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?

Ipilimumab and Nivolumab Combination Therapy in Patients With Selected Immunotherapy Sensitive Advanced Rare Cancers

Next Previous
X
Search
Trial Profile

Ipilimumab and Nivolumab Combination Therapy in Patients With Selected Immunotherapy Sensitive Advanced Rare Cancers

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

Latest Information Update: 14 Mar 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 Ipilimumab (Primary) ; Nivolumab (Primary)
  • Indications Biliary cancer; Carcinoma; Cholangiocarcinoma; Gallbladder cancer; Gynaecological cancer; Leiomyosarcoma; Neuroendocrine carcinoma; Ovarian cancer; Sarcoma; Squamous cell cancer; Uterine cancer; Vaginal intraepithelial neoplasia
  • Focus Therapeutic Use
  • Acronyms MOST-CIRCUIT

    • Most Recent Events

    • 06 Mar 2024 Planned End Date changed from 1 Dec 2024 to 1 Mar 2028.
    • 06 Mar 2024 Planned primary completion date changed from 1 Jun 2024 to 1 Mar 2026.
    • 06 Mar 2024 Status changed from recruiting to active, no longer recruiting.

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