Pharmacokinetic and Dose Response Study of Asfotase Alfa in Adult Patients With Pediatric-Onset Hypophosphatasia (HPP)

Completed · Phase 2

Conditions studied: Hypophosphatasia

In brief

The purpose of this study was to evaluate the pharmacokinetics (PK) and pharmacodynamics (PD) of asfotase alfa in adult participants with pediatric-onset HPP.

Key facts

Study ID

NCT02797821

Run by

Alexion Pharmaceuticals, Inc.

People needed

27

Starts

2016-06-06

Expected to finish

2017-06-21

Last updated by the study team

2019-09-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants or their legal representative(s) provided written informed consent prior to undergoing any study-related procedures.
• Participants were ≥18 years of age at Screening.
• Participant had pediatric-onset hypophosphatasia (HPP), defined as onset of first sign(s)/symptom (s) of HPP prior to 18 years of age.
• Participants had a documented diagnosis of HPP as indicated by a documented history of HPP-related skeletal abnormalities and 1 or more of the following:
• Documented tissue-nonspecific alkaline phosphatase (TNSALP) gene mutation(s) from a certified laboratory.
• Serum alkaline phosphatase (ALP) level below the age-adjusted normal range AND plasma pyridoxal-5'-phosphate (PLP) above the upper limit of normal at Screening.
• Participants had a plasma inorganic pyrophosphate (PPi) level of ≥3.9 micromolar (µM) at Screening.
• Female participants of childbearing potential had a negative pregnancy test at the time of enrollment.
• Sexually active male and female participants of childbearing potential agreed to use a highly effective method of birth control during the study.
• Female participants not of child-bearing potential due to sterilization (at least 6 weeks after surgical bilateral oophorectomy with or without hysterectomy or at least 6 weeks after tubal ligation) confirmed by medical history, or menopause.
• Participants were willing to comply with study procedures and the visit schedule.

You may not qualify if…

• Investigational site personnel directly affiliated with this study and/or their immediate families. Immediate family was defined as a spouse, parent, child, or sibling, whether biological or legally adopted.
• Employees of Alexion Pharmaceuticals.
• Currently enrolled in a clinical study involving another study drug or non-approved use of a drug or device.
• Participated, within the last 30 days, in a clinical study involving a study drug (other than the study drug used in this study).
• Completed or withdrawn from this study or any other study investigating asfotase alfa in the previous 3 years.
• Women who were pregnant, planning to become pregnant, or breastfeeding.
• Serum 25-hydroxy Vitamin D levels below 20 nanogram (ng) per milliliter (mL) at Screening.
• Screening serum creatinine or parathyroid hormone (PTH) levels ≥1.5 times the upper limit of normal.
• Any medical condition, serious concurrent illness and/or injury, recent orthopedic surgery, or other extenuating circumstance that, in the opinion of the Investigator, may have significantly interfered with study compliance or study endpoints.
• Prior treatment with bisphosphonates within 2 years of study entry for any length of time or for more than 2 consecutive years at any prior timepoint.
• Treatment with PTH, strontium, or sclerostin inhibitors within 6 months prior to the first dose of study drug.
• Unwilling or unable to comply with the use of a data collection device on which study participants directly recorded data.

Where it is running

• Shriners Hospitals for Children — St Louis, Missouri, United States
• Duke University Medical Center — Durham, North Carolina, United States
• Vanderbilt Medical Center Endocrinology — Nashville, Tennessee, United States
• University of Würzburg — Würzburg, Germany

Full record on ClinicalTrials.gov

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