News
First-ever patient focused drug development meeting for chronic cough will be held in October 2026.
Washington D.C., June 18, 2026 — For the first time, a coalition of patient advocacy organizations is uniting to bring the voice of the chronic cough community directly to the U.S. Food and Drug Administration (FDA). The Asthma and Allergy Foundation of America, COPD Foundation, Global Allergy & Airways Patient Platform, and Pulmonary Fibrosis Foundation announce Let’s Talk Cough, a joint effort to document and elevate the lived experience of chronic cough. This initiative aims to capture the full impact of chronic cough across many conditions, current management strategies, unmet medical needs, and treatment outcomes that matter most patients—with the goal of informing the development of new therapies.
On October 28, 2026, Let’s Talk Cough will culminate in a hybrid, externally-led patient-focused drug development (EL-PFDD) meeting, conducted in parallel with the FDA’s PFDD initiative. The meeting will be streamed live, bringing members of the global chronic cough community together to share their experiences and perspectives. A “Voice of the Patient” report will summarize insights gathered during the Let’s Talk Cough meeting and throughout the planning process, creating a resource for researchers, drug makers, regulators, healthcare professionals, and the broader chronic cough community.
Initial discussions about the initiative generated enthusiasm and validated the need for this initiative. “The burden of chronic cough is debilitating. It’s a community that has been systematically dismissed, and Let’s Talk Cough is much needed to elevate the experiences of a community with great unmet needs,” stated Tonya Winders, President of the Global Allergy & Airways Patient Platform.
Chronic cough—defined as a daily or intermittent cough lasting 8 weeks or longer in adults or 4 weeks or longer in children—is commonly associated with chronic lung conditions like asthma, chronic obstructive pulmonary disease (COPD), bronchiectasis, and pulmonary fibrosis. Let’s Talk Cough is designed to capture that shared experience while honoring the distinct perspectives of each community represented.
“Chronic cough is more than a symptom. It can take a significant toll on quality of life for patients living with a range of lung and respiratory conditions,” said Dr. Amy Hajari Case, Chief Medical Officer of the Pulmonary Fibrosis Foundation. “Let’s Talk Cough gives patients a platform to share the daily burden of living with a persistent cough for which effective treatment options remain inadequate.”
Visit letstalkcough.org and complete the sign-up form to receive timely updates about the meeting on October 28, 2026, and other opportunities to participate and spread the word.
Let’s Talk Cough is made possible by support from GSK and Trevi Therapeutics. Sponsor support is independent of all programmatic, scientific, and editorial decisions, which remain solely with the host organizations.
Press Contact:
Andy Spears
Public Affairs Manager
Asthma and Allergy Foundation of America (AAFA)
gro.afaa@aidem
The Patient-Focused Drug Development (PFDD) initiative, initiated by the U.S. FDA in 2013, has been instrumental in providing a comprehensive understanding of the lived experience of more than 150 medical conditions to date. As an externally-led PFDD meeting, the October 28, 2026 Let’s Talk Cough meeting provides a unique opportunity for patients with chronic cough to express their experiences, needs, and priorities directly to FDA staff, researchers, and developers of medical therapies.
Asthma and Allergy Foundation of America (AAFA)
Founded in 1953, AAFA is the oldest and largest non-profit patient organization dedicated to saving lives and improving the quality of life for people affected by asthma and allergic diseases through support, advocacy, education, and research. AAFA offers extensive support for individuals and families affected by asthma and allergic diseases. AAFA is the first asthma and allergy patient advocacy group certified to meet the standards of excellence set by the National Health Council. For more information, visit: aafa.org.
COPD Foundation
The COPD Foundation is a nonprofit organization whose mission is to help millions of people live longer and healthier lives by advancing research, advocacy, and awareness to stop COPD, bronchiectasis, and NTM lung disease. The Foundation does this through scientific research, education, advocacy, and awareness to prevent disease, slow progression, and find a cure. For more information, visit copdfoundation.org.
Global Allergy & Airways Patient Platform (GAAPP)
Global Allergy & Airways Patient Platform (GAAPP) is a not-for-profit organization whose mission is to globally support and empower patients with allergies, airways and atopic diseases by protecting their rights and insisting on the duties of governments, healthcare professionals and the general public. With more than 200 organizations throughout 80 countries, GAAPP works to create a world where people live & breathe better. For more information, visit www.gaapp.org.
Pulmonary Fibrosis Foundation (PFF)
The Pulmonary Fibrosis Foundation (PFF) is a 501(c)(3) nonprofit organization committed to accelerating research, empowering the pulmonary fibrosis and interstitial lung disease community, and transforming care so that everyone with pulmonary fibrosis can live a better life. Its ultimate goal is to find a cure for pulmonary fibrosis. For more information, visit https://www.pulmonaryfibrosis.org/.













