100 Active Studies

Atopic Dermatitis Clinical Trials Near You

Also searched as: eczema, skin, itchy skin clinical trials

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

100
Active Trials
278+
Locations
63,708
Participants Needed

Recruiting Studies

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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RecruitingNCT05882877

A Study to Assess Long-term Safety, Tolerability, and Efficacy of Rocatinlimab in Adult and Adolescent Participants With Moderate-to-severe Atopic Dermatitis (AD)

The primary objective of this study is to describe the long-term safety and tolerability of rocatinlimab in participants with moderate-to-severe AD....

10 locations(Birmingham, Phoenix, Phoenix)
2,200 participants
Amgen
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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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RecruitingNCT05492578

Long-Term Safety and Efficacy Evaluation of Amlitelimab in Participants of Previous Amlitelimab Moderate to Severe Atopic Dermatitis Clinical Trials

This is an open-label, Phase 2/Phase 3, long-term extension study for treatment of participants of previous amlitelimab clinical trials in moderate to severe atopic dermatitis. The purpose of this st...

10 locations(Birmingham, Scottsdale, Anaheim)
1,551 participants
Sanofi
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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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RecruitingNCT06407934

A Study to Evaluate the Treatment Response and Safety of Two Dose Regimens of Subcutaneous Amlitelimab Compared With Treatment Withdrawal in Participants Aged 12 Years and Older With Moderate-to-severe Atopic Dermatitis

This is a multinational, multicenter, randomized, double-blind, placebo-controlled, parallel, Phase 3 study for treatment of participants aged 12 years and older diagnosed with moderate-to-severe atop...

10 locations(Scottsdale, Scottsdale, Tempe)
961 participants
Sanofi
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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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RecruitingNCT05769777

Open Label, Long-term Study Evaluating Safety and Efficacy of Subcutaneous Amlitelimab in Participants Aged 12 Years and Older With Moderate to Severe Atopic Dermatitis

This is a single group, 1-arm, long-term safety study for treatment of participants with moderate to severe atopic dermatitis (AD). The purpose of this study is to characterize the long-term safety a...

10 locations(Birmingham, Litchfield Park, Phoenix)
901 participants
Sanofi
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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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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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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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RecruitingNCT06461897

A Study to Assess Adverse Events and Change in Disease Activity Comparing Oral Upadacitinib to Subcutaneous Dupilumab in Children From 2 to Less Than 12 Years of Age With Moderate to Severe Atopic Dermatitis

Atopic dermatitis (AD) is a skin condition that may cause a rash and itching due to inflammation of the skin. Topical therapies applied over the skin may not be enough to control the AD in trial parti...

10 locations(Little Rock, Sacramento, Boca Raton)
675 participants
AbbVie
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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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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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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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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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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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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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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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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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RecruitingNCT06395948

A Study Evaluating APG777 in Atopic Dermatitis

This is a two-part study that will evaluate the safety and efficacy of APG777 in participants with moderate-to-severe Atopic Dermatitis (AD). Part A (Proof-of-concept) and Part B (Dose-regimen Finding...

10 locations(Fountain Valley, Los Angeles, San Diego)
431 participants
Apogee Therapeutics, Inc.
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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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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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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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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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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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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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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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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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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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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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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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RecruitingNCT05559359

A Study of Lebrikizumab (LY3650150) in Participants 6 Months to <18 Years of Age With Moderate-to-Severe Atopic Dermatitis

The main purpose of this study is to measure the effect, safety and how well the body absorbs lebrikizumab in pediatric participants 6 months to \<18 years of age with moderate-to-severe atopic dermat...

10 locations(Birmingham, Phoenix, North Little Rock)
360 participants
Eli Lilly and Company
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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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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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RecruitingNCT07003425

A Long-term Safety and Efficacy Study Evaluating APG777 in Atopic Dermatitis

This is a multicenter, double-blind, Long-Term Extension (LTE) study to evaluate the long-term safety and efficacy of APG777 in patients with moderate-to-severe AD who have completed treatment in an A...

10 locations(Fountain Valley, Coral Gables, Margate)
350 participants
Apogee Therapeutics, Inc.
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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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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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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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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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RecruitingNCT05995964

A Study To Learn About Two Study Medicines (PF-07275315 And PF-07264660) In People Who Have Moderate To Severe Atopic Dermatitis

The purpose of this study is to learn about the safety and effects of 2 study medicines (PF-07275315 and PF-07264660) for the treatment of atopic dermatitis (AD). AD is a long- lasting itchy red rash,...

10 locations(Birmingham, Peoria, Phoenix)
340 participants
Pfizer
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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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RecruitingNCT06241118

A Study to Evaluate the Efficacy and Safety of Subcutaneous Amlitelimab on Background Topical Corticosteroids Therapy in Participants Aged 12 Years and Older With Moderate-to-severe AD Who Have Had an Inadequate Response to Prior Biologic Therapy or an Oral JAK Inhibitor

This is a parallel group, Phase 3, multinational, multicenter, randomized, double-blind, placebo-controlled, 3-arm study for treatment of participants diagnosed with moderate-to-severe AD on backgroun...

10 locations(Birmingham, Scottsdale, North Little Rock)
330 participants
Sanofi
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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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RecruitingNCT04561362

Study BT8009-100 in Subjects With Nectin-4 Expressing Advanced Malignancies

This study is a Phase I/II, multicenter, first-in-human, open-label dose-escalation study of BT8009 given as a single agent and in combination with pembrolizumab in participants with advanced solid tu...

10 locations(Denver, Ocala, Orlando)
329 participants
BicycleTx Limited
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RecruitingNCT06567743

Phase 2 Study to Evaluate Safety and Efficacy of Cretostimogene Grenadenorepvec in High-Risk NMIBC

This is a Phase 2, Multi-Arm, Multi-Cohort, Open-Label Study to Evaluate the Safety and Efficacy of Cretostimogene Grenadenorepvec in Participants with High-Risk Non-Muscle-Invasive Bladder Cancer....

10 locations(Phoenix, Tucson, Little Rock)
325 participants
CG Oncology, Inc.
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RecruitingNCT05541016

De-Escalated Adjuvant and Definitive Radiation Therapy Informed by DART 2.0 ctHPV-DNA

This phase II trial examines the use of blood-based biomarkers is to help inform decision making for treatment and radiation therapy for patients with human papillomavirus (HPV) positive oropharyngeal...

3 locations(Scottsdale, Jacksonville, Rochester)
320 participants
Mayo Clinic
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RecruitingNCT05434234

A Study of YL201 in Patients With Advanced Solid Tumors

This is a phase 1, multicenter, nonrandomized, open-label, first-in-human study of YL201 conducted in China and the United States. The study will include 2 parts: a dose escalation part (Part 1) follo...

10 locations(Fair Oaks, La Jolla, Lone Tree)
312 participants
MediLink Therapeutics (Suzhou) Co., Ltd.
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RecruitingNCT05544552

Safety and Preliminary Anti-Tumor Activity of TYRA-300 in Advanced Urothelial Carcinoma and Other Solid Tumors With FGFR3 Gene Alterations

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of TYRA-300 in cancers with FGFR3 activating gene alterations, including lo...

10 locations(Ocala, Boston, Worcester)
310 participants
Tyra Biosciences, Inc
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RecruitingNCT06973577

P3b Short-term Study of CTN in Patients With ADHD and Comorbid Anxiety

Primary: To evaluate the efficacy of CTN in adults ages with ADHD and comorbid anxiety (AISRS) Key Secondary: To assess the efficacy of CTN in adults ages with ADHD and comorbid anxiety...

10 locations(Dothan, Little Rock, Rogers)
308 participants
Otsuka Pharmaceutical Development & Commercialization, Inc.
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RecruitingNCT06833073

A Clinical Study of Intismeran Autogene (V940) and BCG in People With Bladder Cancer (V940-011/INTerpath-011)

Researchers are looking for new ways to treat people with high-risk non-muscle invasive bladder cancer (HR NMIBC). NMIBC is cancer in the tissue that lines the inside of the bladder but has not spread...

10 locations(Bakersfield, Los Alamitos, Los Angeles)
308 participants
Merck Sharp & Dohme LLC
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RecruitingNCT06188702

S095035 as a Single Agent and in Combination in Adult Participants With Advanced or Metastatic Solid Tumors With Deletion of MTAP

This is a first-in-human Phase 1/2, multicenter, open-label study of S095035 as single-agent, or in combination with TNG462 in adult participants with advanced or metastatic solid tumors with homozygo...

10 locations(Los Angeles, San Francisco, Lake Mary)
308 participants
Servier Bio-Innovation LLC
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RecruitingNCT06439277

A Study of Tirzepatide in Adolescents With Obesity and Weight-Related Comorbidities (SURMOUNT-ADOLESCENTS-2)

The goal of the study is to assess how tirzepatide impacts bodyweight and cardiovascular risk factors when used in conjunction with healthy nutrition and physical activity in adolescents with obesity ...

10 locations(Los Angeles, Sacramento, Wilmington)
300 participants
Eli Lilly and Company
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RecruitingNCT05398484

Psilocybin Therapy in Advanced Cancer

The purpose of this research is to study the safety and effects of single-dose psilocybin 25mg versus an active placebo (single dose niacin 100mg) in the treatment of anxiety, depression, and existent...

2 locations(Aurora, New York)
300 participants
NYU Langone Health
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RecruitingNCT05941507

A Study to Evaluate TROP2 ADC LCB84 Single Agent and in Combination With an Anti-PD-1 Ab in Advanced Solid Tumors

This is a first-in-human, Phase 1/2 study to evaluate LCB84, a TROP2-directed antibody-drug conjugate, alone and in combination with an anti-PD-1 Ab, in dose escalation (Phase 1) followed by dose expa...

