Skip to content

Open-Label Treatment With MPC-7869 for Patients With Alzheimer's Who Previously Participated in an MPC-7869 Protocol

Open Label Study of the Effect of Daily Treatment With MPC-7869 in Subjects With Dementia of the Alzheimer's Type

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00380276
Enrollment
1000
Registered
2006-09-25
Start date
2006-09-30
Completion date
2008-12-31
Last updated
2008-08-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's Disease

Keywords

Alzheimer's, Dementia, Dementia of Alzheimer Type

Brief summary

Open-label treatment with MPC-7869 for participants in a previous randomized study.

Interventions

800 mg BID Oral dosing

Sponsors

Myrexis Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participation in a previous MPC-7869 randomized protocol * Have had a diagnosis of probable Alzheimer's disease. * Men or women ages 55 years or greater and living in the community at the time of enrollment (i.e., not living in a rest home or nursing care facility). * Signed the subject Informed Consent Form and is willing and able to participate for the duration of the study. * Female subjects must be surgically sterile or postmenopausal for \> 1 year. * Subjects must have a reliable caregiver who can read, understand and speak English or Spanish.

Exclusion criteria

* History or evidence of, active malignancy, except for basal cell carcinoma or squamous cell carcinoma of the skin, within the 24 months prior to entry. Men with prostate cancer may be enrolled at the discretion of the sponsor. * Chronic or acute renal, hepatic or metabolic disorder. * Use of any investigational therapy within 30 days, or 5 half-lives, whichever is longer, and/or use of AD immunotherapy prior to screening.

Design outcomes

Primary

MeasureTime frame
Primary SafetyFor study duration

Countries

Canada, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026