Pure Global

Oral Inulin in Combination With Fruquintinib Plus Sintilimab as Third- or Further-line Treatment in Metastatic Colorectal Cancer - Trial NCT06347198

Access comprehensive clinical trial information for NCT06347198 through Pure Global AI's free database. This Phase 1 trial is sponsored by Wuhan Union Hospital, China and is currently Recruiting. The study focuses on Metastatic Colorectal Cancer. Target enrollment is 30 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

Free Database
Powered by Pure Global AI
840K+ Trials
NCT06347198
Phase 1
Recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06347198
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Oral Inulin in Combination With Fruquintinib Plus Sintilimab as Third- or Further-line Treatment in Metastatic Colorectal Cancer
A Single-center Exploratory Clinical Study of Oral Inulin in Combination With Fruquintinib Plus Sintilimab as Third- or Further-line Treatment in Metastatic Colorectal Cancer

Study Focus

Fruquintinib

Interventional

drug

Sponsor & Location

Wuhan Union Hospital, China

Wuhan, China

Timeline & Enrollment

Phase 1

Apr 10, 2024

May 01, 2025

30 participants

Primary Outcome

Intestinal microbiota diversity, abundance and taxonomic information,adverse events

Summary

This is a single-center exploratory clinical study to explore the efficacy and safety of Oral
 Inulin in Combination With Fruquintinib Plus Sintilimab as Third- or Further-line Treatment
 in Metastatic Colorectal Cancer.

ICD-10 Classifications

Malignant neoplasm of colon
Malignant neoplasm: Colon, unspecified
Malignant neoplasm: Descending colon
Malignant neoplasm: Ascending colon
Malignant neoplasm: Overlapping lesion of colon

Data Source

ClinicalTrials.gov

NCT06347198

Non-Device Trial