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Pembrolizumab Combined With Preoperative Chemotherapy (Albumin Paclitaxel+Carboplatin) Neoadjuvant Therapy for Resectable Locally Advanced (Stage II/III) Esophageal Squamous Cell Carcinoma - Trial NCT06304350

Access comprehensive clinical trial information for NCT06304350 through Pure Global AI's free database. This Phase 2 trial is sponsored by Tongji University and is currently Recruiting. The study focuses on Esophageal Cancer. Target enrollment is 25 participants.

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NCT06304350
Phase 2
Recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06304350
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Pembrolizumab Combined With Preoperative Chemotherapy (Albumin Paclitaxel+Carboplatin) Neoadjuvant Therapy for Resectable Locally Advanced (Stage II/III) Esophageal Squamous Cell Carcinoma
A Single Arm, Single Center, Phase II Clinical Study of Pembrolizumab Combined With Preoperative Chemotherapy (Albumin Paclitaxel+Carboplatin) Neoadjuvant Therapy for Resectable Locally Advanced (Stage II/III) Esophageal Squamous Cell Carcinoma

Study Focus

Esophageal Cancer

Combination of pembrolizumab and platinum containing dual drugs

Interventional

drug

Sponsor & Location

Tongji University

Shanghai, China

Timeline & Enrollment

Phase 2

Feb 17, 2024

Dec 31, 2026

25 participants

Primary Outcome

Pathological complete remission (pCR)

Summary

This study is a prospective, single center, open label, single arm clinical study. Select
 resectable locally advanced (cT3-4aN0M0, cT1-3N1-2M0, cII/III stage) esophageal cancer with
 pathological diagnosis of squamous cell carcinoma for inclusion, receive pembrolizumab
 combined with platinum containing dual drug (albumin paclitaxel+carboplatin) treatment for 2
 courses, and undergo surgery. After surgery, continue pembrolizumab immunotherapy. Using pCR
 as the main endpoint of the study

ICD-10 Classifications

Carcinoma in situ: Oesophagus
Malignant neoplasm of oesophagus
Malignant neoplasm: Middle third of oesophagus
Malignant neoplasm: Overlapping lesion of oesophagus
Malignant neoplasm: Upper third of oesophagus

Data Source

ClinicalTrials.gov

NCT06304350

Non-Device Trial