100 Active Studies

Alzheimers Disease Clinical Trials Near You

Also searched as: dementia, memory loss, cognitive decline clinical trials

Find 100 actively recruiting alzheimers disease research studies near you. Connect with study sites, check eligibility, and explore new treatment options.

100
Active Trials
282+
Locations
86,110
Participants Needed

Recruiting Studies

RecruitingNCT07177352

Screening Study to Determine Individuals With Potential Trial Eligibility for Alzheimer's Disease Studies

This study is a pre-screening process used to assess participants' potential eligibility for Roche interventional Alzheimer's disease studies....

10 locations(Imperial, Inglewood, Irvine)
13,000 participants
Hoffmann-La Roche
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RecruitingNCT03848312

Preventing Alzheimer's With Cognitive Training

Dementia is the most expensive medical condition in the US and increases in prevalence with age. More than 5 million Americans have Alzheimer's disease, the most common form of dementia. Mild cognitiv...

7 locations(Gainesville, Jacksonville, Jacksonville)
7,600 participants
University of South Florida
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RecruitingNCT02693535

TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs That Target a Specific Abnormality in a Tumor Gene in People With Advanced Stage Cancer

The purpose of the study is to learn from the real world practice of prescribing targeted therapies to patients with advanced cancer whose tumor harbors a genomic variant known to be a drug target or ...

10 locations(Birmingham, Phoenix, Auburn)
4,200 participants
American Society of Clinical Oncology
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RecruitingNCT03486873

Long-term Safety and Efficacy Extension Study for Participants With Advanced Tumors Who Are Currently on Treatment or in Follow-up in a Pembrolizumab (MK-3475) Study (MK-3475-587/KEYNOTE-587)

The purpose of this study is to evaluate the long-term safety and efficacy of pembrolizumab (MK-3475) in participants from previous Merck pembrolizumab-based parent studies who transition into this ex...

10 locations(Tucson, Bakersfield, Fresno)
3,500 participants
Merck Sharp & Dohme LLC
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RecruitingNCT05026866

A Donanemab (LY3002813) Study in Participants With Preclinical Alzheimer's Disease (TRAILBLAZER-ALZ 3)

The main purpose of this study is to evaluate the safety and efficacy of donanemab in participants with preclinical Alzheimer's Disease (AD). Approximately 800 additional participants will be enrolled...

10 locations(Birmingham, Homewood, Huntsville)
2,996 participants
Eli Lilly and Company
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RecruitingNCT04373564

Effect on Body Movement and Mental Skills in Patients Who Received Gadolinium-based Contrast Media for Magnetic Resonance Examination Multiple Times Within 5 Years

This study is a postmarketing requirement jointly carried out by four NDA holders (Bayer AG, Bracco, GE Healthcare and Guerbet) and the CRO IQVIA. The study aims to create detailed images of the orga...

10 locations(Scottsdale, New Haven, Chicago)
2,076 participants
Guerbet
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RecruitingNCT05050162

Comparing Cisplatin Every Three Weeks to Cisplatin Weekly When Combined With Radiation for Patients With Advanced Head and Neck Cancer

This phase II/III trial compares whether cisplatin given weekly with radiation therapy is better tolerated than cisplatin given every three weeks with radiation therapy for the treatment of head and n...

10 locations(Mobile, Jonesboro, Little Rock)
1,714 participants
NRG Oncology
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RecruitingNCT06653153

A Study of Remternetug (LY3372993) in Early Alzheimer's Disease (TRAILRUNNER-ALZ 3)

The purpose of this study is to measure the difference in time to developing or worsening memory, thinking, or functional problems due to Alzheimer's disease occurring in participants receiving study ...

10 locations(Birmingham, Chandler, Mesa)
1,400 participants
Eli Lilly and Company
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RecruitingNCT05889182

A Study to Assess Change in Disease Activity and Adverse Events of Oral Upadacitinib in Adult and Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-TNF Therapy

Hidradenitis suppurativa (HS) is an inflammatory skin disease that causes painful lesions in the axilla (underarm), inguinal (groin) and anogenital (anal/genital) regions. This study will assess how s...

10 locations(Birmingham, Fountain Hills, Phoenix)
1,328 participants
AbbVie
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RecruitingNCT06468228

A Study to Assess Disease Activity and Safety of Lutikizumab in Adult and Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa

Hidradenitis suppurativa (HS) is a chronic and often painful inflammatory skin disease which includes the forming of lumps, abscesses and scars in areas of the skin such as under the breasts, under ar...

10 locations(Birmingham, Phoenix, Tucson)
1,280 participants
AbbVie
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RecruitingNCT06129864

A Global Study of Volrustomig (MEDI5752) for Participants With Unresected Locally Advanced Head and Neck Squamous Cell Carcinoma Following Definitive Concurrent Chemoradiotherapy

The main purpose of this study is to assess the efficacy and safety of volrustomig compared to observation in participants with unresected locally advanced head and neck squamous cell carcinoma (LA-HN...

10 locations(Birmingham, Phoenix, Prescott Valley)
1,145 participants
AstraZeneca
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RecruitingNCT05438329

First-in-human Study of DB-1305/BNT325 for Advanced/Metastatic Solid Tumors

This is a dose-escalation and dose-expansion Phase 1/2a trial to evaluate the safety and tolerability of DB-1305/BNT325 in subjects with advanced solid tumors....

10 locations(Cerritos, Los Angeles, Margate)
1,123 participants
DualityBio Inc.
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RecruitingNCT06159673

ACP-204 in Adults With Alzheimer's Disease Psychosis

This is a master protocol for 3 independent, seamlessly enrolling, multicenter, randomized, double-blind, placebo-controlled, parallel-group studies in patients with ADP * Substudy 1 (Phase 2) will e...

10 locations(Chandler, Scottsdale, Anaheim)
1,074 participants
ACADIA Pharmaceuticals Inc.
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RecruitingNCT06212999

A Study to Evaluate the Long-Term Safety and Efficacy of Povorcitinib in Participants With Moderate to Severe Hidradenitis Suppurativa

The purpose of this study is to evaluate long-term safety and efficacy of povorcitinib in participants with moderate to severe hidradenitis suppurativa who completed the 54 weeks of study treatment wi...

10 locations(Phoenix, Scottsdale, Fort Smith)
960 participants
Incyte Corporation
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RecruitingNCT06225596

Study BT8009-230 in Participants With Locally Advanced or Metastatic Urothelial Cancer (Duravelo-2)

This is a global, multicenter, randomized, open-label study, with an adaptive design. The main objective of the study is to measure the efficacy and safety of BT8009 (zelenectide pevedotin) as monothe...

10 locations(Little Rock, Fullerton, Orange)
956 participants
BicycleTx Limited
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RecruitingNCT04626635

A Trial to Find Out How Safe REGN7075 is and How Well it Works in Combination With Cemiplimab for Adult Participants With Advanced Cancers

This study is researching an investigational drug called REGN7075 by itself and in combination with cemiplimab with or without chemotherapy. The study is focused on patients with certain solid tumors ...

10 locations(Los Angeles, Los Angeles, San Francisco)
933 participants
Regeneron Pharmaceuticals
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RecruitingNCT05538663

Intravesical BCG vs GEMDOCE in NMIBC

The study hypothesis is that BCG naïve non-muscle invasive bladder cancer (NMIBC) patients treated with intravesical Gemcitabine + Docetaxel (GEMDOCE) will result in a non-inferior event-free survival...

10 locations(Birmingham, Fairbanks, Gilbert)
870 participants
ECOG-ACRIN Cancer Research Group
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RecruitingNCT06256588

A Study of Dostarlimab vs Placebo After Chemoradiation in Adult Participants With Locally Advanced Unresected Head and Neck Squamous Cell Carcinoma

The goal of this study is to assess the safety and effectiveness of Dostarlimab compared to Placebo in adult participants with Head and Neck Squamous Cell Carcinoma (HNSCC)...

10 locations(Jonesboro, Los Angeles, Solvang)
864 participants
GlaxoSmithKline
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RecruitingNCT05980949

Open-Label Extension Study to Assess the Long-Term Safety and Tolerability of KarXT and KarXT + KarX-EC in Subjects With Psychosis Associated With Alzheimer's Disease (ADEPT-3)

This is a Phase 3 global, multicenter, 52-week, open-label extension (OLE) rollover study for subjects completing study CN012-0026, CN012-0027, CN012-0056 or CN012-0034. Subjects (randomized or non-ra...

10 locations(Homewood, Chandler, Chandler)
800 participants
Karuna Therapeutics
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RecruitingNCT07169578

A Study of Trontinemab in Participants With Early Symptomatic Alzheimer's Disease

The purpose of this study is to assess the efficacy and safety of trontinemab in participants with early symptomatic Alzheimer's disease (AD) (mild cognitive impairment \[MCI\] to mild dementia due to...

3 locations(Irvine, Laurelton, Toronto)
800 participants
Hoffmann-La Roche
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RecruitingNCT06876649

A Master Protocol to Evaluate the Long-Term Safety of (LY3527727) Pirtobrutinib

The master protocol study J2N-MC-JZNY provides a framework to enable the evaluation of the long-term safety and efficacy of pirtobrutinib after completion of clinical studies evaluating pirtobrutinib....

10 locations(Miami, Sarasota, Atlanta)
787 participants
Eli Lilly and Company
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RecruitingNCT06709014

A Double-blind Dual Study Assessing Safety and Efficacy of Buntanetap in Participants With Early AD

The goal of this clinical trial is to learn if buntanetap/Posiphen works to treat early Alzheimer's disease in adults aged 55-85. It will also learn about the safety of buntanetap/Posiphen. The main q...

10 locations(Chandler, Phoenix, Scottsdale)
760 participants
Annovis Bio Inc.
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RecruitingNCT06172478

A Study of HER3-DXd in Subjects With Locally Advanced or Metastatic Solid Tumors

This is a proof-of-concept study designed to investigate HER3-DXd monotherapy in locally advanced unresectable or metastatic solid tumors. The study is enrolling cohorts of participants with melanoma ...

10 locations(Duarte, New Haven, Kissimmee)
740 participants
Daiichi Sankyo
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RecruitingNCT05768139

First-in-Human Study of STX-478 as Monotherapy and in Combination With Other Antineoplastic Agents in Participants With Advanced Solid Tumors

Study STX-478-101 is a multipart, open-label, phase 1/2 study evaluating the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of STX-478 (LY4064809) in participants with...

10 locations(Los Angeles, San Francisco, Aurora)
720 participants
Eli Lilly and Company
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RecruitingNCT05417594

Study of AZD9574 as Monotherapy and in Combination With Anti-cancer Agents in Participants With Advanced Solid Malignancies

This study will assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of AZD9574 individually and in combination with anti-cancer agents in participan...

10 locations(La Jolla, Los Angeles, San Francisco)
695 participants
AstraZeneca
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RecruitingNCT06112314

IMC-F106C Regimen Versus Nivolumab Regimens in Previously Untreated Advanced Melanoma (PRISM-MEL-301)

This is a phase 3, randomized, controlled study of brenetafusp (IMC-F106C) plus nivolumab compared to standard nivolumab regimens in HLA-A\*02:01-positive participants with previously untreated advanc...

10 locations(Tucson, La Jolla, Los Angeles)
680 participants
Immunocore Ltd
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RecruitingNCT06788990

FORTIFI-HN01: A Study of Ficerafusp Alfa (BCA101) or Placebo in Combination With Pembrolizumab in First-Line PD-L1-pos, R or M HNSCC

Ficerafusp alfa is directed against two targets, Epidermal Growth Factor Receptor (EGFR) and Transforming Growth Factor beta (TGF-β). This study intends to evaluate the safety and efficacy of ficeraf...

10 locations(Birmingham, La Jolla, Los Angeles)
650 participants
Bicara Therapeutics
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RecruitingNCT05094336

A Study of AMG 193 in Participants With Advanced MTAP-null Solid Tumors (MTAPESTRY 101)

The primary objective of Parts 1 and 2 of this study is to evaluate the safety, tolerability, and to determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) of AMG 193 alone and ...

10 locations(Duarte, Glendale, Oxnard)
649 participants
Amgen
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RecruitingNCT01810913

Testing Docetaxel-Cetuximab or the Addition of an Immunotherapy Drug, Atezolizumab, to the Usual Chemotherapy and Radiation Therapy in High-Risk Head and Neck Cancer

This phase II/III trial studies how well radiation therapy works when given together with cisplatin, docetaxel, cetuximab, and/or atezolizumab after surgery in treating patients with high-risk stage I...

10 locations(Birmingham, Birmingham, Tucson)
613 participants
National Cancer Institute (NCI)
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RecruitingNCT06855498

Rollover Study for Participants Previously Enrolled in Clinical Trials of Povorcitinib

Rollover study for participants from predetermined, Incyte-sponsored parent clinical trials of povorcitinib....

10 locations(Birmingham, Montgomery, Phoenix)
600 participants
Incyte Corporation
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RecruitingNCT05844982

Intravitreal Faricimab Injections or Fluocinolone Acetonide (0.19 Mg) Intravitreal Implants Vs Observation for Prevention of VA Loss Due to Radiation Retinopathy

This randomized controlled trial will evaluate the effect of intravitreal faricimab or fluocinolone acetonide (FAc) intravitreal implant compared with observation on long-term visual acuity following ...

10 locations(Palo Alto, Tampa, Chicago)
600 participants
Jaeb Center for Health Research
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RecruitingNCT02339571

A Phase II/III Trial of Nivolumab, Ipilimumab, and GM-CSF in Patients With Advanced Melanoma

This phase II/III trial studies the side effects of nivolumab and ipilimumab when given together with or without sargramostim and to see how well they work in treating patients with stage III-IV melan...

10 locations(Birmingham, Kingman, Little Rock)
600 participants
National Cancer Institute (NCI)
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RecruitingNCT02138734

A Study of Intravesical BCG in Combination With ALT-803 in Patients With Non-Muscle Invasive Bladder Cancer

This is a Phase Ib/IIb, randomized, two-cohort, open-label, multicenter study of intravesical N-803 plus BCG versus BCG alone, in BCG naïve patients with high-grade NMIBC....

10 locations(Birmingham, Anchorage, Little Rock)
596 participants
ImmunityBio, Inc.
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RecruitingNCT06976203

A Study to Evaluate the Efficacy and Safety of KarXT + KarX-EC for Cognitive Impairment in Alzheimer's Disease (MINDSET 2)

The purpose of this study is to evaluate the efficacy and safety of KarXT + KarX-EC for cognitive impairment in Alzheimer's Disease...

10 locations(Fullerton, Inglewood, Irvine)
586 participants
Bristol-Myers Squibb
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RecruitingNCT06976216

A Study to Evaluate the Efficacy and Safety of KarXT + KarX-EC for Cognitive Impairment in Alzheimer's Disease

The purpose of this study is to evaluate the efficacy and safety of KarXT + KarX-EC for cognitive impairment in Alzheimer's Disease...

10 locations(Long Beach, Redlands, Basalt)
586 participants
Bristol-Myers Squibb
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RecruitingNCT05489211

Study of Dato-Dxd as Monotherapy and in Combination With Anti-cancer Agents in Patients With Advanced Solid Tumours (TROPION-PanTumor03)

TROPION-PanTumor03 will investigate the safety, tolerability, and anti-tumour activity of Datopotamab Deruxtecan (Dato-DXd) as Monotherapy and in Combination with Anticancer Agents in Patients with Ad...

10 locations(Los Angeles, San Diego, Santa Rosa)
582 participants
AstraZeneca
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RecruitingNCT05579366

Rinatabart Sesutecan (Rina-S, PRO1184, GEN1184) for Advanced Solid Tumors (GCT1184-01/ PRO1184-001)

This study will test the safety, including side effects, and determine the characteristics of a drug called Rina-S in participants with solid tumors. Participants will have solid tumor cancer that ha...

10 locations(Phoenix, Tucson, Los Angeles)
569 participants
Genmab
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RecruitingNCT06319820

A Study to Evaluate TAR-210 Versus Single Agent Intravesical Cancer Treatment in Participants With Bladder Cancer

The main purpose of this study is to compare the disease-free survival between participants receiving treatment with TAR-210 versus investigator's choice of intravesical chemotherapy for treatment of ...

10 locations(Little Rock, Los Alamitos, Los Angeles)
560 participants
Janssen Research & Development, LLC
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RecruitingNCT06840392

Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult Patients With Moderate to Severe Hidradenitis Suppurativa

The purpose of this study is to establish the efficacy, safety, and tolerability of remibrutinib (LOU064) Dose A and Dose B compared to placebo in participants with moderate to severe hidradenitis sup...

10 locations(Birmingham, Gilbert, Scottsdale)
555 participants
Novartis Pharmaceuticals
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RecruitingNCT06799000

A Phase 3 Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult Patients With Moderate to Severe Hidradenitis Suppurativa

The purpose of this study is to establish the efficacy, safety, and tolerability of remibrutinib (LOU064) Dose A and Dose B compared to placebo in participants with moderate to severe hidradenitis sup...

10 locations(Fort Smith, North Little Rock, Anaheim)
555 participants
Novartis Pharmaceuticals
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RecruitingNCT07070232

A Clinical Study to Test if an Investigational Treatment Called BNT326 is Safe and Potentially Beneficial When Used Alone or in Combination With Other Investigational Treatments Such as BNT327, for People With Advanced Malignant Tumors

This study will evaluate the safety, efficacy, optimal dose, and pharmacokinetics (PK) of BNT326 as monotherapy (Part 1) and as combination treatment with immunotherapeutic agents (Part 2) in particip...

9 locations(Sarasota, Grand Rapids, San Antonio)
550 participants
BioNTech SE
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RecruitingNCT06703476

A Study of Surgical Techniques During Cystectomy

The purpose of this study is to look at two standard surgical techniques used during a radical cystectomy and see whether they influence outcomes such as length of stay in the hospital and infections ...

7 locations(Basking Ridge, Middletown, Montvale)
530 participants
Memorial Sloan Kettering Cancer Center
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RecruitingNCT03526835

A Study of Bispecific Antibody MCLA-158 in Patients With Advanced Solid Tumors

This is a Phase 1/2 open-label, multi-center, multi-national study with an initial dose escalation part to determine the recommended Phase II dose (RP2D) of MCLA-158 single agent in patients with mCRC...

10 locations(La Jolla, Los Angeles, San Diego)
523 participants
Merus N.V.
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RecruitingNCT06496178

A Phase 3 Study to Evaluate Petosemtamab Compared With Investigator's Choice Monotherapy in Previously Treated Head and Neck Squamous Cell Carcinoma Patients

This is a phase 3 open-label, randomized, controlled, multicenter study to compare petosemtamab vs investigator's choice monotherapy in HNSCC patients for the second- and third-line treatment of incur...

10 locations(Mobile, Prescott, Scottsdale)
500 participants
Merus N.V.
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RecruitingNCT06311214

Personalized Antibody-Drug Conjugate Therapy Based on RNA and Protein Testing for the Treatment of Advanced or Metastatic Solid Tumors (The ADC MATCH Screening and Treatment Trial)

This phase II ADC MATCH screening and multi-sub-study treatment trial is evaluating whether biomarker-directed treatment with one of three antibody-drug conjugates (ADCs) (sacituzumab govitecan, enfor...

10 locations(Encinitas, La Jolla, San Diego)
500 participants
National Cancer Institute (NCI)
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RecruitingNCT06525220

A Phase 3 Study to Evaluate Petosemtamab Plus Pembrolizumab vs Pembrolizumab in First-line Treatment of Head and Neck Cancer (LiGeR - HN1)

This is a Phase 3 randomized, open-label study to evaluate the efficacy and safety of petosemtamab plus pembrolizumab vs pembrolizumab in first-line treatment of recurrent or metastatic PD-L1+ head an...

10 locations(La Jolla, Los Angeles, Palo Alto)
500 participants
Merus N.V.
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RecruitingNCT06380751

Saruparib (AZD5305) Plus Camizestrant Compared With CDK4/6 Inhibitor Plus Endocrine Therapy or Plus Camizestrant in HR-Positive, HER2-Negative (IHC 0, 1+, 2+/ ISH Non-amplified), BRCA1, BRCA2, or PALB2m Advanced Breast Cancer

The primary objective of the study is to measure efficacy of saruparib (AZD5305) plus camizestrant compared with physician's choice CDK4/6i plus ET in patients with BRCA1, BRCA2, or PALB2m, HR-positiv...

10 locations(Gilbert, Glendale, Los Angeles)
500 participants
AstraZeneca
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RecruitingNCT05916339

AWARE: Management of ADHD in Autism Spectrum Disorder

This study is a pragmatic clinical trial examining the comparative effectiveness of two stimulant medications (methylphenidate and amphetamine) in the treatment of ADHD in children and adolescents wit...

10 locations(Irvine, Los Angeles, Portland)
500 participants
Daniel Coury
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RecruitingNCT04892173

JNJ-90301900 (NBTXR3) Activated by Radiotherapy With or Without Cetuximab in LA-HNSCC

This is a global, open-label, randomized, 2-arm, Investigator's choice Phase 3 (Pivotal Stage) study to investigate the efficacy and safety of JNJ-90301900 (NBTXR3) / radiation therapy (RT)±cetuximab ...

10 locations(Duarte, Laguna Hills, Los Angeles)
500 participants
Johnson & Johnson Enterprise Innovation Inc.
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RecruitingNCT03093116

A Study of Repotrectinib (TPX-0005) in Patients With Advanced Solid Tumors Harboring ALK, ROS1, or NTRK1-3 Rearrangements

Phase 1 dose escalation will determine the first cycle dose-limiting toxicities (DLTs), the maximum tolerated dose (MTD), the biologically effective dose and recommended Phase 2 dose (RP2D) of repotre...

10 locations(Duarte, Glendale, La Jolla)
500 participants
Turning Point Therapeutics, Inc.
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RecruitingNCT03781752

Carboxylesterase 1 Genetic Variation and Methylphenidate in ADHD

The study team will determine the association between d,l-methylphenidate (MPH) therapeutic outcomes in ADHD patients and genetic variants of CES1 and reveal key associations between CES1 genotypes an...

4 locations(Gainesville, New York, Cincinnati)
500 participants
Icahn School of Medicine at Mount Sinai
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RecruitingNCT06544616

A Study of JNJ-64042056 in Participants With Preclinical Alzheimer's Disease

The purpose of this study is to assess the effect of JNJ-64042056 on cognitive decline, as measured by Preclinical Alzheimer's disease Cognitive Composite 5 (PACC-5) compared with placebo....

10 locations(Phoenix, Irvine, Riverside)
498 participants
Janssen Pharmaceutica N.V., Belgium
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RecruitingNCT01760005

Dominantly Inherited Alzheimer Network Trial: An Opportunity to Prevent Dementia. A Study of Potential Disease Modifying Treatments in Individuals at Risk for or With a Type of Early Onset Alzheimer's Disease Caused by a Genetic Mutation. Master Protocol DIAN-TU-001

The purpose of this study is to assess the safety, tolerability, biomarker, cognitive and clinical efficacy of investigational products in participants with an Alzheimer's disease-causing mutation by ...

10 locations(Birmingham, La Jolla, Los Angeles)
490 participants
Washington University School of Medicine
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RecruitingNCT05875168

First-in-Human Study of DS-3939a in Participants With Advanced Solid Tumors

This study will evaluate the safety, tolerability, and efficacy of DS-3939a in participants with advanced solid tumors....

10 locations(Sarasota, Portland, Providence)
470 participants
Daiichi Sankyo
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RecruitingNCT06334432

Safety and Efficacy Study of NUV-1511 in Adult Patients With Advanced Solid Tumors

NUV-1511-01 is a first-in human, open- label, Phase 1/2 to evaluate the safety and efficacy of NUV-1511 in patients with advanced solid tumors. The Phase 1 portion include patients with advanced solid...

8 locations(Detroit, Hackensack, New York)
466 participants
Nuvation Bio Inc.
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RecruitingNCT06510374

Trial of Nadofaragene Firadenovec vs. Observation in Participants With Intermediate Risk Non-Muscle Invasive Bladder Cancer

A phase 3b, Randomized, Controlled Trial of Nadofaragene Firadenovec vs. Observation in Participants with Intermediate Risk Non-Muscle Invasive Bladder Cancer (IR NMIBC)...

10 locations(Mobile, Mobile, Fresno)
454 participants
Ferring Pharmaceuticals
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RecruitingNCT06958211

Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa (TRuE-HS2)

The purpose of this study is to evaluate the efficacy and safety of ruxolitinib cream in participants with hidradenitis suppurativa....

10 locations(Birmingham, Birmingham, Montgomery)
450 participants
Incyte Corporation
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RecruitingNCT06032559

Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment

This hybrid implementation-effectiveness trial will evaluate Mindfulness-Oriented Recovery Enhancement (MORE) for patients with opioid use disorder receiving methadone treatment (MT). The investigator...

2 locations(New Brunswick, Salt Lake City)
450 participants
Rutgers, The State University of New Jersey
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RecruitingNCT05410145

A Study of D3S 001 Monotherapy or Combination Therapy in Subjects With Advanced Solid Tumors With a KRAS p.G12C Mutation

This is a first-in-human (FIH), multicenter, open-label, dose-escalation, and dose-expansion Phase 1/2 clinical trial to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and prel...

