New eczema drug shows promise in Mid-Stage trial
NCT ID NCT07277660
First seen Jun 27, 2026 · Last updated Sep 11, 2026 · Updated 7 times
Summary
This study tests a new medicine called galvokimig in 160 adults with moderate-to-severe atopic dermatitis (eczema). The goal is to see if different doses can reduce skin redness, itching, and rash better than a placebo. Participants will receive injections and be monitored for 16 weeks to check safety and effectiveness.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 160 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participant must be aged greater than or equal (≥)18 years at the time of signing the informed consent * Participant has chronic atopic dermatitis (AtD) (according to American Academy of Dermatology Consensus Criteria) that has been present for at least ≥1 year prior to initiating the study (ie, signing of the informed consent form \[ICF\]) and with: 1. validated Investigator Global Assessment (vIGA) score ≥3 at Screening and Baseline 2. Eczema Area and Severity Index (EASI) score ≥16 at both Screening and Baseline 3. Peak Pruritus Numerical Rating Scale (PP-NRS) score of ≥4 at both Screening and Baseline 4. ≥10% body surface area (BSA) of AtD involvement at both Screening and Baseline 5. Documented recent history (within 6 months prior to Screening) of inadequate response to treatment with topical medications, or study participants for whom topical treatments are otherwise medically inadvisable (eg, due to important side effects or safety risks) and who are candidates for systemic therapy Exclusion Criteria: * Participant has any history or presence of any medical or psychiatric condition, physical examination finding, laboratory test result, or electrocardiogram (ECG) signal that, in the opinion of the investigator, could constitute a risk when taking the study intervention; or interfere with the interpretation of data and could jeopardize or would compromise the study participant's ability to participate in this study * Active dermatologic conditions that may confound the diagnosis of AtD or would interfere with assessment of treatment, such as but not limited to scabies, seborrheic dermatitis, cutaneous lymphoma, ichthyosis, psoriasis, active allergic or irritant contact dermatitis * Presence or family history (first degree) of inflammatory bowel disease (includes Crohn's disease and ulcerative colitis) * History of chronic or recurrent infections, or a serious or life-threatening infection within the 6 months prior to the Baseline (including herpes zoster) as judged by the investigator * Participants are not permitted to enroll into the study if they meet tuberculosis (TB) exclusion criteria * Previous treatment with galvokimig * Participant has relevant safety events to one or more interleukin (IL)-13 biologic response modifiers (ie, dupilumab, tralokinumab and lebrikizumab) that resulted in discontinuation and change of treatment * All systemic therapies (other than biologics), topical therapies and other treatments for AtD must be discontinued at least 4 weeks prior to Baseline * Treatment with biologic agents must discontinued at least 3 months prior to baseline
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Get notified about this study
Sign up to get updates when this study changes or when new studies for Atopic dermatitis are added.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
9 sites in 6 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Atd002 21001
ACTIVE_NOT_RECRUITINGHabikino, Japan
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Atd002 21002
RECRUITINGNagasaki, Japan
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Atd002 21004
ACTIVE_NOT_RECRUITINGTachikawa-shi, Japan
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Atd002 21005
ACTIVE_NOT_RECRUITINGSakai, Japan
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Atd002 21006
ACTIVE_NOT_RECRUITINGYokohama, Japan
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Atd002 21007
ACTIVE_NOT_RECRUITINGNagoya, Japan
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Atd002 21008
ACTIVE_NOT_RECRUITINGSapporo, Japan
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Atd002 41001
ACTIVE_NOT_RECRUITINGPleven, Bulgaria
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Atd002 41002
ACTIVE_NOT_RECRUITINGSevlievo, Bulgaria
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Atd002 41003
RECRUITINGSofia, Bulgaria
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Atd002 41004
ACTIVE_NOT_RECRUITINGLovech, Bulgaria
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Atd002 41005
ACTIVE_NOT_RECRUITINGSofia, Bulgaria
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Atd002 41006
ACTIVE_NOT_RECRUITINGSofia, Bulgaria
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Atd002 41007
ACTIVE_NOT_RECRUITINGPlovdiv, Bulgaria
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Atd002 42001
ACTIVE_NOT_RECRUITINGPrague, Czechia
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Atd002 42002
ACTIVE_NOT_RECRUITINGNáchod, Czechia
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Atd002 42003
ACTIVE_NOT_RECRUITINGPrague, Czechia
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Atd002 42004
ACTIVE_NOT_RECRUITINGPrague, Czechia
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Atd002 42005
ACTIVE_NOT_RECRUITINGPrague, Czechia
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Atd002 43001
ACTIVE_NOT_RECRUITINGBad Bentheim, Germany
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Atd002 43002
RECRUITINGFrankfurt, Germany
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Atd002 43003
RECRUITINGLübeck, Germany
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Atd002 43004
ACTIVE_NOT_RECRUITINGLeipzig, Germany
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Atd002 43005
RECRUITINGDresden, Germany
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Atd002 43007
ACTIVE_NOT_RECRUITINGMahlow, Germany
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Atd002 44001
ACTIVE_NOT_RECRUITINGDebrecen, Hungary
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Atd002 44003
RECRUITINGBudapest, Hungary
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Atd002 45001
ACTIVE_NOT_RECRUITINGKatowice, Poland
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Atd002 45002
ACTIVE_NOT_RECRUITINGWarsaw, Poland
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Atd002 45003
ACTIVE_NOT_RECRUITINGKrakow, Poland
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Atd002 45004
ACTIVE_NOT_RECRUITINGLodz, Poland
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Atd002 45005
ACTIVE_NOT_RECRUITINGSosnowiec, Poland
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Atd002 45006
ACTIVE_NOT_RECRUITINGWarsaw, Poland
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Atd002 45007
ACTIVE_NOT_RECRUITINGKrakow, Poland
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Atd002 45008
ACTIVE_NOT_RECRUITINGWroclaw, Poland
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Atd002 45009
ACTIVE_NOT_RECRUITINGTarnów, Poland
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Atd002 45010
ACTIVE_NOT_RECRUITINGKrakow, Poland
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Atd002 45011
ACTIVE_NOT_RECRUITINGChorzów, Poland
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Atd002 45013
ACTIVE_NOT_RECRUITINGLodz, Poland
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Atd002 45014
ACTIVE_NOT_RECRUITINGKrakow, Poland
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Atd002 46003
ACTIVE_NOT_RECRUITINGSalford, United Kingdom
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Atd002 46004
ACTIVE_NOT_RECRUITINGLondon, United Kingdom
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Atd002 46006
RECRUITINGSheffield, United Kingdom
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Atd002 46007
RECRUITINGLondon, United Kingdom
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Atd002 51002
ACTIVE_NOT_RECRUITINGEdmonton, Canada
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Atd002 51003
ACTIVE_NOT_RECRUITINGVancouver, Canada
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Atd002 51006
ACTIVE_NOT_RECRUITINGHamilton, Canada
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Atd002 51007
ACTIVE_NOT_RECRUITINGToronto, Canada
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Atd002 52001
RECRUITINGTroy, Michigan, 48084, United States
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Atd002 52003
ACTIVE_NOT_RECRUITINGMiami, Florida, 33133, United States
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Atd002 52004
ACTIVE_NOT_RECRUITINGSugar Land, Texas, 77479, United States
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Atd002 52005
ACTIVE_NOT_RECRUITINGDallas, Texas, 75230, United States
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Atd002 52007
ACTIVE_NOT_RECRUITINGMiami, Florida, 33126, United States
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Atd002 52008
ACTIVE_NOT_RECRUITINGSanta Monica, California, 90403, United States
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Atd002 52009
ACTIVE_NOT_RECRUITINGTroy, Michigan, 48084, United States
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Atd002 52010
ACTIVE_NOT_RECRUITINGOmaha, Nebraska, 68144, United States
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Atd002 52011
ACTIVE_NOT_RECRUITINGFrisco, Texas, 75034, United States
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Atd002 52012
ACTIVE_NOT_RECRUITINGNew Albany, Indiana, 47150, United States
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Atd002 52013
ACTIVE_NOT_RECRUITINGBoca Raton, Florida, 33486, United States
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Atd002 52014
ACTIVE_NOT_RECRUITINGBowling Green, Kentucky, 42104, United States
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Atd002 52015
ACTIVE_NOT_RECRUITINGSavannah, Georgia, 31419, United States
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Atd002 52016
ACTIVE_NOT_RECRUITINGFrisco, Texas, 75033, United States
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Atd002 52017
ACTIVE_NOT_RECRUITINGChicago, Illinois, 60657, United States
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Atd002 52018
ACTIVE_NOT_RECRUITINGWheaton, Illinois, 60189, United States
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Atd002 52019
ACTIVE_NOT_RECRUITINGPhiladelphia, Pennsylvania, 19114, United States
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Atd002 52020
ACTIVE_NOT_RECRUITINGThe Bronx, New York, 10455, United States
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Atd002 52021
ACTIVE_NOT_RECRUITINGOceanside, California, 92056, United States
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Atd002 52022
ACTIVE_NOT_RECRUITINGNew York, New York, 10029-6574, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Skin scans may predict who responds to dupilumab for eczema
- Can a daily liquid medicine calm severe eczema in toddlers and preschoolers?
- Scientists probe whether lebrikizumab rewires diseased skin at the molecular level
- Can a Lab-Made antibody calm severe eczema?
- Is your nose fueling infected eczema and scabies sores?
- Can an eczema drug reshape the Skin's microbial community?