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Placebo matching with Abatacept
Placebo matching with Abatacept is a CTLA-4 fusion protein; T-cell costimulation inhibitor Small molecule drug developed by Bristol-Myers Squibb. It is currently FDA-approved for Rheumatoid arthritis, Polyarticular juvenile idiopathic arthritis, Psoriatic arthritis.
Abatacept is a fusion protein that blocks T-cell costimulation by binding to CD80/CD86 on antigen-presenting cells, thereby inhibiting T-cell activation and reducing inflammatory responses.
Abatacept is a fusion protein that blocks T-cell costimulation by binding to CD80/CD86 on antigen-presenting cells, thereby inhibiting T-cell activation and reducing inflammatory responses. Used for Rheumatoid arthritis, Polyarticular juvenile idiopathic arthritis, Psoriatic arthritis.
At a glance
| Generic name | Placebo matching with Abatacept |
|---|---|
| Sponsor | Bristol-Myers Squibb |
| Drug class | CTLA-4 fusion protein; T-cell costimulation inhibitor |
| Target | CD80, CD86 |
| Modality | Small molecule |
| Therapeutic area | Immunology |
| Phase | FDA-approved |
Mechanism of action
Abatacept works by interrupting the second signal required for full T-cell activation. It consists of the extracellular domain of CTLA-4 fused to the Fc portion of IgG1, allowing it to bind CD80 and CD86 molecules on antigen-presenting cells. This prevents the interaction between these molecules and CD28 on T cells, effectively dampening adaptive immune responses in autoimmune conditions.
Approved indications
- Rheumatoid arthritis
- Polyarticular juvenile idiopathic arthritis
- Psoriatic arthritis
- Ankylosing spondylitis
- Systemic lupus erythematosus
Common side effects
- Infections (upper respiratory, urinary tract)
- Headache
- Nausea
- Dizziness
- Hypertension
Key clinical trials
- Study of COYA 302 for the Treatment of ALS (PHASE2)
- Safety and Efficacy of Abatacept for Treating Chronic Cytopenia in Cytotoxic T-Lymphocyte Antigen 4 (CTLA4) Haploinsufficiency (PHASE1, PHASE2)
- Efficacy and Safety of Subcutaneous Abatacept in Adults With Active Psoriatic Arthritis (PHASE3)
- A Study to Evaluate Efficacy and Safety of Abatacept in Participants of Pemphigus Vulgaris (PV) (PHASE4)
- Effects of Abatacept in Patients With Early Rheumatoid Arthritis (PHASE3)
- Efficacy and Safety Study of Abatacept to Treat Lupus Nephritis (PHASE3)
- Abatacept vs Placebo in RA Patients With Hepatitis B on Entecavir Background (NA)
- A Study to Evaluate the Safety and Efficacy of Abatacept in Patients With Diffuse Systemic Sclerosis (Scleroderma) (PHASE1, PHASE2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Placebo matching with Abatacept CI brief — competitive landscape report
- Placebo matching with Abatacept updates RSS · CI watch RSS
- Bristol-Myers Squibb portfolio CI
Frequently asked questions about Placebo matching with Abatacept
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Related
- Drug class: All CTLA-4 fusion protein; T-cell costimulation inhibitor drugs
- Target: All drugs targeting CD80, CD86
- Manufacturer: Bristol-Myers Squibb — full pipeline
- Therapeutic area: All drugs in Immunology
- Indication: Drugs for Rheumatoid arthritis
- Indication: Drugs for Polyarticular juvenile idiopathic arthritis
- Indication: Drugs for Psoriatic arthritis
- Compare: Placebo matching with Abatacept vs similar drugs
- Pricing: Placebo matching with Abatacept cost, discount & access