DS-8201a Versus T-DM1 for Human Epidermal Growth Factor Receptor 2 (HER2)-Positive, Unresectable and/or Metastatic Breast Cancer Previously Treated With Trastuzumab and Taxane [DESTINY-Breast03]

NCT ID: NCT03529110

Last Updated: 2025-10-21

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

PHASE3

Total Enrollment

524 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-08-09

Study Completion Date

2026-07-30

Brief Summary

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This study is designed to compare the anti-tumor activity as well as the safety and efficacy of DS-8201a versus T-DM1 in HER2-positive, unresectable and/or metastatic breast cancer subjects previously treated with trastuzumab and taxane.

Detailed Description

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Conditions

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Breast Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Trastuzumab deruxtecan (T-DXd)

Participants with HER2-positive, unresectable and/or metastatic breast cancer participants previously treated with trastuzumab and taxane who received T-DXd as a sterile intravenous (IV) solution at a dose of 5.4 mg/kg every 3 weeks (Q3W).

Group Type EXPERIMENTAL

Trastuzumab deruxtecan (T-DXd)

Intervention Type DRUG

T-DXd is sterile lyophilized powder reconstituted into a sterile aqueous solution (100 mg/5 mL) to be administered intravenously.

Ado-trastuzumab emtansine (T-DM1)

Participants with HER2-positive, unresectable and/or metastatic breast cancer participants previously treated with trastuzumab and taxane who received T-DM1 in accordance with the approved label.

Group Type ACTIVE_COMPARATOR

Ado-trastuzumab emtansine (T-DM1)

Intervention Type DRUG

The treatment will be in accordance with the approved label.

Interventions

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Trastuzumab deruxtecan (T-DXd)

T-DXd is sterile lyophilized powder reconstituted into a sterile aqueous solution (100 mg/5 mL) to be administered intravenously.

Intervention Type DRUG

Ado-trastuzumab emtansine (T-DM1)

The treatment will be in accordance with the approved label.

Intervention Type DRUG

Other Intervention Names

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DS-8201a T-DM1

Eligibility Criteria

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Inclusion Criteria

1. Must be competent and able to comprehend, sign, and date an Institutional Review Board (IRB) or Ethics Committee (EC) approved ICF before performance of any study-specific procedures or tests.
2. Adults ≥18 y old. (Please follow local regulatory requirements if the legal age of consent for study participation is \>18 y old.)
3. Pathologically documented breast cancer that:

1. is unresectable or metastatic.
2. has confirmed HER2-positive expression as determined according to American Society of Clinical Oncology - College of American Pathologists guidelines evaluated at a central laboratory.23
3. was previously treated with trastuzumab and taxane in the advanced/ metastatic setting or progressed within 6 mo after neoadjuvant or adjuvant treatment involving a regimen including trastuzumab and taxane.
4. Documented radiologic progression (during or after most recent treatment or within 6 mo after completing adjuvant therapy).
5. Subjects must be HER2-positive as confirmed by central laboratory assessment of most recent tumor tissue sample available. If archived tissue is not available, a fresh biopsy is required.
6. Presence of at least 1 measurable lesion per modified Response Evaluation Criteria in Solid Tumors (mRECIST) version 1.1

Exclusion Criteria

1. Prior treatment with an anti-HER2 ADC (such as T-DM1) in the metastatic setting. Prior treatment in the adjuvant/neoadjuvant setting would be allowed if progression of disease did not occur within 12 mo of end of adjuvant therapy.
2. Uncontrolled or significant cardiovascular disease, including any of the following:

1. History of myocardial infarction within 6 mo before randomization;
2. History of symptomatic congestive heart failure (New York Heart Association Class II to IV);
3. Troponin levels consistent with myocardial infarction as defined according to the manufacturer within 28 d prior to randomization;
4. Corrected QT interval (QTc) prolongation to \> 470 ms (females) or \>450 ms (male) based on average of Screening triplicate 12-lead ECG;
5. LVEF \< 50% within 28 d prior to randomization
3. Has a history of (noninfectious) ILD/pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at Screening.
4. Spinal cord compression or clinically active central nervous system (CNS) metastases, defined as untreated or symptomatic, or requiring therapy with corticosteroids or anticonvulsants to control associated symptoms.

* Subjects with clinically inactive brain metastases may be included in the study.
* Subjects with treated brain metastases that are no longer symptomatic and who require no treatment with corticosteroids or anticonvulsants may be included in the study if they have recovered from the acute toxic effect of radiotherapy. A minimum of 2 wk must have elapsed between the end of whole brain radiotherapy and study enrollment.
5. Has a history of severe hypersensitivity reactions to either the drug substances or inactive ingredients in the drug product.
6. History of severe hypersensitivity reactions to other mAbs.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Daiichi Sankyo Co., Ltd.

INDUSTRY

Sponsor Role collaborator

AstraZeneca

INDUSTRY

Sponsor Role collaborator

Daiichi Sankyo

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Global Team Leader

Role: STUDY_DIRECTOR

Daiichi Sankyo

Locations

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UCLA Hematology Oncology

Los Angeles, California, United States

Site Status

Sharp Memorial Hospital

San Diego, California, United States

Site Status

University of California San Francisco

San Francisco, California, United States

Site Status

Innovative Clinical Research Institute

Whittier, California, United States

Site Status

Washington Cancer Institute

Washington D.C., District of Columbia, United States

Site Status

Florida Cancer Specialists-Broadway

Fort Myers, Florida, United States

Site Status

Florida Cancer Specialists NORTH

St. Petersburg, Florida, United States

Site Status

Piedmont Cancer Institute, PC

Atlanta, Georgia, United States

Site Status

Loyola University Health System

Maywood, Illinois, United States

Site Status

Norton Cancer Institute

Louisville, Kentucky, United States

Site Status

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

Site Status

University of Nebraska Medical Center

Omaha, Nebraska, United States

Site Status

North Shore Hematology Oncology Associates, PC

East Setauket, New York, United States

Site Status

University of Rochester

Rochester, New York, United States

Site Status

Wake Forest University Baptist Medical Center

Winston-Salem, North Carolina, United States

Site Status

University of Cincinnati Medical Center

Cincinnati, Ohio, United States

Site Status

Seidman Cancer Center

Cleveland, Ohio, United States

Site Status

The Ohio State University

Columbus, Ohio, United States

Site Status

Dayton Physicians, LLC

Kettering, Ohio, United States

Site Status

Magee-Womens Hospital of UPMC

Pittsburgh, Pennsylvania, United States

Site Status

Tennessee Oncology- St Thomas Location

Nashville, Tennessee, United States

Site Status

Vanderbilt Breast Center at One Hundred Oaks

Nashville, Tennessee, United States

Site Status

UT Southwestern Medical Center

Dallas, Texas, United States

Site Status

Houston Methodist Hospital / Houston Methodist Cancer Center

Houston, Texas, United States

Site Status

MD Anderson Cancer Center

Houston, Texas, United States

Site Status

Millennium Oncology

Houston, Texas, United States

Site Status

The University of Texas Health Science Center at Tyler

Tyler, Texas, United States

Site Status

MultiCare Health System Institute for Research and Innovation

Auburn, Washington, United States

Site Status

The Tweed Hospital

Tweed Heads, New South Wales, Australia

Site Status

Princess Alexandra Hospital

Woolloongabba, Queensland, Australia

Site Status

Box Hill Hospital

Box Hill, Victoria, Australia

Site Status

Peninsula and South Eastern Haematology & Oncology Group

Frankston, Victoria, Australia

Site Status

Peter MacCallum Cancer

Melbourne, Victoria, Australia

Site Status

St John of God Subiaco Hospital

Subiaco, Western Australia, Australia

Site Status

Institut Jules-Bordet

Brussels, , Belgium

Site Status

Universitair Ziekenhuis Brussel

Brussels, , Belgium

Site Status

Universitair Ziekenhuis Antwerpen

Edegem, , Belgium

Site Status

AZ Sint-Lucas - Campus Sint-Lucas

Ghent, , Belgium

Site Status

