A Study to Investigate the Effect of AZD6793 in Participants With Moderate to Very Severe Chronic Obstructive Pulmonary Disease (NCT07082738)
A Multicentre, Parallel-group, Phase IIb, Randomised, Double-blind, Placebo-controlled, 3-Arm, 24-Week Study to Evaluate the Efficacy and Safety of AZD6793 Tablets in Adult Participants With Moderate to Very Severe Chronic Obstructive Pulmonary Disease (PRESTO)
🩺 Plain-English Summary (8th-Grade Level)
This Phase IIb dose-ranging study will evaluate the efficacy and safety of 2 different doses of AZD6793 compared with placebo tablets in participants with moderate to very severe chronic obstructive pulmonary disease.
Who can join: Review the eligibility criteria below.
Location: Research Site — Birmingham, Alabama
Age range: 40 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (368 Sites)
Showing the first 25 of 368 sites.
- Research Site — Birmingham, Alabama
- Research Site — Glendale, Arizona
- Research Site — Phoenix, Arizona
- Research Site — Phoenix, Arizona
- Research Site — Phoenix, Arizona
- Research Site — Canoga Park, California
- Research Site — La Mesa, California
- Research Site — Los Angeles, California
- Research Site — Newport Beach, California
- Research Site — Norco, California
- Research Site — Tustin, California
- Research Site — Lakewood, Colorado
- Research Site — Brandon, Florida
- Research Site — Cape Coral, Florida
- Research Site — Clearwater, Florida
- Research Site — Clearwater, Florida
- Research Site — Jacksonville, Florida
- Research Site — Lake City, Florida
- Research Site — Miami, Florida
- Research Site — Miami, Florida
- Research Site — Miami, Florida
- Research Site — Miami, Florida
- Research Site — Miami, Florida
- Research Site — Miami Lakes, Florida
- Research Site — Naples, Florida
📞 Contact the Study Coordinator
Phone: (877) 240-9479
Email: information.center@astrazeneca.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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Explore by condition: All Chronic Obstructive Pulmonary Disease (COPD) clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.