10 locations(Orange, Denver, Sarasota)
442 participants
D3 Bio (Wuxi) Co., Ltd
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RecruitingNCT06581432

Beamion PANTUMOR-1: A Study to Test Whether Zongertinib Helps People With Advanced Cancers With HER2 Alterations

This is a study for people with advanced cancer for whom previous treatment was not successful. Adults aged 18 and over with advanced cancer with HER2 alterations can join the study. The purpose of th...

10 locations(Anchorage, Tucson, Beverly Hills)
430 participants
Boehringer Ingelheim
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RecruitingNCT04977453

GI-101 as a Single Agent or in Combination With Pembrolizumab, Lenvatinib or Local Radiotherapy in Advanced Solid Tumors

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and therapeutic activity of GI-101/GI-101A as a single agent or in combination with pembrolizumab, lenvatinib or lo...

8 locations(New York, Huntersville, Daejeon)
430 participants
GI Innovation, Inc.
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RecruitingNCT07197827

A Study of YL242 in Subjects With Advanced Solid Tumors

This is a multicenter, open-label study to evaluate the safety and tolerability of YL242 monotherapy and combination in participants with advanced solid malignant tumors....

10 locations(New Haven, Sarasota, Boston)
424 participants
MediLink Therapeutics (Suzhou) Co., Ltd.
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RecruitingNCT06033599

Motivational Interviewing and Mindfulness-Oriented Recovery Enhancement

The purpose of this study is to 1) examine barriers and facilitators to implementation of MI and MORE for polysubstance use and evaluate strategies for optimizing training, fidelity, and clinic uptake...

2 locations(New Brunswick, Salt Lake City)
420 participants
Rutgers, The State University of New Jersey
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RecruitingNCT06697197

A Study of BMS-986482 Alone or as Combination Therapy in Participants With Advanced Solid Tumors

The purpose of this study is to test the safety and efficacy of BMS-986482 alone and as combination therapy in participants with advanced solid tumors....

10 locations(Irvine, Los Angeles, Aurora)
413 participants
Bristol-Myers Squibb
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RecruitingNCT06699212

A Study of ASP-1929 Photoimmunotherapy in Combination With Pembrolizumab in First-line Treatment of Locoregional Recurrent Squamous Cell Carcinoma of the Head and Neck With No Distant Metastases

The goal of this clinical trial is to learn if ASP-1929 photoimmunotherapy (PIT) in combination with pembrolizumab works to treat recurrent squamous cell cancer of the head and neck (HNSCC) with no di...

10 locations(Duarte, Miami, Tampa)
412 participants
Rakuten Medical, Inc.
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RecruitingNCT06295731

INBRX-106 in Combination With Pembrolizumab in First-line PD-L1 CPS≥20 HNSCC

This seamless phase 2/3 randomized controlled study will evaluate the efficacy and safety of the hexavalent OX40 agonist antibody INBRX-106 combined with the anti-PD-1 antibody pembrolizumab versus pe...

10 locations(Duarte, Los Angeles, Sacramento)
410 participants
Inhibrx Biosciences, Inc
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RecruitingNCT06064877

A Study of Ficlatuzumab in Combination With Cetuximab in Participants With Recurrent or Metastatic (R/M) HPV Negative Head and Neck Squamous Cell Carcinoma

The purpose of this study is to compare the efficacy and safety of ficlatuzumab plus cetuximab compared to placebo plus cetuximab in participants with recurrent/metastatic (R/M) HPV-negative Head and ...

10 locations(Gilbert, Tucson, Westwood, Los Angeles)
410 participants
AVEO Pharmaceuticals, Inc.
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RecruitingNCT06585787

A Study to Evaluate KarXT as a Treatment for Psychosis Associated With Alzheimer's Disease (ADEPT-4)

The purpose of this study is to evaluate the safety and efficacy of KarXT in adult participants with mild to severe Alzheimer's Disease (AD) with moderate to severe psychosis related to AD....

10 locations(Chandler, Gilbert, Phoenix)
406 participants
Karuna Therapeutics
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RecruitingNCT06223360

A Trial to Evaluate the Safety and Efficacy of Benfotiamine in Patients With Early Alzheimer's Disease (BenfoTeam)

The purpose of this study is to learn more about the safety, effectiveness and tolerability of the study drug called Benfotiamine which may delay or slow the progression of the symptoms of early Alzhe...

10 locations(Phoenix, Sun City, Chula Vista)
406 participants
Alzheimer's Disease Cooperative Study (ADCS)
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RecruitingNCT05049057

Treatment of Acute PTH With a CGRP Receptor mAb in Military Service Members and Civilians With mTBI

This study aims to assess the effect and safety of erenumab compared to placebo for the treatment of acute posttraumatic headache (PTH) in military service members and civilians with mild traumatic br...

4 locations(Fort Bragg, Pittsburgh, El Paso)
404 participants
Henry M. Jackson Foundation for the Advancement of Military Medicine
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RecruitingNCT06959225

Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa (TRuE-HS1)

The purpose of this study is to evaluate the efficacy and safety of ruxolitinib cream in participants with hidradenitis suppurativa....

10 locations(Phoenix, Scottsdale, Tempe)
400 participants
Incyte Corporation
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RecruitingNCT06351631

A Study to Evaluate Safety and Efficacy of Bomedemstat (MK-3543-017)

The primary purpose of the study is to transition participants into an extension study to collect long-term safety and efficacy data. The study will include participants who are safely tolerating bome...

10 locations(Ann Arbor, Durham, Columbus)
400 participants
Merck Sharp & Dohme LLC
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RecruitingNCT06264180

VO and Nivolumab vs Physician's Choice in Advanced Melanoma That Progressed on Anti-PD-1 & Anti-CTLA-4 Drugs [IGNYTE-3]

This is a randomized, controlled, multicenter, open-label Phase 3 clinical study comparing VO in combination with nivolumab versus Physician's Choice treatment for patients with unresectable Stage III...

10 locations(Gilbert, La Jolla, Los Angeles)
400 participants
Replimune Inc.
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RecruitingNCT05566795

DAY101 vs. Standard of Care Chemotherapy in Pediatric Participants With Low-Grade Glioma Requiring First-Line Systemic Therapy (LOGGIC/FIREFLY-2)

This is a 2-arm, randomized, open-label, multicenter, global, Phase 3 trial to evaluate the efficacy, safety, and tolerability of tovorafenib monotherapy versus standard of care (SoC) chemotherapy in ...

