Viewing Study NCT04145700


Ignite Creation Date: 2025-12-26 @ 12:15 PM
Ignite Modification Date: 2026-01-01 @ 2:14 AM
Study NCT ID: NCT04145700
Status: TERMINATED
Last Update Posted: 2023-09-13
First Post: 2019-10-29
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: CAMPFIRE: A Study of Ramucirumab (LY3009806) in Children and Young Adults With Synovial Sarcoma
Sponsor: Eli Lilly and Company
Organization:

Study Overview

Official Title: A Randomized, Open-Label Phase 1/2 Study Evaluating Ramucirumab in Pediatric Patients and Young Adults With Relapsed, Recurrent, or Refractory Synovial Sarcoma
Status: TERMINATED
Status Verified Date: 2023-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Study terminated for meeting protocol specified futility criteria.
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is being conducted to test the safety and efficacy of ramucirumab in combination with other chemotherapy in the treatment of relapsed, recurrent, or refractory synovial sarcoma (SS) in children and young adults. This trial is part of the CAMPFIRE master protocol (NCT05999994) which is a platform to accelerate the development of new treatments for pediatric and young adult participants with cancer. Your participation in this trial could last 12 months or longer, depending on how you and your tumor respond.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
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?:

Secondary ID Infos

Secondary ID Type Domain Link View
J1S-MC-JV02 OTHER Eli Lilly and Company View
2018-004243-23 EUDRACT_NUMBER None View