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A Study of INCB050465 in Relapsed or Refractory Follicular Lymphoma

NCT03126019 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2025-03-14

Study results available
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Summary

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

Conditions

Interventions

DRUG

Parsaclisib

Parsaclisib tablets administered orally with water and without regard to food

Sponsors & Collaborators

Principal Investigators

  • Fred Zheng, MD, PhD · Incyte Corporation

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-14
Primary Completion
2021-02-26
Completion
2024-06-07
FDA Drug
Yes

Countries

  • United States
  • Australia
  • Canada
  • Czechia
  • Denmark
  • Germany
  • Hungary
  • Israel
  • Italy
  • Poland
  • Spain
  • Sweden
  • United Kingdom

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03126019 on ClinicalTrials.gov