ClinicalTrials.gg
Not yet recruitingNCT07665996Updated Aug 24, 2026

A Phase Ib/IIa Study Assessing the Rapid Onset Characteristics of TLL-018 for Moderate-to-Severe CSU With Inadequate Response to Second-Generation H1 Antihistamines

A Phase 1/2 interventional study of TLL-018 and TLL-018 in Chronic Spontaneous Urticaria (CSU), sponsored by Hangzhou Highlightll Pharmaceutical Co., Ltd. Not yet recruiting at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-08-24.

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

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Phase
Phase 1/2
Study type
Interventional
Enrollment
36
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 34 studies in Chronic Urticaria with a site in China — 16 open to participants now, 20 under way, 5 of them phase 3. Chronic Urticaria · China.

Planned enrollment
27th of 30
36 · median 110
Started
2026
with 10 others
Phase 1/2
4 of 34
4 open now
Primary completion
2027-12
later than 17 of 19 live
Registered
30th of 34
by date
Lead sponsor
3 of 34
Hangzhou Highlightll Pharmaceutical Co., Ltd

Among the 34 studies in Chronic Urticaria with a site in China, this one is the 27th largest by planned enrollment of the 30 interventional ones that give a count, is one of 11 that started in 2026, is one of 4 in phase 1/2, reaches primary completion later than 17 of the 19 other live ones, and was the 30th registered.

Chronic Urticaria

196 studies on the registry are indexed under Chronic Urticaria; 48 are open to participants now.

Browse Chronic Urticaria studies →

Open to participants now

16 of the 34 studies in Chronic Urticaria with a site in China are open now. Recruiting first, the newest first:

10 more — sign in →

All 16 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 25 Chronic Urticaria studies recruiting now, 11 (44%) set no upper age limit and 10 (40%) stop at 75 or younger; 1 takes children under 18; 6 take healthy volunteers.

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

The full table on the hub →

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 34 studies in Chronic Urticaria with a site in China, or all of them as a file.
02

Study summary

The goal of this clinical trial is to evaluate the rapid onset characteristics of TLL-018 in moderate-to-severe CSU with inadequate response to second-generation H1 antihistamines.

The main objectives are:

To evaluate the rapid onset characteristics of TLL-018 in participants with moderate-to-severe chronic spontaneous urticaria.

To evaluate the safety profile of TLL-018 in participants with moderate-to-severe chronic spontaneous urticaria.

To evaluate the pharmacokinetic (PK) profile of TLL-018 in participants with moderate-to-severe chronic spontaneous urticaria.

Participants will be randomly allocated at a 1:1:1 ratio to receive TLL-018 10 mg, TLL-018 20 mg, or placebo orally after meals.

03

Conditions studied

  • Chronic Spontaneous Urticaria (CSU)

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

  • Aged between 18 and 75.
  • Diagnosis of CSU to second-generation H1-AH.
  • CSU diagnosis for ≥ 6 months.
  • The presence of itch and hives despite current use of an approved dose of H1-AH for ≥ 6 weeks prior to screening visit.
  • UAS7 score (range 0-42) ≥ 16 and itch component of UAS7 (ISS range 0-21) ≥ 8 during 7 days prior to randomization (Day 1), and ISS ≥2 on the day of randomization.
  • Participants are required to take a stable standard dose of a second generation H1-AH concomitantly according to local guidelines.
  • Willing and able to to comply with the study protocol and complete the participant diary throughout the study period. Participants shall have no more than one missing urticaria symptom score (morning or evening HSS score and ISS score) within 7 days prior to randomization, and no missing HSS score or ISS score on the day immediately before randomization..
  • Women of Child Bearing Potential () should not be pregnant or breastfeeding and the pregnancy test should be negative before randomization.
  • Participants (whether male or female) should have adequate barrier during the whole treatment period and at least 90 days after treatment; subjects should avoid the sperm or ovum donation for at least six months after treatment.

