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Recruiting Phase 3 NCT07511647

NCT07511647 A Phase 3 Clinical Study of QL2106 Injection

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Clinical Trial Summary
NCT ID NCT07511647
Status Recruiting
Phase Phase 3
Sponsor Qilu Pharmaceutical Co., Ltd.
Condition Plaque Psoriasis
Study Type INTERVENTIONAL
Enrollment 318 participants
Start Date 2026-06-15
Primary Completion 2027-12-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
QL2106 injectionTremfya®

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 3 trials are large pivotal studies comparing the treatment to current standard of care or placebo. Your participation directly contributes to the evidence needed for regulatory approval.

This trial targets 318 participants in total. It began in 2026-06-15 with a primary completion date of 2027-12-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

It is a multicenter randomized, double-blinded, parallel, positive-controlled, Phase 3 comparative study to evaluate the efficacy and safety of QL2106 injection to Tremfya® in Patients with Moderate to Severe Plaque Psoriasis. A total of 318 subjects are planned to be included and randomized at a ratio of 1:1 to receive QL2106 injection orTremfya®

Eligibility Criteria

Inclusion Criteria: * Diagnosis of plaque psoriasis, with or without psoriatic arthritis (PsA), prior to the first administration of study intervention * Total body surface area (BSA) greater than or equal to (\>=)10 percent (%) at screening and baseline * Total psoriasis area and severity index (PASI) \>=12 at screening and baseline * Total investigator global assessment (IGA) \>=3 at screening and baseline * Candidate for phototherapy or systemic treatment for plaque psoriasis Exclusion Criteria: * Nonplaque form of psoriasis (for example \[e.g.\], erythrodermic, guttate, or pustular) * Current drug-induced psoriasis (e.g., a new onset of psoriasis or an exacerbation of psoriasis from beta blockers, calcium channel blockers, or lithium)

Contact & Investigator

Central Contact

Yu ling Shi, Doctor

✉ shiyuling1973@126.com

📞 021-36803000

Frequently Asked Questions

Who can join the NCT07511647 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Plaque Psoriasis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT07511647 trial and what does that mean for participants?

Phase 3 trials are large-scale studies comparing the new treatment to existing standards of care or a placebo. They provide the evidence needed for regulatory approval. This trial targets 318 participants.

Is NCT07511647 currently recruiting?

Yes, NCT07511647 is actively recruiting participants. Contact the research team at shiyuling1973@126.com for enrollment information.

Where is the NCT07511647 trial being conducted?

This trial is being conducted at Jining, China.

Who is sponsoring the NCT07511647 clinical trial?

NCT07511647 is sponsored by Qilu Pharmaceutical Co., Ltd.. The trial plans to enroll 318 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology