A Phase 3 Study to Evaluate Petosemtamab Compared with Investigator's Choice Monotherapy in Previously Treated Head and Neck Squamous Cell Carcinoma Patients

Description

This is a phase 3 open-label, randomized, controlled, multicenter study to compare petosemtamab vs investigator's choice monotherapy in HNSCC patients for the second- and third-line treatment of incurable metastatic/recurrent disease.

Conditions

Head and Neck Squamous Cell Carcinoma

Study Overview

Study Details

Study overview

This is a phase 3 open-label, randomized, controlled, multicenter study to compare petosemtamab vs investigator's choice monotherapy in HNSCC patients for the second- and third-line treatment of incurable metastatic/recurrent disease.

A Phase 3 Open-label, Randomized Controlled Study to Evaluate the Efficacy and Safety of Petosemtamab Compared with Investigator's Choice Monotherapy Treatment in Previously Treated Patients with Incurable, Metastatic/recurrent Head and Neck Squamous Cell Carcinoma

A Phase 3 Study to Evaluate Petosemtamab Compared with Investigator's Choice Monotherapy in Previously Treated Head and Neck Squamous Cell Carcinoma Patients

Condition
Head and Neck Squamous Cell Carcinoma
Intervention / Treatment

-

Contacts and Locations

La Jolla

Site 25, La Jolla, California, United States, 92093

Palo Alto

Site 28, Palo Alto, California, United States, 94304

Bradenton

Site 12, Bradenton, Florida, United States, 34205

Orlando

Site 9, Orlando, Florida, United States, 32827

Indianapolis

Site 31, Indianapolis, Indiana, United States, 46202

Louisville

Site 8, Louisville, Kentucky, United States, 40202

Detroit

Site 5, Detroit, Michigan, United States, 48201

Saint Louis

Site 18, Saint Louis, Missouri, United States, 63110

Albuquerque

Site 15, Albuquerque, New Mexico, United States, 87131

New York

Site 24, New York, New York, United States, 10029

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

  • * Signed ICF before initiation of any study procedures.
  • * Age ≥ 18 years at signing of ICF.
  • * Histologically previously confirmed HNSCC with evidence of metastatic or locally advanced disease not amenable to standard therapy with curative intent.
  • * HNSCC patients progressed on or after anti-PD-1 therapy and platinum-containing therapy.
  • * The eligible HNSCC primary tumor locations are oropharynx, oral cavity, hypopharynx, and larynx.
  • * Documentation of p16 status (positive or negative) by local laboratory IHC for patients with primary oropharyngeal cancer.
  • * A baseline new tumor sample unless the patient has an available tumor sample as an FFPE block with sufficient material.
  • * Measurable disease as defined by RECIST v1.1 by radiologic methods.
  • * ECOG PS of 0 or 1
  • * Life expectancy ≥ 12 weeks, as per investigator
  • * Adequate organ function (as per protocol)
  • * Central nervous system metastases that are untreated or symptomatic, or require radiation, surgery, or continued steroid therapy to control symptoms within 14 days of study entry.
  • * Known leptomeningeal involvement
  • * Any systemic anticancer therapy within 4 weeks of the first dose of study treatment.
  • * Major surgery or radiotherapy within 3 weeks of the first dose of study treatment.
  • * Persistent Grade \>1 clinically significant toxicities related to prior antineoplastic therapies
  • * History of hypersensitivity reaction to any of the excipients of treatment required for this study.
  • * Unstable angina; history of congestive heart failure of Class II-IV New York Heart Association (NYHA) criteria, or serious cardiac arrhythmia requiring treatment or history of myocardial infarction within 6 months of study entry
  • * History of prior malignancies with the exception of excised cervical intraepithelial neoplasia or nonmelanoma skin cancer, or curatively treated cancer deemed at low risk for recurrence with no evidence of disease
  • * Current dyspnea at rest of any origin, or other diseases requiring continuous oxygen therapy
  • * Current serious illness or medical conditions including, but not limited to, uncontrolled active infection, clinically significant pulmonary, metabolic or psychiatric disorders
  • * Patients with known infectious diseases (as per protocol)
  • * Pregnant or breastfeeding patients
  • * Patient has a primary tumor site of nasopharynx (any histology).

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Merus N.V.,

Study Record Dates

2029-03