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A Phase III, Randomised, Open-Label, Multicentre Study of Datopotamab Deruxtecan or Docetaxel in Previously Treated TROP2-positive Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer Without Actionable Genomic Alterations (TROPION-Lung17)

Status: Recruiting
Location: See all (198) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

TROPION-Lung17 will measure the efficacy and safety of datopotamab deruxtecan (Dato-DXd) compared with docetaxel in patients with trophoblast cell surface protein 2 (TROP2) positive advanced or metastatic lung cancer without actionable genomic alterations (AGA).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Pathologically documented Stage IIIB, IIIC, or Stage IV non-squamous non-small cell lung cancer (NSCLC) without actionable genomic alterations (AGA) at the time of randomisation and meets the criteria for NSCLC:

‣ Participants must have documented negative test results for epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), and ROS proto-oncogene 1 (ROS1) genomic alterations.

⁃ Has no known tumour genomic alterations in neurotrophic tyrosine receptor kinase (NTRK), proto-oncogene B-raf (BRAF), rearranged during transfection (RET), mesenchymal-epithelial transition (MET) exon 14 skipping, Kirsten rat sarcoma viral oncogene homolog (KRAS) G12C, human epidermal growth factor receptor 2 (HER2) or any other actionable driver oncogenes for which there are locally approved and available targeted first-line therapies.

⁃ Prospectively assessed trophoblast cell surface protein 2 (TROP2) normalised membrane ratio (NMR) positive.

• Documentation of radiographic disease progression while on or after receiving the most recent treatment regimen for advanced or metastatic NSCLC.

• Participants must have received platinum based chemotherapy (PBC) in combination with anti-programmed death-protein 1 (anti-PD-1)/anti-programmed death-ligand 1 (anti-PD-L1) monoclonal antibody (mAb) as the only prior line of therapy or received PBC and anti-PD-1/anti-PD-L1 monoclonal antibody (in either order) sequentially as the only 2 prior lines of therapy.

• Provision of acceptable formalin fixed and paraffin embedded (FFPE) tumour sample for assessment of TROP2.

• At least one lesion not previously irradiated that qualifies as a Response Evaluation Criteria in Solid Tumours, Version 1.1 (RECIST 1.1) target lesion (TL) at baseline and can be accurately measured at baseline as ≥ 10 mm in the longest diameter (except lymph nodes, which must have short axis ≥ 15 mm) with computed tomography (CT) or magnetic resonance imaging (MRI) and is suitable for accurate repeated measurements.

• Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 or 1.

• Adequate bone marrow reserve and organ function within 7 days before randomisation.

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United States
Arizona
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Chandler
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Gilbert
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Goodyear
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Duarte
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Irvine
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Colorado
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Grand Junction
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Chicago
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Detroit
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Bridgeton
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Columbia
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Lincoln
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Albuquerque
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East Syracuse
Oregon
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Hershey
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Philadelphia
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Austin
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Australia
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Gosford
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South Brisbane
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Wollongong
Austria
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Graz
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Linz
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Rankweil
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Vienna
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Vienna
Belgium
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Hasselt
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La Louvière
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Libramont-chevigny
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Namur
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Sint-niklaas
Brazil
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Porto Alegre
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Porto Alegre
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Salvador
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São Paulo
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Brampton
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Hamilton
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Toronto
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Vancouver
China
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Beijing
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Beijing
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Beijing
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Guangzhou
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Hangzhou
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Harbin
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Shanghai
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Shantou
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Shenyang
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Tianjin
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Wuhan
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Wuhan
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Xuzhou
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Zhengzhou
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Zhengzhou
Germany
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Bad Saarow
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Bielefeld
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Bonn
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Cologne
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Essen
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Frankfurt
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Freiburg Im Breisgau
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Gauting
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Hamburg
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Budapest
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Budapest
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Debrecen
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Gyöngyös - Mátraháza
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Győr
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Gyula
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Szolnok
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India
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Bangalore
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Kolkata
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Monza
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Padova
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Chūōku
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Fukuoka
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Hiroshima
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Kyoto
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Osaka
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Yokohama
Poland
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Lodz
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Olsztyn
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Poznan
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Warsaw
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Incheon
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Seoul
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Suwon
Spain
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A Coruña
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Barcelona
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L'hospitalet De Llobregat
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Madrid
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Málaga
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Seville
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Zaragoza
Taiwan
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Kaohsiung City
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Taichung
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Tainan
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Taipei
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Taipei
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Taipei
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Taoyuan District
Thailand
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Bangkok
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Bangkok
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Bangkok
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Hat Yai
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Muang
Turkey
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Ankara
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Istanbul
United Kingdom
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Huddersfield
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London
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London
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Maidstone
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Norwich
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Stoke-on-trent
Viet Nam
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Hanoi
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Ho Chi Minh City
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Ho Chi Minh City
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Vinh
Contact Information
Primary
AstraZeneca Clinical Study Information Center
information.center@astrazeneca.com
1-877-240-9479
Time Frame
Start Date: 2025-10-31
Estimated Completion Date: 2029-01-29
Participants
Target number of participants: 400
Treatments
Experimental: Arm A: Datopotamab deruxtecan (Dato-DXd) monotherapy
Participants in the Dato-DXd monotherapy group will receive Dato-DXd as intravenous (IV) infusion every 3 weeks (Q3W) on Day 1 of each 21-day cycle.
Active_comparator: Arm B: Docetaxel monotherapy
Participants in the docetaxel monotherapy group will receive docetaxel as intravenous (IV) infusion every 3 weeks (Q3W) on Day 1 of each 21-day cycle.
Sponsors
Leads: AstraZeneca
Collaborators: Daiichi Sankyo

This content was sourced from clinicaltrials.gov