RO7568282 for Early Symptomatic Alzheimer's Disease

Study to Test Effects and Safety of RO7568282 in Early Symptomatic Alzheimer's Disease

Recruiting Phase 2 Interventional Study
Alzheimer's Disease
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
50 – 90
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
450 (estimated)
Sponsor
Hoffmann-La Roche · Industry
Who this trial is looking for

This trial is looking for people in the early stages of Alzheimer's disease to compare a new treatment called RO7568282 with a placebo. Participants will need to meet certain health criteria and have a study partner to help them.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have early Alzheimer's disease confirmed by a medical test.
  • I have mild cognitive impairment or mild dementia due to Alzheimer's.
  • I can swallow whole capsules.
  • My body mass index is between 18 and 34.
  • I have a study partner who can assist me.

You may not be able to join if

  • I have another condition that affects my thinking.
  • I have had serious heart problems in the last year.
  • I have dangerous blood pressure that is hard to control.
  • I have had serious problems with blood vessels in my brain.
  • I have significant brain abnormalities seen on an MRI.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial

This study aims to compare the effects of RO7568282 versus a placebo in people in the early stages of Alzheimer's disease (AD).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Evidence of AD pathological process, as confirmed by either amyloid positron emission tomography (PET) scan or cerebrospinal fluid (CSF) * Mild cognitive impairment (MCI) or mild dementia due to AD * Able to swallow whole capsules * Body mass index (BMI) within the range of 18…
Contacts

Reference Study ID Number: BP46554 https://forpatients.roche.com/ No attachments to email below.

888-662-6728

global-roche-genentech-trials@gene.com

CONTACT

Fastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry

CONTACT