8 locations(Los Angeles, Boston, Ann Arbor)
300 participants
LigaChem Biosciences, Inc.
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Top Cities for Atopic Dermatitis Clinical Trials

Atopic Dermatitis clinical trials are recruiting across 278 cities. Here are the cities with the most active studies:

About Atopic Dermatitis

Atopic dermatitis (eczema) is a chronic inflammatory skin condition causing itchy, red, and dry skin. It is the most common form of eczema, often beginning in childhood. Treatment includes moisturizers, topical corticosteroids, immunomodulators, and newer biologics like dupilumab.

Clinical trials are advancing new treatments for atopic dermatitis. Currently, 100 studies are recruiting a combined 63,708 participants across the United States. Research is being conducted by 67 organizations including American Society of Clinical Oncology, Merck Sharp & Dohme LLC, Amgen and 64 others.

2026 Atopic Dermatitis Treatment Landscape & Drug Pipeline

Atopic dermatitis (eczema) trials in 2026 are riding a wave of innovation that began with dupilumab (Dupixent). JAK inhibitors — abrocitinib (Cibinqo), upadacitinib (Rinvoq), and baricitinib (Olumiant) — offer oral alternatives with rapid itch relief, often within days rather than the weeks required for biologics.

Next-generation biologics targeting OX40 ligand (amlitelimab, rocatinumab), IL-13 alone (tralokinumab, lebrikizumab, cendakimab), and IL-31 (nemolizumab for itch) are in Phase 2–3 trials. Nemolizumab is notable for rapid, dramatic pruritus reduction — addressing what patients often describe as the most debilitating AD symptom.

Topical JAK inhibitors (ruxolitinib cream) are approved for mild-to-moderate AD, with additional topical formulations in development. Tapinarof, a topical aryl hydrocarbon receptor (AhR) agonist approved for psoriasis, is also being studied for AD.

Microbiome-based therapies represent an emerging frontier: trials test whether applying beneficial bacteria (like Roseomonas mucosa) to the skin or modifying the gut microbiome can restore the dysfunctional skin barrier and reduce AD flares without immunosuppression.

Patient considerations: AD trials use standardized scoring systems (EASI, IGA, SCORAD) and often require a washout period from current medications. Photography of affected skin areas is standard. Many trials accept patients who have failed topical steroids — prior biologic experience may be required or excluded depending on the specific trial design.

2026 Atopic Dermatitis Research Landscape

As of March 2026, the atopic dermatitis clinical trial landscape includes 100 actively recruiting studies across 278 cities in the United States. These studies are collectively seeking 63,708 participants, with an average enrollment target of 637 per study.

Research is being led by 67 different organizations, including American Society of Clinical Oncology, Merck Sharp & Dohme LLC, Amgen, Guerbet, NRG Oncology, and 62 others. The large number of sponsors reflects significant research interest and investment in atopic dermatitis treatment advancement.

Geographically, atopic dermatitis trials are most concentrated in Los Angeles, California (57 trials); Birmingham, Alabama (23 trials); Boston, Massachusetts (23 trials); Phoenix, Arizona (20 trials); San Diego, California (19 trials) and 7 other cities.

Featured Atopic Dermatitis Studies

Highlighted recruiting studies for atopic dermatitis, selected by enrollment size and research scope.

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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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 extension study. This study will consist of three phases: 1) First Course Phase, 2) Survival Follow-up Phase or 3) Second Course Phase. Each participant will transition to this extension study in one o...

Sponsor: Merck Sharp & Dohme LLC· 3,500 participants· 10 locations (Tucson, Bakersfield, Fresno, Fullerton)
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RecruitingNCT05882877

A Study to Assess Long-term Safety, Tolerability, and Efficacy of Rocatinlimab in Adult and Adolescent Participants With Moderate-to-severe Atopic Dermatitis (AD)

The primary objective of this study is to describe the long-term safety and tolerability of rocatinlimab in participants with moderate-to-severe AD.

Sponsor: Amgen· 2,200 participants· 10 locations (Birmingham, Phoenix, Phoenix, Scottsdale)
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Frequently Asked Questions About Atopic Dermatitis Clinical Trials

Are there atopic dermatitis clinical trials near me?

Yes, there are 100 atopic dermatitis clinical trials currently recruiting across 278+ cities in the United States, including Los Angeles, California; Birmingham, Alabama; Boston, Massachusetts. Browse the studies above to find one at a location convenient for you.

How do I join a atopic dermatitis clinical trial?

To join a atopic dermatitis 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 atopic dermatitis clinical trials free?

Yes, participation in atopic dermatitis 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 atopic dermatitis treatments are being studied?

Current atopic dermatitis clinical trials are testing a range of approaches. These include new drugs, combination therapies, medical devices, and other interventions sponsored by 67 research organizations.

Is it safe to participate in atopic dermatitis 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