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 study evaluating the pharmacokinetics, safety, and tolerability of enzalutamide monotherapy and in combination with endocrine therapies (anastrozole, exemestane, and fulvestrant) in women with advanced breast cancer.

Next Previous
X
Search
Trial Profile

A study evaluating the pharmacokinetics, safety, and tolerability of enzalutamide monotherapy and in combination with endocrine therapies (anastrozole, exemestane, and fulvestrant) in women with advanced breast cancer.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 14 Mar 2017

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 Enzalutamide (Primary) ; Anastrozole; Exemestane; Fulvestrant
  • Indications Breast cancer
  • Focus Adverse reactions; Pharmacodynamics; Pharmacokinetics; Therapeutic Use
  • Sponsors Astellas Pharma; Medivation

    • Most Recent Events

    • 14 Mar 2017 New trial record
    • 09 Mar 2017 Results published in the Clinical cancer research: an official journal of the American Association for Cancer Research

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