NCT06982521ClinicalTrials.gov

Phase 3 Study of RLY-2608 + Fulvestrant vs Capivasertib + Fulvestrant as Treatment for Locally Advanced or Metastatic PIK3CA-mutant HR+/HER2- Breast Cancer

A Phase 3 Open-Label Randomized Study Assessing the Efficacy and Safety of RLY-2608 + Fulvestrant Versus Capivasertib + Fulvestrant as Treatment for PIK3CA-mutant Hormone Receptor Positive, Human Epidermal Growth Factor Receptor 2 Negative (HR+/HER2-) Locally Advanced or Metastatic Breast Cancer Following Recurrence or Progression On or After Treatment With a CDK4/6 Inhibitor

In reclutamentoAccetta partecipanti ora, secondo la scheda del registro.

Contatta questo studio

In breve

This is a global, multicenter, open-label, randomized Phase 3 study comparing the efficacy and safety of RLY-2608 (zovegalisib) + fulvestrant to capivasertib + fulvestrant for the treatment of patients with HR+/HER2- ABC with PIK3CA mutation following recurrence or progression on…

Fase 3540 partecipanti ricercati231 centri24 paesi

Categorie

Oncologia83%Dermatologia10%Endocrino e metabolico6%

Registrato in 1 registro

ClinicalTrials.govNCT06982521Apri questa scheda su ClinicalTrials.govSincronizzato 3 settimane fa

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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 2025-05-21; recorded start 2025-08-26
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
Present: Participants are randomly assignedAllocation is recorded as randomised
Present: Has a comparison groupThe record lists a placebo or comparator arm, or more than one 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 7 other studies in this databaseCounted from the lead sponsor named in the record (Relay Therapeutics, Inc.)
Not stated: No posted results from this sponsor are in this database yetBased on the sponsor’s studies in this database

The record lists 6 conditions.
Lead sponsor type recorded as: industry.
Intervention regulatory context: investigational, within a phased regulatory pathway.

These are facts from the public registry record, not a judgement about the study. Discuss any trial with your own doctor before taking part.

What these facts mean, and what to ask · ruleset v1

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.

Methodological rigourSTRONG

A strong methodological design for a phase 3 study, judged from its ClinicalTrials.gov record.

How this score is built

Randomised allocation20/20
Participants are randomly allocated between arms
Blinding0/20
Open-label
Control arm15/15
Active-comparator control arm
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: 211 sites
Data monitoring committee0/7
Data monitoring committee not stated in the record
Prospective registration5/5
Registered before the study start date
Protocol / SAP posted0/5
No protocol or SAP posted to the registry

ScaleMEDIUM

A medium-sized study, international in scope: 540 participants (target), run at 231 sites, across 24 countries.

How this score is built

Enrolment27/40
540 participants (target)
Site count25/25
211 sites
Country count15/15
23 countries
Planned duration10/10
Planned over about 77 months
Sponsor scale3/10
Relay Therapeutics, Inc. has led 8 trials in our corpus

Investigator standingUNKNOWN

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.

Sintesi

Patologie

PIK3CA Mutation
HER2- Negative Breast Cancer
Hormone Receptor Positive Tumor
Breast Cancer
Metastatic Breast Cancer
Advanced Breast Cancer

Idoneità

Idoneità
Sesso	Tutti
Età	18 Years – Nessun massimo
Volontari sani	No

Idoneità come riportata nel registro

Inclusion Criteria: * Patient has ECOG performance status of 0-1 * One or more known primary oncogenic PIK3CA mutation(s) * Adult females, pre- and/or post-menopausal, and adult males. Pre-menopausal (and peri-menopausal) women can be enrolled if amenable to treatment with a gonadotropin-releasing hormone (GnRH) agonist. Patients are to have commenced treatment with a GnRH agonist at least 2 weeks prior to randomization and must be willing to continue on it for the duration of the study. * Histologically or cytologically confirmed diagnosis of HR+/HER2- locally advanced or metastatic breast cancer (ABC) with radiological or objective evidence of recurrence or progression; locally advanced disease must not be amenable to resection with curative intent * Measurable disease per RECIST v1.1 or evaluable bone-only disease. * Must have radiological evidence of progression on or after previous treatment for HR+/HER2- ABC with: 1. At least 1 and no more than 2 lines of endocrine therapy (ET) in the (neo)adjuvant setting with recurrence on or within 12 months of completion or in the ABC setting 2. Only 1 prior line of CDK4/6 inhibitor therapy in one of the following settings: 1. CDK4/6 inhibitor + ET in the ABC setting 2. CDK4/6 inhibitor therapy in the adjuvant setting if progression occurred during or within 12 months of completion of adjuvant CDK4/6 inhibitor with ET 3. Patients who progressed during or within 12 months of completion of adjuvant CDK4/6 inhibitor and after receiving CDK4/6 inhibitor therapy in the advanced setting are considered to have had \>1 prior line of CDK4/6 inhibitor and are not eligible Exclusion Criteria: * Prior treatment with any of the following: 1. CDK2 inhibitors. Prior treatment with other investigational CDK inhibitors could be permitted upon discussion and approval from the Sponsor 2. PIK3, AKT, or mTOR inhibitors or any agent whose mechanism of action is the inhibit the PIK3/AKT/mTOR pathway 3. Immunotherapy 4. Antibody drug conjugates * Type 1 diabetes, or Type 2 diabetes requiring antihyperglycemic medication, or fasting plasma glucose ≥ 140 mg/dL (7.8 mmol/L), or glycosylated hemoglobin (HbA1c) ≥7.0% (≥ 53 mmol/mol). * Clinically significant, uncontrolled cardiovascular disease * Any factors that increase the risk of QTc prolongation or risk of arrhythmic events * Known active uncontrolled or symptomatic CNS metastases associated with progressive neurological symptoms or requiring ongoing corticosteroids or anticonvulsants for symptomatic control * Past medical history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis which required steroid treatment, or any evidence of clinically active interstitial lung disease * History of hypersensitivity to fulvestrant or drugs in a similar class as fulvestrant, zovegalisib, or capivasertib, including their excipients * Known activating AKT mutations, loss-of-function PTEN mutations, or loss of PTEN expression resulting in oncogenic pathway activation downstream of PI3K

