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Studie hodnotící účinnost a bezpečnost léčby Alpelisibem plus Fulvestrant u japonských mužů a žen po menopauze s pokročilým karcinomem prsu

17. září 2026 aktualizováno: Novartis Pharmaceuticals

Otevřená, 2dílná, multicentrická studie fáze II BYL719 (Alpelisib) v kombinaci s fulvestrantem pro muže a ženy po menopauze s pozitivním, HER2-negativním, pokročilou rakovinou prsu s mutací PIK3CA receptoru hormonu (HR) Po léčbě inhibitorem aromatázy (AI) v Japonsku

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.

Přehled studie

Postavení

Aktivní, ne nábor

Podmínky

Intervence / Léčba

Detailní popis

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any other reason and will be followed for survival regardless of treatment discontinuation reason (except if consent is withdrawn or participant is lost to follow up).

Typ studie

Intervenční

Zápis (Aktuální)

24

Fáze

  • Fáze 2

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní místa

      • Niigata, Japonsko, 951-8566
        • Novartis Investigative Site
    • Aichi-ken
      • Nagoya, Aichi-ken, Japonsko, 4668560
        • Novartis Investigative Site
      • Nagoya, Aichi-ken, Japonsko, 4678602
        • Novartis Investigative Site
      • Nagoya, Aichi-ken, Japonsko, 4648681
        • Novartis Investigative Site
    • Chiba
      • Kashiwa, Chiba, Japonsko, 2778577
        • Novartis Investigative Site
    • Kanagawa
      • Isehara, Kanagawa, Japonsko, 2591193
        • Novartis Investigative Site
      • Yokohama, Kanagawa, Japonsko, 2418515
        • Novartis Investigative Site
    • Kumamoto
      • Kumamoto, Kumamoto, Japonsko, 8608556
        • Novartis Investigative Site
    • Miyagi
      • Sendai, Miyagi, Japonsko, 9808574
        • Novartis Investigative Site
    • Osaka
      • Osaka, Osaka, Japonsko, 5418567
        • Novartis Investigative Site
      • Osaka, Osaka, Japonsko, 5400006
        • Novartis Investigative Site
      • Suita, Osaka, Japonsko, 5650871
        • Novartis Investigative Site
    • Tokyo
      • Bunkyo Ku, Tokyo, Japonsko, 1138677
        • Novartis Investigative Site
      • Koto Ku, Tokyo, Japonsko, 1358550
        • Novartis Investigative Site
      • Meguro-ku, Tokyo, Japonsko, 1528902
        • Novartis Investigative Site

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

18 let až 100 let (Dospělý, Starší dospělý)

Přijímá zdravé dobrovolníky

Ne

Pohlaví způsobilá ke studiu

Všechno

Popis

Inclusion Criteria:

  • Japanese man or postmenopausal woman
  • Participant has adequate tumor tissue for the analysis of PIK3CA mutational status by a Novartis designated laboratory.
  • Participant has identified PIK3CA mutation (as determined by a Novartis designated laboratory)
  • 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 (FISH, CISH or SISH) test is required by local laboratory testing
  • Participant has measurable disease, i.e., at least one measurable lesion as per RECIST 1.1
  • Participant has advanced breast cancer
  • Participant has ECOG performance status 0 or 1

Exclusion Criteria:

  • Participant with symptomatic visceral disease or any disease burden that makes the participant ineligible for endocrine therapy per the investigator's best judgment
  • Participant has received prior treatment;
  • with chemotherapy (except for neoadjuvant/ adjuvant chemotherapy), fulvestrant, any PI3K, mTOR or AKT inhibitor for Cohort 1 and 3
  • with chemotherapy (except for neoadjuvant/ adjuvant chemotherapy), fulvestrant, any PI3K, mTOR, AKT inhibitor or CDK 4/6 inhibitor for Cohort 2
  • Participant has a known hypersensitivity to alpelisib or fulvestrant, or to any of the excipients of alpelisib or fulvestrant
  • Participant with inflammatory breast cancer at screening
  • Participant is concurrently using other anti-cancer therapy
  • Participant has had surgery within 14 days prior to starting study drug or has not recovered from major side effects
  • Participant with an established diagnosis at screening of diabetes mellitus type I or not controlled type II (based on FPG and HbA1c)
  • Participant has currently documented pneumonitis /interstitial lung disease
  • History of acute pancreatitis within 1 year of screening or past medical history of chronic pancreatitis
  • Participant with unresolved osteonecrosis of the jaw
  • Participant has a history of severe cutaneous reactions

Other protocol-defined inclusion/exclusion criteria may apply

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Léčba
  • Přidělení: Nerandomizované
  • Intervenční model: Paralelní přiřazení
  • Maskování: Žádné (otevřený štítek)

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: Cohort 1:CDK4/6 inhibitor naive or pre-treated (Part 1)

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).

[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.

Ostatní jména:
  • BYL719

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).

Ostatní jména:
  • Faslodex
Experimentální: Cohort 2: CDK4/6 inhibitor naive (Part 2)

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).

[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.

Ostatní jména:
  • BYL719

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).

Ostatní jména:
  • Faslodex
Experimentální: Cohort 3: CDK4/6 inhibitor pre-treated (Part 2)

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).

[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.

Ostatní jména:
  • BYL719

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).

Ostatní jména:
  • Faslodex

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
[Part 1] The incidence of Dose Limiting Toxicities (DLTs) of alpelisib in combination with fulvestrant
Časové okno: From Cycle 1 Day 1 to Cycle 2 Day 28 (Cycle = 28 days)

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
Časové okno: Up to approximately 36 months

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

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
[Part 1] Number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)
Časové okno: Up to approximately 37 months

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
[Part 1] Number of participants with dose adjustments
Časové okno: Up to approximately 37 months

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
Časové okno: Up to approximately 37 months

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
Časové okno: Up to approximately 37 months

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
Časové okno: 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)

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
Časové okno: Up to approximately 36 months

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)
Časové okno: Up to approximately 36 months

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)
Časové okno: Up to approximately 60 months

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)
Časové okno: Up to approximately 36 months

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)
Časové okno: Up to approximately 36 months

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)
Časové okno: Up to approximately 36 months

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
Časové okno: Up to approximately 36 months

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)
Časové okno: Up to approximately 37 months

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
Časové okno: Up to approximately 37 months

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
Časové okno: Up to approximately 37 months

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
Časové okno: Up to approximately 37 months

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
Časové okno: 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)

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)

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Sponzor

Vyšetřovatelé

  • Ředitel studie: Novartis Pharmaceuticals, Novartis Pharmaceuticals

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Aktuální)

8. ledna 2021

Primární dokončení (Odhadovaný)

26. února 2027

Dokončení studie (Odhadovaný)

27. února 2027

Termíny zápisu do studia

První předloženo

19. srpna 2020

První předloženo, které splnilo kritéria kontroly kvality

19. srpna 2020

První zveřejněno (Aktuální)

24. srpna 2020

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

18. září 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

17. září 2026

Naposledy ověřeno

1. září 2026

Více informací

Termíny související s touto studií

Další identifikační čísla studie

  • CBYL719C1201

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

ANO

Popis plánu IPD

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

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

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