Exclusion criteria

Exclusion Criteria:

  1. Participants who meet the diagnostic criteria for chronic spontaneous urticaria (CSU) shall be excluded if they present with any of the following conditions:

    • Progressive or uncontrolled symptoms of renal, hepatic, hematologic, gastrointestinal, endocrine, pulmonary, cardiovascular, neurological, psychiatric or cerebral disorders that, in the investigator's judgment, would expose the patient to unacceptable risk from study participation.
    • A well-defined underlying etiology of chronic urticaria other than CSU, such as inducible urticaria, including but not limited to dermatographism, cold contact urticaria, heat contact urticaria, delayed pressure urticaria, solar urticaria, vibratory angioedema, cholinergic urticaria, aquagenic urticaria, and contact urticaria.
    • Other diseases presenting with urticaria or angioedema symptoms, including but not limited to urticarial vasculitis, urticaria pigmentosa, erythema multiforme, mastocytosis, hereditary urticaria, drug-induced urticaria, and hereditary or acquired angioedema.
    • Other chronic pruritic diseases that may interfere with efficacy outcome assessment, such as psoriasis, atopic dermatitis, bullous pemphigoid, dermatitis herpetiformis, and senile pruritus.
    • History of any malignant neoplasm prior to screening, with the exception of non-melanoma skin cancer (NMSC) or basal cell carcinoma that has been adequately treated and deemed cured, cervical carcinoma in situ, or ductal carcinoma in situ of the breast.
    • History of lymphoproliferative disorders (including but not limited to Epstein-Barr virus-related lymphoproliferative disorders, lymphoma, leukemia, etc.); or signs or symptoms suggestive of active lymphoproliferative disorder.
    • History of cardiovascular or cerebrovascular events or related surgical procedures within 12 months prior to screening, including but not limited to myocardial infarction, unstable angina pectoris, acute coronary syndrome, cerebral hemorrhage, stroke, coronary artery stent implantation, percutaneous transluminal coronary angioplasty, and coronary artery bypass graft surgery.
    • History of thromboembolic events within 12 months prior to screening (e.g., pulmonary thromboembolism, deep vein thrombosis, mesenteric artery embolism); or current high-risk factors for thromboembolic diseases (e.g., immobilization within 12 weeks prior to screening, congenital or hereditary thrombophilia, antiphospholipid antibody syndrome, etc.).
    • History of gastrointestinal perforation, except for cases caused by appendicitis or trauma.
    • History of herpes zoster within 1 year prior to randomization; history of disseminated herpes zoster or recurrent herpes zoster at any time prior to randomization; history of disseminated herpes simplex at any time prior to randomization.
    • Positive prior to randomization (or negative HBsAg with positive HBcAb and abnormal HBV-DNA test results), positive antibody (with abnormal HCV-RNA test results), positive antibody, or positive syphilis serological antibody; or known HIV infection or known immunodeficiency status.
    • Any severe or systemic infection (bacterial, fungal, viral, parasitic, etc.) requiring intravenous antimicrobial therapy or resulting in hospitalization within 4 weeks prior to randomization; or any other active or recent infection that, in the investigator's judgment, would expose the participating patient to unacceptable risk.
    • Tuberculosis-related exclusion: Medical history, symptoms and relevant test results (e.g., tuberculosis screening test, chest X-ray) at screening suggest active tuberculosis.
    • History of severe hematologic disorders (e.g., aplastic anemia, myelodysplastic syndrome) or any disease that may cause hemolysis or erythrocyte instability, such as malaria and hemolytic anemia.
  2. Participants with any of the following prior therapies or concomitant medications cannot be enrolled:

