Completed Lungs & Breathing Mental Health

MRC/ABPI COPD Consortium Work Package 1: COPD Phenotyping

In plain English

AI plain-English summary

COPD patients often respond very differently to the same drug, and many promising treatments fail in human trials because they were tested on the wrong group of people. This matters because the pharmaceutical industry has struggled to bring new COPD treatments to market. The core problem is that COPD—formerly called chronic bronchitis and emphysema—is not a single disease. Patients vary widely in how their lungs deteriorate and which symptoms dominate. Without knowing which patient subgroup a drug targets, clinical trials become a gamble. This project aims to identify biological markers in blood and sputum that distinguish these subgroups, linking specific disease patterns to specific drug responses. If successful, this work could change how clinical trials are designed. Instead of testing a drug on a broad, mixed group of COPD patients—where it may appear ineffective—researchers could recruit only those whose biomarker profile matches the drug’s mechanism. This would reduce the number of failed late-stage trials, speed up the approval of effective treatments, and give clinicians a practical tool for matching existing therapies to the patients most likely to benefit. The result would be fewer patients receiving drugs that do not work for them, and a more efficient pipeline for new COPD medicines.

View original technical description
COPD (which used to be called chronic bronchitis and emphysema) is a common disease which causes considerable difficulty to sufferers. The pharmaceutical industry has been relatively unsuccessful in bringing new treatments to the marketplace for COPD, with many products failing when they are first given to patients. This is largely because not all COPD sufferers are the same and it is likely that drugs will treat certain aspects of the disease and therefore are more likely to benefit some but not all patients. We propose to try to understand what makes people with COPD different from each other and to use these differences to further our understanding of which types of drugs will benefit which types of people. Using this approach we aim to identify markers in blood and sputum that will help us to predict the progression of COPD and response to therapy.

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Researchers

Anthony Brookes (Co-Investigator)Christopher Brightling (Principal Investigator)Dave Singh (Co-Investigator)Jadwiga Wedzicha (Co-Investigator)Jorgen Vestbo (Co-Investigator)Martin Tobin (Co-Investigator)Paul Burton (Co-Investigator)Robert Stockley (Co-Investigator)

Related Research

Grants with similar aims, by meaning.

Reducing the burden of COPD by targeting skeletal muscle mass and function. Targets and endpoints for drug development
The British Early COPD Network cohort (BEACON)
Molecular phenotyping of participants with severe asthma to determine response to biologic therapies and stability
Phenotyping of Chronic Obstructive Pulmonary Disease (COPD) and other destructive lung diseases
The British Early (Chronic Obstructive Pulmonary Disease) COPD Network cohort (BEACON)

Original classification

Research Grant

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