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 1b Study of Safety and Immune Response to PVX-410 Vaccine Alone and in Combination with Durvalumab in Human Leukocyte Antigen (HLA)-A2+ Subjects Following Standard Treatment of Stage II or III Triple Negative Breast Cancer

Next Previous
X
Search
Trial Profile

A Phase 1b Study of Safety and Immune Response to PVX-410 Vaccine Alone and in Combination with Durvalumab in Human Leukocyte Antigen (HLA)-A2+ Subjects Following Standard Treatment of Stage II or III Triple Negative Breast Cancer

Status: Active, no longer recruiting
Phase of Trial: Phase I

Latest Information Update: 30 Sep 2024

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 PVX 410 (Primary) ; Durvalumab; Poly ICLC
  • Indications Advanced breast cancer; Early breast cancer; Triple negative breast cancer
  • Focus Adverse reactions

    • Most Recent Events

    • 23 Sep 2024 Planned End Date changed from 1 Sep 2025 to 1 Sep 2026.
    • 23 Sep 2024 Planned primary completion date changed from 1 Jun 2024 to 1 Jun 2025.
    • 13 Nov 2023 Planned End Date changed from 1 Sep 2023 to 1 Sep 2025.

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