    • Receipt of treatment with JAK inhibitors (e.g., tofacitinib, baricitinib, ruxolitinib, etc.) or BTK inhibitors (e.g., remibrutinib) within 4 weeks prior to randomization.
    • Receipt of any medicinal product within 4 weeks or 5 elimination half-lives prior to randomization, whichever is longer.
    • Prior exposure to omalizumab or omalizumab biosimilars.
    • Use of biologic agents with potential therapeutic effect on chronic spontaneous urticaria (CSU) (e.g., dupilumab, GR1802, SYB507, etc.) within 3 months or 5 elimination half-lives prior to randomization, whichever is longer.
    • Receipt of or immunomodulatory agents within 4 weeks prior to randomization, including but not limited to systemic , ciclosporin, Tripterygium wilfordii tablets, Tripterygium glycosides tablets, methotrexate, mycophenolate mofetil, azathioprine, tacrolimus, dapsone, sulfasalazine and hydroxychloroquine.
    • Receipt of Traditional Chinese Medicine (TCM) or Chinese patent medicine explicitly indicated for urticaria per the package insert, clinical practice guidelines or prescription, within 4 weeks prior to randomization.
    • Receipt of topical therapy or phototherapy for CSU within 2 weeks prior to randomization.
    • Underwent major surgery within 4 weeks prior to randomization, or is scheduled to undergo major surgery after study enrollment.
    • Received any within 2 months prior to screening, or plans to receive any live vaccine during the study period.
    • Donated a total of ≥400 mL of blood, or received blood transfusion, within 3 months prior to randomization.
    • History of drug or alcohol abuse within 6 months prior to screening (defined as 14 units of alcohol per week; 1 unit = 17.7 mL of pure ethanol, equivalent to 357 mL of 5% ABV beer, 43 mL of 40% ABV liquor, or 147 mL of 12% ABV wine).
  3. History of allergy to any component of the investigational medicinal product or H1-antihistamines, or history of anaphylactic shock.
  4. Abnormal findings at screening that meet any of the following criteria:

    • Complete blood count (CBC): (Hb) \< 90 g/L; or white blood cell (WBC) count \< 2.5 × 10⁹/L; or (ANC) \< 1.5 × 10⁹/L; or absolute lymphocyte count (ALC) \< 0.8 × 10⁹/L; or (PLT) count \< 100 × 10⁹/L.
    • Liver function: (AST) or alanine aminotransferase (ALT) > 2 × (ULN), or total (TBIL) > 2 × ULN.
    • nSerum creatinine ≥ 1.2 × ULN.
    • Coagulation function: either (PT) or activated partial thromboplastin time (APTT) exceeds the ULN and is .
    • Uncontrolled hypertension (systolic blood pressure [SBP] ≥ 160 mmHg and/or diastolic blood pressure [DBP] ≥ 100 mmHg). One repeat measurement shall be performed for confirmation: if the initial blood pressure reading exceeds the above threshold, a repeat test will be conducted after the participant has rested for at least 10 minutes; if the repeat result is below the threshold, the second measurement value shall be adopted.
    • Uncontrolled hyperlipidemia (fasting total cholesterol ≥ 7.2 mmol/L, or fasting low-density lipoprotein cholesterol [LDL-C] ≥ 4.9 mmol/L, or fasting triglycerides [TG] > 5.6 mmol/L).
    • Abnormal cardiac function, or clinically significant abnormal (ECG) findings that are assessed by the investigator to pose unpredictable risks, such as severe arrhythmia.
    • Other abnormal examination findings that, in the investigator's judgment, may impair the participant's ability to complete the study or interfere with study outcomes.
  5. Any other condition or circumstance that, in the investigator's judgment, renders the participant unsuitable for participation in this study.
Terms in these criteria, in plain language(19)

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.

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

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.

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.

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.

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.

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.

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.

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.

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.

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).

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.

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.

INR, PT and aPTT (clotting tests)

Blood tests of how long blood takes to clot. The INR is the prothrombin time (PT) put on a common scale; about 1 is usual for someone not taking a blood thinner.

Criteria often make an exception for people on a blood thinner such as warfarin, whose INR is raised on purpose.

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.

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.

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
36 participants (estimated)

Study arms

  • Experimental
    Arm 1

    TLL-018 10 mg

    Drug: TLL-018 · Drug: Placebo

  • Experimental
    Arm 2

    TLL-018 20 mg

    Drug: TLL-018

  • Placebo comparator
    Arm 3

    Placebo

    Drug: Placebo

Interventions

  • Participants will receive TLL-018 10 mg (1 tablet) and placebo (1 tablet) orally after meals, with a dosing interval of 12 hours (±15 minutes)

  • Participants will receive TLL-018 20 mg (2 tablets) orally after meals, with a dosing interval of 12 hours (±15 minutes)

  • DrugPlacebo

    Participants will receive placebo (2 tablets) orally after meals, with a dosing interval of 12 hours (±15 minutes)

06

What researchers measure

Primary outcomes

  1. Time to first achievement of ≥1-point reduction from baseline in in-clinic Itch Severity Scale after first dose

    Time from first dose until the first clinic assessment where a ≥1-point reduction from baseline in Itch Severity Scale (ISS, range 0-3; higher = worse itch) at in-clinic evaluation.

    Time frame: First dose up to day 2

  2. Time to first ≥1-point reduction from baseline in in-clinic Hive Severity Scale after first dose

    Time from first dose to the first in-clinic assessment with ≥1-point reduction from baseline on Hive Severity Scale (HSS, 0-3).

    Time frame: First dose up to day 2

  3. Change from baseline in in-clinic Itch Severity Scale post first dose

    Mean change from baseline of in-clinic ISS (0-3) at scheduled timepoints after first dose.

    Time frame: First dose up to 8 hours post first dose

  4. Change from baseline in in-clinic Hive Severity Scale post first dose

    Mean change from baseline of in-clinic Hive Severity Scale (0-3) at scheduled timepoints after first dosing.

    Time frame: First dose up to 8 hours post first dose

  5. Change from baseline in in-clinic Numeric Rating Scale post first dose

    Mean change from baseline of in-clinic Numeric Rating Scale (clinic NRS, 0-10) at scheduled timepoints after first dosing.

    Time frame: First dose up to 8 hours post first dose

  6. Proportion of participants with ≥1-point reduction from baseline in in-clinic Itch Severity Scale post first dose

    Percentage of participants achieving ≥1-point reduction from baseline on in-clinic Itch Severity Scale (0-3) at each in-clinic timepoint post first dose.

    Time frame: First dose up to 8 hours post first dose

  7. Proportion of participants with ≥1-point reduction from baseline in in-clinic Hive Severity Scale post first dose

    Hive Severity Scale (HSS, range 0-3; higher = worse hive)

    Time frame: First dose up to 8 hours post first dose

  8. Proportion of participants with ≥3-point reduction from baseline in in-clinic Numeric Rating Scale post first dose (baseline clinic Numeric Rating Scale ≥3)

    Percentage of participants with baseline NRS score ≥3 who attain ≥3-point reduction from baseline on NRS (0-10) at each in-clinic assessment after first dose.

    Time frame: First dose up to 8 hours post first dose

  9. Proportion of participants with ≥4-point reduction from baseline in in-clinic Numeric Rating Scale post first dose (baseline clinic Numeric Rating Scale ≥4)

    Percentage of participants with baseline Numeric Rating Scale score ≥4 who attain ≥4-point reduction from baseline on NRS (0-10) at each in-clinic assessment after first dose.

    Time frame: First dose up to 8 hours post first dose

  10. Change from baseline in Itch Severity Scale at Day 0.5, Day 1, Day 1.5 post first dose

    Itch Severity Scale (ISS, range 0-3; higher = worse itch)

    Time frame: First dose up to 1.5 days post first dose

  11. Change from baseline in Hive Severity Scale at Day 0.5, Day 1, Day 1.5 post first dose

    Hive Severity Scale (HSS, range 0-3; higher = worse hive)

    Time frame: First dose up to 1.5 days post first dose

  12. Change from baseline in Worst Itch Numeric Rating Scale at Day 0.5, Day 1, Day 1.5 post first dose

    Itch Numeric Rating Scale (NRS): from 0 (no itch) to 10 (worst imaginable itch)

    Time frame: First dose up to 1.5 days post first dose

  13. Change from baseline in in-clinic Itch Severity Scale at 2 hours post second dose

    Itch Severity Scale (ISS, range 0-3; higher = worse itch)

    Time frame: 2 hours post second dose

  14. Change from baseline in in-clinic Hive Severity Scale at 2 hours post second dose

    Hive Severity Scale (HSS, range 0-3; higher = worse hive)

    Time frame: 2 hours post second dose

  15. Change from baseline in in-clinic Numeric Rating Scale at 2 hours post second dose

    Itch Numeric Rating Scale (NRS): from 0 (no itch) to 10 (worst imaginable itch)

    Time frame: 2 hours post second dose

  16. Proportion of participants with ≥1-point reduction from baseline in in-clinic Itch Severity Scale at 2 hours post second dose

