Study of PF-07220060 With Letrozole in Adults With HR-positive HER2-negative Breast Cancer Who Have Not Received Anticancer Treatment for Advanced/Metastatic Disease
- Summary
- The purpose of this study is to determine the safety and efficacy of PF-07220060 with letrozole compared to approved treatments (ie, palbociclib, ribociclib or abemaciclib with letrozole) in people with breast cancer: * HR-positive (breast cancer cells that need estrogen or progesterone to grow) * HER2-negative (cells that have a small amount or none of a protein called HER2 on their surface); * locally advanced (that has spread from where it started to nearby tissue or lymph nodes) or metastatic disease (the spread of cancer to other places in the body) * who have not received any prior systemic anti-cancer treatment for advanced/metastatic disease. Approximately half of the participants will receive PF-07220060 plus letrozole while the other half of participants will receive the investigator's choice of treatment plus letrozole. The study team will monitor how each participant is doing with the study treatment during regular visits at the study clinic.
- Acronym
- FourLight-3
- Short title
- Study of PF-07220060 With Letrozole in Adults With HR-positive HER2-negative Breast Cancer Who Have Not Received Anticancer Treatment for Advanced/Metastatic Disease
- Official title
- AN INTERVENTIONAL, OPEN-LABEL, RANDOMIZED, MULTICENTER PHASE 3 STUDY OF PF-07220060 PLUS LETROZOLE COMPARED TO CDK4/6 INHIBITOR PLUS LETROZOLE IN PARTICIPANTS OVER 18 YEARS OF AGE WITH HORMONE RECEPTOR (HR)-POSITIVE, HER2-NEGATIVE ADVANCED/METASTATIC BREAST CANCER WHO HAVE NOT RECEIVED ANY PRIOR SYSTEMIC ANTICANCER TREATMENT FOR ADVANCED/METASTATIC DISEASE (FOURLIGHT-3)
- Control arm
- Active comparator
- Registry reports results
- Listing at source
- Listed
- Recruitment status
- Active, not recruiting
- Phase
- Phase 3
- Study type
- Interventional
- Completion date
- 2037-12-29
- First posted
- 2025-01-07
- Registry last updated
- 2026-05-19
- Primary completion date
- 2029-01-02
- Start date
- 2025-01-06
- Actual participants
- 1,035
- Participants
- 1,035
- Participant count basis
- Actual
- Protocol amendments
- Number of sites
- Data monitoring committee
- Registry sponsor category
- Industry
- Lead sponsor
- Pfizer
- Source registry
- ClinicalTrials.gov
- Registry ID
- NCT06760637
- ClinicalTrials.gov ID
- NCT06760637
- Registry record
- Open registry record
- Allocation
- Randomised
- Model
- Parallel groups
- Purpose
- Treatment
- Masking
- No masking
Progression Free Survival (PFS) by BICR
Timeframe: From the date of randomization until disease progression or death due to any cause (up to approximately 4 years)
Time from the date of randomization to the date of the first documentation of objective progressive disease as determined by blinded independent central review (BICR) per RECIST v1.1, or death due to any cause, whichever occurs first
Overall Survival (OS)
Timeframe: From the date of randomization until death due to any cause (up to approximately 13 years).
Time from the date of randomization to the date of death due to any cause
Progression Free Survival (PFS) by Investigator
Timeframe: From the date of randomization until disease progression or death due to any cause (up to approximately 4 years)
Time from the date of randomization to the date of the first documentation of objective progressive disease as determined by investigator per RECIST v1.1, or death due to any cause, whichever occurs first
OR by BICR and by investigator
Timeframe: From randomization to progression or death whichever occurs first (up to approximately 4 years)
Time from randomization date (every 8 weeks during the first 48 weeks and then every 12 weeks) to the date of progression OR death whichever occurs first
Duration of Response (DoR) by BICR and by investigator
Timeframe: From the date of CR or PR until objective progressive disease, or death (up to approximately 4 years)
Time from the date of CR or PR to the first documentation of objective progressive disease, or death due to any cause, whichever occurs first
Incidence of treatment emergent treatment related adverse events (AE)
Timeframe: Duration of the study approximately up to 13 years.
