Cypress, California, United States
NCT Number: NCT02563938
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AK001
This first-in-human study will evaluate the safety and tolerability of single doses of AK001 across a range of potentially active doses. Early signals of pharmacodynamic activity will also be evaluated.
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
About this study
AK001 is a monoclonal antibody which may be useful in the treatment of patients with severe allergic diseases.
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- BMI between 18-30
- Determined to be in good health
- Clinical laboratory values within limits of normal values
- Normal 12-lead ECG
- Stool sample negative for parasites
- Non-smoker
- Consumed an average of no more than 2 drinks per day within 6 months
- Subjects of reproductive age must use a highly effective method of contraception
- Positive skin test in certain cohorts
- Elevated total eosinophil counts in certain cohorts
Exclusion criteria
- Clinically significant medical history conditions or laboratory values
- Receipt of investigational drug, biologic or medical device within 30 days prior to Screening
- New drug therapy within 1 week of study drug administration
- Antihistamine use within 2 weeks prior to Screening
- Consumption of alcohol within 48 hours of study drug administration
- Positive urine drug test or cotinine test at Screening or Day -1
- History, within the last 2 years, of alcohol abuse, illicit drug use, or significant mental illness
- Demonstration of veins unsuitable for repeated venipuncture or IV infusion
- Recent treatment with alternative therapies which may confound clinical or laboratory assessments
- Donation or loss of more than 500 mL of blood within 56 days prior to study drug administration
- History of malignancy within last 5 years
- History of severe allergic or anaphylactic reactions
- Females who are pregnant or breastfeeding
Treatment and study plan
AK001
DrugGiven parenterally.
Placebo
DrugOther names: Saline solution
Primary outcomes
-
Evaluation of safety and tolerability of AK001 measured by number of subjects with adverse events and dose limiting toxicities (DLTs) respectively
Time frame: Within 86 days
Secondary outcomes
-
Immediate hypersensitivity skin testing
Time frame: Within 28 days
-
Peripheral blood counts for eosinophils and basophils
Time frame: Within 28 days
-
Serum eosinophilic cationic protein (ECP) and tryptase levels
Time frame: Within 28 days
-
24-hour urine measurement of histamine, N-methylhistamine, and 11-beta-prostaglandin F2
Time frame: Within 28 days
Sponsors and collaborators
Lead sponsor
Allakos Inc.
Industry
Registry information
Official study title
A Phase 1, Randomized, Double-Blind, Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AK001 in Subjects With Atopic Disease
Important dates
- Study start
- 2015
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Sep 30, 2015
- Registry last updated
- Jun 29, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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