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?

An Open-label, Phase IB Study of NEO-PV-01 + Adjuvant With Nivolumab in Patients With Melanoma, Non-Small Cell Lung Carcinoma or Transitional Cell Carcinoma of the Bladder

Trial Profile

An Open-label, Phase IB Study of NEO-PV-01 + Adjuvant With Nivolumab in Patients With Melanoma, Non-Small Cell Lung Carcinoma or Transitional Cell Carcinoma of the Bladder

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 06 Nov 2021

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 NEO-PV 01 (Primary) ; Nivolumab (Primary) ; Poly ICLC (Primary)
  • Indications Bladder cancer; Carcinoma; Malignant melanoma; Non-small cell lung cancer; Transitional cell carcinoma
  • Focus Adverse reactions
  • Sponsors BioNTech; Neon Therapeutics

Most Recent Events

  • 10 Jun 2020 Status changed from active, no longer recruiting to completed.
  • 08 Nov 2019 According to a Neon Therapeutics media release, updated results (n=82, August 2019 data cut) from the trial were presented at the Society for Immunotherapy of Cancer's (SITC) 34th Annual Meeting in National Harbor, MD
  • 08 Nov 2019 Results presented in the Neon Therapeutics media release.

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

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: 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