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Completed Phase 3 Interventional

PK Subtrial in Adolescent Patients With HAE Type I or II Participating in the KVD900-302 Trial

ClinicalTrials.gov ID: NCT05511922

Public ClinicalTrials.gov record NCT05511922. 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, 7:38 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 Pharmacokinetic Subtrial in Adolescent Patients With Hereditary Angioedema Type I or II Participating in the KVD900-302 Trial

Study identification

NCT ID
NCT05511922
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
KalVista Pharmaceuticals, Ltd.
Industry
Enrollment
11 participants

Conditions and interventions

Interventions

  • KVD900 600 mg Drug
  • Drug: KVD900 300 mg Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 17 Years
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
Oct 23, 2022
Primary completion
May 26, 2026
Completion
May 26, 2026
Last update posted
Jun 7, 2026

2022 – 2026

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
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 Evansville Indiana 47715
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 63141
KalVista Investigative Site Charlotte North Carolina 28277
KalVista Investigative Site Cincinnati Ohio 45236
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 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 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05511922, 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 Jun 7, 2026 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05511922 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →