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A Study of Toripalimab in Combination With Cisplatin and Gemcitabine in Participants With Recurrent Metastatic Nasopharyngeal Cancer
RECRUITINGPhase 4Sponsored by Coherus Oncology, Inc.
Actively Recruiting
PhasePhase 4
SponsorCoherus Oncology, Inc.
Started2024-11-01
Est. completion2027-12
Eligibility
Age12 Years+
Healthy vol.Accepted
Locations12 sites
View on ClinicalTrials.gov →
NCT06457503
Summary
This study aims to investigate toripalimab with chemotherapy in participants with nasopharyngeal cancer.
Eligibility
Age: 12 Years+Healthy volunteers accepted
Key Inclusion Criteria: * 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.
Conditions2
CancerNasopharyngeal Cancer Recurrent
Interventions4
Locations12 sites
University of Arkansas for Medical Sciences
Little Rock, Arkansas, 72205
Constance Brownbrownconstance@uams.edu
University of California, San Francisco
Luchia AndemicaelLuchia.Andemicael@ucsf.edu
Emory Winship Cancer Institute
Madison Stallingsmadison.miller.stallings@emory.edu
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
PhasePhase 4
SponsorCoherus Oncology, Inc.
Started2024-11-01
Est. completion2027-12
Eligibility
Age12 Years+
Healthy vol.Accepted
Locations12 sites
View on ClinicalTrials.gov →
NCT06457503