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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 Oct 27, 2026, 7:40 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A study to assess whether different doses of KVD824 are effective in preventing attacks of Hereditary Angiodedema Type I or Type 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

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 18, 2021 (Actual)
Primary completion
Oct 27, 2022 (Actual)
Completion
Oct 27, 2022 (Actual)
Last update posted
May 6, 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 6, 2026 · Synced Oct 27, 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 public registry record, listed eligibility criteria, and available contact information for NCT05055258 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →