Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07000136 · ClinicalTrials.gov registry record · Phase 3

A Phase III Study to Assess the Effect of AZD0780 on LDL-C in Patients With HeFH

A Phase 3 study of Heterozygous Familial Hypercholesterolaemia, sponsored by AstraZeneca.

Active
Registry status
Phase 3
Development phase
455
Enrollment target
20
Study locations

NCT07000136: Active Phase 3 study of Heterozygous Familial Hypercholesterolaemia, sponsored by AstraZeneca.

NCT07000136 is a Phase 3 study of Heterozygous Familial Hypercholesterolaemia that is active but no longer recruiting, run by AstraZeneca. The registered enrollment target is 455 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (41% lower). The trial reports 20 study locations across 13 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07000136, a Phase 3 study of Heterozygous Familial Hypercholesterolaemia, is active but no longer recruiting, sponsored by AstraZeneca.

ACTIVE NOT RECRUITING
Registry status
Phase 3
Development phase
455 participants
Enrollment target
20
Study locations

Study Summary

This is a study to evaluate the efficacy and safety of AZD0780 in adults with HeFH and elevated LDL-C, either with clinical ASCVD and LDL-C levels of 55 mg/dL or higher or without clinical ASCVD and LDL-C levels of 70 mg/dL or higher. AZD0780 is a small molecule that reduces the amount of LDL-C in the blood. Placebo will be used for comparison, and neither the participants nor the Investigators will know who is receiving the AZD0780 medication and who is receiving the placebo until the end of study. The total length of the study for an individual participant will be up to approximately 56 weeks, including a screening period of up to 14 days, treatment with AZD0780 or placebo for 52 weeks, and a safety follow-up period of 10 days.

Primary Outcome

To compare the effect of treatment with AZD0780 versus placebo on LDL-C at 12 weeks

Interventions

  • DRUG Placebo
  • DRUG AZD0780

Study Locations (20)

Texas

  • Research Site - Houston
  • Research Site - Humble
  • Research Site - Kingwood
  • Research Site - McAllen
  • Research Site - Mesquite

California

  • Research Site - Garden Grove
  • Research Site - San Diego

Florida

  • Research Site - Hialeah
  • Research Site - Orlando

Ohio

  • Research Site - Cincinnati
  • Research Site - Lima

Georgia

  • Research Site - Peachtree Corners

Illinois

  • Research Site - Chicago

Louisiana

  • Research Site - Hammond

Nevada

  • Research Site - Las Vegas

Trial Details

FieldValue
Enrollment Target 455 participants
Start Date 2025-06-10
Est. Completion 2027-01-04
Phase Phase 3
AstraZeneca

1,285 total trials

What the registry record for NCT07000136 still lists

NCT07000136 is an interventional study that assigns participants to a tested intervention. The registered 455 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (41% lower).

The record links to 1 condition, with Heterozygous Familial Hypercholesterolaemia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07000136 names 20 study sites across 13 states, led by Texas, California, Florida.

Frequently Asked Questions

What is clinical trial NCT07000136 about?

NCT07000136 is a clinical study titled "A Phase III Study to Assess the Effect of AZD0780 on LDL-C in Patients With HeFH". This is a study to evaluate the efficacy and safety of AZD0780 in adults with HeFH and elevated LDL-C, either with clinical ASCVD and LDL-C levels of 55 mg/dL or higher or without clinical ASCVD and LDL-C levels of 70 mg/dL or higher. AZD0780 is a small molecule that reduces the amount of LDL-C in t...

What is the current status of trial NCT07000136?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 455 participants. The study started on 2025-06-10. Estimated completion is 2027-01-04.

What conditions does trial NCT07000136 study?

This clinical trial studies the following conditions: Heterozygous Familial Hypercholesterolaemia.

What interventions are being tested in trial NCT07000136?

The interventions under investigation include: Placebo (DRUG), AZD0780 (DRUG).

Who is sponsoring clinical trial NCT07000136?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07000136 being conducted?

This trial has 20 study locations across California, Florida, Georgia, Illinois, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT07000136's enrollment target sits among peer trials

455 829th of 2000 higher than 1,170 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05541016 · 455 participants · Phase 2

    De-Escalated Adjuvant and Definitive Radiation Therapy Informed by DART 2.0 ctHPV-DNA

  • NCT06079346 · 455 participants · Phase 2

    A Study of OT-101 With mFOLFIRINOX in Patients With Advanced and Unresectable or Metastatic Pancreatic Cancer

  • NCT06504446 · 455 participants · Phase 2

    Study to Assess the Efficacy, Safety, and Tolerability of NOC-110 in Adults With Refractory or Unexplained Chronic Cough

  • NCT06725030 · 455 participants

    A Post-market, Real-world Experience: Expanding Access to Care by Incorporating the Symani® Surgical System and Enabling Surgeons

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07000136, the US trial registry maintained by the National Library of Medicine. NCT07000136 (mid enrollment · wide site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.