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OncoMatch/Clinical Trials/NCT07361497

A Study to Evaluate Pumitamig Versus Durvalumab Following Concurrent Chemoradiation Therapy in Participants With Unresectable Stage III Non-small Cell Lung Cancer (NSCLC) (ROSETTA Lung-201)

Is NCT07361497 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments including Pumitamig and Durvalumab for non-small cell lung cancer (nsclc).

Phase 3RecruitingBristol-Myers SquibbNCT07361497Data as of May 2026

Treatment: Pumitamig · DurvalumabA study to evaluate Pumitamig versus Durvalumab following concurrent chemoradiation therapy in participants with unresectable stage III Non-small Cell Lung Cancer (NSCLC)

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Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: ALK wild-type

Required: EGFR wild-type

Disease stage

Required: Stage III

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Must have received: platinum-based chemotherapy — concurrent with radiation

at least 2 cycles of platinum-based concurrent chemoradiotherapy (a total dose of radiation of at least 54 Gy)

Must have received: radiation therapy — concurrent with chemotherapy

at least 2 cycles of platinum-based concurrent chemoradiotherapy (a total dose of radiation of at least 54 Gy)

Cannot have received: anticancer therapy (outside of CCRT)

must not have any prior anticancer therapy (outside of CCRT) for locally advanced Stage III disease

Lab requirements

Cardiac function

No significant cardiovascular impairment such as uncontrolled hypertension (despite optimal medical treatment), congestive heart failure, active coronary disease (within 6 months prior to randomization), ventricular arrhythmias, major thrombotic or embolic events or major hemorrhagic events within 6 months prior to randomization, or significant risk of pulmonary hemorrhage

must not have significant cardiovascular impairment such as uncontrolled hypertension (despite optimal medical treatment), congestive heart failure, active coronary disease (within 6 months prior to randomization), ventricular arrhythmias, major thrombotic or embolic events or major hemorrhagic events within 6 months prior to randomization, or significant risk of pulmonary hemorrhage

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Southern Cancer Center Pc · Daphne, Alabama
  • Local Institution - 0780 · Chandler, Arizona
  • Local Institution - 0585 · Golden, Colorado
  • Medical Oncology Hematology Consultants, PA · Newark, Delaware
  • Local Institution - 0711 · Ocala, Florida

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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