NCT05827081ClinicalTrials.gov
Phase IIIb Study of Ribociclib + ET in Early Breast Cancer
A Phase IIIb Study to Characterize the Efficacy and Safety of Adjuvant Ribociclib Plus Endocrine Therapy in a Close-to-clinical Practice Patient Population With HR+ HER2- Early Breast Cancer (Adjuvant WIDER)
בקצרה
The purpose of this open-label, multicenter, phase IIIb, single-arm study is to characterize the efficacy and safety of the combination of ribociclib and standard adjuvant endocrine therapy (ET) on invasive breast cancer-free survival (iBCFS), in a close to clinical practice…
שלב 3דרושים 1,400 משתתפים229 אתרים16 מדינות
קטגוריות
רשום במרשם אחד
- ClinicalTrials.govNCT05827081פתיחת רשומה זו ב־ClinicalTrials.govסונכרן שלשום
מחקר יחיד יכול להיות רשום בכמה מרשמים. אנו מציגים אותו פעם אחת ומקשרים לכל רשומה שברשותנו.
מידע הניסוי מוצג כפי שפורסם על ידי המרשם, בשפת המקור שלו.
מתעניינים במחקר הזה?
התחברות או צרו חשבון כדי לרשום את התעניינותכם ולעקוב אחר המחקר הזה.
How this study is set up
The points below are drawn from the public registry record for this study. Each one cites the field or sentence it came from. A dash (—) means the record does not state something — not that it is missing or wrong. Many well-run studies, especially small ones, leave some of these blank.
- Present: Registered before enrolment beganFirst posted 2023-04-24; recorded start 2024-02-28
- Present: Has a defined primary outcomeA primary outcome measure is listed in the record
- Present: The primary outcome states a time frameThe primary outcome measure records a time frame
- Not stated: Participants are not randomly assignedAllocation is recorded as non-randomised
- Not stated: A comparison group is not stated in the registry recordThe record describes a single study arm
- Not stated: Open label (no blinding)Masking is recorded as none (open label)
- Not stated: An ethics committee is not stated in the registry recordThis registry's ingested record has no ethics-committee field
- Not stated: Regulatory oversight (such as an IND or IDE) is not stated in the registry recordThis registry's ingested record has no regulatory-authorisation field
- Not stated: A data monitoring committee is not stated in the registry recordThis registry's ingested record has no data-monitoring-committee fieldA data monitoring committee is not required for many smaller studies, and its absence here is not unusual.
- Present: No cost to participants is mentioned in the recordChecked the summary, description and eligibility text; no cost-to-participant phrase found
- Present: Sponsor has 1128 other studies in this databaseCounted from the lead sponsor named in the record (Novartis Pharmaceuticals)
- Present: Sponsor has posted results for at least one studyBased on the sponsor’s studies in this database
- The record lists 1 condition.
- Lead sponsor type recorded as: industry.
- Intervention regulatory context: investigational, within a phased regulatory pathway.
Trial stature
Three independent measures of this study, described from its registry record — not a recommendation about it. A rigorous study by investigators nobody has heard of is better evidence than a weak study led by a famous one. How these are scored.
An exploratory-stage design for a phase 3 study, judged from its ClinicalTrials.gov record.
How this score is built
- Randomised allocation0/20
Allocation not stated in the record
- Blinding0/20
Open-label
- Control arm0/15
No comparator arm stated in the record
- Primary-outcome specificity10/10
Named primary outcome with a defined time frame
- Endpoint type10/10
Mortality / MACE endpoint (hard clinical outcome)
- Multi-centre8/8
Multi-centre: 229 sites
- Data monitoring committee0/7
No data monitoring committee stated
- Prospective registration5/5
Registered before the study start date
- Protocol / SAP posted0/5
No protocol or SAP posted to the registry
A large study, international in scope: 1,400 participants (target), run at 229 sites, across 16 countries.
How this score is built
- Enrolment31/40
1,400 participants (target)
- Site count25/25
229 sites
- Country count15/15
16 countries
- Planned duration10/10
Planned over about 80 months
- Sponsor scale10/10
Novartis Pharmaceuticals has led 1,104 trials in our corpus
We have no verifiable track record for the investigator named on this trial. That is common for early-career investigators and for records held outside ClinicalTrials.gov — it is not a negative signal.
