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 IIb Trial of an Encapsulated Cell Therapy Product in Locally Advanced, Inoperable Pancreatic Cancer (LAPC)

Trial Profile

A Phase IIb Trial of an Encapsulated Cell Therapy Product in Locally Advanced, Inoperable Pancreatic Cancer (LAPC)

Status: Planning
Phase of Trial: Phase II

Latest Information Update: 28 Jul 2022

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 Ifosfamide (Primary) ; Microencapsulated CYP2B1-expressing cells+ifosfamide PharmaCyte Biotech (Primary) ; Capecitabine
  • Indications Pancreatic cancer
  • Focus Adverse reactions; Registrational; Therapeutic Use
  • Sponsors PharmaCyte Biotech
  • Most Recent Events

    • 21 Jul 2022 According to a PharmaCyte media release, the company has commenced the pilot phase of its two-phase pig study which is the last of several requirements PharmaCyte has complied with related to the requests from the U.S. Food and Drug Administration (FDA) to lift the clinical hold from this study.
    • 19 Aug 2021 According to a PharmaCyte Biotech media release, the company intends to use the net proceeds from the institutional investors offerings to fully fund and conduct this study.
    • 02 Aug 2021 According to a PharmaCyte Biotech media release, company announced uplist to the nasdaq capital market and launch of public offering, company intends to use the net proceeds of this offering to complete activities requested by the U.S. Food and Drug Administration (FDA) in order to address the FDA clinical hold on its Investigational New Drug application (IND) with respect to this trial and to begin to fund and conduct this trial, if and when the clinical hold on the IND is lifted.
Subscriber content

You need to be a logged in subscriber to view this content.

If your organization has a subscription then there are several options available to help you access AdisInsight, even while working remotely.

  • IP authentication when working within your organization’s network.
  • with username/password or try via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days.
  • Contact us at AsktheExpert.AdisInsight@springer.com for assistance.

If your organization does not have a subscription to this content. To gain full access to the content and functionality of the AdisInsight database try one of the following.

  • Contact your organization’s admin about adding this content to your AdisInsight subscription
  • Buy a PDF version of the profile.
  • Request a free trial
Back to top