10 locations(Birmingham, Phoenix, Los Angeles)
400 participants
Day One Biopharmaceuticals, Inc.
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RecruitingNCT05911295

Disitamab Vedotin With Pembrolizumab vs Chemotherapy in Previously Untreated Urothelial Cancer Expressing HER2

This study will enroll participants with urothelial cancer (UC). UC can include cancer of the bladder, kidney, or the tubes that carry pee through the body (ureter, urethra). This study will try to fi...

10 locations(Gilbert, Gilbert, Alhambra)
400 participants
Seagen, a wholly owned subsidiary of Pfizer
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RecruitingNCT05511363

A Study to Assess Efficacy and Safety of KarXT for the Treatment of Psychosis Associated With Alzheimer's Disease (ADEPT-1)

This is a Phase 3, 38-week, randomized, double-blind, placebo-controlled, multicenter, outpatient study in subjects with psychosis associated with Alzheimer's Disease. The primary objective of the st...

10 locations(Homewood, Phoenix, Encino)
380 participants
Karuna Therapeutics
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RecruitingNCT06998407

Study of AVZO-023 as a Single Agent and in Combination With AVZO-021, and/or Endocrine Therapy in Advanced Solid Tumors

This study, the first clinical trial of AVZO-023, aims to determine the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, maximum tolerated dose, and anti-tumor effects of AVZO-023 in pat...

8 locations(Los Angeles, New Haven, Boston)
380 participants
Avenzo Therapeutics, Inc.
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RecruitingNCT04143711

Study of DF1001 in Patients with Advanced Solid Tumors

DF1001-001 is a study of a new molecule that targets natural killer (NK) cells and T-cell activation signals to specific receptors on cancer cells. The study will occur in two phases. The first phase ...

10 locations(Irvine, Los Angeles, San Diego)
378 participants
Dragonfly Therapeutics
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RecruitingNCT05397639

Masupirdine for the Treatment of Agitation in Dementia of the Alzheimer's Type

This study will be conducted to evaluate the efficacy, safety, tolerability, and pharmacokinetics of masupirdine compared to placebo for the treatment of agitation in participants with dementia of the...

10 locations(Anaheim, Costa Mesa, Encino)
375 participants
Suven Life Sciences Limited
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RecruitingNCT04879329

A Study of Disitamab Vedotin Alone or With Pembrolizumab in Urothelial Cancer That Expresses HER2

This study is being done to see if a drug called disitamab vedotin, alone or with pembrolizumab, works to treat HER2 expressing urothelial cancer. It will also test how safe the drug is for participan...

10 locations(Gilbert, Gilbert, Anaheim)
372 participants
Seagen, a wholly owned subsidiary of Pfizer
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RecruitingNCT06540833

A Study to Assess the Efficacy and Safety of ITI-1284 in the Treatment of Psychosis Associated With Alzheimer's Disease

This is a multicenter, randomized, double-blind, parallel-group, placebo-controlled, flexible-dose study evaluating the efficacy, safety, and tolerability of ITI-1284 compared with placebo in the trea...

10 locations(Anaheim, Costa Mesa, Los Alamitos)
370 participants
Intra-Cellular Therapies, Inc.
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RecruitingNCT05123482

A Phase I/IIa Study of AZD8205 Given Alone or in Combination With Anticancer Drugs, in Participants With Advanced or Metastatic Solid Malignancies

This research study is studying a new compound, AZD8205, as a possible treatment for advanced or metastatic solid tumours alone or in combination with anti-cancer agents...

10 locations(Duarte, Irvine, Santa Monica)
370 participants
AstraZeneca
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RecruitingNCT05592626

A Study of a Selective T Cell Receptor (TCR) Targeting, Bifunctional Antibody-fusion Molecule STAR0602 in Participants With Advanced Solid Tumors

This is an open label, multicenter, phase 1/2 study to assess the safety/tolerability and preliminary clinical activity of STAR0602 as a single agent administered intravenously in participants with ad...

10 locations(Loma Linda, Sacramento, Denver)
365 participants
Marengo Therapeutics, Inc.
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RecruitingNCT06534983

A Study to Evaluate the Efficacy and Safety of Autogene Cevumeran With Nivolumab Versus Nivolumab Alone in Participants With High-Risk Muscle-Invasive Urothelial Carcinoma (MIUC)

The main purpose of the study is to evaluate the efficacy of adjuvant treatment with autogene cevumeran plus nivolumab compared with nivolumab in participants with high risk MIUC. In this study parti...

10 locations(Springdale, Duarte, Riverside)
362 participants
Hoffmann-La Roche
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RecruitingNCT06730750

A Study of BMS-986490 With or Without Bevacizumab in Advanced Solid Tumors

This is a study of BMS-986490 as a monotherapy and in combination with bevacizumab in participants with select advanced solid tumors known to express CEACAM5....

6 locations(Los Angeles, Grand Rapids, Hackensack)
360 participants
Bristol-Myers Squibb
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RecruitingNCT06062420

A Platform Study of Novel Immunotherapy Combinations as First-Line Treatment in Participants With PD-L1 Positive Recurrent/Metastatic Squamous Cell Carcinoma of the Head and Neck- GALAXIES H&N-202

The primary purpose of the study is to evaluate the antitumor activity and safety of novel immunotherapy combinations compared with dostarlimab in participants with Programmed death ligand 1 (PD-L1) p...

10 locations(New Haven, Columbus, Chicago)
360 participants
GlaxoSmithKline
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RecruitingNCT05684965

XTX301 in Patients With Advanced Solid Tumors

This is a first-in-human, multicenter, Phase 1/2, open-label study designed to evaluate the safety and tolerability of XTX301 as monotherapy in patients with advanced solid tumors....

10 locations(Sacramento, New Haven, Saint Louis Park)
358 participants
Xilio Development, Inc.
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RecruitingNCT05824975

A Study to Evaluate the Safety and Therapeutic Activity of GI-102 As a Single Agent and in Combination with Conventional Anti-cancer Drugs, Pembrolizumab or Trastuzumab Deruxtecan(T-DXd) in Patients with Advanced Solid Tumors (KEYNOTE-G08)

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and therapeutic activity of GI-102 as a single agent and in combination with conventional anti-cancer drugs, pembro...