Idoneità in frasi semplici

I criteri di questa scheda non sono ancora stati suddivisi in affermazioni distinte. Il testo del registro qui sopra è completo ed è la versione autorevole.

Disegno dello studio

Disegno dello studio
Tipo di studio	Interventistico
Fase	Fase 3
Assegnazione	Randomizzata
Modello di intervento	PARALLEL
Finalità principale	TREATMENT
Mascheramento	NONE (0)
Arruolamento	540 partecipanti ricercati

Sponsor e collaboratori

Relay Therapeutics, Inc. Sponsor

Bracci e interventi

Zovegalisib + fulvestrantEXPERIMENTAL
Zovegalisib + fulvestrant combination for participants with HR+/HER2- advanced breast cancer
capivasertib + fulvestrantACTIVE_COMPARATOR
capivasertib + fulvestrant combination for participants with HR+/HER2- advanced breast cancer

Interventi

Farmaco Capivasertib
400mg orally BID administered on an intermittent weekly dosing schedule. Patients will dose on Days 1 through 4 each week of a 28-day treatment cycle
Farmaco Fulvestrant
500 mg intramuscularly administered on Cycle 1 Day 1, Day 15, and Day 1 of each subsequent cycle (28-day treatment cycle)
Farmaco Zovegalisib
400 mg orally BID administered daily on a 28-day treatment cycle

Esiti misurati

Esito primario
Progression-Free Survival (PFS) within the overall and kinase population by blinded independent central review (BICR)
Orizzonte temporale The time from date of randomization until radiographic progression per RECIST v1.1, or death due to any cause, up to approximately 77 months
Esito secondario
Overall Survival (OS) within the overall and kinase populations
Orizzonte temporale The time from randomization to the date of death by any cause, up to approximately 77 months
Esito secondario
PFS by Investigator within the overall and kinase populations
Orizzonte temporale The time from date of randomization until radiographic progression per RECIST v1.1, or death due to any cause, up to approximately 77 months
Esito secondario
Objective Response Rate (ORR) within the overall and kinase populations
Orizzonte temporale Up to approximately 77 months
Esito secondario
Duration of Response (DOR) within the overall and kinase populations
Orizzonte temporale Up to approximately 77 months
Esito secondario
Clinical Benefit Rate (CBR) within the overall and kinase populations
Orizzonte temporale Up to approximately 77 months
Esito secondario
Occurrence/frequency of Adverse Events (AEs) and its relationship to the study drugs (safety and tolerability) within the overall and kinase populations
Orizzonte temporale Up to approximately 77 months
Esito secondario
Plasma concentrations of zovegalisib (and its metabolites as appropriate)
Orizzonte temporale Approximately every 2 weeks in Cycle 1 (4-week cycle) and during Cycles 2 and 3
Esito secondario
European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (EORTC QLQ-C30) scale/item scores including change from baseline and time to deterioration within overall and kinase populations
Orizzonte temporale Up to approximately 77 months
Esito secondario
EORTC Quality of Life Questionnaire Breast Cancer-Specific Module (EORTC QLQ-BR23) scale/item scores including change from baseline and time to deterioration within the overall and kinase populations
Orizzonte temporale Up to approximately 77 months
Esito secondario
Health state utility data for economic evaluation by EQ-5D-5L health state utility index within the overall and kinase populations
Orizzonte temporale Up to approximately 77 months

Date

Date
Data di inizio	26 agosto 2025 (effettiva)
Conclusione primaria	30 aprile 2028 (stimata)
Conclusione	31 dicembre 2031 (stimata)
Prima pubblicazione	21 maggio 2025 (effettiva)
Ultimo aggiornamento	3 settembre 2026
Risultati pubblicati	Non indicato nella scheda del registro
Stato verificato l'ultima volta	luglio 2026

«Effettiva» significa che l'evento è avvenuto. «Stimata» significa che lo sponsor lo prevede. Le due cose non sono equivalenti.

