Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING Phase 1

Datopotamab Deruxtecan (Dato-DXd) in Combination With Pembrolizumab With or Without Platinum Chemotherapy in Subjects With Advanced or Metastatic Non-Small Cell Lung Cancer (TROPION-Lung02)

NCT04526691 · View on ClinicalTrials.gov ↗

Study Summary

This study will assess safety and treatment activity of datopotamab deruxtecan (Dato-DXd) in combination with pembrolizumab with or without platinum chemotherapy in participants with advanced or metastatic non-small cell lung cancer.

Interventions

  • DRUG Carboplatin
  • DRUG Cisplatin
  • DRUG Datopotamab deruxtecan
  • DRUG KEYTRUDA®

Study Locations (20)

Other

  • Instituto Europeo Di Oncologica — Milan
  • Azienda Ospedaliera San Gerardo — Monza
  • Istituto Nazionale Tumori Fondazione G. Pascale di Napoli Struttura di Oncologia — Naples
  • National Cancer Center Hospital East — Chiba
  • National Cancer Center Hospital — Tokyo
  • Showa Medical University Hospital — Tokyo
  • H. Vall Hebrón (Vall Hebron Institut de Oncologia - VHIO) — Barcelona
  • START Madrid - Hospital Universitario Fundacion Jimenez Diaz — Madrid
  • Hospital Universitario 12 de Octubre — Madrid
  • (CIOCC-START) Hospital Universitario HM Sanchinarro — Madrid
  • Hospital Puerta de Hierro — Majadahonda

Maryland

  • Johns Hopkins Kimmel Cancer Center at Bayview — Baltimore
  • The Skip Viragh Outpatient Cancer Building — Baltimore

Arizona

  • Mayo Clinic — Scottsdale

California

  • City of Hope — Duarte

District of Columbia

  • Johns Hopkins Kimmel Cancer Center — Washington D.C.

Florida

  • Mayo Clinic — Jacksonville

Minnesota

  • Mayo Clinic — Rochester

New Mexico

  • Quantum Santa Fe — Santa Fe

Trial Details

FieldValue
Enrollment Target 145 participants
Start Date 2020-09-15
Est. Completion 2026-04-15
Phase Phase 1

Sponsor

Daiichi Sankyo

157 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04526691

The ClinicalTrials.gov registry entry for NCT04526691 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 145 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Daiichi Sankyo, which has 157 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Advanced or Metastatic NSCLC appearing as the primary indexed condition, and to 4 interventions — of which Carboplatin is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04526691 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Other, Maryland, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04526691 about?

NCT04526691 is a clinical study titled "Datopotamab Deruxtecan (Dato-DXd) in Combination With Pembrolizumab With or Without Platinum Chemotherapy in Subjects With Advanced or Metastatic Non-Small Cell Lung Cancer (TROPION-Lung02)". This study will assess safety and treatment activity of datopotamab deruxtecan (Dato-DXd) in combination with pembrolizumab with or without platinum chemotherapy in participants with advanced or metastatic non-small cell lung cancer.

What is the current status of trial NCT04526691?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 145 participants. The study started on 2020-09-15. Estimated completion is 2026-04-15.

What conditions does trial NCT04526691 study?

This clinical trial studies the following conditions: Advanced or Metastatic NSCLC. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04526691?

The interventions under investigation include: Carboplatin (DRUG), Cisplatin (DRUG), Datopotamab deruxtecan (DRUG), KEYTRUDA® (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04526691?

This trial is sponsored by Daiichi Sankyo, which has 157 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04526691 being conducted?

This trial has 20 study locations across Arizona, California, District of Columbia, Florida, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial