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 Single Dose, Double-Blind, Parallel Arm, Comparative Pharmacokinetic Study of Three Bevacizumab Preparations, Administered by the Intravenous Route to Male Normal Healthy Volunteers

Next Previous
X
Search
Trial Profile

A Single Dose, Double-Blind, Parallel Arm, Comparative Pharmacokinetic Study of Three Bevacizumab Preparations, Administered by the Intravenous Route to Male Normal Healthy Volunteers

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 16 Jul 2019

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 Bevacizumab (Primary)
  • Indications Advanced breast cancer; Cancer; Colorectal cancer; Male breast cancer; Non-small cell lung cancer
  • Focus Pharmacokinetics
  • Sponsors Dr Reddys Laboratories

    • Most Recent Events

    • 26 Jun 2018 Results published in the British Journal of Clinical Pharmacology
    • 26 Jun 2018 Status changed from not yet recruiting to completed, as per the results published in the British Journal of Clinical Pharmacology
    • 05 Jul 2016 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