10 locations(Scottsdale, Jacksonville, Rochester)
358 participants
GI Innovation, Inc.
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RecruitingNCT07011745

A Phase 3 Study to Evaluate the Safety and Efficacy of KarXT + KarX-EC for the Treatment of Agitation Associated With Alzheimer's Disease (ADAGIO-2)

The purpose of this study is to evaluate the efficacy and safety of KarXT + KarX-EC in adult participants with agitation related to Alzheimer's Disease....

10 locations(Chandler, Chandler, Long Beach)
352 participants
Bristol-Myers Squibb
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RecruitingNCT07011732

A Phase 3 Study to Evaluate the Safety and Efficacy of KarXT + KarX-EC for the Treatment of Agitation Associated With Alzheimer's Disease (ADAGIO-1)

The purpose of this study is to evaluate the efficacy and safety of KarXT + KarX-EC in adult participants with agitation related to Alzheimer's Disease....

10 locations(Scottsdale, Anaheim, La Jolla)
352 participants
Bristol-Myers Squibb
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RecruitingNCT06790966

Phase 3 Study of PDS0101 and Pembrolizumab in HPV16+ Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma

This is a global, multi-center, Phase 3 study that is randomized 2:1, controlled, and open label to evaluate PDS0101 (Versamune + HPVMix) in combination with pembrolizumab vs. pembrolizumab monotherap...

10 locations(Phoenix, Greenbrae, Jacksonville)
351 participants
PDS Biotechnology Corp.
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RecruitingNCT06721156

A Study to Evaluate the Efficacy and Safety of MK-1167 in Participants With Alzheimer's Disease Dementia (MK-1167-008)

Researchers want to learn if giving MK-1167 (the study medicine) along with acetylcholinesterase inhibitor (AChEI) therapy can improve symptoms of Alzheimer's disease dementia (AD dementia), such as m...

10 locations(Phoenix, Irvine, Redlands)
350 participants
Merck Sharp & Dohme LLC
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RecruitingNCT05315700

Study of ORIC-114 in Patients With Advanced Solid Tumors Harboring an EGFR or HER2 Alteration

The purpose of this study is to establish the recommended Phase 2 dose (RP2D) and/or maximum tolerated dose (MTD), safety, pharmacokinetics (PK), pharmacodynamics (PD), and antitumor activity of ORIC-...

10 locations(Duarte, Huntington Beach, Irvine)
350 participants
ORIC Pharmaceuticals
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RecruitingNCT04752722

LEGEND Study: EG-70 in NMIBC Patients BCG-Unresponsive and High-Risk NMIBC Incompletely Treated With BCG or BCG-Naïve

This study will evaluate the safety and efficacy of intravesical administration of EG-70 in the bladder and its effect on bladder tumors in patients with NMIBC. This study study consists of two phase...

10 locations(Birmingham, Scottsdale, Tucson)
350 participants
enGene, Inc.
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RecruitingNCT04534205

A Clinical Trial Investigating the Safety, Tolerability, and Therapeutic Effects of BNT113 in Combination With Pembrolizumab Versus Pembrolizumab Alone for Patients With a Form of Head and Neck Cancer Positive for Human Papilloma Virus 16 and Expressing the Protein PD-L1

An open-label, controlled, multi-site, interventional, 2-arm, Phase II/III trial of BNT113 in combination with pembrolizumab vs pembrolizumab monotherapy as first line treatment in patients with unres...

10 locations(Los Angeles, Los Angeles, Palo Alto)
350 participants
BioNTech SE
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RecruitingNCT05081609

A Study to Investigate Safety and Tolerability of TransCon IL-2 β/γ Alone or in Combination With Pembrolizumab and/or TransCon TLR7/8 Agonist or Other Anticancer Therapies in Adult Participants With Locally Advanced or Metastatic Solid Tumor Malignancies

TransCon IL-2 β/γ is an investigational drug being developed for treatment of locally advanced or metastatic solid tumors. This is a first-in-human, open-label, Phase 1/2, dose escalation and dose exp...

10 locations(Los Angeles, Los Angeles, Springfield)
345 participants
Ascendis Pharma Oncology Division A/S
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RecruitingNCT07033494

A Clinical Study of MK-2214 in People With Early Alzheimer's Disease (MK-2214-004)

Researchers want to know if the study treatment called MK-2214 works to slow certain changes in the brains of people with Alzheimer's disease (AD). AD is a type of dementia that can cause loss of memo...

10 locations(Inglewood, Irvine, Long Beach)
340 participants
Merck Sharp & Dohme LLC
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RecruitingNCT05320588

A Study in Patients With Advanced Cancers

A first-in-human study using BIO-106 as a single agent and in combination with pembrolizumab in advanced cancers....

3 locations(Austin, Houston, Fairfax)
332 participants
BiOneCure Therapeutics Inc.
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RecruitingNCT07000084

Testing the Addition of an Anti-Cancer Drug, Gemcitabine, to Usual Treatment (BCG Alone) in People Whose Non-Muscle Invasive Bladder Cancer (NMIBC) Came Back After Prior BCG Therapy

This phase III trial compares the effect of adding gemcitabine to intravesical Bacillus Calmette Guerin (BCG) versus intravesical BCG alone in patients with non-muscle invasive bladder cancer that has...

10 locations(Birmingham, Gilbert, Gainesville)
330 participants
Alliance for Clinical Trials in Oncology
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RecruitingNCT04983810

A Study to Investigate Fadraciclib (CYC065), in Subjects With Advanced Solid Tumors and Lymphoma

This is a 2-part, phase 1/2, open-label, multicenter study designed to evaluate the safety, tolerability, PK, pharmacodynamics, PGx, and efficacy of fadraciclib administered orally BID. This study con...

4 locations(Duarte, Houston, Seoul)
330 participants
Cyclacel Pharmaceuticals, Inc.
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Top Cities for Alzheimers Disease Clinical Trials

Alzheimers Disease clinical trials are recruiting across 282 cities. Here are the cities with the most active studies:

About Alzheimers Disease

Alzheimer's disease is a progressive brain disorder that destroys memory, thinking skills, and the ability to carry out daily tasks. It is the most common cause of dementia, affecting over 6.7 million Americans age 65 and older. The disease is characterized by amyloid-beta plaques and tau tangles in the brain. Recent FDA approvals of anti-amyloid antibodies like lecanemab (Leqembi) and donanemab have opened a new era of disease-modifying treatments. Clinical trials are now exploring next-generation amyloid-clearing therapies, tau-targeting treatments, anti-inflammatory approaches, and combination strategies. Early-stage patients with mild cognitive impairment or early Alzheimer's are frequently sought for enrollment, and many trials now use blood-based biomarkers for screening.

