Evaluation of Biomarkers Associated With Response to Subsequent Therapies in Subjects With HER2-Positive Metastatic Breast Cancer
17. september 2021 opdateret af: Novartis Pharmaceuticals
An Open-Label, Phase II, Study to Evaluate Biomarkers Associated With Response to Subsequent Therapies in Subjects With HER2-Positive Metastatic Breast Cancer Receiving Treatment With Trastuzumab in Combination With Lapatinib or Chemotherapy (EGF117165)
This was a multicenter, open-label, Phase II study in subjects with Human epidermal growth factor receptor (HER2)-positive metastatic breast cancer who received at least 2 prior lines of anti-HER2-targeted therapies of which at least one included a Trastuzumab-containing regimen.
This study was a post-approval commitment with regulatory authorities.
It was designed to evaluate whether treatment with Dual blockade promoted changes to biomarkers associated with immunomodulation.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This study was designed to address the post-authorization measures as agreed with the Committee for Medicinal Products for Human Use (CHMP). Recruitment of subjects into this study was challenging, and following agreement with the European Medicines Agency (EMA) enrollment into this study was halted after the enrollment of 42 of the 225 planned subjects.
The primary endpoint of the study evaluated changes in expression of biomarkers associated with immunomodulation between a pre-treatment biopsy and the disease progression biopsy. Secondary efficacy endpoints included overall response rate, clinical benefit rate and progression-free survival (PFS), as well as safety/tolerability. All subjects received study treatment until disease progression, death, unacceptable toxicity, or subject withdrawal. In case of disease progression during the treatment period, the subject was followed-up for 30 days for safety evaluation. In case of study treatment discontinuation for any reasons other than disease progression, the subject was followed-up for safety and efficacy assessments until disease progression, new anticancer therapy, death, withdrawal of consent or end of study, whichever came first.
This study supported a better understanding of the rapidly accumulating evidence for the importance of the immune microenvironment in HER2-positive breast cancer and the observed immunomodulation in the neoadjuvant setting could be confirmed in the advanced setting and supported the putative mechanism of action of HER2 dual blockade and its potential function on the tumor microenvironment. No formal comparisons between treatment arms were undertaken.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
42
Fase
- Fase 2
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Ciudad Autonoma de Buenos Aires, Argentina, C1025ABI
- Novartis Investigative Site
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Cordoba, Argentina, X5004FHP
- Novartis Investigative Site
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La Rioja, Argentina, F5300COE
- Novartis Investigative Site
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San Miguel de Tucuman, Argentina, T4000IAK
- Novartis Investigative Site
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Buenos Aires
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Berazategui, Buenos Aires, Argentina, B1880BBF
- Novartis Investigative Site
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Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina, C1125ABD
- Novartis Investigative Site
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Río Negro
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Viedma, Río Negro, Argentina, R8500ACE
- Novartis Investigative Site
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Santa Fe
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Rosario, Santa Fe, Argentina, S2000KZE
- Novartis Investigative Site
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Sao Jose do Rio Preto, Brasilien, 15090-000
- Novartis Investigative Site
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Bahía
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Salvador, Bahía, Brasilien, 41825-010
- Novartis Investigative Site
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Minas Gerais
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Belo Horizonte, Minas Gerais, Brasilien, 30130-090
- Novartis Investigative Site
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Rio Grande Do Sul
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Porto Alegre, Rio Grande Do Sul, Brasilien, 90430-090
- Novartis Investigative Site
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Porto Alegre, Rio Grande Do Sul, Brasilien, 90610-000
- Novartis Investigative Site
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Porto Alegre, Rio Grande Do Sul, Brasilien, 90470-340
- Novartis Investigative Site
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Santa Catarina
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Itajai, Santa Catarina, Brasilien, 88301220
- Novartis Investigative Site
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São Paulo
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Barretos, São Paulo, Brasilien, 14784-400
- Novartis Investigative Site
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Sao Paulo, São Paulo, Brasilien, 01317-001
- Novartis Investigative Site
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Sao Paulo, São Paulo, Brasilien, 01236030