Incidence and severity of AEs graded according to the NCI CTCAE v5.0
Incidence of treatment emergent treatment related serious adverse events
Timeframe: Duration of the study approximately up to 13 years.
Incidence and severity of AEs graded according to NCI CTCAE v5.0
Estimated mean change from baseline in EORTC QLQ C30
Timeframe: Baseline to end of treatment (up to approximately 4 years)
Estimated mean change from baseline in BPI-SF
Timeframe: Baseline to end of treatment (up to approximately 4 years)
Estimated mean change from baseline in EQ-5D-5L
Timeframe: Baseline to end of treatment (up to approximately 4 years)
Estimated mean change from baseline in EORTC Breast Cancer Module (BR42)
Timeframe: Baseline to end of treatment (up to approximately 4 years)
Mean change from baseline of ctDNA
Timeframe: Baseline to end of treatment (up to approximately 4 years)
- Sex
- All
- Age groups
- Adults, Older adults
- Minimum age
- 18 Years
- Healthy volunteers
- No
- Histological confirmation of breast cancer with evidence of locally advanced or metastatic disease, which is not amenable to surgical resection or radiation therapy with curative intent.
- Documented estrogen receptor (ER) and/or progesterone receptor (PR)-positive tumor
- Documented HER2-negative tumor
- Previously untreated with any systemic anticancer therapy for their locally advanced or metastatic disease.
- Measurable disease or non-measurable bone only disease as defined by RECIST version 1.1
- In visceral crisis at risk of immediately life-threatening complications in the short term.
- Current or past history of central nervous system metastases.
- Have received prior (neo)adjuvant endocrine therapy (ET) and had recurrence during or within 12 months after the last dose of ET.
- Have received prior (neo)adjuvant CDK4/6i and had recurrence during or within 12 months after the last dose of CDK4/6i.
- Inadequate renal function, hepatic dysfunction, or hematologic abnormalities.
- The Kirklin Clinic of UAB HospitalBirmingham, United States
- The University of Alabama at BirminghamBirmingham, United States
- University of Alabama at Birmingham HospitalBirmingham, United States
- Ironwood Cancer & Research CentersChandler, United States
- Ironwood Cancer & Research CentersGilbert, United States
- Ironwood Cancer & Research CentersGlendale, United States
- Ironwood Cancer & Research CentersGoodyear, United States
- Ironwood Cancer & Research CentersMesa, United States
- Ironwood Cancer & Research CentersMesa, United States
- Ironwood Cancer & Research CentersPhoenix, United States
- Ironwood Cancer & Research CentersScottsdale, United States
- CARTI Cancer Center Saline CountyBryant, United States
- CARTI Cancer Center ConwayConway, United States
- Highlands OncologyFayetteville, United States
- CARTI Cancer CenterLittle Rock, United States
- CARTI Cancer Center North Little Rock UrologyNorth Little Rock, United States
- CARTI Cancer Center North Little RockNorth Little Rock, United States
- CARTI Cancer Center Pine BluffPine Bluff, United States
- Highlands OncologyRogers, United States
- Highlands Oncology GroupSpringdale, United States
- Providence Medical FoundationAnaheim, United States
- Sutter Auburn Faith HospitalAuburn, United States
- Sutter Health Alta BatesBerkeley, United States
- Cedars-Sinai Cancer Beverly Hills (drug treatment and dispensing location)Beverly Hills, United States
- Cedars-Sinai Cancer Beverly HillsBeverly Hills, United States
And 438 more, listed on the interactive page.
- Related resource (pmiform.com)
Other registry identifiers
- 2024-512925-95-00
Related records
Drugs (5)
Lead sponsors (1)
Conditions (2)
- Breast cancer Primary condition
- Breast neoplasm