    Itch Severity Scale (ISS, range 0-3; higher = worse itch)

    Time frame: 2 hours post second dose

  17. Proportion of participants with ≥1-point reduction from baseline in in-clinic Hive Severity Scale at 2 hours post second dose

    Hive Severity Scale (HSS, range 0-3; higher = worse hive)

    Time frame: 2 hours post second dose

  18. Proportion of participants with ≥3-point reduction from baseline in in-clinic Numeric Rating Scale at 2 hours post second dose (baseline clinic Numeric Rating Scale ≥3)

    Itch Numeric Rating Scale (NRS): from 0 (no itch) to 10 (worst imaginable itch)

    Time frame: 2 hours post second dose

  19. Proportion of participants with ≥4-point reduction from baseline in in-clinic Numeric Rating Scale at 2 hours post second dose (baseline clinic Numeric Rating Scale ≥4)

    Itch Numeric Rating Scale (NRS): from 0 (no itch) to 10 (worst imaginable itch)

    Time frame: 2 hours post second dose

Secondary outcomes

  1. Change from baseline in in-clinic Itch Severity Scale within 1 hour prior to third dose and at 2 hours post third dose

    Itch Severity Scale (ISS, range 0-3; higher = worse itch)

    Time frame: Within 1 hour prior to third dose to 2 hours post third dose

  2. Change from baseline in in-clinic Hive Severity Scale within 1 hour prior to third dose and at 2 hours post third dose

    Hive Severity Scale (HSS, range 0-3; higher = worse hive)

    Time frame: Within 1 hour prior to third dose to 2 hours post third dose

  3. Change from baseline in in-clinic Numeric Rating Scale within 1 hour prior to third dose and at 2 hours post third dose

    Itch Numeric Rating Scale (NRS): from 0 (no itch) to 10 (worst imaginable itch)

    Time frame: Within 1 hour prior to third dose to 2 hours post third dose

  4. Proportion of participants with ≥1-point reduction from baseline in in-clinic Itch Severity Scale within 1 hour prior to third dose and at 2 hours post third dose

    Itch Severity Scale (ISS, range 0-3; higher = worse itch)

    Time frame: Within 1 hour prior to third dose to 2 hours post third dose

  5. Proportion of participants with ≥1-point reduction from baseline in in-clinic Hive Severity Scale within 1 hour prior to third dose and at 2 hours post third dose

    Hive Severity Scale (HSS, range 0-3; higher = worse hive)

    Time frame: Within 1 hour prior to third dose to 2 hours post third dose

  6. Proportion of participants with ≥3-point reduction from baseline in in-clinic Numeric Rating Scale within 1 hour prior to third dose and at 2 hours post third dose (participants with baseline in-clinic Numeric Rating Scale ≥3)

    Itch Numeric Rating Scale (NRS): from 0 (no itch) to 10 (worst imaginable itch)

    Time frame: Within 1 hour prior to third dose to 2 hours post third dose

  7. Proportion of participants with ≥4-point reduction from baseline in in-clinic Numeric Rating Scale within 1 hour prior to third dose and at 2 hours post third dose (participants with baseline clinic Numeric Rating Scale ≥4)

    Itch Numeric Rating Scale (NRS): from 0 (no itch) to 10 (worst imaginable itch)

    Time frame: Within 1 hour prior to third dose to 2 hours post third dose

Other outcomes

  1. Incidence of Treatment-Emergent Adverse Events and Serious Adverse Events

    To demonstrate the safety and tolerability of TLL-018 by assessing occurrence of treatment emergent adverse events and serious adverse events during the study.

    Time frame: From the first dosing to Day 3

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Aug 2026; primary completion for Dec 2027, 16 months later.

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

Registered
Jun 18, 2026
First posted
Jun 24, 2026
StartEst.
Aug 15, 2026
Primary completionEst.
Dec 31, 2027
CompletionEst.
Dec 31, 2027
Last update
Aug 24, 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 Aug 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07665996
Responsible party
Sponsor
First posted
Jun 24, 2026
Start date
Aug 15, 2026 (estimated)
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Aug 24, 2026

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: TLL-018

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