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Breast CancerPhase 2NCT05549505

A Trial Using ARV-471 or Anastrozole in Post-Menopausal Women With Breast Cancer Prior to Surgery

A Phase 2 study testing ARV-471, Anastrozole and Surgical resection of breast tumor in people with Breast Cancer, run by Arvinas Inc. at 49 sites in 4 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This trial is a Phase 2 neoadjuvant study evaluating ARV-471 or anastrozole in post-menopausal women with estrogen receptor positive/ human epidermal growth factor receptor 2 (ER+/HER2)- localized breast cancer. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Breast Cancer
What is being tested?
ARV-471, Anastrozole and Surgical resection of breast tumor
Could I receive a placebo?
No, everyone receives an active treatment
How many people
152 participants
Where
49 sitesin 4 countries
Study dates
15 Feb 2023to 25 Jul 2024
Phase
Phase 2
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Post-menopausal females ≥ 18 years.
  • Histologically or cytologically confirmed ER+ and HER2- breast cancer (per local assessment). ER and HER2 status must be documented:
  • ER+ disease, with ER staining of ≥ 10% of tumor cell nuclei by immunohistochemistry (IHC) per American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP) guidelines.
  • HER2- disease by either IHC or in situ hybridization per ASCO/CAP guidelines.
  • Ki-67 score ≥ 5%, analyzed locally.
  • Clinical T1c-T4c, N0-N2, M0 breast cancer amenable to definitive surgical resection, without bilateral breast ductal carcinoma in situ or invasive breast cancer.
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  • The primary tumor must be at least 1.5 cm by imaging.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • Willingness to undergo a screening biopsy, an on-treatment biopsy and surgical resection.

Who cannot join

  • Any other active malignancy within 3 years prior to enrollment, except for adequately treated basal cell or squamous cell skin cancer, or cervical carcinoma in situ.
  • Any of the following in the previous 6 months: Myocardial infarction; Severe unstable angina; Coronary/peripheral artery bypass graft; Symptomatic congestive heart failure (New York Heart Association class III or IV); Cerebrovascular accident; Transient ischemic attack; Symptomatic pulmonary embolism or other clinically significant episode of thromboembolism.
  • Any of the following in the previous 6 months: Congenital long QT syndrome; Torsade de Pointes; Sustained ventricular tachyarrhythmia and ventricular fibrillation; Left anterior hemiblock (bifascicular block); Ongoing cardiac dysrhythmias of NCI CTCAE ≥ Grade 2; Atrial fibrillation of any grade (≥ Grade 2 in the case of asymptomatic lone atrial fibrillation).
  • corrected QT (Fridericia method) (QTcF) > 470 msec.
  • Active, uncontrolled bacterial, fungal or viral infection, including (but not limited to) hepatitis B virus (HBV), hepatitis C virus (HCV), and known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related illness.
  • Active inflammatory gastrointestinal disease, chronic diarrhea, known uncontrolled diverticular disease, or previous gastric resection or lap band surgery.
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  • Cirrhosis meeting criteria for Child Pugh B and C.
  • Prior treatment for breast cancer including systemic therapy (eg, chemotherapy, hormonal therapy), radiation, surgery, or any investigational agents.
  • Any live vaccines within 14 days of planned start of first dose of study drug.
  • Major surgery (as defined by the Investigator) within four weeks of first dose of study drug.

Trial locations and contacts

49 sites in 4 countries.

