Kiniksa Pharmaceuticals

Kiniksa Pharmaceuticals

KNSA
Lexington, Bermuda· Est.
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KNSA · Stock Price

USD 56.93+30.90 (+118.71%)
Market Cap: $2.6B

Historical price data

Market Cap: $2.6BPipeline: 14 drugs (3 Phase 3)Patents: 20Founded: 2015HQ: Lexington, Bermuda

Overview

Kiniksa Pharmaceuticals is a publicly traded biopharma focused on immune modulation for cardiovascular and autoimmune diseases with high unmet need. Founded in 2015, its key achievement is the FDA approval and commercialization of ARCALYST® (rilonacept), the first and only therapy for recurrent pericarditis, providing a foundational revenue stream. The company's strategy leverages strategic in-licensing and targeted development of biologics with strong biologic rationale, building a balanced portfolio that spans commercial and clinical-stage assets. This approach, led by a seasoned team with a proven track record in rare diseases, aims to deliver differentiated therapies rapidly.

CardiovascularAutoimmune

Technology Platform

Kiniksa employs an indication-driven strategic platform focused on in-licensing and developing immune-modulating biologics that target validated pathways (e.g., IL-1, GM-CSF, CD40) for serious diseases with high unmet need, rather than a single proprietary discovery technology.

Pipeline

14
14 drugs in pipeline3 in Phase 3
DrugIndicationStageWatch
Rilonacept + PlaceboRecurrent PericarditisPhase 3
mavrilimumabCOVIDPhase 2/3
KPL-387 + PlaceboPericarditisPhase 2/3
prednisoneGiant Cell ArteritisPhase 2
KPL-914Recurrent PericarditisPhase 2

Funding History

3
Total raised:$300M
IPO$150M
Series B$100M
Series A$50M

FDA Approved Drugs

1
ARCALYSTBLAFeb 27, 2008

Opportunities

Significant opportunity to expand the market for IL-1 inhibition in recurrent pericarditis and potentially other cardiac inflammatory diseases.
The pipeline offers shots on goal in large autoimmune markets (RA) and novel rare disease frontiers, while partnerships provide non-dilutive funding and access to global capabilities.

Risk Factors

Heavy reliance on a single commercial product (ARCALYST) creates concentration risk.
The clinical pipeline faces inherent development failure risk, and the narrow portfolio magnifies the impact of any single setback.
Competition in core and pipeline indications is substantial.

Competitive Landscape

In recurrent pericarditis, ARCALYST is first-in-class with no direct approved competitors, competing against generic standard-of-care. In rheumatoid arthritis, KPL-404 will enter a crowded market dominated by multiple drug classes and must differentiate on mechanism. In rare cardiovascular diseases, competition is nascent but growing as immunology gains traction in cardiology.

Company Timeline

2008FDA Approval

FDA Approval: ARCALYST

2015Founded

Founded in Lexington, Bermuda

2016Series A

Series A: $50.0M

2017Series B

Series B: $100.0M

2018IPO

IPO — $150.0M