ClinicalTrials.gg
RecruitingNCT07629778Updated Jun 23, 2026

HL-300 Ointment in Patients With Mild-to-Moderate Atopic Dermatitis

A Phase 1/2 interventional study of HL-300 and Placebo in Atopic Dermatitis, sponsored by Hangzhou Highlightll Pharmaceutical Co., Ltd. Recruiting at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-06-23.

Sponsored by Hangzhou Highlightll Pharmaceutical Co., Ltd · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Started May 2026; still recruiting 5 months later.

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Phase
Phase 1/2
Study type
Interventional
Enrollment
156
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-14

Among 205 studies in Dermatitis, Atopic with a site in China — 64 open to participants now, 81 under way, 29 of them phase 3. Dermatitis, Atopic · China.

Planned enrollment
105th of 189
156 · median 165
Started
2026
with 30 others
Phase 1/2
14 of 205
4 open now
Primary completion
2027-06
later than 47 of 80 live
Registered
193rd of 205
by date

Among the 205 studies in Dermatitis, Atopic with a site in China, this one is the 105th largest by planned enrollment of the 189 interventional ones that give a count, is one of 31 that started in 2026, is one of 14 in phase 1/2, reaches primary completion later than 47 of the 80 other live ones, and was the 193rd registered.

Dermatitis, Atopic

1,592 studies on the registry are indexed under Dermatitis, Atopic; 287 are open to participants now.

Browse Dermatitis, Atopic studies →

Open to participants now

64 of the 205 studies in Dermatitis, Atopic with a site in China are open now. Recruiting first, the newest first:

58 more — sign in →

All 64 open studies →

A study can be open while its sites in China have not opened yet or have stopped. Only those recruiting at a site in China →

Who these studies take

Of the 195 Dermatitis, Atopic studies recruiting now, 83 (43%) set no upper age limit and 96 (49%) stop at 75 or younger; 94 take children under 18; 52 take healthy volunteers.

This study: 18 Years to 75 Years · all sexes · no healthy volunteers.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 205 studies in Dermatitis, Atopic with a site in China, or all of them as a file.
02

Study summary

This study is a randomized, double-blind, placebo-controlled, multicenter Phase Ib/II clinical study designed to evaluate the efficacy, safety, and PK characteristics of HL-300 ointment with different concentration regimens for mild-to-moderate AD.

Read the detailed description

In the study, it is planned to enroll approximately 148-156 trial participants, divided into two cohorts. Cohort 1: a randomized, double-blind, placebo-parallel controlled study design, planning to enroll 140 trial participants, randomized in a 1:1:1:1 ratio to the study group or placebo group, with baseline disease severity (mild [vIGA-AD = 2] and moderate [vIGA-AD = 3]) set as stratification factors to ensure balanced participant status across groups. Cohort 2: an open-label, intensive sampling design, planning to enroll 8 trial participants for each dosage strength, enrolled separately, with continuous dosing for 8 days.

The study includes a screening period, a treatment period, and a follow-up period. The quality management system for this trial aims to prospectively integrate quality by design into all aspects of the trial to ensure the rights and interests, safety, and well-being of trial participants, and to guarantee the reliability of the generated data and the scientific validity of the trial results. This system strictly adheres to the principles of ICH E6(R3) and ICH E8(R1), employing a risk-based and proportionate approach.

During the trial design phase, the investigators have systematically identified the critical to quality (CtQ) factors for ensuring the quality of this trial. Given the known safety profile of JAK inhibitors (e.g., infections, hematologic abnormalities, hepatic and renal function effects, thrombosis, etc.), the CtQ factors for this trial will specifically focus on:

  • Trial participant safety: Identification, recording, assessment, and timely reporting of Adverse Events (AEs) and Serious Adverse Events (SAEs).
  • Key efficacy data: Accuracy and integrity of data collection related to the primary and secondary endpoints of the trial (e.g., vIGA-AD, EASI, BSA, WI-NRS, DLQI, SCORAD, etc.).
  • Critical processes: Strict adherence to inclusion/exclusion criteria during participant screening [e.g., exclusion of severe infections (including herpes zoster, tuberculosis, and other opportunistic infections) and active infections, hematologic toxicity (anemia, neutropenia), elevated transaminases, and high-risk thrombosis population], protocol-mandated laboratory tests (e.g., blood routine, blood biochemistry, urinalysis, coagulation function, etc.), completeness of randomization and blinding, concomitant medication management (e.g., contraindications for topical medications for AD or AD-related skin infections, systemic treatments for AD, systemic immunosuppressants or immunomodulators, other JAK inhibitors, etc.), rules for suspension/termination of dosing.
03

Conditions studied

  • Atopic Dermatitis

Browse trials for

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age ≥18 years and ≤75 years at the time of ICF signing, with no gender restriction
  2. Meeting the Hanifin \& Rajka diagnostic criteria for atopic dermatitis (AD) at screening, with a history of AD ≥ 6 months before screening, and the AD condition judged by the investigator to be stable within 4 weeks prior to ICF signing,.
  3. vIGA-AD score of 2-3 at screening and baseline visits;
  4. EASI score within the range of 5-21 at screening and baseline;
  5. "Body Surface Area (BSA) affected by AD skin lesions meeting one of the following requirements at screening and baseline visits, with skin lesions suitable for topical treatment:

    • Cohort 1: BSA of 5% to 20%;
    • Cohort 2: BSA of 15% to 25%. "
  6. Women of and men willing to use at least one highly effective method of or practice abstinence from the time of signing until 3 months after the last dose of the product
  7. Those who voluntarily participate in the study and sign the informed consent form

Exclusion criteria

Exclusion Criteria:

  1. "Trial participants with any of the following medical histories or abnormal conditions at screening: (1) Skin lesions or abnormalities that may affect the assessment of the product application site; (2) skin diseases that are for the study or affect the assessment of the application site, including but not limited to: psoriasis, acne, skin cancer; (3) Other diseases besides AD, such as inflammatory bowel disease, rheumatoid arthritis, where the investigator believes the disease would unfavorably impact the assessment of this study; (4) Current or history of lymphoproliferative disorders, or signs or symptoms suggestive of possible lymphoproliferative disorders, including lymphadenopathy or splenomegaly; (5) Any , or any history of malignancy within 5 years prior to screening (except for completely resected cervical carcinoma in situ or non- cutaneous squamous cell carcinoma, basal cell carcinoma, or papillary thyroid carcinoma); (6) History of herpes virus infection within the past 6 months, or recurrent herpes zoster (≥2 episodes), disseminated herpes zoster, disseminated herpes simplex, or current inability to rule out herpes zoster or herpes simplex infection; (7) Systemic infection requiring hospitalization within 12 weeks prior to screening to baseline, or active bacterial, viral, fungal, parasitic, or other infections requiring anti-infective treatment within 4 weeks prior to screening to baseline; (8) Local active infection within 1 week prior to screening to baseline, such as active infected AD, or any superficial skin infection requiring oral or intravenous antibiotic, antifungal, or antiviral medication; (9) History of thrombotic events, including deep vein thrombosis and pulmonary embolism, or high-risk factors for thromboembolism (e.g., immobilization or prolonged bed rest), which is judged by the investigator's comprehensive clinical assessment to be unsuitable for participation in this study; (10) History of significant cardiovascular, neurological, respiratory, hematological, digestive, urinary, immune, or psychiatric diseases that the investigator believes may confound study results or affect drug absorption, distribution, metabolism, and excretion, or place the trial participant at undue risk; (11) History of drug abuse or substance abuse."
  2. "Trial participants who have received any of the following treatments: (1) Use of topical skin products for AD or AD-related skin infections at the study application site within 2 weeks prior to baseline, including but not limited to: topical (TCS), topical calcineurin inhibitors (TCI), topical phosphodiesterase 4 (PDE-4) inhibitor ointments, topical antimicrobials, etc.; (2) Use of topical skin products containing chemically active ingredients (including but not limited to vitamin E cream, functional products containing niacinamide/urea/ceramide, excluding emollients without any chemically active ingredients) at the study application site within 1 week prior to baseline; (3) Use of systemic therapeutic drugs for AD within 4 weeks or 5 half-lives (whichever is longer) prior to baseline, including but not limited to systemic anti-infectives, PDE-4 inhibitors, and systemic traditional Chinese medicine or herbal medicines for AD; (4) Use of systemic or topical JAK inhibitors (such as ruxolitinib, tofacitinib, baricitinib, filgotinib, lestaurtinib, pacritinib, delgocitinib, upadacitinib, abrocitinib, etc.) within 12 weeks prior to baseline; (5) Use of sedating antihistamines within 2 weeks prior to baseline (Stable use of non-sedating antihistamines is permitted [dose stable for 2 weeks or 5 half-lives (whichever is longer) before the first study medication]); (6) Use of systemic or immunomodulators (such as oral or injectable corticosteroids, methotrexate, cyclosporine, mycophenolate mofetil, and azathioprine) within 4 weeks or 5 half-lives (whichever is longer) prior to baseline; (7) Use of biologics (such as dupilumab) within 12 weeks or 5 half-lives (whichever is longer) prior to baseline; (8) Use of strong CYP450 inhibitors or inducers within 2 weeks prior to baseline, including but not limited to: nelfinavir, ritonavir, clarithromycin, itraconazole, nevirapine, and barbiturates; (9) Vaccination with live/attenuated within 4 weeks prior to baseline, or planning to receive vaccination during the study period; (10) Sunbathing or phototherapy (including ultraviolet therapy, photochemotherapy, etc.) with AD therapeutic effects within 4 weeks prior to baseline;"
  3. "Trial participants with any of the following laboratory and instrumental examination results:

