib capsules
Altri nomi:
Exemestane tablets.
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SPERIMENTALE: Phase 1 (Part 1): Sapanisertib 5 mg + Fulvestrant
Sapanisertib 5 mg, unmilled API capsule, once daily in a 28-day cycle plus fulvestrant 500 mg, injection, intramuscularly (IM), once on Day 1 of each cycle (Up to 57 cycles).
|
Iniezione intramuscolare di Fulvestrant.
Sapnisertib capsules
Altri nomi:
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SPERIMENTALE: Phase 1 (Part 2): Sapanisertib 3 mg + Exemestane
Sapanisertib 3 mg, milled API capsule, once daily in a 28-day cycle plus exemestane 25 mg, tablets, once daily in a 28-day cycle (Up to 8 cycles).
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Sapnisertib capsules
Altri nomi:
Exemestane tablets.
|
|
SPERIMENTALE: Phase 1 (Part 2): Sapanisertib 3 mg + Fulvestrant
Sapanisertib 3 mg, milled API capsule, once daily in a 28-day cycle up to 14 cycles plus fulvestrant 500 mg, injection, IM, once on Day 1 of each cycle (Up to 14 cycles).
|
Iniezione intramuscolare di Fulvestrant.
Sapnisertib capsules
Altri nomi:
|
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SPERIMENTALE: Phase 1 (Part 2): Sapanisertib 4 mg + Exemestane
Sapanisertib 4 mg, milled API capsule, once daily, in a 28-day cycle plus exemestane 25 mg, tablets, once daily in a 28-day cycle (Up to 18 cycles).
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Sapnisertib capsules
Altri nomi:
Exemestane tablets.
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SPERIMENTALE: Phase 2: Sapanisertib 4 mg + Exemestane (Everolimus Sensitive)
Sapanisertib 4 mg, capsula API macinata una volta al giorno in un ciclo di 28 giorni più exemestane 25 mg, compresse, una volta al giorno in un ciclo di 28 giorni (fino a 14 cicli) in partecipanti sensibili a everolimus.
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Sapnisertib capsules
Altri nomi:
Exemestane tablets.
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SPERIMENTALE: Phase 2:Sapanisertib 4 mg+Fulvestrant (Everolimus Sensitive)
Sapanisertib 4 mg, milled API capsule once daily in a 28-day cycle plus fulvestrant 500 mg, injection IM, once on Day 1 of each cycle (Up to 17 cycles) in everolimus sensitive participants.
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Iniezione intramuscolare di Fulvestrant.
Sapnisertib capsules
Altri nomi:
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SPERIMENTALE: Phase 2: Sapanisertib 4 mg+Exemestane (Everolimus Resistant)
Sapanisertib 4 mg, milled API capsule, once daily, in a 28-day cycle plus once daily in a 28-day cycle (Up to 12 cycles) in everolimus resistant participants.
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Sapnisertib capsules
Altri nomi:
Exemestane tablets.
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SPERIMENTALE: Phase 2: Sapanisertib 4 mg+Fulvestrant (Everolimus Resistant)
Sapanisertib 4 mg, capsula API macinata, una volta al giorno in un ciclo di 28 giorni più fulvestrant 500 mg, iniezione IM, una volta al giorno 1 di ogni ciclo (fino a 9 cicli) nei partecipanti resistenti a everolimus.
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Iniezione intramuscolare di Fulvestrant.
Sapnisertib capsules
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Phase 1: Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
Lasso di tempo: First dose of study drug through 30 days after the last dose (Up to 52 months)
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An AE is defined as any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product whether or not it is related to the medicinal product. This includes any newly occurring event, or a previous condition that has increased in severity or frequency since the administration of study drug. A SAE is any untoward medical occurrence that at any dose results in death, is life-threatening, requires inpatient hospitalization or prolongation of an existing hospitalization, results in persistent or significant disability or incapacity, is a congenital anomaly/birth defect or is a medically important event. Relationship of each AE to study drug will be determined by the Investigator. |
First dose of study drug through 30 days after the last dose (Up to 52 months)
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Phase 2: Clinical Benefit Rate at 16 Weeks (CBR-16)
Lasso di tempo: Week 16
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CBR-16 was defined as the percentage of participants who achieved confirmed complete response (CR) or partial response (PR) of any duration or had confirmed stable disease (SD) as best response and the first 2 or more post baseline scans had PR/SD and the duration of SD was >112 days.
Disease response was assessed for target lesions by computed tomography (CT) or magnetic resonance imaging (MRI) according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 guidelines.
CR is disappearance of all target lesions.
PR is >=30% decrease in the sum of the longest diameter of target lesions.
SD is defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for disease progression (PD).
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Week 16
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Phase 2: Clinical Benefit Rate at 24 Weeks (CBR-24)
Lasso di tempo: Week 24
|
CBR-24 was defined as the percentage of participants who achieved confirmed CR or PR at any time or had confirmed SD as best response and the first 2 or more post baseline scans had PR/SD and the duration of stable disease was >168 days.
Disease response was assessed for target lesions by CT or MRI according to RECIST version 1.1 guidelines.
CR is disappearance of all target lesions.
PR is >=30% decrease in the sum of the longest diameter of target lesions.
SD is defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD.
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Week 24
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Phase 2: Overall Response Rate (ORR)
Lasso di tempo: Baseline then every 2 cycles from Cycles 2 through 6, and every 3 cycles thereafter in a 28-day cycle up to End of Treatment (EOT) (Up to 24 months)
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ORR is defined as the percentage of participants with confirmed CR or PR as per RECIST version1.1 guidelines.
CR is disappearance of all target lesions.
PR is >=30% decrease in the sum of the longest diameter of target lesions.
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Baseline then every 2 cycles from Cycles 2 through 6, and every 3 cycles thereafter in a 28-day cycle up to End of Treatment (EOT) (Up to 24 months)
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Phase 2: Progression-Free Survival (PFS)
Lasso di tempo: Basale quindi ogni 2 cicli dai cicli da 2 a 6 e successivamente ogni 3 cicli in un ciclo di 28 giorni, quindi ogni 3 mesi dopo l'EOT fino alla progressione della malattia o alla morte (fino a 24 mesi)
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PFS is defined as the time in months from the date of first dose of study treatment to the date of the first documented disease progression or death.
Disease progression was defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study, including baseline; an absolute increase of at least 5 mm in the sum of diameters of target lesions; or the appearance of one or more new lesions.
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Basale quindi ogni 2 cicli dai cicli da 2 a 6 e successivamente ogni 3 cicli in un ciclo di 28 giorni, quindi ogni 3 mesi dopo l'EOT fino alla progressione della malattia o alla morte (fino a 24 mesi)
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Phase 2: Overall Survival (OS)
Lasso di tempo: Up to 24 months
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OS is the time in months from start of study treatment to date of death due to any cause.
Data for the analysis of OS included the censored data at the timepoint that the participant was last known to be alive.
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Up to 24 months
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Phase 2: Best Percent Change From Baseline in Tumor Size
Lasso di tempo: Baseline to Month 24
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Baseline to Month 24
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Phase1: Cmax: Maximum Observed Plasma Concentration for Sapanisertib
Lasso di tempo: Cycle 1 Day 15 and Cycle 2 Day 1 pre-dose and multiple timepoints (Up to 8 hours) post-dose
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Cycle 1 Day 15 and Cycle 2 Day 1 pre-dose and multiple timepoints (Up to 8 hours) post-dose
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Phase 1: Tmax: Time to Reach the Maximum Plasma Concentration (Cmax) for Sapanisertib
Lasso di tempo: Cycle 1 Day 15 and Cycle 2 Day 1 pre-dose and multiple timepoints (Up to 8 hours) post-dose
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Cycle 1 Day 15 and Cycle 2 Day 1 pre-dose and multiple timepoints (Up to 8 hours) post-dose
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Phase 1: AUC(0-24): Area Under the Plasma Concentration-time Curve From Time 0 to Time 24 Hours for Sapanisertib
Lasso di tempo: Cycle 1 Day 15 pre-dose and multiple timepoints (Up to 8 hours) post-dose, extrapolated to 24 hours post-dose
|
AUC(0-24) is the area under the plasma concentration-time curve of the samples collected up to 8 hours and extrapolated up to 24 hours.
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Cycle 1 Day 15 pre-dose and multiple timepoints (Up to 8 hours) post-dose, extrapolated to 24 hours post-dose
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Phase 1: AUC(0-last): Area Under the Plasma Concentration-time Curve From Time 0 to Last Extrapolated Concentration Over the Dosing Interval for Sapanisertib
Lasso di tempo: Cycle 1 Day 15 pre-dose and multiple timepoints (Up to 8 hours) post-dose, extrapolated to last timepoint
|
AUC(0-last) is the area under the plasma concentration-time curve of the samples collected up to 8 hours and extrapolated up to last time point.
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Cycle 1 Day 15 pre-dose and multiple timepoints (Up to 8 hours) post-dose, extrapolated to last timepoint
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Phase 1: Terminal Elimination Half-life (T1/2) for Sapanisertib
Lasso di tempo: Ciclo 1 Giorno 15 pre-dose e più punti temporali (fino a 8 ore) post-dose
|
Ciclo 1 Giorno 15 pre-dose e più punti temporali (fino a 8 ore) post-dose
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Collaboratori e investigatori
Sponsor
Pubblicazioni e link utili
Studiare le date dei record
Studia le date principali
Inizio studio (EFFETTIVO)
Completamento primario (EFFETTIVO)
Completamento dello studio (EFFETTIVO)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (STIMA)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (EFFETTIVO)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie della pelle
- Neoplasie
- Neoplasie per sede
- Malattie del seno
- Neoplasie mammarie
- Effetti fisiologici delle droghe
- Meccanismi molecolari dell'azione farmacologica
- Inibitori enzimatici
- Agenti antineoplastici
- Ormoni, sostituti ormonali e antagonisti ormonali
- Agenti antineoplastici, ormonali
- Antagonisti ormonali
- Inibitori dell'aromatasi
- Inibitori della sintesi di steroidi
- Antagonisti degli estrogeni
- Antagonisti del recettore degli estrogeni
- Fulvestrant
- Exemestane
Altri numeri di identificazione dello studio
- C31001
- 2014-001921-34 (EUDRACT_NUMBER)
- U1111-1195-3894 (REGISTRO: WHO)
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Descrizione del piano IPD
Criteri di accesso alla condivisione IPD
Tipo di informazioni di supporto alla condivisione IPD
- STUDIO_PROTOCOLLO
- LINFA
- ICF
- RSI
Informazioni su farmaci e dispositivi, documenti di studio
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