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:

Daniela Zinzi, MD +43 06643582281
DZinzi@f2g.com


Study Location:

Skip to Main Content
English | Cymraeg
Be Part of Research - Trial Details - Olorofim Aspergillus Infection Study

Olorofim Aspergillus Infection Study

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Aspergillosis


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.


The purpose of this study is to compare treatment with olorofim versus treatment with AmBisome® followed by standard of care (SOC) in patients with IFD caused by proven IA or probable lower respiratory tract disease Aspergillus species (invasive aspergillosis, IA).

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:

Mar 2022 Sep 2025

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Loading Dose: 5 tablets (150 mg) to be taken twice daily at a 12-hour (± 1 hour) interval on Day 1 Maintenance Dose: 3 tablets (90 mg) to be taken twice daily at 12-hour (± 1 hour) intervals from Day 2 until Day 84 (± 7 days)

Intervention Arm Group : Olorofim;

Intervention Type : DRUG
Intervention Description : Initial course of at least 10 days of AmBisome® administered daily at a dose of 3 mg/kg by IV infusion over a 30- to 60-minute period or according to local guidelines Administration of SOC will follow international, national, or local guidelines and product labelling.

Intervention Arm Group : AmBisome;



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.

  • Imperial College London
    London
    W6 8RP
  • Kings College Hospital
    London
    SE5 9RS
  • University Hospital of Wales
    Cardiff
    Wales
    CF14 4XW

Daniela Zinzi, MD +43 06643582281
DZinzi@f2g.com



The study is sponsored by F2G Biotech GmbH and is in collaboration with Iqvia Pty Ltd; Shionogi.




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: NCT05101187
Last updated 26 September 2024

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.