Universitaire Ziekenhuizen Leuven

Leuven, , Belgium

Site Status

CHU UCL Namur site de Sainte Elisabeth

Namur, , Belgium

Site Status

NOB - Nucleo de Oncologia da Bahia

Salvador, Estado de Bahia, Brazil

Site Status

Hospital Nossa Senhora da Conceição

Porto Alegre, Rio Grande do Sul, Brazil

Site Status

Catarina Pesquisa Clinica

Itajaí, Santa Catarina, Brazil

Site Status

CEPHO - Centro de Estudos e Pesquisas de Hematologia e Oncologia

Santo André, São Paulo, Brazil

Site Status

ICESP - Instituto do Cancer do Estado de São Paulo Octavio Frias de Oliveira

São Paulo, São Paulo, Brazil

Site Status

Clínica de Pesquisas e Centro de Estudos em Oncologia Ginecológica e Mamária Ltda.

São Paulo, São Paulo, Brazil

Site Status

Instituto Americas

Rio de Janeiro, , Brazil

Site Status

A. C. Camargo Cancer Center

São Paulo, , Brazil

Site Status

Tom Baker Cancer Centre

Calgary, Alberta, Canada

Site Status

Toronto Sunnybrook Hospital

Toronto, Ontario, Canada

Site Status

St. Mary's Hospital

Montreal, Quebec, Canada

Site Status

Cancer Hospital Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, China

Site Status

Beijing Hospital

Beijing, Beijing Municipality, China

Site Status

Sun Yat-sen University, Cancer Center

Guangzhou, Guangdong, China

Site Status

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

Guangzhou, Guangdong, China

Site Status

Harbin Medical University Cancer Hospital

Harbin, Heilongjiang, China

Site Status

The First Hospital of Jilin University

Changchun, Jilin, China

Site Status

Liaoning Cancer Hospital & Institute

Shenyang, Liaoning, China

Site Status

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Site Status

West China Hospital, Sichuan University

Chengdu, Sichuan, China

Site Status

Tianjin Medical University Cancer Institute & Hospital

Tianjin, Tianjin Municipality, China

Site Status

Sir Run Run Shaw Hospital Xiasha Branch, Zhejiang University, School of Medicine

Hangzhou, Zhejiang, China

Site Status

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, China

Site Status

Centre Paul Strauss

Strasbourg, Bas Rhin, France

Site Status

Hôpital Nord - CHU Marseille

Marseille, Bouches-du-Rhone, France

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Centre François Baclesse

Caen, Calvados, France

Site Status

Clinique Victor Hugo - Centre Jean Bernard

Le Mans, Cedex 02, Sarthe, France

Site Status

CARIO - Centre Armoricain de Radiothérapie, Imagerie médicale et Oncologie

Plérin, Cotes d'Armor, France

Site Status

Centre Georges François Leclerc

Dijon, Côte-d'Or, France

Site Status

CHRU Jean Minjoz

Besançon, Doubs, France

Site Status

Institut Bergonié

Bordeaux, Gironde, France

Site Status

Centre René Huguenin

Saint-Cloud, Hauts De Seine, France

Site Status

ICM Val d'Aurelle

Montpellier, Herault, France

Site Status

CRLCC Eugene Marquis

Rennes, Ille Et Vilaine, France

Site Status

ICO - Site René Gauducheau

Saint-Herblain, Loire Atlantique, France

Site Status

ICO - Site Paul Papin

Angers, Maine Et Loire, France

Site Status

Centre de cancerologie les Dentellieres

Valenciennes, Nord, France

Site Status

Centre Leon Berard

Lyon, Rhone, France

Site Status

Centre Hospitalier Lyon Sud

Pierre-Bénite, Rhone, France

Site Status

Institut Sainte Catherine

Avignon, Vaculuse, France

Site Status

Hôpital d'Instruction des Armees Begin

Saint-Mandé, Val De Marne, France

Site Status

Institut Gustave Roussy

Villejuif, Val De Marne, France

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Institut Curie - site de Paris

Paris, , France

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Hôpital Saint-Louis

Paris, , France

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Hopital Tenon

Paris, , France

Site Status

Universitaetsklinikum Erlangen

Erlangen, Bavaria, Germany

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Rotkreuzklinikum Muenchen gGmbH

Munich, Bavaria, Germany

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Klinikum rechts der Isar der TU Muenchen

Munich, Bavaria, Germany

Site Status

Universitaetsklinikum Duesseldorf AoeR

Düsseldorf, North Rhine-Westphalia, Germany

Site Status

Haematologisch-Onkologische Schwerpunktpraxis

Troisdorf, North Rhine-Westphalia, Germany

Site Status

Marienhospital Bottrop gGmbH

Bottrop, Rhineland-Palatinate, Germany

Site Status

Universitaetsklinikum Schleswig-Holstein - Campus Luebeck

Lübeck, Schleswig-Holstein, Germany

Site Status

The Chinese

Hong Kong, , Hong Kong

Site Status

The University of Hong Kong

Shatin, , Hong Kong

Site Status

Azienda Ospedaliera Universitaria Arcispedale Sant'Anna

Cona, Ferrara, Italy

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Azienda Socio Sanitaria Territoriale di Monza (Presidio San Gerardo), U.O Oncologia Medica

Monza, Milano, Italy

Site Status

Istituto Clinico Humanitas

Rozzano, Milano, Italy

Site Status

IRCCS Centro di Riferimento Oncologico

Aviano, Pordenone, Italy

Site Status

Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII (Presidio Papa Giovanni XXIII)

Bergamo, , Italy

Site Status

Azienda Ospedaliera Universitaria Policlinico Sant'Orsola Malpighi

Bologna, , Italy

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Istituto Nazionale per la Ricerca sul Cancro di Genova

Genova, , Italy

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Azienda Ospealiera della Provincia di Lecco

Lecco, , Italy

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Azienda Ospedaliera Ospedali Riuniti Papardo-Piemonte

Messina, , Italy

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Ospedale San Raffaele

Milan, , Italy

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IEO Istituto Europeo di Oncologia

Milan, , Italy

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A.O.U. Policlinico di Modena

Modena, , Italy

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Istituto Nazionale Tumori Fondazione G. Pascale

Napoli, , Italy

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Azienda Ospedaliero Universitaria di Parma

Parma, , Italy

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Fondazione IRCCS Policlinico San Matteo

Pavia, , Italy

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Azienda Ospedaliera Città della Salute e della Scienza di Torino

Torino, , Italy

Site Status

Center Hospital of the National Center for Global Health and Medicine

Shinjuku-Ku, Tokyo-To, Japan

Site Status

Aichi Cancer Center Hospital

Aichi, , Japan

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NHO Shikoku Cancer Center

Ehime, , Japan

Site Status

NHO Kyushu Cancer Center

Fukuoka, , Japan

Site Status

Hiroshima City Hiroshima Citizens Hospital

Hiroshima, , Japan

Site Status

NHO Hokkaido Cancer Center

Hokkaido, , Japan

Site Status

Kanagawa Cancer Center

Kanagawa, , Japan

Site Status

Kumamoto University Hospital

Kumamoto, , Japan

Site Status

Niigata Cancer Center

Niigata, , Japan

Site Status

Okayama University Hospital

Okayama, , Japan

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NHO Osaka National Hospital

Osaka, , Japan

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Osaka International Cancer Institute

Osaka, , Japan

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Saitama Cancer Center

Saitama, , Japan

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Shizuoka Cancer Center

Shizuoka, , Japan

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National Cancer Center Hospital

Tokyo, , Japan

Site Status

The Cancer Institute Hospital of JFCR

Tokyo, , Japan

Site Status

Showa University Hospital

Tokyo, , Japan

Site Status

Seoul National University Bundang Hospital

Seongnam-si, Gyeonggi-do, South Korea

Site Status

Seoul National University Hospital

Seoul, , South Korea

Site Status

Severance Hospital, Yonsei University

Seoul, , South Korea

Site Status

Asan Medical Center

Seoul, , South Korea

Site Status

Samsung Medical Center

Seoul, , South Korea

Site Status

ICO l'Hospitalet - Hospital Duran i Reynals

L'Hospitalet de Llobregat, Barcelona, Spain

Site Status

Complejo Hospitalario Universitario A Coruña

A Coruña, La Coruña, Spain

Site Status

Complejo Hospitalario Universitario de Santiago

Santiago de Compostela, La Coruña, Spain

Site Status

Hospital Universitario Puerta de Hierro Majadahonda

Majadahonda, Madrid, Spain

Site Status

Hospital Universitario Virgen Macarena

Seville, Sevill, Spain

Site Status

Hospital Universitario de Canarias

San Cristóbal de La Laguna, Tenerife, Spain

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Hospital Infanta Cristina

Badajoz, , Spain

Site Status

Hospital Universitari Vall d'Hebron

Barcelona, , Spain

Site Status

Hospital Clinic de Barcelona

Barcelona, , Spain

Site Status

IOB-Institute of Oncology

Barcelona, , Spain

Site Status

Hospital General Universitario Gregorio Maranon

Madrid, , Spain

Site Status

MD Anderson Cancer Centre

Madrid, , Spain

Site Status

Hospital Universitario Ramon y Cajal

Madrid, , Spain

Site Status

Hospital Universitario Clinico San Carlos

Madrid, , Spain

Site Status

Hospital Universitario 12 de Octubre

Madrid, , Spain

Site Status

Hospital Clinico Universitario Virgen de la Victoria

Málaga, , Spain

Site Status

Hospital Universitario Virgen del Rocio

Seville, , Spain

Site Status

China Medical University Hospital

Taichung, , Taiwan

Site Status

National Cheng Kung University Hospital

Tainan City, , Taiwan

Site Status

National Taiwan University Hospital

Taipei, , Taiwan

Site Status

Taipei Veterans General Hospital

Taipei, , Taiwan

Site Status

Koo Foundation, Sun Yat-Sen Cancer Center

Taipei, , Taiwan

Site Status

Royal Devon and Exeter Hospital (Wonford)

Exeter, Devon, United Kingdom

Site Status

Aberdeen Royal Infirmary

Aberdeen, Grampian Region, United Kingdom

Site Status

Queen Mary University of London

London, Greater London, United Kingdom

Site Status

University College London Hospitals

London, Greater London, United Kingdom

Site Status

Guy's Hospital

London, Greater London, United Kingdom

Site Status

Sarah Cannon Research Institute UK

London, Greater London, United Kingdom

Site Status

The Christie Hospital

Manchester, Greater Manchester, United Kingdom

Site Status

Western General Hospital

Edinburgh, Lothian Region, United Kingdom

Site Status

Nottingham University Hospitals City Campus

Nottingham, Nottinghamshire, United Kingdom

Site Status

Royal Surrey County Hospital

Guildford, Surrey, United Kingdom

Site Status

Countries

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United States Australia Belgium Brazil Canada China France Germany Hong Kong Italy Japan South Korea Spain Taiwan United Kingdom

References

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Iwata H, Xu B, Kim SB, Chung WP, Park YH, Kim MH, Tseng LM, Chung CF, Huang CS, Kim JH, Chiu JWY, Yamashita T, Li W, Egorov A, Nishijima S, Nakatani S, Nishiyama Y, Sugihara M, Cortes J, Im SA. Trastuzumab deruxtecan versus trastuzumab emtansine in Asian patients with HER2-positive metastatic breast cancer. Cancer Sci. 2024 Sep;115(9):3079-3088. doi: 10.1111/cas.16234. Epub 2024 Jul 9.

Reference Type DERIVED
PMID: 38979893 (View on PubMed)

Cortes J, Hurvitz SA, Im SA, Iwata H, Curigliano G, Kim SB, Chiu JWY, Pedrini JL, Li W, Yonemori K, Bianchini G, Loi S, Borges GS, Wang X, Bachelot T, Nakatani S, Ashfaque S, Liang Z, Egorov A, Hamilton E. Trastuzumab deruxtecan versus trastuzumab emtansine in HER2-positive metastatic breast cancer: long-term survival analysis of the DESTINY-Breast03 trial. Nat Med. 2024 Aug;30(8):2208-2215. doi: 10.1038/s41591-024-03021-7. Epub 2024 Jun 2.

Reference Type DERIVED
PMID: 38825627 (View on PubMed)

Ma R, Shi Y, Yan R, Yin S, Bu H, Huang J. Efficacy and safety of trastuzumab deruxtecan in treating human epidermal growth factor receptor 2-low/positive advanced breast cancer:A meta-analysis of randomized controlled trials. Crit Rev Oncol Hematol. 2024 Apr;196:104305. doi: 10.1016/j.critrevonc.2024.104305. Epub 2024 Mar 3.