49 sites in 4 countries

Spain20 sites
  • Clinical Trial Site

    A Coruña, Galicia, 15006

  • Clinical Trial Site

    Alicante, 03010

  • Clinical Trial Site

    Barcelona, 08025

  • Clinical Trial Site

    Barcelona, 08036

  • Clinical Trial Site

    Barcelona, 08916

  • Clinical Trial Site

    Castelló, 12002

  • Clinical Trial Site

    Córdoba, 14004

  • Clinical Trial Site

    Granada, 18005

  • Clinical Trial Site

    Granada, 18014

  • Clinical Trial Site

    Lleida, 25198

  • Clinical Trial Site

    Madrid, 28034

  • Clinical Trial Site

    Madrid, 28040

  • Clinical Trial Site

    Madrid, 28922

  • Clinical Trial Site

    Manresa, 08243

  • Clinical Trial Site

    San Cristóbal de La Laguna, Santa Cruz De Tenerife, 38320

  • Clinical Trial Site

    Seville, 41009

  • Clinical Trial Site

    Seville, 41013

  • Clinical Trial Site

    Valencia, 46009

  • Clinical Trial Site

    Valencia, 46010

  • Clinical Trial Site

    Zaragoza, 50009

Other trials in Spain

United States13 sites
  • Clinical Trial Site

    Fort Lauderdale, Florida, 33308

  • Clinical Trial Site

    Fort Myers, Florida, 33901

  • Clinical Trial Site

    Iowa City, Iowa, 52242

  • Clinical Trial Site

    Los Angeles, California, 90095

  • Clinical Trial Site

    Nashville, Tennessee, 37203

  • Clinical Trial Site

    Orlando, Florida, 32806

  • Clinical Trial Site

    Springdale, Arkansas, 72762

  • Clinical Trial Site

    Springfield, Massachusetts, 01199

  • Clinical Trial Site

    St Louis, Missouri, 63110

  • Clinical Trial Site

    Tacoma, Washington, 98405

  • Clinical Trial Site

    Torrance, California, 90505

  • Clinical Trial Site

    Van Nuys, California, 91405

  • Clinical Trial Site

    West Palm Beach, Florida, 33401

Other trials in United States

Germany12 sites
  • Clinical Trial Site

    Augsburg, 86156

  • Clinical Trial Site

    Berlin, 13125

  • Clinical Trial Site

    Bonn, 53111

  • Clinical Trial Site

    Bottrop, 46236

  • Clinical Trial Site

    Chemnitz, 09116

  • Clinical Trial Site

    Dresden, 01307

  • Clinical Trial Site

    Erlangen, 91054

  • Clinical Trial Site

    Essen, 451136

  • Clinical Trial Site

    Essen, 45147

  • Clinical Trial Site

    Esslingen am Neckar, 73730

  • Clinical Trial Site

    Mannheim, 68167

  • Clinical Trial Site

    Paderborn, 33098

Other trials in Germany

Georgia4 sites
  • Clinical Trial Site

    Batumi, 6000

  • Clinical Trial Site

    Tbilisi, 0112

  • Clinical Trial Site

    Tbilisi, 0144

  • Clinical Trial Site

    Tbilisi, 0159

Other trials in Georgia

About this study

Official title: An Open-label, Randomized, Non-comparative Phase 2 Study of ARV-471 or Anastrozole in Post-menopausal Women With ER+/HER2- Breast Cancer in the Neoadjuvant Setting

This trial is a Phase 2 neoadjuvant study evaluating ARV-471 or anastrozole in post-menopausal women with estrogen receptor positive/ human epidermal growth factor receptor 2 (ER+/HER2)- localized breast cancer.

Read the detailed description

This is a Phase 2, open-label, randomized, non-comparative proof of concept study of ARV-471 or anastrozole in participants with ER+/HER2- breast cancer amenable to definitive surgical resection. The main goal of this study is to evaluate the biological activity of ARV-471 and anastrozole, respectively.

Conditions
Breast Cancer
Being tested
ARV-471, Anastrozole, Surgical resection of breast tumor
Keywords
Early breast cancer, Localized breast cancer, Untreated breast cancer, Pre-operative breast cancer, Treatment-naïve breast cancer, Neoadjuvant, Estrogen receptor, Estrogen receptor positive, ER+, Hormone positive, Hormone receptor positive, HR+, human epidermal growth factor receptor 2 negative, HER2-, ARV-471, Anastrozole, Arimidex, Aromatase inhibitor, Vepdegestrant, PF-07850327
Medical subject headings
Breast Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ARV-471Drug

    Also called Vepdegestrant, PF-07850327

    100 mg tablet

  • AnastrozoleDrug

    Also called Arimidex

    1 mg tablet

  • Surgical resection of breast tumorProcedure or surgery

    Surgical resection approximately 5.5 months after starting treatment (C6D18 ± 14 days)

Study groups in NCT05549505
Study groupRoleWhat they receive
Arm A: ARV-471 (Experimental)ExperimentalParticipants received 200 mg ARV-471 (2*100 mg tablets) once daily for approximately 5.5 months prior to undergoing surgical resection (no later than Cycle 6 Day 18 [C6D18] + 14 days).
Receives: Drug: ARV-471; Procedure: Surgical resection of breast tumor
Arm B: AnastrozoleActive comparatorParticipants received 1 mg Anastrozole tablet orally once daily for approximately 5.5 months prior to undergoing surgical resection (no later than C6D18 + 14 days).
Receives: Drug: Anastrozole; Procedure: Surgical resection of breast tumor

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percent Reduction in Ki-67 Expression From Baseline to Day 15 in Tumor Biopsies

    Tumor biopsy Ki-67 expression (% of tumor cells that are positive for Ki-67) at baseline and Cycle 1 Day 15 (C1D15) was collected. Ki-67 expression was assessed by immunohistochemical staining in a central laboratory. The log-transformed Ki-67 after approximately 2 weeks of treatment as a percentage of the baseline value, ie, the ratio between the Ki-67 measurements obtained from C1D15 visit and baseline was modelled using a generalized linear model (GLM) with both stratification factors (ie, baseline Ki-67 score and the tumor size) and treatment as co-variates. The treatment effects were back transformed into geometric means and their Confidence Intervals. The percent change, in other words, relative reduction, of Ki-67 after 2 weeks of treatment is reported as the complement of the ratio between the Ki-67 measurement from C1D15 and baseline, that is 100% × (1 - geometric mean ratio between Ki-67 at C1D15 and Ki-67 at baseline).

    Measured: Baseline (during screening, prior to Day 1) and Day 15

Secondary outcomes (7)
  1. Number of Participants With Treatment Emergent Adverse Events (TEAEs), Serious TEAEs and TEAEs Leading to Study Drug Discontinuation

    An AE is any untoward medical occurrence in a participant or clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of study intervention. A serious adverse event (SAE) was an AE that resulted in any of the following outcomes: death; life threatening; persistent/significant disability/incapacity; initial or prolonged inpatient hospitalization; congenital anomaly/birth defect or was otherwise considered medically important. A TEAE is an AE that emerges or worsens on/after the first dose of ARV-471/Anastrozole to 30 days after the last administration of the study intervention (ie, study drug treatment or surgical resection, whichever occurs last).

    Measured: From signing of consent to minimum of 30 days after last administration of study drug (up to approximately 6.5 months)

  2. Pathologic Stage at the Time of Surgical Resection

    Local pathological assessment of the tissue from surgical resection (performed after approximately 5.5 months of treatment), at minimum, included pathologic stage (ypT and ypN stage) as described in the Laboratory Manual. Participants were analysed based on the current American Joint Committee on Cancer (AJCC) staging system as follows:

    • Pathologic Tumor - post-neoadjuvant therapy pathologic tumor categorization (ypT): (ypTx, ypT0, ypTis, ypT1mi, ypT1a, ypT1b, ypT1c, ypT2, ypT3, ypT4a, ypT4b, ypT4c).
    • Pathological Lymph Nodes - post-neoadjuvant therapy pathologic node categorization (ypN): (ypNX, ypN0, ypN0(i+), ypN0(mol+), ypN1, ypN1mi, ypN1a, ypN1b, ypN1c, ypN2, ypN2a, ypN2b, ypN3, ypN3a, ypN3b, ypN3c).
    • ypT0 / ypN0 indicates no evidence of disease and the progressive grades indicate increasing size of tumor and increasing area of lymph node involvement respectively and ypTx/ypNX indicates non-measurable disease.

