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NCT02274155CompletedPhase 1

Anti-OX40 Antibody in Head and Neck Cancer Patients

Phase Ib Study of a Monoclonal Antibody to OX40 (MEDI6469) Administered Prior to Definitive Surgical Resection Patients With Locoregionally Advanced, Oral Head and Neck Squamous Cell Carcinoma

Source: ClinicalTrials.gov · Last updated 7 Feb 2024

Brief summary (registry, in English)

The purpose of this study is to test the safety of the anti-OX40 antibody, MEDI6469, given prior to surgery in patients with advanced head and neck squamous cell carcinoma.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
17 (actual)
First submitted
14 Oct 2014
Start date
12 Nov 2014
Primary completion date
17 Sept 2017
Lead sponsor
Providence Health & Services
NCT number
NCT02274155

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 17
  • From 12 Nov 2014 to the primary completion date, 17 Sept 2017
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous treatment with mouse monoclonal antibodies
  • Need for chronic maintenance oral steroids \> 5mg prednisone daily equivalent.

Other illness

  • Locoregionally unresectable or Metastatic disease (stage IVB)
  • Active infection.
  • Active autoimmune disease including patients with Inflammatory Bowel Disease as determined by an autoimmune questionnaire.
  • Any medical or psychiatric condition that in the opinion of the investigator would preclude compliance with study procedures.

Who the study is looking for

  • Patients with treatment naive, resectable, stage III or IV squamous cell carcinoma of the oral cavity, oropharynx, hypopharynx or larynx who are candidates for definitive surgical resection followed by standard risk adapted adjuvant therapy.
  • Histologic or cytologic diagnosis of a primary OHNSCC with no radiological evidence of metastatic disease is acceptable. Patients with bone or cartilage invasion and any T or N stage are acceptable.
  • Patients with oral cavity primaries will be managed using conventional transoral or transcervical techniques; oropharynx or hypopharynx tumor will be managed with transoral robotic surgery; and larynx tumors (T3/T4 with thyroid cartilage invasion) will be managed by either total laryngectomy or larynx preservation surgery.
  • Eastern Cooperative Oncology Group (ECOG) performance status 0, 1, or 2
  • Laboratory values (performed within 28 days prior to enrollment) within protocol defined range
  • Ability to give informed consent and comply with the protocol. Patients with a history of psychiatric illness must be judged able to understand the investigational nature of the study and the risks associated with the therapy.
  • No active gastrointestinal bleeding.
  • Anticipated lifespan greater than 12 weeks.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Portland Providence Medical Center
Coordinator of this site? Confirm its status
PortlandUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.