Study to Assess the Efficacy and Safety of Alpelisib Plus Fulvestrant in Participants With HR-positive (HR+), HER2-negative, Advanced Breast Cancer After Treatment With a CDK4/6 Inhibitor and an Aromatase Inhibitor.
Alpelisib: Alpelisib (tablets) administered at 300mg orally once daily on a continuous dosing schedule starting on Cycle 1 Day 1 in a 28 day cycle.
Fulvestrant: Fulvestrant (prefilled syringe) 500mg administered intramuscularly at Cycle 1 Day 1 and 15 and then at Day 1 of each subsequent cycle (each cycle is 28 days).
Alpelisib-matching placebo: Alpelisib-matching placebo (tablets) administered orally once daily on a continuous dosing schedule starting on Cycle 1 Day 1 in a 28 day cycle.
After Protocol Amendment 5 is implemented, alpelisib matching-placebo will no longer be supplied or administered once participants have been unblinded.
Study summary
The purpose of this study is to complement Study CBYL719C2301 (SOLAR-1) and obtain more comprehensive data on the efficacy and safety of alpelisib (BYL719) in combination with fulvestrant compared with placebo plus fulvestrant in men or postmenopausal women with HR-positive, HER2-negative advanced breast cancer with a PIK3CA mutation who progressed or relapsed on or after treatment with an AI plus a CDK4/6 inhibitor.
Eligibility
Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Key Inclusion Criteria:
* Participant is an adult ≥ 18 years old at the time of informed consent and has signed informed consent before any trial related activities and according to local guidelines.
* Participant has a histologically and/or cytologically confirmed diagnosis of ER+ and/or PgR+ breast cancer by local laboratory.
* Participant has HER2-negative breast cancer defined as a negative in situ hybridization test or an IHC status of 0, 1+ or 2+. If IHC is 2+, a negative in situ hybridization (Fluorescent in situ hybridization (FISH), Chromogenic in situ hybridization (CISH), or Silver-enhanced in situ hybridization (SISH)) test is required by local laboratory testing.
* Participant has at least one measurable lesion as per RECIST v1.1 criteria as assessed by Investigator (a lesion at a previously irradiated site may only be counted as a target lesion if there is clear sign of progression since the irradiation).
* Participant has recurrence or progression of disease during or after combined AI (i.e. letrozole, anastrozole, exemestane) and CDK4/6 inhibitor therapy. The combined AI and CDK4/6 inhibitor therapy does not need to be the latest treatment regimen (including adjuvant setting).
* Participant has received ≤ 2 prior lines of systemic therapies overall in the metastatic setting, of which a maximum of 1 line of prior treatment with chemotherapy (except for neoadjuvant/ adjuvant chemotherapy) is permitted.
* The presence of PIK3CA mutation(s) determined in tumor tissue prior to enrollment either by a Novartis designated laboratory or in tumor tissue or plasma ctDNA by a local laboratory using a Food and Drug Administration (FDA)-approved PIK3CA Companion Diagnostics (CDx) test for alpelisib or the CE-IVD QIAGEN Therascreen® PIK3CA RGQ PCR test.
* If female, then the participant must be in postmenopausal status.
Key Exclusion Criteria:
* Participant with symptomatic visceral disease or any disease burden that makes the participant ineligible for endocrine therapy (ET) per the Investigator's best judgment.
* Participant who relapsed with documented evidence of progression more than 12 months from completion of (neo)adjuvant endocrine/endocrine-based therapy with no treatment for metastatic disease.
* Participant has received prior treatment with fulvestrant, any oral selective estrogen receptor degrader (SERD), any Phosphatidylinositol-3-Kinase (PI3K), mammalian Target of Rapamycin (mTOR) or Protein Kinase B (AKT) inhibitor.
Other Inclusion and Exclusion Criteria do apply
Primary outcome measure(s)
Progression-free survival (PFS) based on BIRC assessments and using RECIST v1.1 criteria — From randomization to date of the first documented progression or death due to any cause, assessed up to a maximum duration of 60 months. Progression-free survival (PFS) is defined as the time from the date of randomization to the date of the first documented progression or death due to any cause. PFS will be assessed by the Blinded Independent Review Committee (BIRC) according to RECIST 1.1.
Trial sites (68)
Facility
City
Region
Status
Novartis Investigative Site
Sint-Niklaas
Oost Vlaanderen
Novartis Investigative Site
Brussels
Belgium
Novartis Investigative Site
Brussels
Belgium
Novartis Investigative Site
Ghent
Belgium
Novartis Investigative Site
Leuven
Belgium
Novartis Investigative Site
Liège
Belgium
Novartis Investigative Site
Plovdiv
Bulgaria
Novartis Investigative Site
Sofia
Bulgaria
Novartis Investigative Site
Calgary
Alberta
Novartis Investigative Site
Ottawa
Ontario
Novartis Investigative Site
Brno
Czechia
Novartis Investigative Site
Nový Jičín
Czechia
Novartis Investigative Site
Prague
Czechia
Novartis Investigative Site
Prague
Czechia
Novartis Investigative Site
Prague
Czechia
Novartis Investigative Site
Aalborg
Denmark
Novartis Investigative Site
Helsinki
Finland
Novartis Investigative Site
Tampere
Finland
Novartis Investigative Site
Besançon
France
Novartis Investigative Site
Clermont-Ferrand
France
Novartis Investigative Site
La Roche-sur-Yon
France
Novartis Investigative Site
Lyon
France
Novartis Investigative Site
Marseille
France
Novartis Investigative Site
Montpellier
France
Novartis Investigative Site
Paris
France
Novartis Investigative Site
Paris
France
Novartis Investigative Site
Valenciennes
France
Novartis Investigative Site
Cologne
North Rhine-Westphalia
Novartis Investigative Site
Augsburg
Germany
Novartis Investigative Site
Berlin
Germany
Novartis Investigative Site
Essen
Germany
Novartis Investigative Site
Lübeck
Germany
Novartis Investigative Site
Athens
Greece
Novartis Investigative Site
Pátrai
Greece
Novartis Investigative Site
Budapest
Hungary
Novartis Investigative Site
Dublin
Ireland
Novartis Investigative Site
Bari
BA
Novartis Investigative Site
Bergamo
BG
Novartis Investigative Site
Bologna
BO
Novartis Investigative Site
Florence
FI
+ 28 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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