Phase III Study to Assess AZD9833+ CDK4/6 Inhibitor in HR+/HER2-MBC With Detectable ESR1m Before Progression (SERENA-6)

NCT ID: NCT04964934

Last Updated: 2025-12-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

PHASE3

Total Enrollment

315 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-30

Study Completion Date

2027-11-26

Brief Summary

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The study is intended to show superiority of AZD9833 in combination with CDK4/6 inhibitor (palbociclib, abemaciclib or ribociclib) versus aromatase inhibitors (anastrozole or letrozole) in combination with CDK4/6 inhibitor in patients with hormone receptor-positive (HR-positive), human epidermal growth factor receptor 2-negative (HER2-negative) metastatic breast cancer with detectable ESR1 mutation.

Detailed Description

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Breast cancer is the most common type of cancer among women. In people with breast cancer, the body is not able to control the growth of some cells. These extra cells can form tumors in the breast. When tumor cells move to different parts of the body this is called advanced cancer. Researchers are looking for better ways to treat advanced breast cancer.

This trial will look at six drugs: palbociclib, abemaciclib, ribociclib, letrozole, anastrozole, and AZD9833. AZD9833 is the trial drug, and is the only drug not yet approved for use. Palbociclib, abemaciclib and ribociclib work in the same way and are a type of cancer drug called a CDK4/6 inhibitor. Letrozole and anastrozole work in the same way and are both a type of cancer drug called an aromatase inhibitor (AI). CDK4/6 inhibitors and AIs work together to block the tumor's ability to grow. These drugs have been approved for combined use in people with advanced breast cancer that is HR-positive and HER2-negative. But if people get mutations in the ESR1 gene, it can make the AI and CDK4/6 inhibitor treatment work less well.

The trial drug, AZD9833, is designed to work with a CDK4/6 inhibitor in the same way that an AI does. Researchers think that AZD9833 might work better with a CDK4/6 inhibitor than an AI does in people who get mutations in their ESR1 gene.

Participants in this trial will have already been receiving one of the following combinations of a CDK4/6 inhibitor and an AI:

* palbociclib + anastrozole
* palbociclib + letrozole
* abemaciclib + anastrozole
* abemaciclib + letrozole
* ribociclib + anastrozole
* ribociclib + letrozole

During the trial, participants will remain on the same CDK4/6 inhibitor that they were taking before the trial.

In this trial, the researchers want to find out how well switching a participant with an ESR1 gene mutation from an AI (letrozole or anastrozole) to AZD9833 works in the treatment of advanced breast cancer that is HR-positive and HER2-negative.

The researchers will look at which trial treatment helps the participants live longer with the cancer before it gets worse.

The researchers also want to know more about how safe AZD9833 is.

The trial participants will be split into 2 groups:

* Participants in Group A will receive AZD9833, a CDK4/6 inhibitor, and a placebo
* Participants in Group B will receive an AI, a CDK4/6 inhibitor, and a placebo

A placebo looks like a treatment but does not have any medicine in it.

A computer program will be used to randomly choose the treatments each participant gets. This helps make sure the groups are chosen fairly. Researchers do this so that comparing the results of each treatment will be as accurate as possible.

The participants will take their trial treatments over 28-day cycles, with a placebo and either AZD9833 or an AI taken once daily by mouth for all 28 days. If the participant is taking abemaciclib, they will take it twice daily by mouth for all 28 days. If the participant is taking palbociclib or ribociclib, they will take it once daily by mouth for 21 days and then stop taking it for the final 7 days of the cycle. The participant will then repeat the 28-day cycle receiving the trial treatment in the same way for as long as they are in the trial.

Participants will visit their trial site regularly throughout the trial. At these visits, the trial doctors will check the health of the participants. They will also take blood samples and do scans of the participants' tumors.

Participants will take their trial treatment until their cancer gets worse or they decide to leave the trial.

