ClinicalTrials.gov record
Terminated Phase 2 Interventional Results available

A Trial to Evaluate the Efficacy and Safety of Different Doses of KVD824 for Prophylactic Treatment of HAE Type I or II

ClinicalTrials.gov ID: NCT05055258

Public ClinicalTrials.gov record NCT05055258. 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 May 19, 2026, 9:07 PM EDT

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

Official title

Randomized, Double-Blind, Placebo-Controlled, Phase 2 Trial to Evaluate the Efficacy and Safety of 3 Dose Levels of KVD824, an Oral Plasma Kallikrein Inhibitor, for Long-Term Prophylactic Treatment of Hereditary Angioedema Type I or II

Study identification

NCT ID
NCT05055258
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
KalVista Pharmaceuticals, Ltd.
Industry
Enrollment
33 participants

Conditions and interventions

Interventions

  • KVD824 Drug
  • Placebo to KVD824 Drug

Drug

Eligibility (public fields only)

Age range
18 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
Nov 17, 2021
Primary completion
Oct 26, 2022
Completion
Oct 26, 2022
Last update posted
May 5, 2026

2021 – 2022

United States locations

U.S. sites
13
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
KalVista Investigative Site Birmingham Alabama 35294
KalVista Investigative Site Scottsdale Arizona 85251
KalVista Investigative Site La Jolla California 92093
KalVista Investigative Site Santa Monica California 90404
KalVista Investigative Site Centennial Colorado 80112
KalVista Investigative Site Tampa Florida 33620
KalVista Investigative Site Chevy Chase Maryland 20815
KalVista Investigative Site Boston Massachusetts 02114
KalVista Investigative Site St Louis Missouri 63110
KalVista Investigative Site Cincinnati Ohio 45231
KalVista Investigative Site Hershey Pennsylvania 17033
KalVista Investigative Site Dallas Texas 75390
KalVista Investigative Site Spokane Washington 99204

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05055258, 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 5, 2026 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05055258 live on ClinicalTrials.gov.

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