Safety and Efficacy of Asfotase Alfa in Juvenile Patients With Hypophosphatasia (HPP)

Alexion Pharmaceuticals

Status and phase: Completed; Phase 2

Conditions: Hypophosphatasia (HPP)

Treatments: Biological: asfotase alfa

Study type: Interventional

Funder types: Industry

Identifiers

NCT00952484

ENB-006-09

Details and patient eligibility

About

This clinical trial studied the safety and efficacy of asfotase alfa in children with HPP compared to a historical control group.

Full description

Asfotase Alfa was formerly referred to as ENB-0040

Hypophosphatasia (HPP) is a life-threatening, genetic, and ultra-rare metabolic disease characterized by defective bone mineralization and impaired phosphate and calcium regulation that can lead to progressive damage to multiple vital organs, including destruction and deformity of bones, profound muscle weakness, seizures, impaired renal function, and respiratory failure. There are no approved disease-modifying treatments for patients with this disease. There is also limited data available on the natural course of this disease over time, particularly in patients with the juvenile-onset form.

Efficacy analyses were prospectively defined in the protocol with a comparison to historical controls. The historical control group came from patients whose characteristics matched as closely as possible the entry criteria for the trial. The control group included all patients who had x-rays within the age range defined by the inclusion criteria of this study (5 to 12 years of age, inclusive, with open growth plates).

The pre-specified plan for analysis was to combine the two asfotase alfa treated groups (asfotase alfa 2 mg/kg subcutaneous (SC) injection three times per week or 3 mg/kg subcutaneous (SC) injection three times per week) and compare them to historical controls.

Enrollment: 13 patients

Sex: All

Ages: 5 to 12 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Written informed consent from parent or legal guardian prior to participation

2. Patients > 5 and < 12 years of age with open growth plates at time of enrollment

3. Tanner stage of 2 or less indicating pre-pubescence

4. Documented history of HPP, as evidenced by:

   • Presence of HPP-related rickets on skeletal radiographs of the wrist and knee
   • Serum alkaline phosphatase (ALP) below age-adjusted normal range
   • Plasma PLP at least twice the upper limit of normal

5. 25(OH) vitamin D level > 20 ng/mL

6. Ability of patient and parent/guardian to comply with study requirements

Exclusion criteria

1. Serum calcium or phosphorus below age-adjusted normal range
2. History of sensitivity to any study drug constituent
3. Medical condition, serious intercurrent illness, or other extenuating circumstance that, in the opinion of the Investigator, may significantly interfere with study compliance, including all prescribed evaluations and follow-up activities
4. Treatment with an investigational drug within 1 month before start of study drug
5. Current enrollment in any other study involving an investigational new drug, device, or treatment for HPP (e.g., bone marrow transplantation)
6. Current evidence of a treatable form of rickets
7. Prior treatment with bisphosphonates
8. Bone fracture or orthopedic surgery within the past 12 months that, in the opinion of the Investigator would interfere with the ability of study patient to comply with study protocol
9. Major congenital abnormality other than those associated with HPP

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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13 participants in 2 patient groups

2 mg/kg

Active Comparator group

Description:

2 mg/kg subcutaneous injection three times per week.

Treatment:

Biological: asfotase alfa

Biological: asfotase alfa

3 mg/kg

Active Comparator group

Description:

3 mg/kg subcutaneous injection three times per week.

Treatment:

Biological: asfotase alfa

Biological: asfotase alfa