- Novartis Investigative Site
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Kazan, Den Russiske Føderation, 420029
- Novartis Investigative Site
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Moscow, Den Russiske Føderation, 115 478
- Novartis Investigative Site
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Ryazan, Den Russiske Føderation, 390011
- Novartis Investigative Site
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St. Petersburg, Den Russiske Føderation, 197758
- Novartis Investigative Site
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St. Petersburg, Den Russiske Føderation, 197022
- Novartis Investigative Site
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Volzhskiy, Den Russiske Føderation, 404130
- Novartis Investigative Site
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Cebu, Filippinerne, 6000
- Novartis Investigative Site
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Manila, Filippinerne, 1000
- Novartis Investigative Site
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Alabama
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Mobile, Alabama, Forenede Stater, 36608
- Novartis Investigative Site
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Massachusetts
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Boston, Massachusetts, Forenede Stater, 02114
- Novartis Investigative Site
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Texas
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Houston, Texas, Forenede Stater, 77030
- Novartis Investigative Site
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Pok Fu Lam, Hong Kong
- Novartis Investigative Site
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Pokfulam, Hong Kong
- Novartis Investigative Site
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Lombardia
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Milano, Lombardia, Italien, 20133
- Novartis Investigative Site
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Milano, Lombardia, Italien, 20141
- Novartis Investigative Site
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Mexico, Mexico, 06760
- Novartis Investigative Site
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Arequipa, Peru
- Novartis Investigative Site
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Lima, Peru, Lima 34
- Novartis Investigative Site
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Barcelona, Spanien, 08035
- Novartis Investigative Site
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Barcelona, Spanien, 08036
- Novartis Investigative Site
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Donostia, Spanien, 20014
- Novartis Investigative Site
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Madrid, Spanien, 28041
- Novartis Investigative Site
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Madrid, Spanien, 28034
- Novartis Investigative Site
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Madrid, Spanien, 28040
- Novartis Investigative Site
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Malaga, Spanien, 29010
- Novartis Investigative Site
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Sevilla, Spanien, 41013
- Novartis Investigative Site
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Valencia, Spanien, 46010
- Novartis Investigative Site
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Valencia, Spanien, 46015
- Novartis Investigative Site
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Bangkok, Thailand, 10330
- Novartis Investigative Site
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Chiangmai, Thailand, 50200
- Novartis Investigative Site
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Phitsanulok, Thailand, 65000
- Novartis Investigative Site
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Salzburg, Østrig, A-5020
- Novartis Investigative Site
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Wien, Østrig, 1090
- Novartis Investigative Site
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
- Signed written informed consent
- Female >=18 years
- Histologically or cytologically confirmed invasive breast cancer with distant metastasis
- Subjects must have at least one measurable lesion per RECIST 1.1
- Note: Biopsied lesions should not be used as target lesions.
- Documentation of HER2 overexpression or gene amplification, in the invasive component of either the primary tumor or metastatic disease site as defined as: 3+ by Immunohistochemistry (IHC) and/or
- HER2/neu gene amplification by fluorescence, chromogenic, or silver in situ hybridization [FISH, CISH or SISH;>=6 HER2/neu gene copies per nucleus or a FISH, CISH, or SISH test ratio (HER2 gene copies to chromosome 17 signals) of >=2.0 OR HER2/chromosome 17 ratio <=2.0 with average HER2 copy number >=6 signals/cell nucleus]
- Centrally determined HER2-positive, hormone receptor status, breast molecular subtype by Prediction Analysis of Microarray 50 (PAM50) on the pre-treatment biopsy of metastatic lesion obtained during screening
- Note: Biopsied lesions should not be used as target lesions.
- Progression on at least 2 lines of anti-HER2-targeted therapies for metastatic breast cancer (MBC)
- Documented radiological disease progression during the most recent treatment regimen for metastatic disease
- Most recent treatment regimen for metastatic disease must include Trastuzumab and chemotherapy.
