KalVista Pharmaceuticals

KalVista Pharmaceuticals

KALVApproved
Cambridge, United StatesFounded 2011250+ employeeskalvista.com

KalVista Pharmaceuticals is dedicated to advancing oral small molecule medicines for rare diseases with significant unmet needs, with its primary focus on hereditary angioedema (HAE). The company achieved a major milestone with the FDA approval of EKTERLY® (sebetralstat), the first oral on-demand treatment for HAE attacks, which is now commercially launched. Beyond its commercial product, KalVista maintains an innovative pipeline including oral Factor XIIa inhibitors for prophylactic HAE treatment and is exploring applications in thrombosis and inflammation. With over 250 employees worldwide, the company combines scientific expertise with commercial execution to transform patient care.

Market Cap
$839.1M
+32.8% period
Pipeline
13
4 in Phase 3
Patents
20
granted
Publications
20
indexed

KALV · Stock Price

USD 16.60+4.10 (+32.80%)

Historical price data

AI Company Overview

KalVista Pharmaceuticals is dedicated to advancing oral small molecule medicines for rare diseases with significant unmet needs, with its primary focus on hereditary angioedema (HAE). The company achieved a major milestone with the FDA approval of EKTERLY® (sebetralstat), the first oral on-demand treatment for HAE attacks, which is now commercially launched. Beyond its commercial product, KalVista maintains an innovative pipeline including oral Factor XIIa inhibitors for prophylactic HAE treatment and is exploring applications in thrombosis and inflammation. With over 250 employees worldwide, the company combines scientific expertise with commercial execution to transform patient care.

Rare DiseasesHereditary Angioedema (HAE)InflammationThrombosis

Technology Platform

Oral small molecule inhibitors targeting the kallikrein-kinin system (KKS), specifically plasma kallikrein and Factor XIIa, to control inflammation and vascular leakage for diseases like HAE.

Pipeline

13
13 drugs in pipeline4 in Phase 3
DrugIndicationStageWatch
KVD900 600 mg + KVD900 300 mgHereditary AngioedemaPhase 3
Placebo + KVD900 600 mg + KVD900 300 mgHereditary AngioedemaPhase 3
KVD900 150 mg + KVD900 300 mg + KVD900 600 mgHereditary AngioedemaPhase 3
KVD900 600 mg + Drug: KVD900 300 mgHereditary AngioedemaPhase 3
KVD001 InjectionDiabetic Macular EdemaPhase 2

Funding History

4
Total raised:$200M
PIPE$75MFeb 15, 2021
IPO$60MJul 22, 2015
Series B$35MMar 15, 2014
Series A$30MMay 15, 2011

FDA Approved Drugs

1
EKTERLYNDAJul 3, 2025

Opportunities

Major growth opportunities include capturing significant market share in the HAE on-demand treatment space with its first-to-market oral therapy, expanding into the larger prophylactic HAE market with its oral Factor XIIa inhibitor program, and leveraging its kallikrein-kinin system expertise to develop treatments for other inflammatory and thrombotic disorders.

Risk Factors

Key risks include commercial execution challenges in launching EKTERLY® against established injectable competitors, clinical and competitive risks associated with developing a successful oral prophylactic therapy, and financial risks related to funding pipeline development and achieving profitability.

Competitive Landscape

KalVista competes in the HAE market against Takeda, CSL Behring, and BioCryst. Its primary differentiation is EKTERLY® as the first and only oral on-demand therapy. Future competition in oral prophylaxis will be direct with BioCryst's Orladeyo, requiring KalVista's Factor XIIa inhibitor to demonstrate superior efficacy, safety, or convenience.