Study of AZD6793 tablets to reduce flare-ups in adults with moderate to very severe chronic obstructive pulmonary disease (COPD)
- Participants:Adults
Rare diseases
Investigational molecules
Locations
AZD6793 is an investigational substance, meaning it has not yet received a marketing authorisation and is not available as a prescribed medicine. It is a chemically synthesised substance, classified as a small-molecule chemical compound. The product records in the EU Clinical Trials Information System (CTIS) list AstraZeneca AB as the authorisation holder and supplier of the product.[1] The substance appears under the name AZD6793, which is both its development code and the name used in the trial records; no trade name or other name is given in the registry data.[1] In the therapeutic area classification, AZD6793 sits within respiratory tract diseases, reflecting the condition it is being studied for.[1]
The registry data provided for this page do not state the mechanism of action of AZD6793, such as the molecular target it binds to or the biological pathway it affects. What is known from the trial record is that the substance is being tested for its effect on the rate of moderate or severe COPD exacerbations, which are episodes where breathing symptoms suddenly worsen.[1] The specific way in which AZD6793 might influence these exacerbations is not described in the sources available here.
AZD6793 is given as a film-coated tablet for oral use, meaning it is swallowed.[1] The trial record lists two AZD6793 arms and one placebo arm, all oral; the dose in milligrams is not reported in the register and is therefore not stated here.[1] The placebo is a tablet that looks the same but contains no active substance, used as a comparison.
One clinical trial of AZD6793 is present in the data, registered in the EU Clinical Trials Information System under the identifier 2025-520473-40-00.[1] It is a Phase 2, interventional study with a planned enrolment of 970 participants, and its status is authorised, meaning it has received the approvals needed to proceed.[1] The trial compares AZD6793 with placebo in adults with moderate to very severe COPD. The primary outcome is the annualised rate of moderate or severe COPD exacerbations, which counts how many flare-ups of the disease a person has per year on average.[1] The trial does not report a dose in milligrams, and no results are yet available in the registry record.
The sources provided for this page do not include information on side effects of AZD6793. No adverse event data are available from the trial record or from supplementary sources.
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