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NCT06218004

Envafolimab Combined With Chemotherapy in Neoadjuvant and Conversion Therapy for Head and Neck Squamous Cell Carcinoma

Status unknown Phase 2 Last updated 23 January 2024
What this trial tests

Phase 2 trial testing Envafolimab combined with chemotherapy in Efficacy and Safety in 40 participants. Status unknown.

Timeline
25 January 2024
Primary endpoint
31 December 2025
31 December 2025

Quick facts

Lead sponsorHairong Liu
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment40
Start date25 January 2024
Primary completion31 December 2025
Estimated completion31 December 2025

Drugs / interventions tested

Conditions studied

Sponsor

Hairong Liu — full company profile →

Who can join

Adults 18 to 80, any sex, with Efficacy and Safety. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a prospective clinical study. The purpose is to explore the efficacy and safety of Envafolimab combined with chemotherapy for neoadjuvant treatment or conversion treatment of locally advanced head and neck squamous cell carcinoma, and to observe the correlation between the immune microenvironment and the efficacy of immune checkpoint inhibitors, genetic changes and the efficacy in head and neck squamous cell carcinoma .

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Efficacy and Safety

Currently open trials in the same condition.

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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/NCT06218004.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing