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 for evaluation of the safety, tolerability and pharmacokinetics of dose-escalation ACT001 in patients with advanced glioblastoma

X
Trial Profile

A phase I study for evaluation of the safety, tolerability and pharmacokinetics of dose-escalation ACT001 in patients with advanced glioblastoma

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 10 Jul 2021

Price : $35 *
  • 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 ACT 001 (Primary)
  • Indications Astrocytoma; Choroid neoplasms; Ependymoma; Glioblastoma; Glioma; Oligodendroglioma
  • Focus Adverse reactions; Pharmacokinetics; Therapeutic Use
  • Most Recent Events

    • 08 Jun 2021 Results (n=16) assessing the Pharmacokinetics, adverse events, therapeutic efficacy of ACT001 in patients with advanced glioma, presented at the 57th Annual Meeting of the American Society of Clinical Oncology.
    • 01 Dec 2017 New trial record

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

If your organization or you do not have a subscription, try one of the following:
  • Contacting your organization’s admin about adding this content to your AdisInsight subscription
  • Buying a PDF version of any individual profile
  • Request a free trial
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