How this score is built
- Investigator standing0/100
No investigator recorded in the registry for this trial
These describe the registry record only, and today we hold ClinicalTrials.gov data. Absent fields lower a score, and absence often reflects registration practice rather than study quality. A high-stature trial is not necessarily safer or a better choice for you — enrolling in a large definitive trial can mean a higher chance of receiving placebo, while a small early-phase study may be the only route to a new therapy.
תקציר
The purpose of this open-label, multicenter, phase IIIb, single-arm study is to characterize the efficacy and safety of the combination of ribociclib and standard adjuvant endocrine therapy (ET) on invasive breast cancer-free survival (iBCFS), in a close to clinical practice patient population with HR-positive (HR+), HER2-negative (HER2-), Anatomic Stage Group III, IIB, and a subset of Stage IIA Early Breast Cancer (EBC).
מצבים רפואיים
- Early Breast Cancer
זכאות
| מין | הכול |
|---|---|
| גילאים | 18 Years – 100 Years |
| מתנדבים בריאים | לא |
זכאות כפי שנכתבה במרשם
זכאות במשפטים פשוטים
הקריטריונים של רשומה זו טרם פורקו למשפטים נפרדים. טקסט המרשם שלמעלה שלם והוא הגרסה המחייבת.
תכנון המחקר
| סוג המחקר | התערבותי |
|---|---|
| שלב | שלב 3 |
| הקצאה | לא רלוונטי |
| מודל ההתערבות | SINGLE_GROUP |
| מטרה ראשית | TREATMENT |
| הסתרה | NONE (0) |
| גיוס | דרושים 1,400 משתתפים |
נותן חסות ושותפים
- Novartis Pharmaceuticals נותן חסות
זרועות והתערבויות
- Ribociclib + endocrine therapyEXPERIMENTAL
Participants will receive ribociclib 400 mg orally once daily on days 1 to 21 of a 28-day cycle, in combination with daily endocrine therapy (ET) for 36 months (approximately 39 cycles). ET consists of: * For postmenopausal women: letrozole 2.5 mg orally once daily continuously, anastrozole 1 mg orally once daily continuously, or exemestane 25 mg once daily continuously. * For pre/perimenopausal women, and men: letrozole 2.5 mg orally once daily continuously, anastrozole 1 mg orally once daily continuously, or exemestane 25 mg once daily continuously, combined with goserelin subcutaneously (at 3.6 mg once every 4 weeks if the one-month depot formulation is used or at 10.8 mg once every 3 months if the three-month depot formulation is used) or leuprolide subcutaneously (at 3.75 mg once every 4 weeks if the one-month depot formulation is used or at 11.25 mg once every 3 months if the three-month depot formulation is used)
התערבויות
- תרופה Ansastrozole
Anastrozole 1 mg orally once daily continuously.
- תרופה Exemestane
Exemestane 25 mg once daily continuously
- תרופה Goserelin
Goserelin administered subcutaneously at 3.6 mg once every 4 weeks if the one-month depot formulation is used or at 10.8 mg once every 3 months if the three-month depot formulation is used
- תרופה Letrozole
Letrozole 2.5 mg orally once daily continuously
- תרופה Leuprolide
Leuprolide administered subcutaneously at 3.75 mg once every 4 weeks if the one-month depot formulation is used or at 11.25 mg once every 3 months if the three-month depot formulation is used
- תרופה Ribociclib
Ribociclib 400 mg orally once daily on days 1-21 of a 28 day cycle followed by 7 days rest
מדדי תוצאה
מדד תוצאה ראשוני
Invasive Breast Cancer Free Survival (iBCFS) rate at 3 years
iBCFS is defined as the time from the date of first dose to the date of the first event of invasive ipsilateral breast tumor recurrence, local/regional invasive recurrence, distant recurrence, death (any cause), or contralateral invasive BC. iBCFS will be assessed using STEEP criteria version 2.0 (Standardized Definitions for Efficacy End Points in Adjuvant Breast Cancer Trials), as assessed by Investigator. The iBCFS rate at 3 years will be assessed.
מסגרת זמן At 3 years
מדד תוצאה משני
Incidence and severity of adverse events (AEs) using CTCAE v4.03
To evaluate Safety of ribociclib + ET
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Invasive Disease-Free Survival (iDFS)
iDFS is defined as the time from the date of first dose of study treatment to the date of the first event of invasive ipsilateral breast tumor recurrence, local/regional invasive recurrence, distant recurrence, death (any cause), contralateral invasive BC, or second primary non-breast invasive cancer (excluding basal and squamous cell carcinomas of the skin). iDFS will be assessed using STEEP 2.0 as assessed by the investigator.
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Distant Disease-Free Survival (DDFS)
Distant Disease-Free Survival (DDFS) is defined as the time from the date of first dose of study treatment to the date of the first event of recurrence at a distant site, death (any cause), or second primary non-breast invasive cancer (excluding in situ/non-invasive cancers and basal and squamous cell carcinomas of the skin). DDFS will be assessed using STEEP 2.0 as assessed by the investigator.
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Distant Relapse-Free Survival (DRFS)
Distant Relapse Free Survival (DRFS) is defined as the time from the date of first dose of study treatment to the date of the first event of recurrence at a distant site or death (any cause). DRFS will be assessed using STEEP 2.0 as assessed by the investigator.
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Recurrence-Free Interval (RFI)
RFI is defined as the time from date of first dose to date of first event of invasive recurrence in the ipsilateral breast or locoregionally, at a distant site, or death from breast cancer. RFI will be assessed using STEEP 2.0 as per investigator assessment.
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Relative dose intensity (RDI) of ribociclib
RDI is defined as the ratio of the dose intensity delivered to the planned dose intensity.
מסגרת זמן Up to 3 years
מדד תוצאה משני
Overall Survival (OS)
OS is defined as time from the start of study treatment to date of death due to any cause.
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Time To Discontinuation (TTD) of ribociclib
TTD is defined as the time from starting ribociclib to the time to treatment discontinuation due to any cause.
מסגרת זמן Up to 3 years
מדד תוצאה משני
Changes from baseline in Functional Assessment of Cancer Therapy - Breast (FACT-B) score
The FACT-B is a questionnaire that consists of 37 items with items from FACT-General (FACT-G) questionnaire (27 items) and from the Breast Cancer Subscale (BCS, 10 items). FACT-B consists of five subscales that address different aspects of the participant's quality of life: physical well-being (PWB), social/family well-being (SWB), emotional well-being (EWB), functional well-being (FWB), and BCS.
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Changes from baseline in Functional Assessment of Cancer Therapy - Endocrine Symptoms (FACT-ES) score
The FACT-ES is a questionnaire that consists of 19 items which assesses endocrine complaints and adverse events.
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Changes from baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F) score
The FACIT-F is a 13-item questionnaire designed to assess self-reported fatigue and its impact on daily activities and functions.
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Changes from baseline in European Quality of Life-5 Dimensions (EQ-5D-5L) score
EQ-5D-5L is a standardized participant completed questionnaire that measures health-related quality of life and translates that score into an index value or utility score. EQ-5D-5L consists of two components: a health state profile and an optional visual analogue scale (VAS). EQ-5D-5L health state profile is comprised of 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
מסגרת זמן Up to approximately 6 years
מדד תוצאה משני
Changes from baseline in Work Productivity and Activity Impairment Questionnaire (WPAI-GH) score
WPAI-GH measures the impact of health problems on the participant's productivity, in paid or unpaid activities, in the last 7 days. It is 6-item scale measuring absenteeism, presenteeism, and impairments in unpaid activity.
מסגרת זמן Up to approximately 6 years
תאריכים
| תאריך התחלה | 28 בפברואר 2024 (בפועל) |
|---|---|
| סיום ראשוני | 7 בספטמבר 2029 (משוער) |
| סיום | 20 בספטמבר 2030 (משוער) |
| פורסם לראשונה | 24 באפריל 2023 (בפועל) |
| עודכן לאחרונה | 18 בספטמבר 2026 |
| התוצאות פורסמו | לא צוין ברשומת המרשם |
| המצב אומת לאחרונה | ספטמבר 2026 |
בפועל פירושו שהאירוע התרחש. משוער פירושו שנותן החסות צופה אותו. שתי המשמעויות שונות זו מזו.
