Datopotamab Deruxtecan (Dato-DXd) in Combination With Durvalumab With or Without Platinum Chemotherapy in Subjects With Advanced or Metastatic Non-Small Cell Lung Cancer (TROPION-Lung04)

  • End date
    Dec 17, 2024
  • participants needed
  • sponsor
    Daiichi Sankyo, Inc.
Updated on 26 September 2021
Daiichi Sankyo Contact for Clinical Trial Information
Primary Contact
The Cancer Institute Hospital of Japanese Foundation For Cancer Research (6.7 mi away) Contact
+21 other location


This study will assess safety, tolerability, and treatment activity of datopotamab deruxtecan (Dato-DXd) in combination with durvalumab in participants with advanced or metastatic non-small cell lung cancer (NSCLC).


The primary objective of this study will assess the safety and tolerability of datopotamab deruxtecan (Dato-DXd) in combination with durvalumab with or without 4 cycles of platinum chemotherapy in participants with advanced or metastatic NSCLC who have either been previously treated or are treatment nave in a metastatic setting.

Two dose levels of Dato-DXd (4.0 mg/kg and 6.0 mg/kg) will be studied in combination with 1120 mg fixed dose of durvalumab, with or without 4 cycles of platinum chemotherapy in 6 study cohorts. This study will be conducted sequentially and dose escalation will occur according to lower dose to higher dose in the same combination regimen (4.0 mg/kg to 6.0 mg/kg) and from 2-drug combination (Dato-DXd and durvalumab) to 3-drug combination regimen (Dato-DXd, durvalumab, and carboplatin or cisplatin).

Condition Advanced or Metastatic NSCLC
Treatment cisplatin, carboplatin, durvalumab, DS-1062a, Datopotamab deruxtecan
Clinical Study IdentifierNCT04612751
SponsorDaiichi Sankyo, Inc.
Last Modified on26 September 2021


Yes No Not Sure

Inclusion Criteria

Men or women 20 years old in Japan, 18 years old in the United States on the day of signing the informed consent form (for the other countries, local regulatory requirements to consent should be followed)
Advanced or metastatic NSCLC, histologically confirmed at diagnosis of NSCLC, documented negative test results for EGFR and ALK genomic alterations, and no known genomic alterations in ROS1, NTRK, BRAF, RET, MET, or other driver oncogenes with approved therapies (actionable genomic alterations)
Is not a candidate for surgical resection or chemoradiation with curative intent
Documentation of radiological disease progression while on or after receiving the most recent treatment regimen, if any, for advanced or metastatic NSCLC
Must meet the following prior therapy requirements for advanced or metastatic NSCLC
Dose escalation (all cohorts): Has received 2 lines of prior anticancer therapy for advanced/metastatic disease
Archival tumor tissue from initial diagnosis, to the extent that archival tumor tissue is available, for measurement of TROP2 expression levels or other biomarkers
Has adequate bone marrow reserve and organ function at baseline within 7 days prior to Cycle 1 Day 1
Dose expansion (cohorts with 4.0 mg/kg or 6.0 mg/kg Dato-DXd in combination with 1120 mg durvalumab Q3W): Has not received immune checkpoint inhibitor (ICI) including PD-1/PD-L1, PD-L2, CTLA-4, and may or may not have been treated with systemic chemotherapy for advanced or metastatic NSCLC
Dose expansion (cohorts with 4.0 mg/kg or 6.0 mg/kg Dato-DXd in combination with 1120 mg durvalumab and 4 cycles of AUC 5 carboplatin or cisplatin 75 mg/m^2 Q3W): ICI nave and has not been treated with systemic anticancer therapy for advanced or metastatic NSCLC
Willing and able to undergo a mandatory tumor biopsy. There is no requirement for PD-L1 protein expression for inclusion

Exclusion Criteria

Experienced grade 3 or higher immune-related adverse events with prior immunotherapy treatment
Received a live vaccine within 30 days prior to the first dose of study treatment
Active, known, or suspected autoimmune disease
Has a condition requiring systemic treatment with either corticosteroids (>10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of Cycle 1 Day 1
Prior allogenic organ transplantation
Uncontrolled or significant cardiac disease
Has spinal cord compression or clinically active central nervous system metastases, defined as untreated and symptomatic, or requiring therapy with corticosteroids or anticonvulsants to control associated symptoms
History of (non-infectious) interstitial lung disease (ILD)/pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/ pneumonitis cannot be ruled out by imaging at screening
Clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses
Has a history of severe hypersensitivity reactions to either the drug substances or inactive ingredients (including but not limited to polysorbate 80) of Dato-DXd or durvalumab, and carboplatin or cisplatin for participants to be enrolled in those relevant cohorts)
Has a history of malignancy, other than NSCLC, except (a) adequately resected nonmelanoma skin cancer, (b) curatively treated in situ disease, or (c) other solid tumors curatively treated, with no evidence of disease for 3 years
Toxicities from previous anticancer therapy, defined as toxicities (other than alopecia) not yet improved to the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0 Grade 1 or baseline
Clear my responses

How to participate?

Step 1 Connect with a site
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact


Preferred Language
Other Language
Please verify that you are not a bot.

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider


Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 



Reply by • Private

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note