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A PHASE 3, RANDOMIZED, OPEN-LABEL, MULTICENTER TRIAL OF ARV-471 (PF-07850327) VS FULVESTRANT IN PARTICIPANTS WITH ESTROGEN RECEPTOR-POSITIVE, HER2-NEGATIVE ADVANCED BREAST CANCER WHOSE DISEASE PROGRESSED AFTER PRIOR ENDOCRINE BASED TREATMENT FOR ADVANCED DISEASE (VERITAC-2)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT05654623-Aug 04, 2026
NCT ID
NCT05654623
Status
ACTIVE_NOT_RECRUITING
Phase
Phase 3
Sponsor
Pfizer
Executive brief
Investment-Ready Snapshot
ARV-471 (PF-07850327) is being evaluated against fulvestrant in patients with ER+/HER2- advanced breast cancer who have progressed after prior endocrine therapy. The trial aims to establish ARV-471 as a superior treatment option, potentially capturing market share from existing therapies like fulvestrant. Given the increasing prevalence of advanced breast cancer and the need for effective treatments post-endocrine therapy, successful outcomes could position ARV-471 favorably in a competitive landscape dominated by CDK4/6 inhibitors and other SERDs. Diligence should focus on market access strategies and potential partnerships, especially considering the collaboration with Arvinas Estrogen Receptor, Inc.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05654623
Indication
Advanced Breast Cancer
Modality
small molecule
Target
Estrogen Receptor (ER) degradation via PROTAC mechanism.
Intervention
ARV-471, Fulvestrant
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.