Safety Tolerability and Pharmacokinetics of ALD403

Alder Biopharmaceuticals

Status and phase: Completed; Phase 1

Conditions: Migraine Disorders

Treatments: Biological: ALD403; Biological: Sumatriptan

Study type: Interventional

Funder types: Industry

Identifiers

NCT01579383

ALD403-CLIN-001

Details and patient eligibility

About

The purpose of this study is to determine the safety, tolerability and pharmacokinetics of ALD403, a monoclonal antibody, administered by intravenous infusion and subcutaneous injection.

Enrollment: 104 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria Part A:

• Healthy males and females between the ages of 18 and 65 (inclusive).
• Normal renal function as calculated by the Cockcroft- Gault equation at screening.
• Body Mass Index (BMI) between 18.0 and 30.0 kg/m2, and a total body weight of 50 to 100kg inclusive.
• No clinically significant disease or abnormal laboratory values as determined by medical history, physical examination, electrocardiogram, and laboratory evaluations

Exclusion Criteria Part A:

• History of febrile illness within 5 days prior to the first dose
• Any clinically significant laboratory findings
• Any clinically significant physical exam abnormalities
• Hospitalization for any reason within 30 days of the screening visit.
• History of or positive human immunodeficiency virus (HIV) screen result
• History of positive Hepatitis B surface antigen (HBsAg), and/or positive Hepatitis C antibody (HCV) at screening.
• History of malignancy within five years prior to screening.
• History of leukemia, myeloproliferative disorder or lymphoproliferative disorder
• History of rubber, latex allergy or allergy to medical adhesives
• Positive urine, drug or alcohol screen result
• Current smokers
• Previous treatment or clinical trial with a monoclonal antibody.
• Participation in any clinical research study evaluating another investigational drug or therapy within 30 days or at least 5 half-lives

Inclusion Criteria Part B:

• Healthy females between the ages of 18 and 65 (inclusive).
• Male and female migraine patients with clinically diagnosed migraine not attributed to another cause with or without aura based on International Headache Society criteria.
• Migraine patients must have a history of migraine with or without aura for more than 1 year with 1-8 moderate or severe migraine attacks per month in the 2 months prior to starting in the study.
• Normal renal function as defined by Cockcroft- Gault equation at screening.
• Body Mass Index (BMI) between 18.0 and 30.0 kg/m2, and a total body weight of 50 to 100kg inclusive.
• No clinically significant disease or abnormal laboratory values as determined by medical history, physical examination, electrocardiogram, and laboratory evaluations conducted at the screening visit or at the time of admission

Exclusion Criteria Part B:

• For migraine patients: patient is not able to refrain from use of their usual triptan therapy (if applicable) from 48 hours (Day -2) prior to dosing on Day 1 until the morning of discharge (Day 3).
• Migraine patients who experience migraine with prolonged aura, familiar hemiplegic migraine, migrainous infarction or basilar migraine
• For migraine patients: patient has more than 8 headache-days per month or has taken medication for acute headache on more than 8 days a month in the past 3 months
• For migraine patients: patient was greater than 50 years old at the age of migraine onset
• History of febrile illness within 5 days prior to the first dose
• Any clinically significant laboratory findings
• Any clinically significant physical exam abnormalities
• Previous treatment or clinical trial with a monoclonal antibody.
• Hospitalization for any reason within 30 days of the screening visit.
• History of or positive human immunodeficiency virus (HIV) screen result
• History of positive Hepatitis B surface antigen (HBsAg), and/or positive Hepatitis C antibody (HCV
• History of malignancy within five years prior to screening.
• History of leukemia, myeloproliferative disorder or lymphoproliferative disorder
• Positive urine drug or alcohol screen result
• Current smokers.
• Known contraindication to sumatriptan
• Participation in any clinical research study evaluating another investigational drug or therapy within 30 days or at least 5 half-lives

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: Triple Blind

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104 participants in 3 patient groups

Part A, Cohorts A - H

Experimental group

Description:

ALD403/Placebo

Treatment:

Biological: ALD403

Biological: ALD403

Part A, Cohort I

Experimental group

Description:

ALD403/Placebo

Treatment:

Biological: ALD403

Biological: ALD403

Part B

Experimental group

Description:

ALD403/Placebo/Sumatriptan

Treatment:

Biological: ALD403

Biological: ALD403

Biological: Sumatriptan