HOVON HO162 AML

Cancelled
Go to eCRF

Main info

Identifier:
HO162 AML
Sponsor:
HOVON
Working group party:
Leukemia
Stage:
1st Line
Echelon:
Level A
Included patients:
0
(of 25)
Active sites:
0
(of 4)
4 sites are pending
Title:

A phase II multicenter study to assess the feasibility and efficacy of the addition of an interphase cycle with flotetuzumab prior to start conditioning for an allogeneic HCT in AML with detectable MRD after 2 cycles of intensive chemotherapy

Timeline

Scheduled
Actual
2021
05 Jan
Opportunity
2021
02 Feb
Development
2021
29 Oct
Submission in Progress
2021
15 Nov
Submission in Progress
2021
20 Dec
Cancelled
2022
16 Jan
Activated
2022
16 Jan
EC Approval
2022
15 Feb
First Site
2022
15 Mar
FPI
2024
01 Aug
Endpoint Analysis

News

20 Dec 2021: The pharmaceutical company MacroGenics no longer wants to support the HO162 study.

Details

Phase:
Prospective Phase II study
Monitoring Type:
Site Evaluation Visit
Objectives:

Registration Details

Go to eCRF

Participating Sites

Site
4 results
Order by
Accrual rate
Activation date
NL-Rotterdam-ERASMUSMC
NL-Maastricht-MUMC
NL-Groningen-UMCG
NL-Amsterdam-VUMC
= Active hospitals
= Inactive hospitals

Participating Parties

Up