A Phase III, Crossover Trial Evaluating the Efficacy and Safety of KVD900 (Sebetralstat) for On-Demand Treatment of Angioedema Attacks in Adolescent and Adult Patients With Hereditary Angioedema (HAE)

Last updated:
2026-08-15
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View trial details

Overview

Official protocol title:

A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PHASE 3, THREE-WAY CROSSOVER TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF TWO DOSE LEVELS OF KVD900, AN ORAL PLASMA KALLIKREIN INHIBITOR, FOR ON-DEMAND TREATMENT OF ANGIOEDEMA ATTACKS IN ADOLESCENT AND ADULT PATIENTS WITH HEREDITARY ANGIOEDEMA TYPE I OR II

Intervention/treatment:
SEBETRALSTAT (KVD900)
Medical condition:
HEREDITARY ANGIOEDEMA
Protocol code:
KVD900-301
Control number:
262896
Status:
Closed
Approved:
April 29, 2022
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT05259917
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
12 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Vice President Clinical
Organization
KalVista Pharmaceuticals Ltd.
Phone:
1 (857) 999-0075
Sponsor
KALVISTA PHARMACEUTICALS LTD.

Locations

Ontario

KalVista Investigative Site
Toronto, Ontario, M3B 3S6

Results

See the results from the trial NCT05259917. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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