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NCT06811844

Two-cycle and Three-cycle Induction Therapy With Modified TPF Regimen Combined and Camrelizumab for LANPC

Recruiting now Phase 2 Last updated 1 July 2025
What this trial tests

Phase 2 trial testing Two-cycle induction chemotherapy + immunotherapy in Nasopharyngeal Neoplasms in 208 participants. Currently enrolling.

Timeline
25 February 2025
Primary endpoint
31 December 2027
31 December 2029

Quick facts

Lead sponsorThe First Affiliated Hospital of Xiamen University
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment208
Start date25 February 2025
Primary completion31 December 2027
Estimated completion31 December 2029
Sites3 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

The First Affiliated Hospital of Xiamen University

Who can join

Adults 18 to 65, any sex, with Nasopharyngeal Neoplasms or PD-1 Inhibitor. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This prospective, phase II, multicenter, randomized controlled study aims to compare the complete response rate and long-term survival outcomes of two-cycle and three-cycle induction therapy with modified TPF regimens combined with camrelizumab in patients with locally advanced nasopharyngeal carcinoma.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Divergent immuno-landscapes: comparing the tumor microenvironment of Indian and Western HNSCC patients.
    Kumar Rai P, Choudhary B. · · 2026 · PMID 42111272 · DOI 10.3389/fcell.2026.1725978

Verify or expand the search:

Other recruiting trials for Nasopharyngeal Neoplasms

Currently open trials in the same condition.

Other The First Affiliated Hospital of Xiamen University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06811844.

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