Conditions

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ER-Positive HER2-Negative Breast Cancer

Keywords

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Neoplasms Metastatic Breast Neoplasms Neoplasms by Site Breast Diseases Physiological Effects of Drugs Randomised Multicentre Double-Blind Phase III AZD9833 Next Generation Oral SERD Anastrozole Letrozole Palbociclib Abemaciclib Ribociclib Antagonists Antineoplastic Agents Estrogen Receptor Antagonists Hormone Antagonists camizestrant ESR1m Switch Treatment Endocrine Therapy Endocrine Resistance

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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AZD9833 + palbociclib, abemaciclib or ribociclib

The patients will receive AZD9833 (75 mg, PO, once daily) + palbociclib (PO, once daily, 125, 100 or 75 mg for 21 consecutive days followed by 7 days off treatment), abemaciclib (PO, twice daily, 150,100 or 50 mg) or ribociclib (To Be Determined, PO, once daily for 21 consecutive days followed by 7 days off treatment) + anastrozole placebo (PO, once daily) or letrozole placebo (PO, once daily)

Group Type EXPERIMENTAL

AZD9833

Intervention Type DRUG

Dosage formulation: AZD9833 tablets will be administered orally

Anastrozole placebo

Intervention Type DRUG

Dosage formulation: anastrozole placebo tablets will be administrated orally.

Letrozole placebo

Intervention Type DRUG

Dosage formulation: letrozole placebo tablets will be administered orally.

Palbociclib

Intervention Type DRUG

Dosage formulation: palbociclib tablets/capsules will be administered orally

Abemaciclib

Intervention Type DRUG

Dosage formulation: abemaciclib tablets will be administered orally

Luteinizing hormone-releasing hormone (LHRH) agonist

Intervention Type DRUG

Men (when medically applicable) and pre- or peri-menopausal women are required to receive a monthly LHRH agonist.

Ribociclib

Intervention Type DRUG

Dosage formulation: ribociclib tablets will be administered orally

Anastrozole or letrozole + palbociclib, abemaciclib or ribociclib

The patients will recieve anastrozole (1 mg, PO, once daily) or letrozole (2.5 mg, PO, once daily) + palbociclib (PO, once daily, 125, 100 or 75 mg for 21 consecutive days followed by 7 days off treatment), abemaciclib (PO, twice daily, 150, 100 or 50 mg) or ribociclib (To Be Determined, PO, once daily for 21 consecutive days followed by 7 days off treatment) + AZD9833 placebo (PO, once daily)

Group Type ACTIVE_COMPARATOR

AZD9833 Placebo

Intervention Type DRUG

Dosage formulation: AZD9833 placebo tablets will be administrated orally.

Anastrozole

Intervention Type DRUG

Dosage formulation: anastrozole tablets will be administered orally.

Letrozole

Intervention Type DRUG

Dosage formulation: letrozole tablets will be administered orally.

Palbociclib

Intervention Type DRUG

Dosage formulation: palbociclib tablets/capsules will be administered orally

Abemaciclib

Intervention Type DRUG

Dosage formulation: abemaciclib tablets will be administered orally

Luteinizing hormone-releasing hormone (LHRH) agonist

Intervention Type DRUG

Men (when medically applicable) and pre- or peri-menopausal women are required to receive a monthly LHRH agonist.

Ribociclib

Intervention Type DRUG

Dosage formulation: ribociclib tablets will be administered orally

Interventions

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AZD9833

Dosage formulation: AZD9833 tablets will be administered orally

Intervention Type DRUG

AZD9833 Placebo

Dosage formulation: AZD9833 placebo tablets will be administrated orally.

Intervention Type DRUG

Anastrozole

Dosage formulation: anastrozole tablets will be administered orally.

Intervention Type DRUG

Anastrozole placebo

Dosage formulation: anastrozole placebo tablets will be administrated orally.

Intervention Type DRUG

Letrozole

Dosage formulation: letrozole tablets will be administered orally.

Intervention Type DRUG

Letrozole placebo

Dosage formulation: letrozole placebo tablets will be administered orally.

Intervention Type DRUG

Palbociclib

Dosage formulation: palbociclib tablets/capsules will be administered orally

Intervention Type DRUG

Abemaciclib

Dosage formulation: abemaciclib tablets will be administered orally

Intervention Type DRUG

Luteinizing hormone-releasing hormone (LHRH) agonist

Men (when medically applicable) and pre- or peri-menopausal women are required to receive a monthly LHRH agonist.

Intervention Type DRUG

Ribociclib

Dosage formulation: ribociclib tablets will be administered orally

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

INFORMATION FOR TRIAL PARTICIPANTS - Participants can join the trial if they:

* Have advanced breast cancer that is not able to be treated with surgery or radiation;
* Have an ESR1 mutation in their cancer;
* Have breast cancer that is HR-positive and HER2-negative;
* Are currently being treated with a CDK4/6 inhibitor and an AI and have been taking these drugs for at least 6 months;
* Have not had their cancer get worse after taking an AI and CDK4/6 inhibitor;
* Are able to do their daily activities;
* Are at least 18.


