What to Expect

01

Informed Consent

Informed Consent

Participants are required to review and sign a consent form confirming their understanding of their study information and rights.
02

Screening

Screening

Participants are screened against strict criteria through various medical tests (e.g., blood test, physical exams) to ensure the study is safe for them and that the results are reliable.
03

Assessments

Assessments

Comprehensive eye exams, vision tests and retinal imaging are routinely performed to check eye structure and function.
04

Study Treatment

Study Treatment

Once enrolled, participants will receive treatment as outlined in the protocol. Some may receive a placebo or standard care for comparison.
05

Monitoring

Monitoring

The team will monitor your response to the treatment and any side effects. Expect regular follow-up visits for continued monitoring and data collection.

Why Participate?

  • Access to new treatments
  • Expert care and close monitoring
  • Contributre to medical progress
  • Reduce future treatment burden
  • Make a difference
Why Participate

Clinical Trial FAQs

If you think you may be eligible to participate in a trial, it is best to email us at info@cureos.com.au for further discussions.

Your doctor and trial team will explain the details of the specific study. After you have been provided with all the necessary information and have consented, you may be asked about your general health and medical history. You may also be required to undergo various assessments and health checks during your visit to assess your eligibility.

A referral is not required but it will help our team in their assessment of your eligibility for a trial.

Participation in a clinical trial is completely voluntary, you may choose to withdraw your consent at any-time, and this will not affect your current or future care from your doctor.

This will depend on the clinical trial; some studies may restrict the use of concurrent medications which may interact or confound the efficacy of the drug being tested. This will be discussed with you at your trial assessment.

Investigational products used in trials are only permitted to be assessed in humans after ethical approval with extensive safety results.

You may have early access to an investigational treatment, including for conditions with limited or no approved therapies.

Increased drug durability → Reduce need for frequent injections and clinic visits + Improved efficacy → Can potentially treat the disease better

No, your appointment fees are covered by the sponsor. In cases where additional treatments are required, payments may be needed.

Travel-related expenses may be reimbursed for eligible studies.

Contact Us

Any questions about Clinical Trials or want more information? Feel free to message or call us below and we will get back to you as soon as we can.

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If you would like to discuss a clinical trial, please contact us.