(1) Any significant clinical and laboratory abnormalities that the investigator believes may affect trial participant safety, including but not limited to:

  1. White blood cell count (WBC) \< 3×109/L, (ANC) \< 1.5×109/L, absolute lymphocyte count (ALC) \< 0.8×109/L, count (PLT) \< 100×109/L, (Hb) \< 100 g/L;
  2. (AST) or alanine aminotransferase (ALT) > 2× , or total (TBIL) ≥ 1.5× ULN;
  3. Blood creatinine > 1.5× ULN; (2) Confirmed or suspected active tuberculosis, incompletely cured tuberculosis, or active Mycobacterium tuberculosis infection (except for trial participants with documented treatment proving adequate therapy, who may enter this study based on the medical judgment of the investigator and/or infectious disease specialist) judged by the investigator and/or infectious disease specialist (combining medical history, symptoms, signs, laboratory tests, tuberculosis screening tests, and imaging findings); (3) corrected by Fridericia formula (QTcF) ≥500 ms in 12- results at screening; (4) surface antigen (HBsAg) positive; HBsAg negative but hepatitis B core antibody (HBcAb) positive and HBV-DNA above detection limit, or antibody (HIV) positive, or anti- virus (HCV) antibody positive and HCV-RNA positive, or Treponema pallidum antibody positive (excluding trial participants with negative non-specific syphilis antibody results and judged by the investigator to have a past history of syphilis infection that has been cured);" 4.Known or suspected allergy to the investigational product or in the investigational product; 5.Female trial participants who are suspected or known to be pregnant, breastfeeding, or planning pregnancy during the trial period; 6.History of major surgery within 4 weeks prior to baseline or planned surgery during the study; 7.Significant blood loss, received blood transfusion, or donated blood (≥400 mL) within 3 months prior to baseline; 8.Participation in other clinical trials within 3 months prior to baseline; 9.Weekly alcohol consumption greater than 14 units within 3 months prior to screening (1 unit of alcohol ≈ 360 mL beer or 45 mL spirits with 40% alcohol content or 150 mL wine); 10.Other conditions judged by the investigator to be unsuitable for participation in the study.
Terms in these criteria, in plain language(24)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Live vaccines

Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.

Absolute neutrophil count (ANC)

The number of neutrophils, white blood cells that help fight infection, in a given amount of blood. Too few raises the risk of infection.

It is a count, not a percentage of the white cells. Limits are written in units that mean the same: ≥ 1.5 × 10⁹/L is ≥ 1,500 per mm³ (µL). Each lab has its own reference range.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
156 participants (estimated)

Study arms

  • Placebo comparator
    Group D

    Drug: Placebo

  • Experimental
    Group A

    Group A:0.25%

    Drug: HL-300

  • Experimental
    Group B

    Group B:0.5%

    Drug: HL-300

  • Experimental
    Group C

    Group C:1.0%

    Drug: HL-300

Interventions

  • DrugHL-300

    Group A receives the investigational product at a concentration of 0.25%, BID,4 weeks.

  • DrugPlacebo

    BID, day 7.

  • DrugHL-300

    Group B receives the investigational product at a concentration of 0.5%, BID,4 weeks.

  • DrugHL-300

    Group A receives the investigational product at a concentration of 1.0%, BID,4 weeks.

06

What researchers measure

Primary outcomes

  1. Eczema Area and Severity Index (EASI)

    Percentage change from baseline in Eczema Area and Severity Index (EASI) score at Week 4 (W4). The EASI score ranges from 0 to 72, with higher scores indicating more severe AD.

    Time frame: 4 weeks

Secondary outcomes

  1. Eczema Area and Severity Index(EASI)

    Change from baseline in EASI score at Weeks 1, 2, 3, 4, and 6 after treatment. The EASI score ranges from 0 to 72, with higher scores indicating more severe AD.

    Time frame: at Weeks 1, 2, 3, and 6 after treatment.

  2. EASI50(≥50% improvement from baseline in EASI score)

    Proportion of trial participants with ≥50% improvement from baseline in EASI score (EASI50) at Weeks 1, 2, 3, 4, and 6 after treatment. The EASI score ranges from 0 to 72, with higher scores indicating more severe AD.

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment

  3. EASI75(≥75% improvement from baseline in EASI score)

    Proportion of trial participants with ≥75% improvement from baseline in EASI score (EASI75) at Weeks 1, 2, 3, 4, and 6 after treatment. The EASI score ranges from 0 to 72, with higher scores indicating more severe AD.

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment

  4. EASI90(≥90% improvement from baseline in EASI score)

    Proportion of trial participants with ≥90% improvement from baseline in EASI score (EASI90) at Weeks 1, 2, 3, 4, and 6 after treatment. The EASI score ranges from 0 to 72, with higher scores indicating more severe AD.

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment.

  5. Validated Investigator Global Assessment for Atopic Dermatitis(vIGA-AD)

    Proportion of trial participants achieving vIGA-AD score of 0 (clear) or 1 (almost clear) and ≥2-point improvement from baseline at Weeks 1, 2, 3, 4, and 6 after treatment. The vIGA-AD scale divides disease severity into 5 grades (0 = clear; 1 = almost clear; 2 = mild; 3 = moderate; 4 = severe), each corresponding to specific skin lesion morphological characteristics. A higher grade indicates greater severity.

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment.

  6. Validated Investigator Global Assessment for Atopic Dermatitis(vIGA-AD)

    Proportion of trial participants achieving vIGA-AD score of 0 or 1 at Weeks 1, 2, 3, 4, and 6 after treatment. The vIGA-AD scale divides disease severity into 5 grades (0 = clear; 1 = almost clear; 2 = mild; 3 = moderate; 4 = severe), each corresponding to specific skin lesion morphological characteristics. A higher grade indicates greater severity.

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment.

  7. Numeric Rating Scale (NRS)

    Change from baseline in weekly average itch Numeric Rating Scale (NRS) at Weeks 1, 2, 3, 4, and 6 after treatment. This scale assesses the most severe itch intensity subjectively felt by the trial participant due to AD in the past 24 h. The scale rates itch intensity on 10 levels (0 means no itch, 10 means the worst itch imaginable), with integer scores.The higher the score, the greater the disease severity.

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment.

  8. Numeric Rating Scale (NRS)

    Percentage of trial participants with ≥4-point improvement from baseline in weekly average itch NRS at Weeks 1, 2, 3, 4, and 6 after treatment. This scale assesses the most severe itch intensity subjectively felt by the trial participant due to AD in the past 24 h. The scale rates itch intensity on 10 levels (0 means no itch, 10 means the worst itch imaginable), with integer scores.The higher the score, the greater the disease severity.

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment

  9. Scoring Atopic Dermatitis(SCORAD)

    \]Change from baseline and percentage change from baseline in Scoring Atopic Dermatitis (SCORAD) at Weeks 1, 2, 3, 4, and 6 after treatment. The SCORAD score ranging from 0 to 103 points. Based on the score, the condition is classified as mild (0-24 points), moderate (25-50 points), and severe (\>50 points).

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment.

  10. Body Surface Area (BSA)

    Change from baseline and percentage change from baseline in Body Surface Area (BSA) affected by AD at Weeks 1, 2, 3, 4, and 6 after treatment. The BSA ranges from 0% to 100%. The larger the range, the more severe the affected area.

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment.

  11. Dermatology Life Quality Index (DLQI)

    Change from baseline in Dermatology Life Quality Index (DLQI) score at Weeks 1, 2, 3, 4, and 6 after treatment. DLQI contains 10 questions, with a total score ranging from 0 to 30.The higher the score, the greater the impact on quality of life.

    Time frame: at Weeks 1, 2, 3, 4, and 6 after treatment.

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started May 2026 (actual). Primary completion is estimated for Jun 2027, 13 months after the start.

Of 25 industry-sponsored phase 1/2 interventional studies under Dermatitis, Atopic, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 8 and three quarters within 38. This study's planned 13 months is below that.

Counting every sponsor, half of 29 studies reached it within 22 months; a quarter within 8 and three quarters within 38.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 1, 2026
First posted
Jun 5, 2026
StartActual
May 26, 2026
Primary completionEst.
Jun 30, 2027
CompletionEst.
Dec 31, 2027
Last update
Jun 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07629778
Responsible party
Sponsor
First posted
Jun 5, 2026
Start date
May 26, 2026
Primary completion
Jun 30, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Jun 23, 2026

Study contacts

Wu Liming NA, Doctor of Medicine
principal investigator · First People's Hospital of Hangzhou

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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