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Evaluation of 611 in Chinese Adults With Moderate to Severe Chronic Obstructive Pulmonary Disease - Trial NCT06099652

Access comprehensive clinical trial information for NCT06099652 through Pure Global AI's free database. This Phase 2 trial is sponsored by Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd. and is currently Not yet recruiting. The study focuses on Pulmonary Disease, Chronic Obstructive. Target enrollment is 150 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.

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NCT06099652
Phase 2
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06099652
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Evaluation of 611 in Chinese Adults With Moderate to Severe Chronic Obstructive Pulmonary Disease
A Multi-Centered, Randomized, Double-Blinded, Placebo-Controlled Phase II Clinical Trial, to Evaluate the Efficacy and Safety of 611 in Chinese Adults With Moderate to Severe Chronic Obstructive Pulmonary Disease.

Study Focus

611 300 mg Q2W

Interventional

drug

Sponsor & Location

Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.

Beijing,Shenzhen,Shanghai, China

Timeline & Enrollment

Phase 2

Nov 01, 2023

May 01, 2025

150 participants

Primary Outcome

Change from baseline in pre-bronchodilator FEV1 at Week 16

Summary

The primary objective of the study was to evaluate the efficacy and safety of 611 in Chinese
 adults with moderate to severe COPD.

ICD-10 Classifications

Chronic obstructive pulmonary disease, unspecified
Other chronic obstructive pulmonary disease
Other specified chronic obstructive pulmonary disease
Chronic obstructive pulmonary disease with acute exacerbation, unspecified
Chronic obstructive pulmonary disease with acute lower respiratory infection

Data Source

ClinicalTrials.gov

NCT06099652

Non-Device Trial