Activity and Safety of Danvatirsen and Pembrolizumab in HNSCC

Description

Open-label, Phase II, randomized, controlled study evaluating the efficacy and safety of danvatirsen in combination with pembrolizumab compared with pembrolizumab alone as first-line treatment of patients with recurrent/metastatic (R/M) HNSCC. Two-thirds of patients will be randomized to receive danvatirsen and pembrolizumab and one-third will be randomized to receive pembrolizumab alone.

Conditions

HNSCC

Study Overview

Study Details

Study overview

Open-label, Phase II, randomized, controlled study evaluating the efficacy and safety of danvatirsen in combination with pembrolizumab compared with pembrolizumab alone as first-line treatment of patients with recurrent/metastatic (R/M) HNSCC. Two-thirds of patients will be randomized to receive danvatirsen and pembrolizumab and one-third will be randomized to receive pembrolizumab alone.

An Open-Label, Phase II, Randomized, Controlled Study of Danvatirsen Plus Pembrolizumab Compared to Pembrolizumab Alone in Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC)

Activity and Safety of Danvatirsen and Pembrolizumab in HNSCC

Condition
HNSCC
Intervention / Treatment

-

Contacts and Locations

Tucson

The University of Arizona Cancer Center, Tucson, Arizona, United States, 85719

Irvine

University of California Irvine (UCI), Irvine, California, United States, 92617

Torrance

TMPN Hunt Cancer Care, Torrance, California, United States, 90505

Westwood

University of California Los Angeles, Westwood, California, United States, 90024

Aurora

University of Colorado Hospital (UCH) Anschutz Cancer Pavilion, Aurora, Colorado, United States, 80045

Miami

Miami Cancer Institute, Miami, Florida, United States, 33176

Chicago

University of Illinois Cancer Center, Chicago, Illinois, United States, 60612

Merriam

AMR Kansas City Oncology, Merriam, Kansas, United States, 66204

Westwood

University of Kansas Medical Center, Westwood, Kansas, United States, 66205

Baton Rouge

Mary Bird Perkins Cancer Center, Baton Rouge, Louisiana, United States, 70809

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Must have given written informed consent (signed and dated).
  • 2. Aged ≥18 years at the time of informed consent.
  • 3. Recurrent/metastatic histologically or cytologically proven squamous cell carcinoma of the head and neck that is considered incurable by local therapy. Eligible primary tumor locations are oropharynx, oral cavity, hypopharynx, and larynx.
  • 4. Presence of measurable tumor per RECIST v1.1 criteria.
  • 5. Detectable PD-L1 expression in tumor, defined as CPS ≥1 determined by a FDA or national regulatory agency of the country in which the patient resides.-approved test.
  • 6. Baseline fresh tumor biopsy or archival specimen.
  • 7. ECOG performance status of 0 or 1.
  • 8. Adequate organ function within 10 days of study treatment,
  • 9. Oxygen saturation on room air ≥92% by pulse oximetry.
  • 10. Females must be non-pregnant and non-lactating and either be postmenopausal or agree to adequate birth control.
  • 11. Males must be surgically sterile or agree to adequate birth control.
  • 12. Has an estimated life expectancy of at least 3 months.
  • 13. Has recovered from all complications or surgery and all toxicities of prior therapy
  • 1. Prior therapy for metastatic HNSCC.
  • 2. Has disease suitable for local therapy with curative intent.
  • 3. Primary tumor of the nasopharynx.
  • 4. Has received prior therapy with an anti-programmed death 1 (PD-1), anti PD L1, or anti-programmed death-ligand-2 (PD-L2).
  • 5. Radiation therapy (or other non-systemic therapy) within 2 weeks of Day 1 of study treatment.
  • 6. Known autoimmune disease that has required systemic treatment
  • 7. Known immunodeficiency or receiving systemic steroid therapy that would be the equivalent of \>10 mg prednisone daily
  • 8. Prior allogeneic tissue/solid organ transplant.
  • 9. Has significant cardiovascular disease
  • 10. Has received a live vaccine within 30 days
  • 11. Active infection requiring systemic antiviral or antimicrobial therapy
  • 12. History of (non-infectious) pneumonitis that required steroids or current pneumonitis.
  • 13. History of other malignancies
  • 14. Active HIV infection except patients who are currently stable on antiretroviral therapy for at least 4 weeks
  • 15. Active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.
  • 16. Treated or untreated parenchymal brain metastases or leptomeningeal disease.
  • 17. Treatment with another investigational drug, biological agent, or device within 1 month of screening, or 5 half-lives of investigational agent (if known), whichever is longer.
  • 18. Hypersensitivity to any component of danvatirsen or pembrolizumab.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Flamingo Therapeutics NV,

Study Record Dates

2026-05-30