🏛️ Verified NIH Record • Updated 2026-07-17

A Study of Lurbinectedin in Combination With Durvalumab for the Treatment of Participants With ES-SCLC (NCT07459634)

A Phase 2, Multicenter, Open-Label, Single-Arm Study of Lurbinectedin in Combination With Durvalumab as First-line Maintenance Therapy in Participants With Extensive-Stage Small-Cell Lung Cancer Following Induction Treatment With Platinum Based Chemotherapy and Durvalumab

🟢 Recruiting Phase2 💊 Investigational Drug / Biologic Sponsor: Jazz Pharmaceuticals

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this study is to evaluate the efficacy and safety of lurbinectedin in combination with durvalumab for the treatment of participants with extensive stage small cell lung cancer (ES-SCLC) whose disease has not progressed after first line (1L) induction therapy.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (7 items) and avoid the listed exclusions (12 items).

Location: Valkyrie Clinical Trials, Inc. — Los Angeles, California

Age range: 18 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Usually NOT eligible if any of the following apply:

  • Exclusion Criteria:
  • History of leptomeningeal carcinomatosis.
  • Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures
  • History of another primary malignancy
  • Presence or history of Central Nervous System (CNS) metastases
  • History of allogeneic organ transplantation.
  • History of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on the screening chest CT scan.
  • Any concurrent chemotherapy, study intervention, biologic, or hormonal therapy for cancer treatment.
  • Receipt of live attenuated vaccine within 30 days prior to the first dose of study intervention.
  • Concurrent enrollment in another clinical study
  • Prior enrollment or treatment in a previous durvalumab clinical study regardless of treatment arm assignment.
  • Pregnant or breastfeeding or intending to become pregnant during the study or within 6 months after the last dose of study intervention.

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (4 Sites)

  • Valkyrie Clinical Trials, Inc. — Los Angeles, California
  • Cancer Specialists of North Florida — Jacksonville, Florida
  • Emory University — Atlanta, Georgia
  • Carolina Blood and Cancer Care — Rock Hill, South Carolina

📞 Contact the Study Coordinator

Phone: (215) 832-3750

Email: ClinicalTrialDisclosure@JazzPharma.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