* Proven diagnosis of adenocarcinoma of the breast with evidence of locoregionally recurrent or metastatic disease not amenable to resection or radiation therapy with curative intent;
* Documentation of histologically confirmed diagnosis of estrogen receptor positive (ER+) /HER2- breast cancer based on local laboratory results;
* Currently on AI (letrozole or anastrozole) + CDK4/6 inhibitor (palbociclib, abemaciclib or ribociclib) ± LHRH as the initial endocrine based treatment for advanced disease;
* Eastern Cooperative Oncology Group performance status of 0 or 1;
* ESR1m detected by central testing of ctDNA with Guardant360® CDx;
* Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures;
* Adequate organ and marrow function.

Exclusion Criteria

INFORMATION FOR TRIAL PARTICIPANTS - Participants cannot join the trial if they:

* Had certain types of tumors in the past that may come back;
* Are currently taking any other treatments for their cancer or other conditions including hormone replacements, medications, or supplements that could interfere with the trial treatment;
* Have or have had any major health problem, infection, or recent surgery that could make it difficult or dangerous to participate in this trial.


* Advanced, symptomatic, visceral spread, that are at risk of life-threatening complications in the short term;
* Known active uncontrolled or symptomatic CNS metastases, carcinomatous meningitis, or leptomeningeal disease;
* Any evidence of severe or uncontrolled systemic diseases which, in the investigator's opinion, makes it undesirable for the participant to participate in the study or that would jeopardize compliance with the protocol;
* Patient with known or family history of severe heart disease;
* Previous treatment with AZD9833, investigational SERDs or fulvestrant;
* Currently pregnant (confirmed with positive pregnancy test) or breastfeeding;
* Persistent non-haematological toxicities (CTCAE Grade \> 2) caused by CDK4/6 inhibitor and/or AI treatment.
Minimum Eligible Age

18 Years

Maximum Eligible Age

130 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Phoenix, Arizona, United States

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Hot Springs, Arkansas, United States

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Little Rock, Arkansas, United States

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Long Beach, California, United States

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San Diego, California, United States

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Santa Rosa, California, United States

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Grand Junction, Colorado, United States

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Lone Tree, Colorado, United States

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Fort Myers, Florida, United States

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Jacksonville, Florida, United States

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Jacksonville, Florida, United States

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St. Petersburg, Florida, United States

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Atlanta, Georgia, United States

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Atlanta, Georgia, United States

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Atlanta, Georgia, United States

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Park Ridge, Illinois, United States

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Fort Wayne, Indiana, United States

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Indianapolis, Indiana, United States

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Baltimore, Maryland, United States

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Boston, Massachusetts, United States

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Fairhaven, Massachusetts, United States

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Foxborough, Massachusetts, United States

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Milford, Massachusetts, United States

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South Weymouth, Massachusetts, United States

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Detroit, Michigan, United States

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Grand Rapids, Michigan, United States

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Rochester, Minnesota, United States

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Oxford, Mississippi, United States

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Kansas City, Missouri, United States

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St Louis, Missouri, United States

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Billings, Montana, United States

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Omaha, Nebraska, United States

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Camden, New Jersey, United States

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Ridgewood, New Jersey, United States

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Brooklyn, New York, United States

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East Syracuse, New York, United States

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New Hyde Park, New York, United States

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New York, New York, United States

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New York, New York, United States

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Shirley, New York, United States

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Goldsboro, North Carolina, United States

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Canton, Ohio, United States

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Cincinnati, Ohio, United States

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Columbus, Ohio, United States

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Portland, Oregon, United States

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Philadelphia, Pennsylvania, United States

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Pittsburgh, Pennsylvania, United States

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York, Pennsylvania, United States

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Greenville, South Carolina, United States

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West Columbia, South Carolina, United States

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Knoxville, Tennessee, United States

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Memphis, Tennessee, United States

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Nashville, Tennessee, United States

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Bedford, Texas, United States

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Houston, Texas, United States

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Irving, Texas, United States

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Longview, Texas, United States

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San Antonio, Texas, United States

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Salt Lake City, Utah, United States