- Note: Trastuzumab emtansine (T-DM1) is considered acceptable as prior Trastuzumab/chemotherapy regimen
- Agreement to provide 2 tumor biopsies
- Prior treatment with pertuzumab, Lapatinib, and/or Trastuzumab emtansine is allowed; however, the last treatment for MBC must not include Trastuzumab in combination with pertuzumab.
- Subjects with radiographically stable Central nervous system (CNS) metastases, defined as radiographically stable on the previous 2 brain imaging scans, asymptomatic, and off systemic steroids and anticonvulsants for at least 1 month are eligible; treatment with prophylactic anticonvulsants is permitted unless listed under Prohibited Medications
- Discontinuation of all prior chemotherapy, immunotherapy, or biological therapy at least 3 weeks prior to the first dose of investigational product is required.
- Note: Discontinuation of Trastuzumab is not necessary.
- All treatment related toxicities, except alopecia, must have recovered to Grade 1 or better (Common Terminology Criteria for Adverse Events (CTCAE); version 4.0) prior to administration of the first dose of study treatment.
- Baseline Left ventricular ejection fraction (LVEF) >=50% as measured by Echocardiogram (ECHO) or Multigated acquisition (MUGA) and above the testing institution's lower limit of normal
- QT interval corrected (QTc) <450 millisecond (msec) or QTc <480 msec for patients with bundle branch block.
- The QTc is the QT interval corrected for heart rate according to either Bazett's formula (QTcB)
- Fridericia's formula (QTcF), or another method, machine or manual overread.
- For subject eligibility and withdrawal, QT correction formula QTcB will be used.
- For purposes of this data analysis, Bazett's formula will be used as the primary method of calculating the corrected QT interval. The QTc should be based on either a single Electrocardiogram (ECG) or an average of 3 sequential ECGs obtained within 24 hours of each other.
- The QTc should be based on single or averaged QTc values of triplicate ECGs obtained over a brief recording period.
- Women of childbearing potential must have a negative serum pregnancy test within 7 days prior to the first dose of study treatment and agree to use effective contraception, during the study and for 30 days following the last dose of study treatment.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Completion of screening and baseline assessments
- Able to swallow and retain orally administered medication and does not have any clinically significant gastrointestinal abnormalities that may alter absorption such as malabsorption syndrome or major resection of the stomach or bowels.
- At least 4 weeks must have elapsed since the last surgery and 2 weeks must have elapsed since radiotherapy
- Adequate baseline organ function as defined below
- Screening laboratory values should be used to confirm subject eligibility. Laboratory results may be retested if necessary to confirm eligibility.
- Hematologic(These values must be independent of growth factor support and stable for at least one week post transfusion)
- Absolute neutrophil count >=1.5 x 10^9/litre (L)
- Hemoglobin >=9.0 grams/decilitre(g/dL) (after transfusion if needed)
- Platelets>=100 x 10^9/L
- Hepatic
- Albumin >=2.5 g/dL
- Serum bilirubin <=1.25 x upper limit of normal (ULN)( These values must be independent of growth factor support and stable for at least one week post transfusion)
- Alanine aminotransferase; and, Aspartate aminotransferase AST and ALT<=2.5 x ULN
- Renal
- Calculate creatinine clearance >=40 millilitre/ minute (mL/min) (With the exception of those subjects who have Gilbert's syndrome; the bilirubin in these subjects should be at their baseline)
Exclusion Criteria:
- Lactating female
- Note: Women with potential to have children must be willing to practice acceptable methods of birth control during the study
- Bone-only disease and/or disease that cannot be biopsied.
- Unstable CNS metastases or leptomeningeal carcinomatosis not considered radiographically stable
- Note: Subjects with radiographically stable CNS metastases are defined as radiographically stable on the previous 2 brain imaging studies, asymptomatic, and off systemic steroids and anticonvulsants for at least 1 month; treatment with prophylactic anticonvulsants is permitted unless listed under prohibited medications
- Any serious and/or unstable pre-existing medical, psychiatric disorder, or other conditions including concurrent disease that could interfere with subject's safety, obtaining informed consent, or compliance with the study procedures.
