Evidence map›Paper›PMID 41304975›Full record

ReviewPharmaceuticals (Basel, Switzerland)2025

Targeting Amyloid-β Proteins as Potential Alzheimer's Disease Therapeutics: Anti-Amyloid Drug Discovery, Emerging Therapeutics, Clinical Trials and Implications for Public Health.

Asaad Abdulrahman Abduljawad, Khadijah B Alkinani, Aysha Zaakan, Abeer S AlGhamdi, Alashary Adam Eisa Hamdoon, Batool H Alshanbari, Ahmed Abdullah Alshehri, Badria Bakheet Alluhaybi, Shahad Othman Ibrahim Alqashi, Ryan Abdulrahman Abduljawad

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Limitations of Current Therapies and Barriers in Alzheimer's Disease.Archives of internal medicine research · 2026
    Article
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Asaad Abdulrahman AbduljawadDepartment of Public Health, College of Health Sciences, Umm Al-Qura University, Makkah 21955, Saudi Arabia.ORCID 0000-0002-1894-5382
Khadijah B AlkinaniDepartment of Public Health, College of Health Sciences, Umm Al-Qura University, Makkah 21955, Saudi Arabia.ORCID 0000-0003-4895-9803
Aysha ZaakanDepartment of Chemistry, Faculty of Sciences, Taibah University, Madinah 42353, Saudi Arabia.
Abeer S AlGhamdiDepartment of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0009-0005-5932-8742
Alashary Adam Eisa HamdoonDepartment of Public Health, College of Health Sciences, Umm Al-Qura University, Makkah 21955, Saudi Arabia.ORCID 0000-0001-9068-3818
Batool H AlshanbariDepartment of Public Health, College of Health Sciences, Umm Al-Qura University, Makkah 21955, Saudi Arabia.
Ahmed Abdullah AlshehriHealth Management and Medical Informatics Department, College of Health Sciences, Umm Al-Qura University, Makkah 21955, Saudi Arabia.ORCID 0009-0000-5994-0492
Badria Bakheet AlluhaybiMedical Complex at the Public Services Center in Alshumaisy-Ministry of Health, Mecca 24231, Saudi Arabia.
Shahad Othman Ibrahim AlqashiPublic Health Department, King Abdulaziz Airport, Ministry of Health, Jeddah 21442, Saudi Arabia.
Ryan Abdulrahman AbduljawadKing Salman Bin Abdulaziz Hospital, Ministry of Health, Riyadh 12769, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD), a neurodegenerative disorder of the aging brain, is associated with behavioral and cognitive issues and poses a huge burden on the global health care system. One of the key features of AD is the deposition of abnormal proteins called amyloid-beta (Aβ) in the brain, causing inflammatory changes, oxidative stress, and neuronal loss. Recent advancements in the anti-Aβ therapies have considerably improved the management of AD, resulting in better clinical outcomes for patients and caregivers. This review offers an inclusive update on current drug discovery efforts, innovative approaches, and ongoing clinical trials targeting Aβ, a key player in AD pathogenesis. We have evaluated the most recent developments in monoclonal antibodies, including aducanumab (discontinued November 2024), lecanemab, and donanemab, emerging therapeutic options, as well as emerging strategies such as tau-targeting therapies, gene therapy, and small molecule inhibitors. Moreover, we highlighted the challenges and opportunities in AD research, including the need for early diagnosis, personalized medicine, and combination therapies. Our review will offer a concise and informative overview of the current landscape and future directions in anti-Aβ therapeutics for AD, shedding light on potential treatments and prospects for improving patient outcomes.

Indexed as

Alzheimer’s diseaseanti-amyloid therapeuticsclinical trialsdrug discoveryinnovative approachesmonoclonal antibodiespublic health

Identifiers

PMID41304975
PMCPMC12655499

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.