Becotatug Vedotin (MRG003) With PD-1 Blockade and Chemoradiotherapy in High-Risk Locoregionally Advanced Nasopharyngeal Carcinoma

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorSun Yat-sen University

About this trial

This randomized controlled trial aims to evaluate the efficacy and safety of Becotatug Vedotin (MRG003), an antibody-drug conjugate (ADC), combined with the PD-1 inhibitor Pucotenlimab as induction therapy for high-risk locoregionally advanced nasopharyngeal carcinoma (NPC), compared to the standard gemcitabine and cisplatin (GP) regimen combined with Pucotenlimab, followed by concurrent chemoradiotherapy (CCRT) and adjuvant immunotherapy.

Eligibility criteria

Qualifiers

1. Age ≥ 18 years at the time of diagnosis, regardless of sex

Disqualifiers

1. History of any other malignancy within the past 5 years, with the exception of curatively treated cervical carcinoma in situ, papillary thyroid carcinoma, or basal cell carcinoma of the skin

Trial design

Treatments tested in this trial

  • Becotatug Vedotin
  • Pucotenlimab
  • Gemcitabine + cisplatin (GP)
  • intensity-modulated radiotherapy
  • Cisplatin

Treatment groups

514 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators