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Clinical Trials in the UK / NCT03975647
Active, not recruiting Phase 3

A Study of Tucatinib vs. Placebo in Combination With Ado-trastuzumab Emtansine (T-DM1) for Patients With Advanced or Metastatic HER2+ Breast Cancer

NCT03975647 · tracked via the Priya Life Science UK tracker
Sponsor
Seagen, a wholly owned subsidiary of Pfizer
Phase
Phase 3
Started
2019-10-02
Last updated
2026-07-23

Condition(s) studied

HER2-positive Breast Cancer

Investigational drug(s) / intervention(s)

tucatinibplaceboT-DM1

tucatinib: 300mg given twice per day by mouth (orally)

placebo: Given twice per day orally

T-DM1: 3.6 mg/kg given into the vein (IV; intravenously) every 21 days

Study summary

This study is being done to see if tucatinib with ado-trastuzumab emtansine (T-DM1) works better than T-DM1 alone to help patients who have a specific type of breast cancer called HER2 positive breast carcinoma. The breast cancer in this study is either metastatic (spread into other parts of the body) or cannot be removed completely with surgery.

Patients in this study will be randomly assigned to get either tucatinib or placebo (a pill with no medicine). This is a blinded study, so neither patients nor their doctors will know whether a patient gets tucatinib or placebo. All patients in the study will get T-DM1, a drug that is often used to treat this cancer.

Each treatment cycle lasts 21 days. Patients will swallow tucatinib pills or placebo pills two times every day. Patients will get T-DM1 injections from the study site staff on the first day of every cycle.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
* Inclusion Criteria: * Histologically confirmed HER2+ breast carcinoma as determined by a sponsor-designated central laboratory * History of prior treatment with a taxane and trastuzumab in any setting, separately or in combination * Have progression of unresectable locally advanced/metastatic breast cancer after last systemic therapy, or be intolerant of last systemic therapy * Measurable or non-measurable disease assessable by RECIST v1.1 * ECOG performance status score of 0 or 1 * CNS Inclusion - Based on screening contrast brain magnetic resonance imaging (MRI), participants must have at least one of the following: (a) No evidence of brain metastases (b) Untreated brain metastases not needing immediate local therapy (c) Previously treated brain metastases 1. Brain metastases previously treated with local therapy may either be stable since treatment or may have progressed since prior local CNS therapy, provided that there is no clinical indication for immediate re-treatment with local therapy 2. Participants treated with CNS local therapy for newly identified lesions or previously treated and progressing lesions may be eligible to enroll if all of the following criteria are met: (i) Time since SRS is at least 7 days prior to first dose of study treatment, time since WBRT is at least 14 days prior to first dose, or time since surgical resection is at least 28 days. (ii) Other sites of evaluable disease are present 3. Relevant records of any CNS treatment must be available to allow for classification of target and non-target lesions * Exclusion Criteria: * Prior treatment with tucatinib, afatinib, trastuzumab deruxtecan (DS-8201a), or any other investigational anti-HER2, anti-EGFR, or HER2 TKI agent. Prior treatment with lapatinib or neratinib within 12 months of starting study treatment (except in cases where they were given for ≤21 days and was discontinued for reasons other than disease progression or severe toxicity). Prior treatment with pyrotinib for recurrent of mBC (except in cases where pyrotinib was given for ≤21 days and was discontinued for reasons other than disease progression or severe toxicity). * CNS Exclusion - Based on screening contrast brain magnetic resonance imaging (MRI), participants must not have any of the following: 1. Any untreated brain lesions \>2 cm in size 2. Ongoing use of corticosteroids for control of symptoms of brain metastases at a total daily dose of \>2 mg of dexamethasone (or equivalent). 3. Any brain lesion thought to require immediate local therapy 4. Known or concurrent leptomeningeal disease as documented by the investigator 5. Poorly controlled generalized or complex partial seizures

Primary outcome measure(s)

Trial sites (490)

FacilityCityRegionStatus
University of South Alabama Health Children's and Women's Hospital Mobile Alabama
University of South Alabama Mitchell Cancer Institute Mobile Alabama
University of South Alabama Health University Hospital Mobile Alabama
Banner Gateway Medical Center Gilbert Arizona
Banner MD Anderson Cancer Center Gilbert Arizona
Western Regional Medical Center, LLC Goodyear Arizona
Arizona Oncology Associates, PC - HOPE. Tucson Arizona
Arizona Oncology Associates, PC - HOPE Tucson Arizona
Arizona Oncology Associates, PC - HOPE Tucson Arizona
UCLA Hematology/Oncology - Alhambra Alhambra California
Kaiser Permanente Medical Center Lab Drawing Station Antioch California
Kaiser Permanente Medical Center Lab Drawing Station Antioch California
UCLA Hematology/Oncology- Beverly Hills Beverly Hills California
UC Irvine Health Cancer Center - Newport Costa Mesa California
City of Hope Investigational Drug Services (IDS) Duarte California
City of Hope(City of Hope National Medical Center,City of Hope Medical Center) Duarte California
Kaiser Permanente Medical Center (Radiology) Dublin California
UCLA Hematology/Oncology - Encino Encino California
Kaiser Permanente Medical Center Lab Drawing Station Fairfield California
Kaiser Permanente Medical Center Lab Drawing Station Gilroy California
UCLA Hematology/Oncology- Irvine Irvine California
Drug Management Only: UCLA West Medical Pharmacy, Attn: Steven L Wong, Pharm.D. Los Angeles California
Regulatory Management only: TRIO-US Central Administration Los Angeles California
Ronald Reagan UCLA Medical Center Los Angeles California
UCLA Hematology/Oncology Los Angeles California
UCLA West Medical Pharmacy Los Angeles California
Kaiser Permanente Medical Center Lab Drawing Station Martinez California
Kaiser Permanente Medical Center Lab Drawing Station Milpitas California
Kaiser Permanente Medical Center Lab Drawing Station Modesto California
Kaiser Permanente Medical Center Lab Drawing Station Mountain View California
Kaiser Permanente Medical Center Lab Drawing Station Napa California
Kaiser Permanente Medical Center (clinic+DSL) Oakland California
Kaiser Permanente Medical Center (Radiology) Oakland California
Chao Family Comprehensive Cancer Center University of California Irvine Orange California
UC Irvine Medical Center Attn: Trisha Maris Orange California
UCI Medical Center - Chao Family Comprehensive Cancer Center Orange California
Kaiser Permanente Medical Center Lab Drawing Station Pleasanton California
UCLA Hematology/Oncology - Porter Ranch Porter Ranch California
Kaiser Permanente Medical Center Lab Drawing Station Redwood City California
Kaiser Permanente Medical Center (clinic+DSL) Roseville California

+ 450 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03975647 on ClinicalTrials.gov ↗ ← All trials in the UK