Phase 2 Alzheimer's Disease Trial, Recruiting NCT06582706 Sponsor: Indiana University Condition: Alzheimer's Disease
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Phase 2 Alzheimer's Disease Trial, Recruiting

NCT06582706
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are between 60 and 85 years old (male or female)
  • You have been diagnosed with Alzheimer's disease in the mild to moderate range, confirmed by a standard memory test score between 14 and 24
  • You are either taking a stable dose of an approved Alzheimer's medication (such as donepezil or memantine) for at least 30 days, or you are not taking any such medication
  • You have a reliable person (such as a family member or caregiver) who sees you face-to-face at least 3 days a week and can help make sure you take the study medication
  • You have had a brain scan (MRI or CT) done within the past year, or one can be arranged before the study begins

Who may not be able to join:

  • You have a condition that makes a lumbar puncture (spinal tap) unsafe, such as increased pressure in the brain, a growth at the base of the brain, a bleeding disorder, or you take blood-thinning medications (other than aspirin)
  • You have severe disease affecting the blood vessels in your brain
  • You have had a major stroke in the past
  • You have a known allergy or sensitivity to B-vitamins or nicotinic acid (a form of Vitamin B3)
  • You have a history of abnormal liver test results or known liver disease
  • You are currently taking Vitamin B3 in any form — including in multivitamins or energy drinks — unless you are able to stop taking it for at least 4 weeks before the study begins
  • You have moderate or worse kidney disease (stage 2 or higher) (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 30 June 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
19 December 2024
Est. completion
1 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in nicotinic acid levels in blood and CSF

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov