Ask to take part

Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

ORIC Clinical 650-388-5600
clinical@oricpharma.com


Study Location:

Skip to Main Content
English | Cymraeg
Be Part of Research - Trial Details - Study of ORIC-944 in Patients with Metastatic Prostate Cancer

Study of ORIC-944 in Patients with Metastatic Prostate Cancer

Recruiting

Open to: MALE

Age: 18.0 - N/A

Medical Conditions

Prostatic Neoplasms


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


The purpose of this study is to establish the safety and preliminary antitumor activity of ORIC-944 as a single agent and in combinations with ARPIs in patients with metastatic prostate cancer.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Jun 2022 Dec 2025

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Oral, once daily, continuous

Intervention Arm Group : Combination Dose Escalation;Combination Dose Optimization;Single Agent Dose Escalation;

Intervention Type : DRUG
Intervention Description : Oral, 1000 mg once daily, continuous

Intervention Arm Group : Combination Dose Escalation;

Intervention Type : DRUG
Intervention Description : Oral, 240 mg once daily, continuous

Intervention Arm Group : Combination Dose Escalation;Combination Dose Optimization;

Intervention Type : DRUG
Intervention Description : Oral, 600 mg twice daily, continuous

Intervention Arm Group : Combination Dose Escalation;Combination Dose Optimization;

Intervention Type : DRUG
Intervention Description : Oral, 160 mg once daily, continuous

Intervention Arm Group : Combination Dose Escalation;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Royal Marsden NHS Foundation Trust
    Sutton
    Surrey


The study is sponsored by ORIC Pharmaceuticals





We'd like your feedback

Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.


Is this study information helpful?

What will you do next?

Read full details for Trial ID: NCT05413421
Last updated 17 March 2025

This page is to help you find out about a research study and if you may be able to take part

You can print or share the study information with your GP/healthcare provider or contact the research team directly.