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NCT07561645Not yet recruitingPhase 2

A Trial for the Treatment of Advanced Large-Cell Neuroendocrine Cancer of the Lung

A Phase II, Single-arm Trial on the Addition of the DLL3xCD3 Bispecific T-cell Engager Obrixtamig (BI 764532) to Standard-of-care Platinum-based First-line Treatment of Advanced Large-cell Neuroendocrine Carcinoma of the Lung

Source: ClinicalTrials.gov · Last updated 26 Aug 2026

Brief summary (registry, in English)

This phase II clinical trial evaluates the efficacy, safety and tolerability of Obrixtamig in addition to standard of care chemotherapy (Platinum/Etoposide) in LCNEC.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
75 (estimated)
First submitted
15 Apr 2026
Start date
Sept 2026
Primary completion date
Apr 2032
Lead sponsor
Technische Universität Dresden
NCT number
NCT07561645
EU CT number
2025-524345-28-00

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 75
  • From Sept 2026 to the primary completion date, Apr 2032
  • 11 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Symptomatic brain metastases (Patients with asymptomatic brain metastases are allowed provided they are clinically stable, receiving no or a stable dose of anticonvulsants without steroid treatment for at least 3 weeks.)
  • Any prior systemic treatment for metastatic disease, except for one cycle of SoC as described under inclusion criteria
  • Previous treatment with obrixtamig or any anti-DLL3 compound including T-cell engagers and antibody-drug conjugates

Other illness

  • Known leptomeningeal disease

Who the study is looking for

  • Patient has provided written informed consent and is able to consent
  • Patients with pulmonary large-cell neuroendocrine carcinoma (LCNEC) defined by local histology and immunohistochemistry; patients with mixed histology are eligible if LCNEC is the predominant histology, i.e. ≥50%
  • Patients with locally advanced or metastatic disease without curative treatment options
  • All patients must have received one, but not more than one, cycle of platinum/etoposide chemotherapy with or without immune checkpoint inhibitor (standard-of-care; SoC). Other than that, patients must be previously untreated with systemic therapy.
  • Measurable disease according to RECIST v1.11

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (11)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Evangelische Lungenklinik Berlin Krankenhausbetriebs gGmbH
Coordinator of this site? Confirm its status
BerlinGermanyNot yet recruiting
Technische Universitaet Dresden
Coordinator of this site? Confirm its status
DresdenGermanyNot yet recruiting
Universitaetsklinikum Essen (AoR)
Coordinator of this site? Confirm its status
EssenGermanyNot yet recruiting
Goethe University Frankfurt
Coordinator of this site? Confirm its status
Frankfurt Am MainGermanyNot yet recruiting
Asklepios Klinik Gauting GmbH
Coordinator of this site? Confirm its status
GautingGermanyNot yet recruiting
LungenClinic Grosshansdorf GmbH
Coordinator of this site? Confirm its status
GrosshansdorfGermanyNot yet recruiting
Thoraxklinik Heidelberg gGmbH
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HeidelbergGermanyNot yet recruiting
Lungenklinik Hemer Deutscher Gemeinschafts-Diakonieverband GmbH
Coordinator of this site? Confirm its status
HemerGermanyNot yet recruiting
Universitaetsmedizin der Johannes Gutenberg-Universitaet Mainz KöR
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MainzGermanyNot yet recruiting
Pius Hospital Oldenburg
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OldenburgGermanyNot yet recruiting
Robert Bosch Gesellschaft fuer medizinische Forschung mbH
Coordinator of this site? Confirm its status
StuttgartGermanyNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.