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Midlothian, Virginia, United States

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Norfolk, Virginia, United States

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Tacoma, Washington, United States

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Waukesha, Wisconsin, United States

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Birtinya, , Australia

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Darlinghurst, , Australia

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Graz, , Austria

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Innsbruck, , Austria

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Salzburg, , Austria

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Vienna, , Austria

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Leuven, , Belgium

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Liège, , Belgium

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Namur, , Belgium

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Haskovo, , Bulgaria

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Panagyurishte, , Bulgaria

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Pleven, , Bulgaria

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Plovdiv, , Bulgaria

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Sofia, , Bulgaria

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Sofia, , Bulgaria

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Sofia, , Bulgaria

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Sofia, , Bulgaria

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Sofia, , Bulgaria

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Calgary, Alberta, Canada

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Vancouver, British Columbia, Canada

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Ottawa, Ontario, Canada

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Lévis, Quebec, Canada

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Montreal, Quebec, Canada

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Montreal, Quebec, Canada

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Montreal, Quebec, Canada

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Québec, Quebec, Canada

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Avignon, , France

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Brest, , France

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Clermont-Ferrand, , France

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Dijon, , France

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Limoges, , France

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Lorient, , France

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Lyon, , France

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Marseille, , France

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Metz-Tessy, , France

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Nîmes, , France

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Paris, , France

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Rouen, , France

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Saint-Cloud, , France

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Saint-Herblain, , France

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Toulouse, , France

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Tours, , France

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Vandœuvre-lès-Nancy, , France

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Vantoux, , France

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Villejuif, , France

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Ansbach, , Germany

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Aschaffenburg, , Germany

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Augsburg, , Germany

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Bonn, , Germany

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Chemnitz, , Germany

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Dresden, , Germany

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Erlangen, , Germany

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Essen, , Germany

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Freiburg im Breisgau, , Germany

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Immenstadt im Allgäu, , Germany

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Koblenz, , Germany

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Leipzig, , Germany

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Mannheim, , Germany

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München, , Germany

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Paderborn, , Germany

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Ratingen, , Germany

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Ravensburg, , Germany

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Regensburg, , Germany

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Stade, , Germany

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Tübingen, , Germany

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Ulm, , Germany

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Budapest, , Hungary

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Budapest, , Hungary

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Miskolc, , Hungary

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Szekszárd, , Hungary

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Szolnok, , Hungary

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Zalaegerszeg, , Hungary

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Beersheba, , Israel

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Haifa, , Israel

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Jerusalem, , Israel

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Petah Tikva, , Israel

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Ramat Gan, , Israel

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Bergamo, , Italy

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Bologna, , Italy

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Florence, , Italy

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Meldola, , Italy

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Milan, , Italy

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Milan, , Italy

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Misterbianco, , Italy

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Napoli, , Italy

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Padua, , Italy

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Roma, , Italy

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Rozzano, , Italy

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Chiba, , Japan

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Chūōku, , Japan

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Hidaka-shi, , Japan

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Hirakata-shi, , Japan

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Kitaadachi-gun, , Japan

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Kōtoku, , Japan

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Kumamoto, , Japan

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Matsuyama, , Japan

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Nagoya, , Japan

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Nagoya, , Japan

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Niigata, , Japan

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Osaka, , Japan

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Osaka, , Japan

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Ota-shi, , Japan

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Sapporo, , Japan

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Shinagawa-ku, , Japan

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Shinjuku-ku, , Japan

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Takasaki-shi, , Japan

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Takatsuki-shi, , Japan

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Tsukuba, , Japan

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Yokohama, , Japan

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Drammen, , Norway

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Oslo, , Norway

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Bydgoszcz, , Poland

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Gdynia, , Poland

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Koszalin, , Poland

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Lodz, , Poland

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Poznan, , Poland

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Rzeszów, , Poland

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Tomaszów Mazowiecki, , Poland

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Warsaw, , Poland

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Guimarães, , Portugal

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Lisbon, , Portugal

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Lisbon, , Portugal

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Lisbon, , Portugal

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Lisbon, , Portugal

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Loures, , Portugal

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Porto, , Portugal

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Porto, , Portugal

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Porto, , Portugal

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Vila Nova de Gaia, , Portugal

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Moscow, , Russia

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Moscow, , Russia

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Moscow, , Russia

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Nizhny Novgorod, , Russia

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Podolsk, , Russia

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Saint Petersburg, , Russia

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Saint Petersburg, , Russia

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Banská Bystrica, , Slovakia

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Bratislava, , Slovakia

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Košice, , Slovakia

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Michalovce, , Slovakia

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Partizánske, , Slovakia

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Cheonan-si, , South Korea

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Daegu, , South Korea

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Goyang-si, , South Korea

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Seongnam-si, , South Korea

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Seongnam-si, , South Korea

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Seoul, , South Korea

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Seoul, , South Korea

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Seoul, , South Korea

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Seoul, , South Korea

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Seoul, , South Korea

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Seoul, , South Korea

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Seoul, , South Korea

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A Coruña, , Spain

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Badalona, , Spain

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Barcelona, , Spain

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L'Hospitalet de Llobregat, , Spain

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Madrid, , Spain

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Madrid, , Spain

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Málaga, , Spain

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Murcia, , Spain

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Sant Joan Despí, , Spain

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Seville, , Spain

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Valencia, , Spain

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Bern, , Switzerland

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Chur, , Switzerland

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Winterthur, , Switzerland

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Kaohsiung City, , Taiwan

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Taichung, , Taiwan

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Tainan, , Taiwan

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Tainan, , Taiwan

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Taipei, , Taiwan

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Taipei, , Taiwan

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Taipei, , Taiwan

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Taipei, , Taiwan

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Taipei, , Taiwan

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Taipei, , Taiwan

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Taoyuan District, , Taiwan

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Adana, , Turkey (Türkiye)

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Ankara, , Turkey (Türkiye)

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Ankara, , Turkey (Türkiye)

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Ankara, , Turkey (Türkiye)

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Ankara, , Turkey (Türkiye)

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Izmir, , Turkey (Türkiye)

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Izmir, , Turkey (Türkiye)

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Kadıkoy/Istanbul, , Turkey (Türkiye)

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Karşıyaka, , Turkey (Türkiye)

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Kayseri, , Turkey (Türkiye)

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Blackpool, , United Kingdom

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Cambridge, , United Kingdom

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London, , United Kingdom

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London, , United Kingdom

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Manchester, , United Kingdom

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Newport, , United Kingdom

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Nottingham, , United Kingdom

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Portsmouth, , United Kingdom

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Reading, , United Kingdom

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Sheffield, , United Kingdom

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Sutton, , United Kingdom

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Taunton, , United Kingdom

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Countries

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United States Australia Austria Belgium Bulgaria Canada France Germany Hungary Israel Italy Japan Norway Poland Portugal Russia Slovakia South Korea Spain Switzerland Taiwan Turkey (Türkiye) United Kingdom

References

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Bidard FC, Mayer EL, Park YH, Janni W, Ma C, Cristofanilli M, Bianchini G, Kalinsky K, Iwata H, Chia S, Fasching PA, Brufsky A, Nowecki Z, Pascual J, Moreau L, Chen SC, Karadurmus N, Gal-Yam EN, Jung KH, Pernas S, McClain S, He W, Klinowska T, Huang-Bartlett C, Turner NC; SERENA-6 Study Group. First-Line Camizestrant for Emerging ESR1-Mutated Advanced Breast Cancer. N Engl J Med. 2025 Aug 7;393(6):569-580. doi: 10.1056/NEJMoa2502929. Epub 2025 Jun 1.

Reference Type DERIVED
PMID: 40454637 (View on PubMed)

Turner N, Huang-Bartlett C, Kalinsky K, Cristofanilli M, Bianchini G, Chia S, Iwata H, Janni W, Ma CX, Mayer EL, Park YH, Fox S, Liu X, McClain S, Bidard FC. Design of SERENA-6, a phase III switching trial of camizestrant in ESR1-mutant breast cancer during first-line treatment. Future Oncol. 2023 Mar;19(8):559-573. doi: 10.2217/fon-2022-1196. Epub 2023 Apr 18.

Reference Type DERIVED
PMID: 37070653 (View on PubMed)

Related Links

Access external resources that provide additional context or updates about the study.

https://www.breastcancerstudylocator.com/trial/listing/296201

Breast Cancer Study Locator details (for US)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

D8534C00001

Identifier Type: -

Identifier Source: org_study_id

2023-503990-39-00

Identifier Type: OTHER

Identifier Source: secondary_id

2021-000546-17

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id