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 1, Open-Label, Multiple-Ascending Dose Study of the Safety and Tolerability of CTX-8371 in Patients With Advanced Malignancies

Trial Profile

A Phase 1, Open-Label, Multiple-Ascending Dose Study of the Safety and Tolerability of CTX-8371 in Patients With Advanced Malignancies

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 15 May 2025

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 CTX-8371 (Primary)
  • Indications Head and neck cancer; Hodgkin's disease; Hypopharyngeal cancer; Laryngeal cancer; Malignant melanoma; Non-small cell lung cancer; Oropharyngeal cancer; Squamous cell cancer; Triple negative breast cancer
  • Focus Adverse reactions; First in man
  • Sponsors Compass Therapeutics

Most Recent Events

  • 08 May 2025 Results (toxicity data) presented in a Compass Therapeutics media release
  • 08 May 2025 According to a Compass Therapeutics media release, company advanced the Phase 1 dose-escalation study of CTX-8371 and evaluating the fourth dosing cohort with preliminary data. The company looks forward to sharing data from the study later this year.
  • 30 Apr 2025 Trial design presented at the 116th Annual Meeting of the American Association for Cancer Research

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