ClinicalTrials.gov record
Recruiting Phase 1 Interventional Accepts healthy volunteers

A Phase I Study Comparing the Relative Bioavailability of a Fixed-Dose Combination of Laroprovstat/Rosuvastatin vs Their Single Therapy Products in Healthy Adults

ClinicalTrials.gov ID: NCT07316608

Public ClinicalTrials.gov record NCT07316608. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 22, 2026, 9:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I, Randomized, Open-label, 3 or 4-period, 7-treatment, Single-dose, Two Cohort, Crossover Study to Assess the Relative Bioavailability of Laroprovstat/Rosuvastatin Fixed Combination Drug Products to the Single Therapy Products in Healthy Adults

Study identification

NCT ID
NCT07316608
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
AstraZeneca
Industry
Enrollment
44 participants

Conditions and interventions

Interventions

  • Laroprovstat Dose X STP Drug
  • Laroprovstat Dose X/Rosuvastatin Dose 1 FCDP test formulation 1 Drug
  • Laroprovstat Dose X/Rosuvastatin Dose 1 FCDP test formulation 2 Drug
  • Laroprovstat Dose X/Rosuvastatin Dose 2 FCDP test formulation 1 Drug
  • Laroprovstat Dose X/Rosuvastatin Dose 2 FCDP test formulation 2 Drug
  • Rosuvastatin Dose 1 STP Drug
  • Rosuvastatin Dose 2 STP Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 55 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 15, 2026
Primary completion
May 28, 2026
Completion
May 28, 2026
Last update posted
Apr 21, 2026

2026

United States locations

U.S. sites
2
U.S. states
2
U.S. cities
2
Facility City State ZIP Site status
Research Site Glendale California 91206 Recruiting
Research Site Brooklyn Maryland 21225 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07316608, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 21, 2026 · Synced Apr 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07316608 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →