A Safety and Dose-Finding Study of SYNT001 in Subjects With Pemphigus (Vulgaris or Foliaceus)

Phase 2TerminatedNCT03075904

Alexion Pharmaceuticals, Inc.8 enrolled

Overview

This was a multicenter, open-label safety study to determine the dose regimen of SYNT001 (ALXN1830) administered intravenously in participants with pemphigus (vulgaris or foliaceus).

This study planned to evaluate 2 cohorts: up to 8 participants to receive 5 weekly intravenous (IV) doses of ALXN1830 at 10 milligram/kilogram (mg/kg) (Cohort 1) and up to 12 participants to receive 3 x 30 mg/kg weekly doses of ALXN1830 IV (loading) followed by 5 x 10 mg/kg doses of ALXN1830 IV every other week or 10 weekly doses of ALXN1830 IV (maintenance) (Cohort 2). This study was terminated after the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and efficacy were characterized in participants with pemphigus at a single dose level (10 mg/kg) in Cohort 1, before any participants were enrolled in Cohort 2. The study consisted of 3 periods: Screening, Treatment, and Follow-Up.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Pemphigus Pemphigus Vulgaris Pemphigus Foliaceus

Interventions

ALXN1830DRUG

Administered via IV infusion.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: Participants must have meet the following criteria to be included: * Were willing and able to read, understand and sign an informed consent form * Documented diagnosis of pemphigus vulgaris or foliaceus * Were required to use medically acceptable contraception Exclusion Criteria: Participants meeting any of the following criteria were excluded: * Were unable or unwilling to comply with the protocol * Active non-hematologic malignancy or history of non-hematologic malignancy in the 3 years prior to screening (exclusive of non-melanoma skin cancer and cervical cancer in situ) * Positive for human immunodeficiency virus (HIV) or hepatitis C antibody * Positive for hepatitis B surface antigen * IV immunoglobulin treatment within 30 days of screening * Any exposure to an investigational drug or device within the 30 days prior to screening * Plasmapheresis or immunoadsorption within 30 days of screening * Participant had any current medical condition that, in the opinion of the Investigator, may have compromised their safety or compliance, preclude successful conduct of the study, or interfere with interpretation of the results

Locations (3)

Alexion Study Site

Chapel Hill, North Carolina, United States

Alexion Study Site

Durham, North Carolina, United States

Alexion Study Site

Philadelphia, Pennsylvania, United States

Outcomes

Primary Outcomes

Count Of Participants Reporting Treatment-emergent Adverse Events (TEAEs)

A TEAE was defined as any adverse event (AE) that starts on or after the first dose of study drug or occurs prior to the first dose and worsens in severity on or after the first dose of study drug, during the Treatment Period and Follow-up Period. A TEAE was considered "serious" (Grade 3) if, in the view of either the investigator or sponsor, it resulted in any of the following outcomes: death, life-threatening adverse drug event, inpatient hospitalization or prolongation of existing hospitalization, persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions, congenital anomaly/birth defect, or an event that may have jeopardized the participant and may have required medical or surgical intervention to prevent one of the previously listed outcomes. A summary of serious and all other non-serious adverse events, regardless of causality, is located in the Reported Adverse Events module.

Time frame: Day 1 (after first dose) through Day 112

Secondary Outcomes

Maximum Percent Reduction Of Mean Total Immunoglobulin G (IgG) Levels From Baseline

Pharmacodynamic samples were collected for analysis throughout the study. The maximum percent reduction of mean serum total IgG levels from Baseline observed during the study is presented.

Time frame: Baseline through Day 112

Maximum Percent Reduction In Mean Pemphigus Disease Area Index (PDAI) Total Activity Score From Baseline

Pemphigus severity and disease activity was measured using the PDAI in regions where a validated questionnaire was available. The PDAI was administered during Treatment Period and Follow-up Period. PDAI total activity was comprised of scores for the skin, mucous membrane, and scalp subscales. The investigator determined a PDAI score as 0 to 250 points for total activity score (0 to 120 for skin, 0 to 10 for scalp, and 0 to 120 for mucosa). A higher score indicated higher impact on skin disease. The maximum percent reduction in PDAI total activity score from Baseline observed during the study is presented.

Time frame: Baseline through Day 112

Data from ClinicalTrials.gov

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