A Phase I Randomized, Single-blind, Placebo-controlled Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AZD8233 Following Multiple Ascending Subcutaneous Dose Administration in Subjects With Dyslipidemia With or Without Type 2 Diabetes
This is a Phase I study to assess the safety, tolerability and pharmacokinetics (PK), and pharmacodynamics (PD) of AZD8233, following subcutaneous (SC) administration of multiple ascending doses (MAD) of AZD8233 in subjects with confirmed dyslipidemia with or without type 2 diabetes.
Indication: Dyslipidemia
Modality: small molecule
Target: AZD8233 subcutaneous injection, Placebo
Sponsor: AstraZeneca
Source URL: ClinicalTrials.gov
Source updated: Jun 30, 2021
Ingested: Jun 11, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: AZD8233 subcutaneous injection, Placebo
View original source fields
Condition raw: Dyslipidemia
Condition normalized: Dyslipidemia
Modality raw: small molecule
Modality normalized: small molecule
Target raw: AZD8233 subcutaneous injection, Placebo
Target normalized: AZD8233 subcutaneous injection, Placebo