Investigator Initiated Trial of Galcanezumab Treatment in Alzheimer's Disease

NCT ID: NCT07323927

Last Updated: 2026-01-07

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-08-01
• Study Completion Date: 2027-03-31

Brief Summary

This single-arm, open-label clinical study systematically evaluates the efficacy and safety of Galcanezumab in patients with mild-to-moderate Alzheimer's disease (AD). Eligible participants who provided written informed consent were screened and enrolled to receive Galcanezumab treatment. The therapeutic regimen involved subcutaneous administration of Galcanezumab with an initial 240 mg loading dose followed by 120 mg maintenance doses every four weeks for six total administrations over a 24-week treatment period. All study procedures were conducted at the Advanced Innovation Center for Neurological Disorders, Xuanwu Hospital, Capital Medical University. Comprehensive data collection and clinical assessments were performed at baseline (pre-treatment), week 12 (Visit 3), week 24 (Visit 4), and week 36 (Visit 5, 12 weeks after the final dose) to evaluate treatment outcomes and safety profiles. The study design incorporates standardized clinical trial methodology while maintaining the flexibility required for exploratory therapeutic evaluation.

Conditions

Alzheimer Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Galcanezumab Treatment Arm (Open-label)

Subcutaneous Galcanezumab administration with an initial dose of 240 mg (single injection), followed by 120 mg every 4 weeks for a total of 6 doses (24-week treatment duration).

Group Type: EXPERIMENTAL

Galcanezumab

Intervention Type: DRUG

Subcutaneous injection; monotherapy (administered at the designated study site: Advanced Innovation Center for Neurological Disorders, Xuanwu Hospital, Capital Medical University); initial dose: 240 mg (single administration) followed by 120 mg every 4 weeks for 6 total doses

Interventions

Galcanezumab

Subcutaneous injection; monotherapy (administered at the designated study site: Advanced Innovation Center for Neurological Disorders, Xuanwu Hospital, Capital Medical University); initial dose: 240 mg (single administration) followed by 120 mg every 4 weeks for 6 total doses

Intervention Type: DRUG

Other Intervention Names

Emgality

Eligibility Criteria

Inclusion Criteria

1. Age between 50 and 90 years at enrollment, regardless of gender;

2. Meeting the NIA-AA core clinical criteria for probable Alzheimer's disease;

3. Clinical Dementia Rating - Global Score (CDR-GS) between ≥1 and ≤2; Clinical Dementia Rating - Memory Box (CDR-Memory box) ≥0.5;

4. Amyloid PET or cerebrospinal fluid (CSF) biomarkers consistent with AD pathology;

5. Mini-Mental State Examination (MMSE) score between ≥12 and ≤26;

6. Non-illiterate or with at least 4 to 6 years of formal education;

7. If currently taking psychiatric or cognitive-enhancing medications, the dosage must have been stable for at least 3 months prior to the study and remain unchanged during the study. Unless otherwise specified, all permitted concomitant medications (non-AD related) must have been stable for at least 4 weeks prior to baseline;

8. Availability of a reliable caregiver or legal guardian able to support the participant throughout the study, defined as spending at least 8 hours per week with the participant;

9. Willingness to participate in the clinical trial, maintain existing interventions during the study period, and provision of signed informed consent.

Exclusion Criteria

1. Presence of neuropsychiatric symptoms outside the typical spectrum of Alzheimer's disease;

2. History of transient ischemic attack (TIA), stroke, or seizure within the past 12 months;

3. Known allergy to gantenerumab or its excipients, or severe allergic reactions to monoclonal antibodies;

4. Cardiovascular or gastrointestinal diseases including severe arrhythmias, uncontrolled hypertension (systolic >180 mmHg or diastolic >110 mmHg), or active peptic ulcer disease, inflammatory bowel disease, or other conditions likely to exacerbate gastrointestinal adverse reactions;

5. MRI contraindications such as cardiac pacemaker/defibrillator or ferromagnetic metal implants;

6. MRI evidence of other clinically significant lesions suggesting dementia diagnoses other than AD;

7. MRI findings of other important pathologies, including but not limited to: single hemorrhagic lesions >10 mm in diameter; evidence of vasogenic edema; brain contusions, softening, aneurysms, vascular malformations, or infectious lesions; strokes involving major vascular territories; severe small vessel or white matter disease; space-occupying lesions; or brain tumors (meningiomas or arachnoid cysts with a maximum diameter <1 cm may be allowed);

8. Current participation in another clinical trial targeting AD improvement;

9. Any unstable or inadequately controlled medical condition, or other situations deemed by investigators to compromise participant safety or study assessments;

10. Other investigator-determined reasons precluding participant inclusion.

• Minimum Eligible Age: 50 Years
• Maximum Eligible Age: 90 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Xuanwu Hospital, Beijing

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yi Tang

Role: STUDY_CHAIR

M.D., Ph.D.

Locations

Xuanwu Hospital, Capital Medical University

Beijing, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Yi Tang, M.D., Ph.D.

Role: CONTACT

tangyi@xwhosp.org

00861083199456

Ouyang Chen, Ph.D.

Role: CONTACT

chenouyang@xwhosp.org

15652888562

Facility Contacts

Yi Tang, M.D., Ph.D.

Role: primary

tangyixw@vip.163.com

00861083199456

Other Identifiers

2025162

Identifier Type: -

Identifier Source: org_study_id