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Completed Phase 2 Interventional Results available

Safety, Tolerability and Pharmacodynamic Effect of Fazirsiran (TAK-999, ARO-AAT)

ClinicalTrials.gov ID: NCT03945292

Public ClinicalTrials.gov record NCT03945292. 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 Oct 26, 2026, 4:52 AM 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 Placebo-Controlled, Multi-dose, Phase 2 Study to Determine the Safety, Tolerability and Pharmacodynamic Effect of Fazirsiran (TAK-999, ARO-AAT) in Patients With Alpha-1 Antitrypsin Deficiency (AATD) [SEQUOIA]

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of AROAAT2001 (SEQUOIA) is to evaluate the safety, efficacy and tolerability of multiple doses of the investigational product, Fazirsiran Injection, administered subcutaneously to participants with alpha-1 antitrypsin deficiency (AATD).

Study identification

NCT ID
NCT03945292
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Arrowhead Pharmaceuticals
Industry
Enrollment
40 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Aug 7, 2019 (Actual)
Primary completion
Nov 8, 2021 (Actual)
Completion
Sep 18, 2023 (Actual)
Last update posted
Nov 4, 2025

2019 – 2023

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Research Site 5 Birmingham Alabama 35233 —
Research Site 9 Phoenix Arizona 85054 —
Research Site 14 La Jolla California 92037 —
Research Site 17 Los Angeles California 90095 —
Research Site 11 Sacramento California 95817 —
Research Site 15 San Francisco California 94158 —
Research Site 13 Stanford California 94305 —
Research Site 2 Gainesville Florida 32610 —
Research Site 7 Indianapolis Indiana 46202 —
Research Site 3 Iowa City Iowa 52242 —
Research Site 10 St Louis Missouri 63104 —
Research Site 12 New York New York 10032 —
Research Site 1 Charleston South Carolina 29425 —
Research Site 4 Nashville Tennessee 37232 —
Research Site 19 Houston Texas 77030 —
Research Site 16 Salt Lake City Utah 84132 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03945292, 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 Nov 4, 2025 · Synced Oct 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03945292 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →