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Completed Phase 2 Interventional Results available

A Study of INCB050465 in Relapsed or Refractory Follicular Lymphoma

ClinicalTrials.gov ID: NCT03126019

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT03126019. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 14, 2026, 2:16 AM EST

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Official title

A Phase 2, Multicenter, Open-Label Study of INCB050465, a PI3Kδ Inhibitor in Relapsed or Refractory Follicular Lymphoma (CITADEL-203)

Brief summary

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

The purpose of this study is to assess the objective response rate of parsaclisib treatment in participants with relapsed or refractory follicular lymphoma.

Study identification

NCT ID
NCT03126019
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Incyte Corporation
Industry
Enrollment
126 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years 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
Mar 14, 2018 (Actual)
Primary completion
Feb 26, 2021 (Actual)
Completion
Jun 7, 2024 (Actual)
Last update posted
Mar 14, 2025

2018 – 2024

United States locations

U.S. sites
22
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
Arizona Oncology Associates - Biltmore Cancer Center Phoenix Arizona 85016 —
Beverly Hills Cancer Center Beverly Hills California 90211 —
Synergy Hematology and Oncology Medical Associates Los Angeles California 90036 —
St. Joseph Heritage Healthcare Santa Rosa California 95403 —
American Institute of Research Corporate Office Whittier California 90603 —
Cancer Center of Central Connecticut Southington Connecticut 06489 —
Florida Cancer Specialists & Research Institute Fort Myers Florida 33901 —
Asclepes Research Centers Spring Hill Florida 34606 —
Clinical Trials of Swla Llc Lake Charles Louisiana 70601 —
Saint Agnes Hospital Baltimore Maryland 21229 —
Barbara Ann Karmanos Cancer Hospital Detroit Michigan 48201 —
Hattiesburg Clinic Hematology Hattiesburg Mississippi 39401 —
Saint Luke'S Hospital Kansas City Missouri 64111 —
Sarah Cannon Research Institute Kansas City Missouri 64132 —
Clinical Research Alliance, Inc. New Hyde Park New York 11042 —
Duke University Medical Center Durham North Carolina 27710 —
Gabrail Cancer Center Canton Ohio 44718 —
University of Pennsylvania Health System Philadelphia Pennsylvania 19104 —
Charleston Hematology Oncology Associates Pa Charleston South Carolina 29414 —
Tennessee Oncology Nashville Tennessee 37203 —
Renovatio Clinical Consultants Llc Spring Texas 77380 —
University of Washington Seattle Washington 98109 —

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 61 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03126019, 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 14, 2025 · Synced Nov 14, 2026

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