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The purpose of this study is to assess the safety and efficacy of alpelisib plus fulvestrant in men and postmenopausal women with hormone receptor (HR) positive, human epidermal growth factor 2 (HER2)-negative, advanced breast cancer harboring a PIK3CA mutation in Japan, whose disease has progressed on or after aromatase inhibitor (AI) treatment regardless of prior CDK4/6 inhibitor use.
This is a Phase II open-label, 2-Part, multi-center study in Japan. The study will be conducted in two parts: Part 1 (Cohort 1) includes participants regardless of prior CDK4/6 inhibitor use and is designed to determine the recommended dose (RD), evaluate the tolerability and safety of alpelisib in combination with fulvestrant. Part 2 consists of 2 cohorts (the CDK4/6 inhibitor naive participants are in Cohort 2 and the CDK4/6 inhibitor pre-treated participants are in Cohort 3) which are designed to assess the efficacy and safety of alpelisib in combination with fulvestrant, will start once the RD of alpelisib is established.
Participants will be treated until disease progression, unacceptable toxicity, death or discontinuation from the study treatment for any other reason and will be followed for survival regardless of treatment discontinuation reason (except if consent is withdrawn or participant is lost to follow up).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cohort 1:CDK4/6 inhibitor naive or pre-treated (Part 1) | Experimental | Participants regardless of prior CDK4/6 inhibitor will be treated at escalating doses (200 mg, 250 mg and 300 mg, orally) of BYL719 in combination with Fulvestrant (500 mg, intramuscular). |
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| Cohort 2: CDK4/6 inhibitor naive (Part 2) | Experimental | Participants who are CDK4/6 inhibitor naive will be treated with BYL719 at the recommended dose identified in Part 1 in combination with Fulvestrant (500 mg, intramuscular). |
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| Cohort 3: CDK4/6 inhibitor pre-treated (Part 2) | Experimental | Participants who are CDK4/6 inhibitor pre-treated will be treated with BYL719 at the recommended dose identified in Part 1 in combination with Fulvestrant (500 mg, intramuscular). |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Alpelisib | Drug | [Part 1] Alpelisib administered at 200 mg (DL 1), 250 mg (DL 2) or 300mg (DL 3) orally once daily on a continuous dosing schedule starting on Cycle 1 Day 1 in a 28 day cycle. If DL 1 is tolerated, the alpelisib doses of 250 mg will be investigated. If DL 2 is tolerated, the alpelisib doses of 300 mg will be investigated. [Part 2] In the Part 2, participants will be enrolled into Cohort 2 (CDK4/6 inhibitor naive) and Cohort 3 (CDK4/6 inhibitor pre-treated) in parallel and alpelisib will be administered at the recommended dose identified in Part 1. |
| Measure | Description | Time Frame |
|---|---|---|
| [Part 1] The incidence of Dose Limiting Toxicities (DLTs) of alpelisib in combination with fulvestrant | A DLT is defined as an AE or abnormal laboratory value assessed as unrelated to disease, disease progression, inter-current illness, or concomitant medications that occurs within the first 2 cycles (the first 56 days) of treatment with alpelisib in combination with fulvestrant and meets any of the criteria specified in the protocol . | From Cycle 1 Day 1 to Cycle 2 Day 28 (Cycle = 28 days) |
| [Part 2] Overall Response Rate (ORR) in CDK4/6 inhibitor naive participants | ORR is defined as the proportion of participants with best overall response (BOR) of confirmed complete response (CR) or confirmed partial response (PR) based on local investigator assessment per RECIST 1.1. | Up to approximately 36 months |
| Measure | Description | Time Frame |
|---|---|---|
| [Part 1] Number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) | Safety is determined by incidence, type, and severity of adverse events per CTCAE v4.03 criteria including changes in laboratory values, vital signs, liver assessments, renal and cardiac assessments. | Up to approximately 37 months |
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Inclusion Criteria:
Exclusion Criteria:
Other protocol-defined inclusion/exclusion criteria may apply
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| Name | Affiliation | Role |
|---|---|---|
| Novartis Pharmaceuticals | Novartis Pharmaceuticals | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Novartis Investigative Site | Nagoya | Aichi-ken | 4648681 | Japan | ||
| Novartis Investigative Site |
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
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Part 1 of the study has a "Single group" design and the Part 2 has a "Parallel" design.
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| Fulvestrant | Drug | Fulvestrant is administered at a dose of 500 mg intramuscular on Cycle 1 Day 1, Day 15, and Day 1 of every cycle thereafter (where a cycle is 28 days). |
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| [Part 1] Number of participants with dose adjustments |
The number of participants with dose adjustments (reductions, interruption, or permanent discontinuation) and the reasons |
| Up to approximately 37 months |
| [Part 1] Dose intensity for alpelisib and fulvestrant | The dose intensity (computed as the ratio of actual cumulative dose received and actual duration of exposure) and the relative dose intensity (computed as the ratio of dose intensity and planned dose intensity) | Up to approximately 37 months |
| [Part 1] Duration of exposure for alpelisib and fulvestrant | The duration of exposure (in months) to alpelisib and fulvestrant | Up to approximately 37 months |
| [Part 1] Plasma concentrations of alpelisib in combination with fulvestrant | Summary statistics of alpelisib plasma concentrations by time point and dose level | Cycle 1 Day 8 (pre-dose), 15 (pre-dose, post-dose 1 hour, 3 hours) and Day 1 of Cycles 2, 4, 6, 8 (pre-dose) (Cycle = 28 days) |
| [Part 2] Overall Response Rate (ORR) for CDK4/6 inhibitor pre-treated participants | ORR is defined as the proportion of participants with best overall response (BOR) of confirmed complete response (CR) or confirmed partial response (PR) based on local investigator assessment per RECIST 1.1. | Up to approximately 36 months |
| [Part 2] Progression Free Survival (PFS) | PFS is defined as the time from the date of first administration of study treatment until the date of the first documented progression or death due to any cause. PFS will be assessed based on local investigator assessment per RECIST 1.1. | Up to approximately 36 months |
| [Part 2] Overall Survival (OS) | OS is defined as the time from date of first administration of study treatment until date of death due to any cause. | Up to approximately 60 months |
| [Part 2] Clinical Benefit Rate (CBR) | CBR is defined as the proportion of participants with a best overall response of confirmed CR, or confirmed PR, or an overall response of confirmed stable disease (SD), lasting for a duration of at least 24 weeks. CR, PR, and SD are defined based on local investigator assessment per RECIST 1.1. | Up to approximately 36 months |
| [Part 2] Duration of Response (DOR) | DOR only applies to participants whose best overall response is CR or PR based on local investigator assessment per RECIST 1.1. The start date is the date of first documented response of CR or PR (i.e. the start date of response, not the date when response was confirmed), and the end date is defined as the date of the first documented progression or death due to underlying cancer. | Up to approximately 36 months |
| [Part 2] Time to Response (TTR) | TTR is defined as the time from the date of first administration of study treatment until the date of the first documented response of either CR or PR, which must be subsequently confirmed (although date of initial response is used, not date of confirmation). | Up to approximately 36 months |
| [Part 2] Time to definitive deterioration of Eastern Cooperative Oncology Group (ECOG) performance status | Time to definitive deterioration in ECOG performance status is defined as the time from the date of first administration to the date when ECOG performance status has definitively deteriorated by at least one category compared with baseline. Deterioration is considered definitive if there is no subsequent improvement in ECOG performance status back to the baseline category or above. | Up to approximately 36 months |
| [Part 2] Number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) | Incidence, type, and severity of adverse events per CTCAE v4.03 criteria including changes in laboratory values, vital signs, liver assessments, renal and cardiac assessments | Up to approximately 37 months |
| [Part 2] Number of participants with dose adjustments | The number and percentage of participants with dose interruptions and dose reductions | Up to approximately 37 months |
| [Part 2] Dose intensity for alpelisib and fulvestrant | The dose intensity (computed as the ratio of actual cumulative dose received and actual duration of exposure) and the relative dose intensity (computed as the ratio of dose intensity and planned dose intensity) | Up to approximately 37 months |
| [Part 2] Duration of exposure for alpelisib and fulvestrant | The duration of exposure (in months) to alpelisib and fulvestrant | Up to approximately 37 months |
| [Part 2] Plasma concentrations of alpelisib in combination with fulvestrant | Summary statistics of alpelisib plasma concentrations by time point and dose level | Cycle 1 Day 8 (pre-dose), 15 (pre-dose, post-dose 1 hour, 3 hours) and Day 1 of Cycles 2, 4, 6, 8 (pre-dose) (Cycle= 28 days) |
| Nagoya |
| Aichi-ken |
| 4668560 |
| Japan |
| Novartis Investigative Site | Nagoya | Aichi-ken | 4678602 | Japan |
| Novartis Investigative Site | Kashiwa | Chiba | 277-8577 | Japan |
| Novartis Investigative Site | Isehara | Kanagawa | 259-1193 | Japan |
| Novartis Investigative Site | Yokohama | Kanagawa | 241-8515 | Japan |
| Novartis Investigative Site | Kumamoto | Kumamoto | 860-8556 | Japan |
| Novartis Investigative Site | Sendai | Miyagi | 9808574 | Japan |
| Novartis Investigative Site | Osaka | Osaka | 5400006 | Japan |
| Novartis Investigative Site | Osaka | Osaka | 5418567 | Japan |
| Novartis Investigative Site | Suita | Osaka | 565-0871 | Japan |
| Novartis Investigative Site | Bunkyo Ku | Tokyo | 1138677 | Japan |
| Novartis Investigative Site | Koto Ku | Tokyo | 1358550 | Japan |
| Novartis Investigative Site | Meguro-ku | Tokyo | 152-8902 | Japan |
| Novartis Investigative Site | Niigata | 951-8566 | Japan |
| ID | Term |
|---|---|
| C585539 | Alpelisib |
| D000077267 | Fulvestrant |
| ID | Term |
|---|---|
| D004958 | Estradiol |
| D004963 | Estrenes |
| D004962 | Estranes |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |
| D045166 | Estradiol Congeners |
| D012739 | Gonadal Steroid Hormones |
| D042341 | Gonadal Hormones |
| D006728 | Hormones |
| D006730 | Hormones, Hormone Substitutes, and Hormone Antagonists |
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