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NCT05919069CompletedPhase 1

A Phase I Study to Investigate the Effect of Hepatic Impairment on the PK, Safety, and Tolerability of AZD2693

A Single Dose, Non-Randomised, Open-Label, Parallel Group Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety and Tolerability of AZD2693.

Source: ClinicalTrials.gov · Last updated 11 May 2026

Brief summary (registry, in English)

Subcutaneous administration of AZD2693 single dose in participants with hepatic impairment

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
35 (actual)
First submitted
16 Jun 2023
Start date
16 Jun 2023
Primary completion date
16 Sept 2024
Lead sponsor
AstraZeneca
NCT number
NCT05919069

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 35
  • From 16 Jun 2023 to the primary completion date, 16 Sept 2024
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of any major surgical procedure within 30 days prior to study intervention

Other illness

  • Positive test for HIV at screening
  • History or presence of clinically significant thyroid disease
  • History or presence of clinically significant or unstable medical or psychiatric condition

Lab values

  • Participant with impaired hepatic function has eGFR \< 60 mL/minute/1.73 m2 and participant with normal hepatic function has eGFR \< 90 mL/minute/1.73 m2

Who the study is looking for

  • For Hepatic:
  • Participant with a diagnosis of chronic and stable hepatic impairment
    • For Healthy:
  • Participant with no clinically significant medical history, physical examination, laboratory profiles, vital signs, or 12-lead ECGs,
    • All participants:
    • \- Body weight ≥ 50 kg; BMI within the range of 18.0 to 40.0 kg/m2 (inclusive) as measured at screening

Age in the registry: 18 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
Miami LakesUnited StatesUnknown status
-
Coordinator of this site? Confirm its status
OrlandoUnited StatesUnknown status
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Coordinator of this site? Confirm its status
RialtoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.