- Serious cardiac illness or medical condition including but not confined to: Uncontrolled arrhythmias (e.g. ventricular tachycardia, high-grade atrioventricular (AV)-block, supraventricular arrhythmias which are not adequately rate-controlled);
- Angina pectoris requiring antianginal medication
- History of congestive heart failure or systolic dysfunction (LVEF <50%)
- Documented myocardial infarction <6 months from study entry
- Evidence of transmural infarction on ECG
- Poorly controlled hypertension (e.g. systolic >160milimiter (mm) Mercury (Hg) or diastolic >100mm Hg)
- Clinically significant valvular heart disease
- Current active hepatic or biliary disease (with exception of subjects with Gilbert's syndrome, asymptomatic gallstones, liver metastases, or stable chronic liver disease per investigator assessment)
- Any clinically significant gastrointestinal abnormalities that may alter absorption such as malabsorption syndrome or major resection of the stomach or bowels as well as subjects with ulcerative colitis are also excluded
- Any prohibited medication
- Prior treatment with Trastuzumab in combination with Lapatinib or prior treatment with an irreversible inhibitor of the intracellular domain of the HER2 receptor such as neratinib
- Last treatment for metastatic disease including Trastuzumab in combination with pertuzumab
- Administration of an investigational drug within 30 days or 5 half-lives, whichever is longer, preceding the first dose of study treatment
- A known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to any of the study drugs or their excipients that, in the opinion of the investigator or medical monitor, contraindicates participation
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Aktiv komparator: Lapatinib 1000mg + Trastuzumab in HER2 Enriched
In subjects with HER2-overexpressing MBC with a molecular subtype of HER2 Enriched, Lapatinib 1000mg once daily orally along with Trastuzumab (loading dose of 8 milligram/ kilogram (mg/kg) followed by the maintenance dose of 6 mg/kg Intravenous (IV) Every 3 weeks (q3weekly)) or Lapatinib 1000 milligram (mg) once daily orally along with Weekly Trastuzumab (loading dose of 4 mg/kg) followed by maintenance dose of 2 mg/kg IV weekly.
For subjects who were hormone receptor positive, an aromatase inhibitor of the investigator's choice was required.
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Lapatinib is available as 250-mg orange tablets.
Subjects randomized to the Lapatinib plus Trastuzumab arm received 1000 mg per day of Lapatinib, so wre instructed to take 4 x 250 mg tablets per day.
Lapatinib was to be taken either 1 hour (or more) before a meal or 1 hour (or more) after a meal
Trastuzumab is a sterile, white to pale yellow, preservative-free lyophilized powder for IV administration.
Trastuzumab was administered on Day 1 of the start of Lapatinib or in conjunction with the first cycle of chemotherapy, as an 8 mg/kg loading dose.
Subsequently, Trastuzumab was administered q3weekly as a 6 mg/kg maintenance dose.
At the discretion of the investigator, weekly Trastuzumab could be given in either of the three treatment arms (loading dose 4mg/kg followed by weekly administration of 2mg/kg).
Subjects who were hormone receptor-positive were required to receive an aromatase inhibitor as combination treatment; however the choice of the aromatase inhibitor selected for each patient was determined by the patients' investigator.
The AIs the Investigator could choose from were anastrozole, exemestane, and letrozole and dosing was per product information.
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Aktiv komparator: Trastuzumab in HER2 Enriched
In subjects with HER2-overexpressing MBC with a molecular subtype of HER2 Enriched, Trastuzumab (loading dose of 8 mg/kg followed by the maintenance dose of 6 mg/kg IV q3weekly) along with chemotherapy of the investigator's choice or Weekly Trastuzumab (loading dose of 4 mg/kg) followed by maintenance dose of 2 mg/kg IV weekly along with chemotherapy of the investigators choice.
Subjects randomized to this arm and hormone receptor positive received an aromatase inhibitor at the discretion of the investigator.
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Trastuzumab is a sterile, white to pale yellow, preservative-free lyophilized powder for IV administration.
