RecruitingPhase 2NCT07690787

JS207 a Bispecific Antibody Against PD1-VEGF in Nasopharyngeal Carcinoma

Phase I-II Study of JS207 a Bispecific Antibody Against PD1-VEGF in the Treatment of Recurrent/Metastatic Nasopharyngeal Carcinoma


Sponsor

Chinese University of Hong Kong

Enrollment

49 participants

Start Date

Jun 29, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study is to determine the activity and tolerability of JS207 as a single agent and in combination cohort with chemotherapy. This is an open-labelled, phase Ib/II study of JS207 in patients with previously treated recurrent or metastatic nasopharyngeal carcinoma. The study will comprise of two phases: * Phase 1b monotherapy: Consisting of a dose escalation and then expansion phase in patients with recurrent/ metastatic (R/M) NPC, who have failed at least 1 prior line of platinum-based chemotherapy, with or without prior treatment with PD1/ PDL1 inhibitor. * Randomized phase II: Combination of JS207 with capecitabine or paclitaxel in platinum-refractory patients: Patients who have failed one prior line of platinum-based chemotherapy for R/M NPC will be treated with JS207 in combination with capecitabine. As phase I portion of the study was completed, the starting dose of JS207 for phase II portion will be 10mg/kg IV every 3 weeks.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called JS207 + capecitabine and a drug called JS207 + paclitaxel for people with recurrent/ metastatic npc. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGJS207

10mg/kg IV every 3 weeks

DRUGPaclitaxel

135 mg/m² b.d. IV at 3-weekly cycle until disease progression or intolerance

DRUGCapecitabine

1000 mg/m² b.d. orally from days 1 to 14 at 3-weekly cycle until disease progression or intolerance


Locations(1)

Department of Clinical Oncology, Prince of Wales Hospital

Hong Kong, Hong Kong

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07690787