    Measured: At Cycle 6 Day 18 (approximately 5.5 months), each cycle is 28 days

  3. Pathological Complete Response(pCR) Rate at the Time of Surgical Resection

    pCR is defined as no invasive cancer in the breast and sampled axillary lymph nodes following completion of neoadjuvant systemic therapy (ie, Pathologic Tumor - ypT = ypT0 or ypTis, and Pathologic Lymph Nodes - ypN = ypN0 in the current American Joint Committee on Cancer (AJCC) staging system). pCR rate is the percentage of participants with pCR.

    Measured: At Cycle 6 Day 18 (approximately 5.5 months), each cycle is 28 days

  4. Number of Participants With Modified Preoperative Endocrine Prognostic Index (mPEPI) Score of 0 at the Time of Surgical Resection

    Modified Pre-operative Endocrine Prognostic Index (mPEPI) score is an investigational prognostic tool used to predict the risk of breast cancer recurrence. It will be derived from factors assigned a numerical score following Neoadjuvant endocrine treatment (NET). The factors include pathologic tumor size, and lymph node status and Ki67 expression in the surgical specimen. Total mPEPI score (mPEPI_T) per participant is the sum of mPEPI score of each factor.

    mPEPI score of 0 indicates Pathological tumor size T1-T2, no lymph nodes and Ki67 level of 0%-2.7%, 1 indicates: Ki67 level >2.7%-7.3%, 2 indicates Ki67 level >19.7%-53.1% and 3 indicates: tumor sizeT3-T4, presence of lymph nodes and Ki67 level >53.1%.

    Measured: At Cycle 6 Day 18 (approximately 5.5 months), each cycle is 28 days

  5. Breast Conserving Surgery (BCS) Rate

    Breast conserving surgery (BCS) Rate is the percentage of participants received breast conserving surgery.

    Measured: At Cycle 6 (from Day 141 to Day 168), each cycle is 28 days

  6. Radiographic Response Per Modified Response Evaluation Criteria in Solid Tumors (mRECIST) in Primary Tumor During Cycle 6

    The number of participants with Complete Response (CR), Partial Response (PR), Stable Disease (SD), Progressive Disease (PD), Not Evaluable (NE) per mRECIST calculated. CR = disappearance of all target lesions, PR is >=30% decrease in sum of diameters of target lesions, progressive disease (PD) is >=20% increase in sum of diameters of target lesions, stable disease (SD) is <30% decrease or <20% increase in sum of diameters of target lesions.

    Measured: At Cycle 6 (from Day 141 to Day 168), each cycle is 28 days

  7. Percentage Change From Baseline at Cycle 6 Day 1 in Caliper Measurement of the Primary Tumor

    The percentage change from the baseline of the primary breast tumor size in physical exam calculated in caliper measurement. Caliper-based response is the maximum percentage decrease or minimum percentage increase if there is no decrease per participant.

    Measured: Baseline (Day 1) and Cycle 6 Day 1 (At Day 141), each cycle is 28 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Sep 2022
  2. Study start15 Feb 2023
  3. Primary completion13 Jul 2024
  4. Study completion25 Jul 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
152 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05549505
Sponsor's protocol ID
ARV-471-BC-201
Other IDs
C4891025
Status last verified
Aug 2025
First submitted
7 Sep 2022
Last updated
29 Aug 2025
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing ARV-471, Anastrozole and Surgical resection of breast tumor in people with Breast Cancer, run by Arvinas Inc. at 49 sites in 4 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 49 sites in Spain, United States, Germany, Georgia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 29 Aug 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percent Reduction in Ki-67 Expression From Baseline to Day 15 in Tumor Biopsies (time frame: Baseline (during screening, prior to Day 1) and Day 15). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Aug 2025.

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