Reference Type DERIVED
PMID: 38442809 (View on PubMed)

Cortes J. Trastuzumab Deruxtecan versus Trastuzumab Emtansine for Breast Cancer: a plain language summary of the DESTINY-Breast03 study. Future Oncol. 2024 Feb;20(4):167-178. doi: 10.2217/fon-2023-0422. Epub 2023 Dec 7.

Reference Type DERIVED
PMID: 38059424 (View on PubMed)

Rugo HS, Crossno CL, Gesthalter YB, Kelley K, Moore HB, Rimawi MF, Westbrook KE, Buys SS. Real-World Perspectives and Practices for Pneumonitis/Interstitial Lung Disease Associated With Trastuzumab Deruxtecan Use in Human Epidermal Growth Factor Receptor 2-Expressing Metastatic Breast Cancer. JCO Oncol Pract. 2023 Aug;19(8):539-546. doi: 10.1200/OP.22.00480. Epub 2023 May 19.

Reference Type DERIVED
PMID: 37207306 (View on PubMed)

Curigliano G, Dunton K, Rosenlund M, Janek M, Cathcart J, Liu Y, Fasching PA, Iwata H. Patient-reported outcomes and hospitalization data in patients with HER2-positive metastatic breast cancer receiving trastuzumab deruxtecan or trastuzumab emtansine in the phase III DESTINY-Breast03 study. Ann Oncol. 2023 Jul;34(7):569-577. doi: 10.1016/j.annonc.2023.04.516. Epub 2023 May 12.

Reference Type DERIVED
PMID: 37179020 (View on PubMed)

Hurvitz SA, Hegg R, Chung WP, Im SA, Jacot W, Ganju V, Chiu JWY, Xu B, Hamilton E, Madhusudan S, Iwata H, Altintas S, Henning JW, Curigliano G, Perez-Garcia JM, Kim SB, Petry V, Huang CS, Li W, Frenel JS, Antolin S, Yeo W, Bianchini G, Loi S, Tsurutani J, Egorov A, Liu Y, Cathcart J, Ashfaque S, Cortes J. Trastuzumab deruxtecan versus trastuzumab emtansine in patients with HER2-positive metastatic breast cancer: updated results from DESTINY-Breast03, a randomised, open-label, phase 3 trial. Lancet. 2023 Jan 14;401(10371):105-117. doi: 10.1016/S0140-6736(22)02420-5. Epub 2022 Dec 7.

Reference Type DERIVED
PMID: 36495879 (View on PubMed)

Rugo HS, Bianchini G, Cortes J, Henning JW, Untch M. Optimizing treatment management of trastuzumab deruxtecan in clinical practice of breast cancer. ESMO Open. 2022 Aug;7(4):100553. doi: 10.1016/j.esmoop.2022.100553. Epub 2022 Aug 11.

Reference Type DERIVED
PMID: 35964548 (View on PubMed)

Cortes J, Kim SB, Chung WP, Im SA, Park YH, Hegg R, Kim MH, Tseng LM, Petry V, Chung CF, Iwata H, Hamilton E, Curigliano G, Xu B, Huang CS, Kim JH, Chiu JWY, Pedrini JL, Lee C, Liu Y, Cathcart J, Bako E, Verma S, Hurvitz SA; DESTINY-Breast03 Trial Investigators. Trastuzumab Deruxtecan versus Trastuzumab Emtansine for Breast Cancer. N Engl J Med. 2022 Mar 24;386(12):1143-1154. doi: 10.1056/NEJMoa2115022.

Reference Type DERIVED
PMID: 35320644 (View on PubMed)

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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2018-000222-61

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

jRCT2080223919

Identifier Type: REGISTRY

Identifier Source: secondary_id

DESTINY-B03

Identifier Type: OTHER

Identifier Source: secondary_id

CTR20190378

Identifier Type: REGISTRY

Identifier Source: secondary_id

2024-511204-16-00

Identifier Type: CTIS

Identifier Source: secondary_id

DS8201-A-U302

Identifier Type: -

Identifier Source: org_study_id

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