מיקומים
118 אתרים מגייסים
Argentina
| מתקן | עיר | מדינה או אזור | מצב |
|---|---|---|---|
| Novartis Investigative Site | Caba | Buenos Aires | פעיל, ללא גיוס |
| Novartis Investigative Site | Córdoba | מגייס | |
| Novartis Investigative Site | La Plata | Buenos Aires | מגייס |
Australia
| מתקן | עיר | מדינה או אזור | מצב |
|---|---|---|---|
| Novartis Investigative Site | Clayton | Victoria | פעיל, ללא גיוס |
| Novartis Investigative Site | East Melbourne | Victoria | פעיל, ללא גיוס |
| Novartis Investigative Site | Gateshead | New South Wales | פעיל, ללא גיוס |
| Novartis Investigative Site | Tiwi | Northern Territory | פעיל, ללא גיוס |
Brazil
| מתקן | עיר | מדינה או אזור | מצב |
|---|---|---|---|
| Novartis Investigative Site | Belo Horizonte | Minas Gerais | מגייס |
| Novartis Investigative Site | Porto Alegre | Rio Grande do Sul | מגייס |
| Novartis Investigative Site | Porto Alegre | Rio Grande do Sul | מגייס |
| Novartis Investigative Site | Porto Alegre | Rio Grande do Sul | מגייס |
| Novartis Investigative Site | Rio de Janeiro | מגייס | |
| Novartis Investigative Site | Rio de Janeiro | מגייס | |
| Novartis Investigative Site | Salvador | Estado de Bahia | מגייס |
| Novartis Investigative Site | São Paulo | São Paulo | מגייס |
| Novartis Investigative Site | São Paulo | São Paulo | מגייס |
| Novartis Investigative Site | São Paulo | מגייס |
Canada
| מתקן | עיר | מדינה או אזור | מצב |
|---|---|---|---|
| Novartis Investigative Site | Halifax | Nova Scotia | פעיל, ללא גיוס |
| Novartis Investigative Site | Montreal | Quebec | מגייס |
| Novartis Investigative Site | Montreal | Quebec | מגייס |
| Novartis Investigative Site | Montreal | Quebec | פעיל, ללא גיוס |
| Novartis Investigative Site | Oakville | Ontario | פעיל, ללא גיוס |
| Novartis Investigative Site | Ottawa | Ontario | פעיל, ללא גיוס |
| Novartis Investigative Site | Québec | Quebec | מגייס |
| Novartis Investigative Site | Saskatoon | Saskatchewan | פעיל, ללא גיוס |
| Novartis Investigative Site | Toronto | Ontario | מגייס |
| Novartis Investigative Site | Toronto | Ontario | מגייס |
| Novartis Investigative Site | Victoria | British Columbia | פעיל, ללא גיוס |
China
| מתקן | עיר | מדינה או אזור | מצב |
|---|---|---|---|
| Novartis Investigative Site | Beijing | פעיל, ללא גיוס | |
| Novartis Investigative Site | Beijing | Beijing Municipality | פעיל, ללא גיוס |
| Novartis Investigative Site | Beijing | פעיל, ללא גיוס | |
| Novartis Investigative Site | Changchun | Jilin | פעיל, ללא גיוס |
| Novartis Investigative Site | Chengdu | Sichuan | פעיל, ללא גיוס |
| Novartis Investigative Site | Chengdu | Sichuan | פעיל, ללא גיוס |
| Novartis Investigative Site | Guangzhou | Guangdong | פעיל, ללא גיוס |
| Novartis Investigative Site | Guangzhou | מגייס | |
| Novartis Investigative Site | Hangzhou | Zhejiang | פעיל, ללא גיוס |
| Novartis Investigative Site | Hangzhou | Zhejiang | פעיל, ללא גיוס |
| Novartis Investigative Site | Harbin | Heilongjiang | מגייס |
| Novartis Investigative Site | Jinan | Shandong | פעיל, ללא גיוס |
| Novartis Investigative Site | Jinan | Shandong | פעיל, ללא גיוס |
| Novartis Investigative Site | Jining | Shandong | פעיל, ללא גיוס |
| Novartis Investigative Site | Nanchang | Jiangxi | פעיל, ללא גיוס |
| Novartis Investigative Site | Nanjing | Jiangsu | מגייס |
| Novartis Investigative Site | Qingdao | פעיל, ללא גיוס | |
| Novartis Investigative Site | Shanghai | פעיל, ללא גיוס | |
| Novartis Investigative Site | Shijiazhuang | פעיל, ללא גיוס | |
| Novartis Investigative Site | Tianjin | פעיל, ללא גיוס | |
| Novartis Investigative Site | Wenzhou | Zhejiang | פעיל, ללא גיוס |
| Novartis Investigative Site | Zhengzhou | Henan | פעיל, ללא גיוס |
179 אתרים נוספים מצוינים ברשומת המרשם.
מסמכי המחקר
לא צורפו מסמכים ברשומת מרשם זו.
שינויים לאורך זמן
- 4 בספטמבר 2026
אתר נוסף
1 site added (229 total)
228229
- 18 באוגוסט 2026
אתר הוסר
1 site removed (228 total)
229228