New hope for kids with severe psoriasis: QLETLI shows promise
NCT ID NCT05803187
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether QLETLI, a biosimilar of adalimumab, is safe and effective for children and teens aged 4 to 17 with severe plaque psoriasis. A total of 80 participants were followed for 24 weeks. The main goal was to see how much their psoriasis symptoms improved, measured by skin clearance scores.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- QLETLI (adalimumab biosimilar)
- What this could lead to
- If successful, this could provide a safe and effective treatment option for children with severe plaque psoriasis who have not responded to other therapies.
- What could go wrong
- This is a small, observational study without a comparison group, so results may not be definitive. As a biosimilar, it may carry similar risks to adalimumab, including infections.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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80 people
The number who actually took part.
- Started
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Apr 2023
- Finished
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Mar 2025
- 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.
Who is studied
A total of 80 children and adolescents with severe plaque psoriasis were enrolled in this study. Selected recipient Candidates must meet all inclusion criteria and not meet any exclusion criteria. Before performing any specific evaluation or Prior to the procedure, all subjects and/or guardians must sign written informed consent.
- Ages
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4 to 18 years
- 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: 1. ) Patients and / or patient guardians voluntarily participated in the study and signed informed consent 2. )Age ≥ 4 years and \< 18 years, male or female 3. ) The weight of patients should be 15 kg or more 4. ) Patients diagnosed with plaque psoriasis for at least 6 months ; at the same time, the researchers clarified the diagnosis of psoriasis 5. ) Patients with poor efficacy or unsuitable for local treatment and / or phototherapy 6. ) For patients with severe plaque psoriasis, the definition should meet one of the following conditions : Psoriasis static clinician overall assessment PGA score ≥ 4 points The body surface area of psoriatic lesions was BSA \> 10 %. Psoriasis area and severity index PASI \> 12 Children 's skin disease quality of life index ( CDLQI ) score \> 10 points. Exclusion Criteria: 1. A history of severe allergies or allergic reactions to monoclonal antibodies 2. Active infectious diseases ( including tuberculosis, hepatitis B, AIDS, syphilis, etc. ) 3. Conform to any of the following criteria associated with latent or active TB infection : A history of active TB ≤3 years prior to screening (but if \> 3 years, and a history of complete treatment Piece record, can also be grouped) During the screening period, there were signs or symptoms indicating active TB during medical history and / or physical examination ; recent close contact with people with active tuberculosis ( TB ) ; At the time of screening the interferon gamma release test tested positive if the subject's first interferon If the gamma release test results are inconclusive, the subject is excluded from the study;For subjects who have completed appropriate standard treatment for latent TB prior to screening and have no additional risk factors, radiographic findings or support for specific signs of latent or active TB,Possible for positive or inconclusive results. Exceptions will be made. The investigator will need to consult with a qualified infectomist to determine the risk of TB (including extra-pulmonary) and Discuss and decide with the sponsor; 4. Two pairs of hepatitis B surface antigen ( HBsAg ) were positive in screening. Or HBsAg negative, HBcAb positive and HBV-DNA positive. 5. There are serious, progressive or uncontrollable kidney, liver, blood, gastrointestinal, lung, heart blood. Tube, nerve or brain disease symptoms. 6. Patients received anti-tumor necrosis factor ( TNF ) or other biological agents with potential therapeutic effects on psoriasis within the previous 12 weeks. 7. Patients received intravenous anti-infective therapy within 30 days or oral anti-infective therapy within 14 days. 8. Local glucocorticoids, vitamin D derivatives, retinoic acid, calcineurin inhibitors ( TCI ) and other topical preparations with pharmacologically active ingredients were received within 7 days. 9. Local or UVB phototherapy within 7 days or psoralen or psoralen combined with ultraviolet A ( UVA ) phototherapy within 14 days. 10. Systemic treatment with non-biological agents for psoriasis including methotrexate, retinoic acids, cyclosporine, apulmiast, azathioprine, hydroxyurea, leflunomide, mexicophenol ester, sulfadiazine, calcineurase inhibitors, 6⁃ thiguanine for 14 days prior to baseline 11. Those who received any live vaccine within 3 months prior to receiving the first dose of the study drug, or during the study period. 12. Patients with erythrodermic psoriasis, pustular psoriasis, drug-induced or aggravated psoriasis, and newly minted guttate psoriasis 13. Patients who were judged unsuitable for inclusion by other investigators
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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.
Contacts and locations
Locations
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Shanghai Tenth People's Hospital
Shanghai, Shanghai Municipality, 200072, China
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