Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A Phase I Study of Human Placental Hematopoietic Stem Cell Derived Natural Killer Cells (CYNK-001) in Adults With Recurrent Glioblastoma Multiforme (GBM)

Trial Profile

A Phase I Study of Human Placental Hematopoietic Stem Cell Derived Natural Killer Cells (CYNK-001) in Adults With Recurrent Glioblastoma Multiforme (GBM)

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 26 May 2022

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Taniraleucel (Primary) ; Taniraleucel (Primary) ; Cyclophosphamide
  • Indications Glioblastoma
  • Focus Adverse reactions; First in man
  • Acronyms CYNK001GBM01
  • Sponsors Celularity

Most Recent Events

  • 24 Jan 2022 Status changed from active, no longer recruiting to discontinued due to business decision.
  • 13 Jul 2021 Status changed from recruiting to active, no longer recruiting.
  • 24 Nov 2020 According to a Celularity media release, abstract highlighting the details of this study were presented at the 25th Annual Meeting and Education Day of the Society for Neuro-Oncology (SNO) 2020.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top