Clinical trials are advancing new treatments for alzheimers disease. Currently, 100 studies are recruiting a combined 86,110 participants across the United States. Research is being conducted by 66 organizations including Hoffmann-La Roche, University of South Florida, American Society of Clinical Oncology and 63 others.

2026 Alzheimers Disease Treatment Landscape & Drug Pipeline

Alzheimer's research has entered a transformative era following the approval of anti-amyloid antibodies. Lecanemab (Leqembi) demonstrated a 27% slowing of cognitive decline in early-stage Alzheimer's, and donanemab showed similar efficacy with the possibility of stopping treatment once amyloid plaques are sufficiently cleared. Current trials are exploring whether these drugs work better when started even earlier — in preclinical Alzheimer's, before memory symptoms appear.

Beyond amyloid, tau-targeted therapies represent the next frontier. Phase 2 trials are testing anti-tau antibodies (semorinemab, zagotenemab, E2814) and tau aggregation inhibitors. Since tau neurofibrillary tangles correlate more closely with cognitive symptoms than amyloid plaques, successful tau therapies could provide more meaningful clinical benefit.

Combination therapy trials — targeting amyloid AND tau simultaneously — are now enrolling. Additionally, GLP-1 receptor agonists (semaglutide, liraglutide) are being tested for neuroprotective effects based on data showing 20–30% lower dementia rates in diabetic patients taking these medications.

Blood-based biomarker screening has revolutionized trial enrollment. Plasma p-tau217 and amyloid beta ratio tests can identify Alzheimer's pathology with a simple blood draw, replacing expensive PET scans ($5,000+) and invasive lumbar punctures.

Patient considerations: Trials typically require a study partner (spouse, adult child) who attends visits and reports on daily functioning. Anti-amyloid therapies carry ARIA risk (amyloid-related imaging abnormalities) — brain edema or microbleeds on MRI — requiring regular brain imaging, especially in the first 6 months. APOE4 gene carriers face higher ARIA risk and should discuss this with the research team.

2026 Alzheimers Disease Research Landscape

As of March 2026, the alzheimers disease clinical trial landscape includes 100 actively recruiting studies across 282 cities in the United States. These studies are collectively seeking 86,110 participants, with an average enrollment target of 861 per study.

Research is being led by 66 different organizations, including Hoffmann-La Roche, University of South Florida, American Society of Clinical Oncology, Merck Sharp & Dohme LLC, Eli Lilly and Company, and 61 others. The large number of sponsors reflects significant research interest and investment in alzheimers disease treatment advancement.

Geographically, alzheimers disease trials are most concentrated in Los Angeles, California (52 trials); Phoenix, Arizona (23 trials); Birmingham, Alabama (20 trials); Boston, Massachusetts (20 trials); Irvine, California (18 trials) and 7 other cities.

Featured Alzheimers Disease Studies

Highlighted recruiting studies for alzheimers disease, selected by enrollment size and research scope.

RecruitingNCT07177352

Screening Study to Determine Individuals With Potential Trial Eligibility for Alzheimer's Disease Studies

This study is a pre-screening process used to assess participants' potential eligibility for Roche interventional Alzheimer's disease studies.

Sponsor: Hoffmann-La Roche· 13,000 participants· 10 locations (Imperial, Inglewood, Irvine, Long Beach)
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RecruitingNCT03848312

Preventing Alzheimer's With Cognitive Training

Dementia is the most expensive medical condition in the US and increases in prevalence with age. More than 5 million Americans have Alzheimer's disease, the most common form of dementia. Mild cognitive impairment is a transitional stage between normal cognitive aging and Alzheimer's disease or another type of dementia, and is indicative of higher risk for dementia. In addition to the obvious healt...

Sponsor: University of South Florida· 7,600 participants· 7 locations (Gainesville, Jacksonville, Jacksonville, Sarasota)
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RecruitingNCT02693535

TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs That Target a Specific Abnormality in a Tumor Gene in People With Advanced Stage Cancer

The purpose of the study is to learn from the real world practice of prescribing targeted therapies to patients with advanced cancer whose tumor harbors a genomic variant known to be a drug target or to predict sensitivity to a drug. NOTE: Due to character limits, the arms section does NOT include all TAPUR Study relevant biomarkers. For additional information, contact TAPUR@asco.org, or if a pat...

Sponsor: American Society of Clinical Oncology· 4,200 participants· 10 locations (Birmingham, Phoenix, Auburn, Berkeley)
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Frequently Asked Questions About Alzheimers Disease Clinical Trials

Are there alzheimers disease clinical trials near me?

Yes, there are 100 alzheimers disease clinical trials currently recruiting across 282+ cities in the United States, including Los Angeles, California; Phoenix, Arizona; Birmingham, Alabama. Browse the studies above to find one at a location convenient for you.

How do I join a alzheimers disease clinical trial?

To join a alzheimers disease clinical trial: 1) Browse the available studies on this page, 2) Click on a study that interests you, 3) Check the study locations to find a site near you, 4) Review the eligibility criteria, and 5) Contact the study site or complete the eligibility form. The process is free and you can withdraw at any time.

Are alzheimers disease clinical trials free?

Yes, participation in alzheimers disease clinical trials is free. Study-related treatments, medical tests, and doctor visits are provided at no cost to participants. Many studies also offer compensation for your time and travel expenses.

What types of alzheimers disease treatments are being studied?

Current alzheimers disease clinical trials are testing a range of approaches. These include new drugs, combination therapies, medical devices, and other interventions sponsored by 66 research organizations.

Is it safe to participate in alzheimers disease clinical trials?

Clinical trials are carefully regulated by the FDA and institutional review boards (IRBs). All trials must follow strict safety protocols, and participants receive close medical monitoring throughout the study. You can withdraw from a trial at any time without penalty.

Data updated March 1, 2026 from ClinicalTrials.gov

About This Data

Clinical trial information on this page is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health (NIH) and National Library of Medicine (NLM). Study data is refreshed every hour to ensure accuracy.

Medical Disclaimer: The information provided on this page is for informational purposes only and does not constitute medical advice. Always consult with a qualified healthcare provider before making decisions about clinical trial participation or changes to your treatment plan.

Page reviewed by the HelloStudys Research Team · Last updated March 1, 2026 · Data from ClinicalTrials.gov