A Randomized, Double-blind, Placebo-controlled, Phase II, Cross-over Clinical Trial Evaluating the Efficacy and Safety of KVD900, an Oral Plasma Kallikrein Inhibitor, in the On-demand Treatment of Angioedema Attacks in Adult Subjects With Hereditary Angioedema Type I or II
Overview
- Phase
- Phase 2
- Intervention
- KVD900
- Conditions
- Hereditary Angioedema
- Sponsor
- KalVista Pharmaceuticals, Ltd.
- Enrollment
- 84
- Locations
- 1
- Primary Endpoint
- Time to Conventional Attack Treatment Use Within 12 Hours of Study Drug (Full Analysis Set)
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
This study is a randomized, double-blind, placebo-controlled, phase II, cross-over clinical trial evaluating the efficacy and safety of KVD900, in the treatment of hereditary angioedema attacks in adult subjects.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Male or female adult subjects 18 years of age and older.
- •Confirmed diagnosis of HAE type I or II at anytime in the medical history
- •At least 3 documented HAE attacks in the past 93 days, as supported by medical history.
- •Access to and ability to use conventional attack treatment for attacks of HAE
- •Adequate organ functions
- •Females of childbearing potential must agree to use highly effective birth control from the Screening visit until the end of the trial follow-up procedures.
- •Females of non-childbearing potential, defined as surgically sterile (status post hysterectomy, bilateral oophorectomy, or bilateral tubal ligation) or post-menopausal for at least 12 months, do not require contraception during the study
- •Males with female partners of childbearing potential must agree to be abstinent or else use a highly effective method of birth control as defined in inclusion 6 from the Screening visit until the end of the trial follow-up procedures
- •Provide signed informed consent and are willing and capable of complying with study requirements and procedures
Exclusion Criteria
- •Any concomitant diagnosis of another form of chronic angioedema, such as acquired C1 inhibitor (C1-INH) deficiency, HAE with normal C1-INH (also known as HAE type III), idiopathic angioedema, or angioedema associated with urticaria
- •Current use of C1INH, androgens, or tranexamic acid for HAE prophylaxis
- •Use of angiotensin-converting enzyme (ACE) inhibitors or any estrogen-containing medications with systemic absorption (such as oral contraceptives or hormonal replacement therapy) within 93 days prior to initial study treatment.
- •Use of androgens (e.g. stanozolol, danazol, oxandrolone, methyltestosterone, testosterone) or antifibrinolytics within 30 days prior to initial study treatment.
- •Use of lanadelumab within 10 weeks prior to initial study treatment.
- •Use of strong CYP3A4/CYP2C9 inhibitors and inducers during participation in the trial
- •Clinically significant abnormal ECG at Visit 1 and pre-dose at Visit
- •This includes, but is not limited to, a QT interval by Fredericia, QTcF \> 470 msec (for women) or \> 450 msec (for men), a PR \> 220 msec or ventricular and/or atrial premature contractions that are more frequent than occasional and/or occur as couplets or higher in grouping
- •Any clinically significant history of angina, myocardial infarction, syncope, clinically significant cardiac arrhythmias, left ventricular hypertrophy, cardiomyopathy, or any other cardiovascular abnormality
- •Any other systemic dysfunction (e.g., gastrointestinal, renal, respiratory, cardiovascular) or significant disease or disorder which, in the opinion of the Investigator, would jeopardize the safety of the subject by taking part in the trial
Arms & Interventions
Part 1
Subjects received a single dose of 600 mg KVD900.
Intervention: KVD900
Part 2 - Sequence 1: 600 mg KVD900, Then Placebo
Subjects received a single dose of 600 mg KVD900 to treat the first eligible HAE attack. Following resolution of this attack, subjects received a second single dose of placebo to treat the second eligible HAE attack.
Intervention: KVD900
Part 2 - Sequence 1: 600 mg KVD900, Then Placebo
Subjects received a single dose of 600 mg KVD900 to treat the first eligible HAE attack. Following resolution of this attack, subjects received a second single dose of placebo to treat the second eligible HAE attack.
Intervention: Placebo
Part 2 - Sequence 2: Placebo, Then 600 mg KVD900
Subjects received a single dose of placebo to treat the first eligible HAE attack. Following resolution of this attack, subjects received a second single dose of 600 mg KVD900 to treat the second eligible HAE attack.
Intervention: KVD900
Part 2 - Sequence 2: Placebo, Then 600 mg KVD900
Subjects received a single dose of placebo to treat the first eligible HAE attack. Following resolution of this attack, subjects received a second single dose of 600 mg KVD900 to treat the second eligible HAE attack.
Intervention: Placebo
Outcomes
Primary Outcomes
Time to Conventional Attack Treatment Use Within 12 Hours of Study Drug (Full Analysis Set)
Time Frame: 12 hours
The primary variable for statistical comparison between treatments in Part 2 of the study was time to use of conventional attack treatment (pdC1INH or rhC1INH intravenous \[iv\] or icatibant) within 12 hours of study drug. Censoring occurs where a subject did not use conventional attack treatment within 12h post-study drug dosing. When an endpoint result was non-calculable (NC) within 12 hours, if the event did occur, the event must have occurred \>12 hours following study drug.
Secondary Outcomes
- Time to Either Worsening in HAE Attack Severity by One Level or More on the PGI-S or to Conventional Attack Treatment Use Within 12 Hours of Study Drug (Full Analysis Set)(12 hours)
- Proportion of HAE Attacks That Worsen in Severity by One Level or More on the PGI-S or Require Conventional Attack Treatment Within 12 Hours of Study Drug (Full Analysis Set)(12 hours)
- Time to Symptom Relief Defined as HAE Attack Rated as "A Little Better" or Higher on the PGI-C for Two Consecutive Time Points Within 12 Hours of Study Drug (Full Analysis Set)(12 hours)
- Time to Symptom Relief Defined as 50% Reduction in Composite VAS Score for Three Consecutive Time Points Within 12 Hours of Study Drug (Full Analysis Set)(12 hours)