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TRANSPARENT: Single-Arm Study of Toripalimab in Combination with Cisplatin and Gemcitabine in Recurrent Metastatic Nasopharyngeal Carcinoma Systemic Treatment Naïve Participants


Primary Investigator
Swiecicki, Paul
Status
OPEN TO ACCRUAL
Phase
IV
NCT Number
NCT06457503
UM Number
2025.037
Age Group
Adults
Management Group
CTSU - Oncology
Oncology Group
Head, Neck, and Endocrine Malignancies
ID (Protocol)
55178
Secondary Protocol No
HUM00269940
Scope
Unspecified
Sponsor Type
Industry

Disease Site
Lip, Oral Cavity and Pharynx

Summary
This study aims to investigate toripalimab with chemotherapy in participants with nasopharyngeal cancer.

Eligibility: Inclusion Criteria
  •   Key
  •   * Histological or cytological confirmation of recurrent/metastatic nasopharyngeal cancer with either EBV or non-EBV-associated cancer. The following subgroups are included:
    •   * EBER/EBV-negative (HPV+/-)
    •   * EBER/EBV-positive (HPV+/-)
  •   * Recurrent/metastatic (stage IV-B as defined by the International Union against Cancer [UICC] and American Joint Committee on Cancer [AJCC] staging system for nasopharyngeal cancer [NPC], eighth edition) or recurrent NPC after curative treatment. For recurrent NPC, more than 6 months between the last dose of radiotherapy or chemotherapy and the date of recurrence.
  •   * Measurable disease based on RECIST v 1.1 as determined by the site. Note: Lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions.
  •   Key
Exclusion Criteria
  •   * Disease that is suitable for local therapy administered with curative intent.
  •   * Prior systemic therapy administered in the recurrent or metastatic setting. Participants who develop disease recurrence within 6 months from curative intent chemoradiation will be excluded.
  •   * Rapidly progressing disease (e.g., tumor bleeding, uncontrolled tumor pain) in the opinion of the treating investigator.
  •   * Active or untreated central nervous system (CNS) metastases (e.g., brain or leptomeningeal), as determined on computerized tomography (CT) or magnetic resonance imaging (MRI) evaluation during screening and prior radiographic assessments. Participants who have prior therapies for brain or leptomeningeal metastasis and have been stabilized >= 1 month and have discontinued systemic steroid therapy (>10 mg/day prednisone or equivalent) >= 1 month prior to enrollment are eligible.
  •   Other protocol-defined inclusion and exclusion criteria apply.