- Home
- Therapeutics
- Internal Medicine & Immunology
- Respiratory
Respiratory
Expertise to navigate the complexities of respiratory research, providing effective solutions across every facet of respiratory drug development
Research into respiratory disease continues to have a high profile due to unmet needs and the large patient populations.
The increased prevalence of allergy and respiratory illnesses in the past 20 years has resulted in a corresponding surge in clinical research. ICON has participated in the development of allergy and respiratory drugs on the market today, and several inhalers for respiratory products. Our services include clinical, operational, and consulting support, from pre-clinical stage through post-registration.
ICON respiratory experience in the last five years
-
123
Studies conducted -
24,000+
Patients involved -
3,500
Sites worldwide
To address the complexity of respiratory research, ICON uses a multi-disciplinary approach. We bring together experts in infectious disease, paediatrics, rare disease, device development, innovation technology, translational, regulatory, and real world evidence, for a comprehensive approach to asset development.
Expertise in a wide range of indications
- Allergic and non-allergic rhinitis
- Asthma
- COPD
- a1-Anti trypsin deficiency
- Respiratory infections
- Cystic fibrosis
- Pulmonary fibrosis
- Pulmonary hypertension
- ARDS/SEPSIS and critically ill (ICU trials)
Incorporating respiratory testing methods
- Sleep disorders
- Biomarkers
- Functional tests
- Imaging
- Nuclear medicine
- Self-assessed scores and patient reported outcome (PRO) questionnaires
- Wearables
- Polysomnography
- Ventilators
- Oxygen therapy
Increasing patient centricity in clinical research
Increasing patient centricity in clinical research is bringing benefits to both patients and sponsors. From our experience in conducting trials during pandemics and in rare disease indications, we know that it is essential to reduce patient burden. Working with the sponsor, patients, and providers, ICON can help to understand how the disease may be affecting a patient’s life and apply innovative solutions that both support patients and improve study compliance.
Accellacare
Accellacare is ICON's a global clinical research network, offering stand-alone and integrated solutions, including patient assessments at sites and in-home as part of decentralised trials.
Accellacare has strong asthma, COPD, smoking cessation, and allergy experience in particular, and provides a range of services for both ICON and sponsor-direct studies:
- Board certified internal medicine physicians, family physicians, and pulmonologists
- Breathing, lung function, and related testing
- Clinical outcomes assessments (Exact, CAT, St. Georges Questionnaires, and others)
- End point collection
- Experience with devices and wearables and expertise in the use of inhalers, steroids, vaccinations and smoking cessation methodologies
In this section
-
Biosimilars
-
Cardiovascular
- Cell and Gene Therapies
- Central Nervous System
- Endocrine & Metabolic Disorders
- Infectious Diseases
- Internal Medicine & Immunology
-
Medical Device
- Oncology
-
Paediatrics
- Rare & Orphan Diseases
- Vaccines
-
Women's Health
-
Therapeutics insights
- Cardiovascular
- Cell and Gene Therapies
- Central Nervous System
-
Glycomics
- Infectious Diseases
- NASH
-
Women's Health Insights
-
Oncology
- Paediatrics
-
Rare and orphan diseases
-
Pushing boundaries in idiopathic pulmonary fibrosis clinical research
-
Advanced therapies for rare diseases
-
Cross-border enrollment of rare disease patients
-
Crossing the finish line: Why effective participation support strategy is critical to trial efficiency and success in rare diseases
-
Diversity, equity and inclusion in rare disease clinical trials
-
Identify and mitigate risks to rare disease clinical programmes
-
Leveraging historical data for use in rare disease trials
-
Natural history studies to improve drug development in rare diseases
-
Patient Centricity in Orphan Drug Development
-
The key to remarkable rare disease registries
-
Pushing boundaries in idiopathic pulmonary fibrosis clinical research