Trastuzumab was administered on Day 1 of the start of Lapatinib or in conjunction with the first cycle of chemotherapy, as an 8 mg/kg loading dose.
Subsequently, Trastuzumab was administered q3weekly as a 6 mg/kg maintenance dose.
At the discretion of the investigator, weekly Trastuzumab could be given in either of the three treatment arms (loading dose 4mg/kg followed by weekly administration of 2mg/kg).
Subjects who were hormone receptor-positive were required to receive an aromatase inhibitor as combination treatment; however the choice of the aromatase inhibitor selected for each patient was determined by the patients' investigator.
The AIs the Investigator could choose from were anastrozole, exemestane, and letrozole and dosing was per product information.
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Aktiv komparator: Lapatinib 1000mg + Trastuzumab in Non- HER2 Enriched
In subjects with HER2-overexpressing MBC with a molecular subtype of Non- HER2 Enriched (luminal A, luminal B or Basal type), Lapatinib 1000mg once daily orally along with Trastuzumab (loading dose of 8 milligram/ kilogram (mg/kg) followed by the maintenance dose of 6 mg/kg Intravenous (IV) Every 3 weeks (q3weekly)) or Lapatinib 1000 milligram (mg) once daily orally along with Weekly Trastuzumab (loading dose of 4 mg/kg) followed by maintenance dose of 2 mg/kg IV weekly.
For subjects who were hormone receptor positive, an aromatase inhibitor of the investigator's choice was required.
|
Lapatinib is available as 250-mg orange tablets.
Subjects randomized to the Lapatinib plus Trastuzumab arm received 1000 mg per day of Lapatinib, so wre instructed to take 4 x 250 mg tablets per day.
Lapatinib was to be taken either 1 hour (or more) before a meal or 1 hour (or more) after a meal
Trastuzumab is a sterile, white to pale yellow, preservative-free lyophilized powder for IV administration.
Trastuzumab was administered on Day 1 of the start of Lapatinib or in conjunction with the first cycle of chemotherapy, as an 8 mg/kg loading dose.
Subsequently, Trastuzumab was administered q3weekly as a 6 mg/kg maintenance dose.
At the discretion of the investigator, weekly Trastuzumab could be given in either of the three treatment arms (loading dose 4mg/kg followed by weekly administration of 2mg/kg).
Subjects who were hormone receptor-positive were required to receive an aromatase inhibitor as combination treatment; however the choice of the aromatase inhibitor selected for each patient was determined by the patients' investigator.
The AIs the Investigator could choose from were anastrozole, exemestane, and letrozole and dosing was per product information.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Fold Change in Expression Profile of Genes and/or Proteins for Arm A (LAP+TRAS±AI (HER2-Enriched)) From Screening to Approx. 3.5 Years
Tidsramme: At screening and at disease progression, assessed up to approx. 3.5 years
|
Evaluate changes in biomarkers associated with immunomodulation between pre-treatment biopsy and disease progression biopsy within each arm. Biomarker analysis was performed using an mRNA gene expression panel derived from Nanostring platform in a total of 20 subjects who received the study treatment as per the study design and with baseline tumor biopsies available. For the selected biomarkers associated with immunomodulation, the median fold changes of gene expression level and 95% confidence interval are presented. The fold change was calculated as the ratio of the expression level of a biomarker at disease progression over the baseline. |
At screening and at disease progression, assessed up to approx. 3.5 years
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Fold Change in Expression Profile of Genes and /or Proteins for Arm B (TRAS+CHEM±AI (HER2-Enriched)) From Screening to Approx. 3.5 Years
Tidsramme: At screening and at disease progression, assessed up to approx. 3.5 years
|
Evaluate changes in biomarkers associated with immunomodulation between pre-treatment biopsy and disease progression biopsy within each arm. Biomarker analysis was performed using an mRNA gene expression panel derived from Nanostring platform in a total of 20 subjects who received the study treatment as per the study design and with baseline tumor biopsies available. For the selected biomarkers associated with immunomodulation, the median fold changes of gene expression level and 95% confidence interval are presented. The fold change was calculated as the ratio of the expression level of a biomarker at disease progression over the baseline. |
At screening and at disease progression, assessed up to approx. 3.5 years
|
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Fold Change in Expression Profile of Genes and /or Proteins for Arm C (Non-HER2- Enriched) From Screening to Approx. 3.5 Years
Tidsramme: At screening and at disease progression, assessed up to approx. 3.5 years
|
Evaluate changes in biomarkers associated with immunomodulation between pre-treatment biopsy and disease progression biopsy within each arm. Biomarker analysis was performed using an mRNA gene expression panel derived from Nanostring platform in a total of 20 subjects who received the study treatment as per the study design and with baseline tumor biopsies available. For the selected biomarkers associated with immunomodulation, the median fold changes of gene expression level and 95% confidence interval are presented. The fold change was calculated as the ratio of the expression level of a biomarker at disease progression over the baseline. |
At screening and at disease progression, assessed up to approx. 3.5 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Progression-free Survival (PFS)
Tidsramme: From randomization to disease progression or death, up to approx. 5.6 years
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PFS was defined as the time from the date of randomization (for Arm A and B) / treatment start date (for Arm C) to the date of the first documented disease progression or death due to any cause, whichever was earlier.
If a subject had not progressed or died at the analysis cutoff date, PFS was censored at the time of the last adequate tumor assessment.
PFS was summarized using Kaplan-Meier estimates.
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From randomization to disease progression or death, up to approx. 5.6 years
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Overall Response Rate (ORR)
Tidsramme: From enrollment/randomization to the end of study, approximately 5.6 years
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Overall response rate was defined as the percentage of subjects achieving either a confirmed complete response (CR) or partial response (PR) and was calculated from the Investigator's assessment of response per RECIST 1.1 criteria. .
The confirmed CR or PR was derived using the following rules: confirmed CR - at least two determinations of CR at least 4 weeks apart before disease progression; confirmed PR - at least two determinations of PR or better at least 4 weeks apart before progression.
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From enrollment/randomization to the end of study, approximately 5.6 years
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Clinical Benefit Rate (CBR)
Tidsramme: From enrollment/randomization the end of study, approximately 5.6 years
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CBR is defined as percentage of subjects with a complete response (CR), partial response (PR), or maintaining stable disease (SD) for at least 24 weeks while on study according to the investigator assessment of response per RECIST 1.1 criteria.
CR and PR are confirmed responses derived using the following rules: Confirmed CR - at least 2 determinations of CR at least 4 weeks apart before disease progression.
Confirmed PR - at least 2 determinations of PR or better at least 4 weeks apart before progression.
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From enrollment/randomization the end of study, approximately 5.6 years
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Association Between Biomarkers and PFS
Tidsramme: From randomization to disease progression or death, up to approx. 5.6 years
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Describe if changes of biomarker expression at disease progression from baseline correlate with PFS.
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From randomization to disease progression or death, up to approx. 5.6 years
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
24. oktober 2014
Primær færdiggørelse (Faktiske)
4. juni 2020
Studieafslutning (Faktiske)
4. juni 2020
Datoer for studieregistrering
Først indsendt
7. august 2014
Først indsendt, der opfyldte QC-kriterier
7. august 2014
Først opslået (Skøn)
11. august 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
13. oktober 2021
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
17. september 2021
Sidst verificeret
1. september 2021
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Hudsygdomme
- Neoplasmer
- Neoplasmer efter sted
- Brystsygdomme
- Brystneoplasmer
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Enzymhæmmere
- Antineoplastiske midler
- Hormoner, hormonsubstitutter og hormonantagonister
- Antineoplastiske midler, immunologiske
- Proteinkinasehæmmere
- Hormonantagonister
- Steroidsyntesehæmmere
- Østrogenantagonister
- Trastuzumab
- Lapatinib
- Aromatasehæmmere
Andre undersøgelses-id-numre
- 117165
- 2014-001220-30 (EudraCT nummer)
- CLAP016A2206 (Anden identifikator: Novartis)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
JA
IPD-planbeskrivelse
Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.
This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ja
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .