Purpose

The sebetralstat Early Access Program (EAP) provides early access to the investigational medicinal product (IMP) sebetralstat to eligible and approved Hereditary Angioedema (HAE) pediatric (ages 2-11) post-trial and naïve patients for the on-demand treatment of angioedema attacks where the treating Physician determines they might benefit from this treatment.

Condition

Eligibility

Eligible Ages
Between 2 Years and 11 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Male or female patients 2 to 11 years of age. - Parent or LAR provides signed informed consent and patient provides assent (when applicable). - Confirmed diagnosis of HAE.

Exclusion Criteria

  • Confirmed diagnosis of HAE with nC1-INH or acquired angioedema - Patient weighs <9.5 kg - Patient participated in the KVD900-303 trial and withdrew prior to trial completion per the protocol or trial closure - Any clinically significant medical condition or medical history that, in the opinion of the Treating Physician, would interfere with the patient's safety. - Known hypersensitivity to sebetralstat or its excipients. - Patient with a medical history or known to have severe hepatic impairment (Child Pugh C). - Patients who require sustained use of strong cytochrome P450 3A4 inhibitors or inducers.

Study Design

Phase
Study Type
Expanded Access

Recruiting Locations

KalVista Investigative Site
Evansville 4257227, Indiana 4921868 47715

KalVista Investigative Site
Wheaton 4373349, Maryland 4361885 20902

KalVista Investigative Site
St Louis 4407066, Missouri 4398678 63110

More Details

Status
Available
Sponsor
KalVista Pharmaceuticals, Ltd.

Study Contact

KalVista Pharmaceuticals Ltd
1 (857) 999-0075
expandedaccess@kalvista.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.