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ACTIVE NOT RECRUITING Phase 3

HERTHENA-Lung02: A Study of Patritumab Deruxtecan Versus Platinum-based Chemotherapy in Metastatic or Locally Advanced EGFRm NSCLC After Failure of EGFR TKI Therapy

NCT05338970 · View on ClinicalTrials.gov ↗

Study Summary

Disease progression is typical for patients with epidermal growth factor receptor mutated (EGFRm) non-small cell lung cancer (NSCLC). Standard platinum-based chemotherapy offers limited efficacy and an unfavorable safety profile.There is an urgent need for more effective and tolerable therapies for patients with EGFRm NSCLC who have exhausted available targeted therapies. Clinical evidence suggest that patritumab deruxtecan constitutes a promising investigational therapy for patients with EGFRm NSCLC.

Interventions

  • DRUG Platinum-based chemotherapy
  • DRUG Patritumab Deruxtecan

Study Locations (20)

California

  • City of Hope — Duarte
  • Moores Cancer Center at the UC San Diego Health — La Jolla
  • Scripps MD Anderson Cancer Center — La Jolla
  • USC Norris Comprehensive Cancer Center — Los Angeles
  • Kaiser Permanente - Vallejo Medical Center — Vallejo
  • Innovative Clinical Research Institute — Whittier

New York

  • Memorial Sloan Kettering Cancer Center — New York
  • Montefiore Medical Center — The Bronx

Alaska

  • Alaska Oncology and Hematology LLC — Anchorage

Arkansas

  • Highlands Oncology — Springdale

Florida

  • Sarah Cannon/Florida Cancer Specialists - FCS South — Port Charlotte

Georgia

  • Emory University — Atlanta

Idaho

  • St Luke's Cancer Institute — Boise

Maryland

  • American Oncology Partners of Maryland — Bethesda

Trial Details

FieldValue
Enrollment Target 586 participants
Start Date 2022-07-08
Est. Completion 2026-06-30
Phase Phase 3

Sponsor

Daiichi Sankyo

157 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05338970

The ClinicalTrials.gov registry entry for NCT05338970 describes a study currently listed as active not recruiting. It is categorized as Phase 3, 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 586 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 3 conditions, with Nonsquamous Non-small Cell Lung Cancer appearing as the primary indexed condition, and to 2 interventions — of which Platinum-based chemotherapy 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: NCT05338970 reports 20 study locations spanning 14 distinct geographic areas — top geographies include California, New York, Alaska. 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 NCT05338970 about?

NCT05338970 is a clinical study titled "HERTHENA-Lung02: A Study of Patritumab Deruxtecan Versus Platinum-based Chemotherapy in Metastatic or Locally Advanced EGFRm NSCLC After Failure of EGFR TKI Therapy". Disease progression is typical for patients with epidermal growth factor receptor mutated (EGFRm) non-small cell lung cancer (NSCLC). Standard platinum-based chemotherapy offers limited efficacy and an unfavorable safety profile.There is an urgent need for more effective and tolerable therapies for ...

What is the current status of trial NCT05338970?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 586 participants. The study started on 2022-07-08. Estimated completion is 2026-06-30.

What conditions does trial NCT05338970 study?

This clinical trial studies the following conditions: Nonsquamous Non-small Cell Lung Cancer, EGFR L858R, EGFR Exon 19 Deletion. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05338970?

The interventions under investigation include: Platinum-based chemotherapy (DRUG), Patritumab Deruxtecan (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05338970?

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 NCT05338970 being conducted?

This trial has 20 study locations across Alaska, Arkansas, California, Florida, Georgia. 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