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OncoMatch/Clinical Trials/NCT06780137

A Study to Evaluate the Safety and Efficacy of Gocatamig (MK-6070) and Ifinatamab Deruxtecan (I-DXd) in Participants With Relapsed/Refractory Extensive-Stage Small Cell Lung Cancer (MK-6070-002)

Is NCT06780137 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including Gocatamig and Ifinatamab Deruxtecan (I-DXd) for small cell lung cancer.

Phase 1/2RecruitingMerck Sharp & Dohme LLCNCT06780137Data as of May 2026

Treatment: Gocatamig · Ifinatamab Deruxtecan (I-DXd) · DurvalumabResearchers are looking for new ways to treat people with extensive-stage small cell lung cancer (SCLC) that has relapsed or is refractory. Gocatamig is a new type of immunotherapy that uses a person's immune system to find and destroy cancer cells. Ifinatamab deruxtecan (also known as I-DXd) is a drug which binds to a specific target on cancer cells and delivers treatment to destroy those cells. Durvalumab is a different type of immunotherapy that also destroys cancer cells. Researchers want to know if giving gocatamig, I-DXd, and gocatamig with I-DXd or durvalumab can treat SCLC that did not respond or stopped responding to a prior treatment. The goals of this study are to learn: * If gocatamig alone, I-DXd alone, and gocatamig with I-DXd or durvalumab are safe and well tolerated * If people who receive gocatamig alone, I-DXd alone, and gocatamig with I-DXd or durvalumab have their SCLC get smaller or go away

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Extracted eligibility criteria

Cancer type

Small Cell Lung Cancer

Disease stage

Required: Stage IV (T ANY, N ANY, M1A/B/C)

Metastatic disease required

extensive stage (defined as Stage IV (T any, N any, M1a/b/c))

Prior therapy

Min 1 prior line

Must have received: platinum-based chemotherapy

following at least 1 prior line of systemic therapy that included platinum-based chemotherapy

Cannot have received: radiation therapy

Received prior radiotherapy within 2 weeks of start of study intervention, or has radiation-related toxicities, requiring corticosteroids

Cannot have received: systemic anticancer therapy (except antibody-based anticancer therapy)

Exception: Part 1 only

Part 1 only: Systemic anticancer therapy (except antibody-based anticancer therapy) or investigational agents within 3 weeks or 5 half-lives, whichever is longer

Cannot have received: antibody-based cancer therapy

Exception: Part 1 only

Part 1 only: Antibody-based cancer therapy within 3 weeks before start of study intervention

Cannot have received: anticancer hormonal treatment (except LHRH)

Exception: Part 1 only

Part 1 only: Anticancer hormonal treatment (except luteinizing hormone-releasing hormone [LHRH]) within 2 weeks before start of study intervention

Cannot have received: chloroquine/hydroxychloroquine (chloroquine, hydroxychloroquine)

Exception: Part 1 only

Part 1 only: Chloroquine/hydroxychloroquine within 2 weeks before start of study intervention

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

US trial sites

  • University of Colorado Anschutz Medical Campus ( Site 1110) · Aurora, Colorado
  • University of Miami Hospital and Clinics, Sylvester Cancer Center ( Site 1111) · Miami, Florida
  • University of Chicago ( Site 1108) · Chicago, Illinois
  • Dana Farber Cancer Institute ( Site 1105) · Boston, Massachusetts
  • John Theurer Cancer Center at Hackensack University Medical Center ( Site 1103) · Hackensack, New Jersey

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

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