Centri

231 centri stanno reclutando

Argentina

Argentina
Struttura	Città	Stato
Organización Médica de Investigación (OMI)	Buenos Aires	In reclutamento
Centro Medico Dr. Doreski- Fundacion Respirar	Buenos Aires	In reclutamento
Hospital Britanico de Buenos Aires	Buenos Aires	In reclutamento
Instituto de Investigaciones Clinicas de Cordoba	Córdoba	In reclutamento
Breast clinica de la mama	La Plata	In reclutamento
Hospital Provincial del Centenario	Rosario	In reclutamento
Instituto de Oncología de Rosario	Rosario	In reclutamento
Centro de Investigaciones Clinicas. Clinica Viedma S.A.	Viedma	In reclutamento

Australia

Australia
Struttura	Città	Stato o regione	Stato
Monash Health	Clayton	Victoria	In reclutamento
St. Vincent's Hospital Sydney	Darlinghurst	New South Wales	In reclutamento
Lake Macquarie Hospital	Gateshead	New South Wales	In reclutamento
Barwon Health	Geelong	Victoria	In reclutamento
Bayside Health (Alfred)	Melbourne	Victoria	In reclutamento
Peter MacCallum Cancer Center	Melbourne	Victoria	In reclutamento
Mater Hospital Sydney	North Sydney	New South Wales	In reclutamento
Sunshine Hospital	Saint Albans	Victoria	In reclutamento
Sydney Adventist Hospital	Wahroonga	New South Wales	In reclutamento
Ballarat Oncology & Haematology Clinical Research Fund	Wendouree	Victoria	In reclutamento

Austria

Austria
Struttura	Città	Stato
Medical University of Graz	Graz	In reclutamento
Ordensklinikum Linz GmbH	Linz	In reclutamento
LKH Feldkirch, Interne E am LKH Rankweil	Rankweil	In reclutamento

Belgium

Belgium
Struttura	Città	Stato
Universitair Ziekenhuis Antwerpen	Antwerp	In reclutamento
Cliniques Universitaires Saint-Luc	Brussels	In reclutamento
Institut Jules Bordet	Brussels	In reclutamento
Ghent University Hospital	Ghent	In reclutamento
Universitair Ziekenhuis Brussel	Jette	In reclutamento
Universitair Ziekenhuis Leuven	Leuven	In reclutamento
Centre Hospitalier de l'Ardenne	Libramont	In reclutamento
Clinique CHC Mont Legia	Liège	In reclutamento
CHU-UCL Namur, Site Sainte-Elisabeth	Namur	In reclutamento
Vitaz	Sint-Niklaas	In reclutamento
CHR de Verviers site Tourelle	Verviers	In reclutamento

Brazil

Brazil
Struttura	Città	Stato
Oncolinicas do Brasil Serviços Médicos S.A (Oncocentro)	Belo Horizonte	In reclutamento
CEMEC CTO (CPAM - Centro de Pesquisas da Amazônia)	Belém	In reclutamento
Instituto do Câncer do Ceará	Fortaleza	In reclutamento
Hospital de Cancer Araujo Jorge/ Associacao de Combate ao Cancer em Goias	Goiânia	In reclutamento
Oncoclinicas Natal- Centro de Pesquisa Oncology Natal	Natal	In reclutamento
Associação Hospitalar Moinhos de Vento	Porto Alegre	In reclutamento
Uniao Brasileira de Educacao e Assistencia/ Hospital Sao Lucas da PUCRS	Porto Alegre	In reclutamento
Centro Gaúcho Integrado - Hospital Mae de Deus	Porto Alegre	In reclutamento
Hospital de Clinicas de Porto Alegre	Porto Alegre	In reclutamento
Irmandade da Santa Casa de Misericórdia de Porto Alegre	Porto Alegre	In reclutamento
Oncoclinicas Rio de Janeiro S.A.	Rio de Janeiro	In reclutamento
Instituto de Educação Pesquisa e Gestão em Saúde	Rio de Janeiro	In reclutamento
Nucleo de Oncologia da Bahia S.A.	Salvador	In reclutamento
Centro de Oncologia do ABC- CEON+ Unidade Sao Caetano do Sul	São Caetano do Sul	In reclutamento
Sociedade Beneficente de Senhora Hospital Sírio-Libanês	São Paulo	In reclutamento
Clinica Onco Star	São Paulo	In reclutamento

Bulgaria

Bulgaria
Struttura	Città	Stato o regione	Stato
MHAT "Dr. Tota Venkova", AD	Gabrovo		In reclutamento
Acibadem City Clinic Tokuda University Hospital EAD	Sofia		In reclutamento

Nella scheda del registro sono indicati altri 181 centri.

Documenti dello studio

In questa scheda del registro non sono collegati documenti.

Modifiche nel tempo

3 settembre 2026
Centro aggiunto
9 sites added (231 total)
222231
5 agosto 2026
Centro aggiunto
11 sites added (222 total)
211222

Registro: ClinicalTrials.gov · NCT########

https://xmedica.io/trials/ctgov/NCT06982521