πŸ›οΈ Verified NIH Record β€’ Updated 2025-10-03

Pembrolizumab and Lenvatinib in Advanced Cervical Cancer (NCT04865887)

A Phase II Trial of Combination Therapy of Pembrolizumab and Lenvatinib in Patients With Locally Advanced or Metastatic Cervical Cancer

🟒 Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: Georgetown University

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

This is a phase II trial of combination therapy of pembrolizumab and lenvatinib in patients with locally advanced or metastatic cervical cancer that had failed first line of therapy. The hypothesis is the combination of lenvatinib and pembrolizumab will overcome vascular endothelial growth factor (VEGF)-mediated immunosuppression to enhance the response of patients with locally advanced or metastatic cervical cancer.

Who can join: Review the eligibility criteria below.

Location: MedStar Georgetown University Hospital β€” Washington D.C., District of Columbia

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (4 Sites)

  • MedStar Georgetown University Hospital β€” Washington D.C., District of Columbia
  • Medstar Washington Hospital Center β€” Washington D.C., District of Columbia
  • Georgia Cancer Center at Augusta University β€” Augusta, Georgia
  • John Theurer Cancer Center at Hackensack UMC β€” Hackensack, New Jersey

πŸ“ž Contact the Study Coordinator

Phone: (202) 687-3937

Email: jm3821@georgetown.edu

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

πŸ’° 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 Β§ 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.

Explore by condition: All Cervical Cancer clinical trials

πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—