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.
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
- Type of treatment
- Pill or oral medicine, Surgery or procedure
- 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.
Show all 9Show fewer
- 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.
Show all 10Show fewer
- 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
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
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
Georgia4 sites
Clinical Trial Site
Batumi, 6000
Clinical Trial Site
Tbilisi, 0112
Clinical Trial Site
Tbilisi, 0144
Clinical Trial Site
Tbilisi, 0159
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 group | Role | What they receive |
|---|---|---|
| Arm A: ARV-471 (Experimental) | Experimental | Participants 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: Anastrozole | Active comparator | Participants 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.
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)
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)
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
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
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
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
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
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.
- First posted22 Sep 2022
- Study start15 Feb 2023
- Primary completion13 Jul 2024
- Study completion25 Jul 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Breast CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Arvinas Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Pfizer
- Responsible party
- Sponsor
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
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Aug 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT05549505
- Acronym / sponsor ID
- ARV-471-BC-201
- Conditions
- Breast Cancer
- Keywords
- Early breast cancer, Localized breast cancer, Untreated breast cancer, Pre-operative breast cancer, Treatment-naïve breast cancer, Neoadjuvant, Estrogen receptor, Estrogen receptor positive
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 152 participants (actual)
- Lead sponsor
- Arvinas Inc.Industry (pharma, biotech, devices)
- Collaborators
- Pfizer
- Study start
- 15 Feb 2023 (actual)
- Primary completion
- 13 Jul 2024 (actual)
- Study completion
- 25 Jul 2024 (actual)
- First posted
- 22 Sep 2022 (actual)
- Results
- Posted 29 Aug 2025
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Arm A: ARV-471 (Experimental) | Experimental | Drug: ARV-471, Procedure: Surgical resection of breast tumorParticipants 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). |
| Arm B: Anastrozole | Active comparator | Drug: Anastrozole, Procedure: Surgical resection of breast tumorParticipants received 1 mg Anastrozole tablet orally once daily for approximately 5.5 months prior to undergoing surgical resection (no later than C6D18 + 14 days). |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (9 listed)
- Post-menopausal females ≥ 18 years.
- Histologically or cytologically confirmed ER+ and HER2- breast cancer (per local assessment). ER and HER2 status must be documented:
- Clinical T1c-T4c, N0-N2, M0 breast cancer amenable to definitive surgical resection, without bilateral breast ductal carcinoma in situ or invasive breast cancer.
- The primary tumor must be at least 1.5 cm by imaging.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
Key exclusion criteria (10 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ARV-471Also: Vepdegestrant, PF-07850327100 mg tablet | Drug | Arm A: ARV-471 (Experimental) |
| AnastrozoleAlso: Arimidex1 mg tablet | Drug | Arm B: Anastrozole |
| Surgical resection of breast tumorSurgical resection approximately 5.5 months after starting treatment (C6D18 ± 14 days) | Procedure or surgery | Arm A: ARV-471 (Experimental), Arm B: Anastrozole |
Primary outcome
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
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).
7 secondary outcomes
Number of Participants With Treatment Emergent Adverse Events (TEAEs), Serious TEAEs and TEAEs Leading to Study Drug Discontinuation
Time frame: From signing of consent to minimum of 30 days after last administration of study drug (up to approximately 6.5 months)
Pathologic Stage at the Time of Surgical Resection
Time frame: At Cycle 6 Day 18 (approximately 5.5 months), each cycle is 28 days
Pathological Complete Response(pCR) Rate at the Time of Surgical Resection
Time frame: At Cycle 6 Day 18 (approximately 5.5 months), each cycle is 28 days
Number of Participants With Modified Preoperative Endocrine Prognostic Index (mPEPI) Score of 0 at the Time of Surgical Resection
Time frame: At Cycle 6 Day 18 (approximately 5.5 months), each cycle is 28 days
Breast Conserving Surgery (BCS) Rate
Time frame: At Cycle 6 (from Day 141 to Day 168), each cycle is 28 days
Radiographic Response Per Modified Response Evaluation Criteria in Solid Tumors (mRECIST) in Primary Tumor During Cycle 6
Time frame: At Cycle 6 (from Day 141 to Day 168), each cycle is 28 days
Percentage Change From Baseline at Cycle 6 Day 1 in Caliper Measurement of the Primary Tumor
Time frame: Baseline (Day 1) and Cycle 6 Day 1 (At Day 141), each cycle is 28 days
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Aug 2025.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
49 sites in 4 countries: see every site and its status.
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.