Viewing Study NCT03164603



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Last Modification Date: 2024-10-26 @ 12:24 PM
Study NCT ID: NCT03164603
Status: COMPLETED
Last Update Posted: 2020-06-04
First Post: 2017-05-22

Brief Title: NLG802 Indoleamine 23-Dioxygenase IDO Inhibitor in Advanced Solid Tumors
Sponsor: NewLink Genetics Corporation
Organization: Lumos Pharma

Study Overview

Official Title: A Phase 1 Study of NLG802 for Adult Patients With Recurrent Advanced Solid Tumors
Status: COMPLETED
Status Verified Date: 2020-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is an open-label Phase I study to evaluate the safety tolerability and pharmacokinetics of escalating oral doses of NLG802 an investigational agent intended to inhibit the indoleamine 23-dioxygenase 1 IDO1 enzyme and help the human immune system attack solid tumor cells more effectively
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None