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Taking people in FrancePhase 1

Tests JNJ-90301900 with chemoradiation for advanced head and neck cancer

Tests an injected drug with chemotherapy and radiation in adults with head and neck cancer.

Plain-language title generated from the registry record
Registry title: A Study of JNJ-90301900 in Combination With Chemoradiation Therapy in Participants With Locally Advanced Head and Neck Squamous Cell Carcinoma

Key facts

Where
Brest, Grenoble Cedex 9, Lille, Marseille, Rouen Cedex, and Villejuif, FranceSee the 6 sites
Phase
Phase 1

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 74 years old?

Source: NCT07219212, who can take part

Where in France

  • Centre Hospitalier Régional et Universitaire de BrestBrest, FranceTaking people
  • Centre Hospitalier Universitaire Grenoble AlpesGrenoble Cedex 9, FranceTaking people
  • Centre Oscar LambretLille, FranceTaking people
  • Centre Hospitalier Regional De MarseilleMarseille, FranceTaking people
  • Centre Henri BecquerelRouen Cedex, FranceTaking people
  • Institut Gustave RoussyVillejuif, FranceTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Johnson & Johnson Enterprise Innovation Inc.
Trial code
NCT07219212EU 2025-522914-22-00
Record updated
3 November 2026
Original description
This global, open-label, single arm, phase 1b study aims to learn more about whether a treatment called JNJ-90301900 is safe and effective when injected directly into tumors, along with standard chemotherapy and radiation therapy, for participants with head and neck squamous cell cancer (HNSCC; a type of solid tumor that begins in outer tissue layer of the mouth \& throat).Read full original descriptionShow less

A Study of JNJ-90301900 in Combination With Concurrent Chemoradiation Therapy in Participants With Locally Advanced Head and Neck Squamous Cell Carcinoma

This global, open-label, single arm, phase 1b study aims to learn more about whether a treatment called JNJ-90301900 is safe and effective when injected directly into tumors, along with standard chemotherapy and radiation therapy, for participants with head and neck squamous cell cancer (HNSCC; a type of solid tumor that begins in outer tissue layer of the mouth \& throat).

Inclusion: Pathologically (histologically or cytologically) proven diagnosis of HNSCC of the oral cavity, oropharynx (p16 negative), hypopharynx, or supraglottic larynx; Stage III, IVA or IVB according to the 8th Edition of the American Joint Committee on Cancer (AJCC) guidelines; A candidate for definitive concurrent chemoradiation therapy treatment as determined by investigator and per local guidelines; Participants must have at least 1 target lesion (primary tumor or involved lymph node) per RECIST v.1.1; Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0 or 1.

Exclusion: Ineligible to receive platinum-based chemotherapy; Suspected or known allergies, hypersensitivity, or intolerance to JNJ-90301900 or its excipients; Primary tumor originating in the nasopharynx, paranasal sinuses, salivary glands, thyroid gland, parathyroid gland, skin, or unknown primary site; Non-squamous histology; Stages 0, I, II, and IVC HNSCC, loco-regionally recurrent HNSCC, or synchronous second primary HNSCC (within 2 months).

ClinicalTrials.gov NCT07219212 · EU CTIS 2025-522914-22-00