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Completed Phase 3 Interventional Results available

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)

ClinicalTrials.gov ID: NCT05259917

Public ClinicalTrials.gov record NCT05259917. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 9:01 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official 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

Study identification

NCT ID
NCT05259917
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
KalVista Pharmaceuticals, Ltd.
Industry
Enrollment
136 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • KVD900 600 mg Drug
  • KVD900 300 mg Drug

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 21, 2022
Primary completion
Dec 30, 2023
Completion
Dec 30, 2023
Last update posted
May 1, 2025

2022 – 2023

United States locations

U.S. sites
22
U.S. states
19
U.S. cities
21
Facility City State ZIP Site status
KalVista Investigative Site Birmingham Alabama 35209
KalVista Investigative Site Scottsdale Arizona 85251
KalVista Investigative Site Little Rock Arkansas 72205
KalVista Investigative Site San Diego California 92122
KalVista Investigative Site San Diego California 92123
KalVista Investigative Site Santa Monica California 90404
KalVista Investigative Site Centennial Colorado 80112
KalVista Investigative Site Colorado Springs Colorado 80907
KalVista Investigative Site Tampa Florida 33613
KalVista Investigative Site Chicago Illinois 60612
KalVista Investigative Site Overland Park Kansas 66211
KalVista Investigative Site Louisville Kentucky 40215
KalVista Investigative Site Chevy Chase Maryland 20815
KalVista Investigative Site Plymouth Minnesota 55446
KalVista Investigative Site St Louis Missouri 61414
KalVista Investigative Site New York New York 10029
KalVista Investigative Site Charlotte North Carolina 28277
KalVista Investigative Site Toledo Ohio 43617
KalVista Investigative Site Hershey Pennsylvania 17033
KalVista Investigative Site Dallas Texas 75231
KalVista Investigative Site Layton Utah 84041
KalVista Investigative Site Spokane Washington 99202

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 44 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05259917, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 1, 2025 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05259917 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →