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?

Phase I Evaluation of Combination CLK/DYRK (Cirtuvivint) Inhibition with PARP Inhibition (Olaparib) in BRCA/HRD Platinum Resistant Ovarian Cancer

Trial Profile

Phase I Evaluation of Combination CLK/DYRK (Cirtuvivint) Inhibition with PARP Inhibition (Olaparib) in BRCA/HRD Platinum Resistant Ovarian Cancer

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 12 Jan 2026

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 Cirtuvivint (Primary) ; Olaparib (Primary)
  • Indications Fallopian tube cancer; Ovarian cancer; Peritoneal cancer
  • Focus Adverse reactions

Most Recent Events

  • 22 Dec 2025 According to Biosplice Therapeutics media release, this trial is sponsored by UCHealth University of Colorado Hospital and led by principal investigator Bradley R. Corr, MD, associate professor and director of clinical research in gynecologic oncology at the University of Colorado Anschutz.
  • 22 Dec 2025 According to Biosplice Therapeutics media release, first patient has been dosed in this Investigator-Initiated Phase 1 trial.
  • 22 Sep 2025 Status changed from not yet recruiting to recruiting.

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