Gemcitabine + Docetaxel + Toripalimab Induction in Epstein-Barr Virus (EBV) Associated Nasopharyngeal Carcinoma(NPC)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorStanford University

About this trial

The purpose of the research is to test the safety and efficacy of the investigational drug in human subjects with cancer.

Eligibility criteria

Qualifiers

Eligible disease(s) / stage(s): Locoregionally advanced EBV positive NPC (T3-4, any N OR any T, N1-3. No M1) per AJCC v 8

Prior therapy: None for NPC permitted

Life expectancy: 3 months at least

Contraception requirements: Women of childbearing potential and male participants who are sexually active must agree to use a medically effective means of birth control during treatment with toripalimab and for 4 months after the last dose.

Disqualifiers

Prior systemic anticancer treatment for NPC

Prior radiation to head and neck region or regions necessitating overlapping fields

Concurrent use of any anti- cancer treatment, standard, alternative or investigational.

History of allergic reactions to any agents in this study

Trial design

Treatments tested in this trial

  • Toripalimab
  • Concurrent Chemoradiation and Adjuvant treatment following Chemoradiation

Treatment groups

24 Participants
are divided into 1 treatment group

Sponsors and collaborators