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Search / Trial NCT06869551

A Study to Evaluate the Drug Levels, Efficacy, and Safety of Deucravacitinib (BMS-986165) in Pediatric Participants With Juvenile Psoriatic Arthritis

Launched by BRISTOL-MYERS SQUIBB · Mar 6, 2025

Trial Information

Current as of May 29, 2025

Recruiting

Keywords

Juvenile Psoriatic Arthritis (J Ps A) Juvenile Idiopathic Arthritis (Jia) Pediatric Ps A Deucravacitinib Bms 986165

ClinConnect Summary

This clinical trial is studying a new medication called Deucravacitinib (BMS-986165) to see how it works in children and teenagers with Juvenile Psoriatic Arthritis (JPsA). The main goals are to check how much of the drug gets into the body, how effective it is at treating the condition, and whether it is safe for young patients. The trial is currently open to participants aged between 6 and 20 years who have been diagnosed with JPsA and have at least three joints affected by arthritis. To qualify, participants must have already tried at least one other treatment for JPsA that didn’t work as well as expected or caused side effects.

If someone is eligible and decides to participate, they will be closely monitored throughout the study. This means they will have regular check-ups to assess how the medication is affecting their condition and to ensure their safety. It’s important to note that the study has specific requirements, such as not allowing participants who have been diagnosed with other types of arthritis or certain eye conditions recently. Overall, this trial aims to find a new treatment option for young people struggling with JPsA, with the hope of improving their quality of life.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria
  • Participants must have been diagnosed with Juvenile Psoriatic Arthritis (JPsA).
  • Participants must have at least three joints that are affected by arthritis.
  • Participants must have tried at least one type of medicine for JPsA for at least three months, but it didn't work well or caused problems.
  • Exclusion Criteria
  • Participants must not have been diagnosed with JPsA before 5 years of age.
  • Participants must not have other types of Juvenile Idiopathic Arthritis (JIA) that aren't JPsA,
  • Participants must not have a history of chronic eye inflammation (uveitis), or were diagnosed with uveitis within the last three months.
  • Other protocol-defined Inclusion/Exclusion criteria apply.

About Bristol Myers Squibb

Bristol-Myers Squibb (BMS) is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a robust portfolio of products across multiple therapeutic areas, including oncology, immunology, cardiovascular, and fibrotic diseases, BMS emphasizes cutting-edge research and a commitment to advancing medical science through clinical trials. The company is driven by a mission to provide transformative therapies, leveraging collaboration and scientific expertise to address unmet medical needs and improve patient outcomes worldwide.

Locations

Plovdiv, , Bulgaria

Olomouc, Olomoucký Kraj, Czechia

València, , Spain

Barcelona, Barcelona [Barcelona], Spain

Praha, Praha 5, Czechia

Firenze, Toscana, Italy

Râmnicu Vâlcea, Vâlcea, Romania

Cuiabá, Mato Grosso, Brazil

Belo Horizonte, Minas Gerais, Brazil

Recife, Pernambuco, Brazil

Porto Alegre, Rio Grande Do Sul, Brazil

Porto Alegre, Rio Grande Do Sul, Brazil

Rio De Janeiro, , Brazil

São Paulo, , Brazil

São Paulo, , Brazil

Plovdiv, , Bulgaria

Sofia, , Bulgaria

Beijing, Beijing, China

Guangzhou, Guangdong, China

Nanjing, Jiangsu, China

Changchun, Jilin, China

Shanghai, Shanghai, China

Hangzhou, Zhejiang, China

Olomouc, Olomoucký Kraj, Czechia

Praha, Praha 5, Czechia

Erlangen, Bayern, Germany

Hamburg, , Germany

Hannover, , Germany

Napoli, Campania, Italy

Firenze, Toscana, Italy

Iasi, Iași, Romania

Râmnicu Vâlcea, Vâlcea, Romania

Barcelona, Barcelona [Barcelona], Spain

Madrid, Madrid, Comunidad De, Spain

València, , Spain

Istanbul Fatih, İstanbul, Turkey

Ankara, , Turkey

Ankara, , Turkey

Istanbul, , Turkey

Chicago, Illinois, United States

Indianapolis, Indiana, United States

Cluj Napoca, Cluj, Romania

Lancaster, California, United States

Austin, Texas, United States

Patients applied

0 patients applied

Trial Officials

Bristol-Myers Squibb

Study Director

Bristol-Myers Squibb

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported