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Terminated Phase 2Phase 3 Interventional Results available

GBT021601-022: A Study of GBT021601 in Participants With Sickle Cell Disease (SCD)

ClinicalTrials.gov ID: NCT05632354

Public ClinicalTrials.gov record NCT05632354. 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 Sep 5, 2026, 7:35 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

An Open-label Extension Study to Evaluate the Long-term Safety of GBT021601 Administered to Participants With Sickle Cell Disease Who Have Participated in a GBT021601 Clinical Trial

Brief summary

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

An Open-label Extension Study of GBT021601 in Participants with Sickle Cell Disease

Study identification

NCT ID
NCT05632354
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
47 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
6 Months and older
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
Jan 4, 2023
Primary completion
Feb 12, 2025
Completion
Feb 12, 2025
Last update posted
Mar 18, 2026

2023 – 2025

United States locations

U.S. sites
6
U.S. states
4
U.S. cities
5
Facility City State ZIP Site status
Our Lady of the Lake Hospital, Inc. Baton Rouge Louisiana 70808
University Medical Center Inpatient Pharmacy New Orleans Louisiana 70112
University Medical Center New Orleans New Orleans Louisiana 70112
Mississippi Center for Advanced Medicine Madison Mississippi 39110
University of Texas Health Science Center Houston Texas 77030
Inova Schar Cancer Institute Fairfax Virginia 22031

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05632354, 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 Mar 18, 2026 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05632354 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →