quecitinib (QY201)
/ E-nitiate Biopharma, VivaVision
- LARVOL DELTA
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August 25, 2026
A Phase 3 Study of VVN461 Ophthalmic Solution for Noninfectious Anterior Uveitis
(clinicaltrials.gov)
- P3 | N=154 | Active, not recruiting | Sponsor: VivaVision Biotech, Inc | Not yet recruiting ➔ Active, not recruiting
Enrollment closed • Ocular Inflammation • Ophthalmology • Uveitis
July 18, 2026
A Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo-Controlled Phase II Clinical Trial to Evaluate the Efficacy and Safety of QY201 Tablets in Subjects With Non-Segmental Vitiligo
(clinicaltrials.gov)
- P2 | N=200 | Recruiting | Sponsor: E-nitiate Biopharmaceuticals (Hangzhou) Co., Ltd.
New P2 trial • Dermatology • Immunology • Vitiligo
July 17, 2026
Phase IIa Study of Pharmacokinetics, Safety and Efficacy of QY201 Tablets in Adolescent Subjects With Moderate to Severe Atopic Dermatitis
(clinicaltrials.gov)
- P2 | N=24 | Completed | Sponsor: E-nitiate Biopharmaceuticals (Hangzhou) Co., Ltd.
New P2 trial • Atopic Dermatitis • Dermatitis • Dermatology • Immunology
September 18, 2025
A Phase III Clinical Study of QY201 Tablet in Subjects With Moderate to Severe Atopic Dermatitis.
(clinicaltrials.gov)
- P3 | N=460 | Enrolling by invitation | Sponsor: E-nitiate Biopharmaceuticals (Hangzhou) Co., Ltd.
New P3 trial • Atopic Dermatitis • Dermatitis • Dermatology • Immunology
May 27, 2025
The Pharmacokinetics, Pharmacodynamics, Tolerability, and Safety of Orally Dosed QY201, a Novel JAK1/TYK2 Inhibitor, in Chinese Healthy Subjects.
(PubMed, J Clin Pharmacol)
- "QY201 was generally safe and well tolerated following oral administration, with dose-limiting toxicity of the highest tested dose of 40 mg being well tolerated. The favorable PK, PD, safety, and tolerability results from these studies supported evaluations of QY201 in future clinical trials."
Clinical • Journal • PK/PD data • Atopic Dermatitis • Dermatitis • Dermatology • Immunology • CRP • JAK1 • TYK2
February 22, 2025
QY201 in adults with moderate-to-severe atopic dermatitis: 12-week results from a dose-finding phase 2 trial
(AAD 2025)
- No abstract available
Clinical • Late-breaking abstract • P2 data • Atopic Dermatitis • Dermatitis • Dermatology • Immunology
September 02, 2022
A Study of QY201 Tablet in Subjects With Moderate to Severe Atopic Dermatitis
(clinicaltrials.gov)
- P1/2 | N=260 | Not yet recruiting | Sponsor: E-nitiate Biopharmaceuticals (Hangzhou) Co., Ltd.
New P1/2 trial • Atopic Dermatitis • Dermatitis • Dermatology • Immunology
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