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.
Treatment: Gocatamig · Ifinatamab Deruxtecan (I-DXd) · Durvalumab — Researchers 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
Check if I qualifyExtracted 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
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 →
Could you qualify for this trial?
Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.
Check if I qualify