Advancing Precision in Respiratory Research

Experience Rapid Study Start-Up & Unmatched Endpoint Quality for Your Respiratory Program

Why Choose Worldwide for Your Respiratory Clinical Trial?

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Expedited Study Start-Up: Your Fast Lane to Breakthroughs

Leverage our ready-to-deploy respiratory team, pre-qualified sites, and existing infrastructure to reduce your study’s start-up period significantly. We can accelerate your first 60-90 days, moving faster than a typical cycle and providing a unique opportunity for rapid deployment of your upcoming respiratory studies.

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Deep Therapeutic Expertise Across Complex Indications

Our dedicated respiratory team brings extensive experience across a broad spectrum of conditions, ready to tackle both established and emerging indications:

  • Interstitial Lung Disease (ILD)
  • Idiopathic Pulmonary Fibrosis (IPF)
  • Asthma
  • Eosinophilic Asthma
  • Cystic Fibrosis
  • COPD-Adjacent Endpoints
  • Bronchiectasis
  • Cough
  • Additional Emerging Respiratory Areas
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Patient-Centric Approach & Sponsor Satisfaction

We conduct qualitative interviews with patients and caregivers to gain a deep understanding of their motivations and needs, ensuring that we design our trials with the patient experience as a top priority. Our sponsors consistently report high satisfaction with our responsiveness, attention to detail, and the overall quality of our respiratory delivery teams.

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Industry-Leading Endpoint Quality & Data Reliability

Our commitment to exceptional data quality sets us apart, and we understand the nuances of pulmonary function testing. We ensure superior pulmonary function data through:

Rigorous Training 

  • Our CRAs and medical experts provide purpose-built training to sites, ensuring accurate and reproducible respiratory endpoints, even in non-specialized settings.

Guideline Adherence

  • Our spirometry execution consistently meets and exceeds industry benchmarks, with a 94% acceptable rate compared with the 91% industry average, aligned with and exceeding ATS/ERS 2019 standards.

Strategic Partnership with Clario 

  • Our integrated partnership enhances equipment quality, data review, and ongoing site proficiency, strengthening endpoint reliability.

Proactive Monitoring

  • We meticulously monitor data for outliers, ensuring the integrity and quality of every endpoint.
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Global Reach with Proven Site Networks

Benefit from our established network of over 100 high-performing sites across North America, Latin America, Europe, and Asia-Pacific. These relationships deliver robust patient recruitment and consistently high-quality data, ensuring the global success of your study.

Meet our team and learn how our approach can transform your Respiratory trial.

Drew Matheson

Franchise Area Lead, Respiratory Medicine

Drew Matheson is Worldwide’s Franchise Area Lead for Respiratory Medicine and has over 25 years experience in clinical trials. He is responsible for the strategy and oversight of our respiratory portfolio and is passionate about bringing new therapies to patients.

Our methodology and delivery puts our partners first in each and every program. We tailor this approach to match the unique medical, scientific, and regulatory needs of everyone we work with.