RESTORE: Mitigate Immune-Mediated Loss of Therapeutic Response to Asfotase Alfa (STRENSIQ®) for Hypophosphatasia

Sponsor

Alexion (Industry)

Overall Status

Not yet recruiting

CT.gov ID

NCT06015750

Collaborator

(none)

Enrollment

Arm

47.9

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

The primary objective of this study is to evaluate the effect of immunosuppressive therapy (IST) in participants treated with asfotase alfa who demonstrate immune-mediated loss of effectiveness (LoE).

Condition or Disease	Intervention/Treatment	Phase
Hypophosphatasia	Drug: methotrexate Drug: rituximab Drug: bortezomib Drug: IVIg Drug: Folic Acid	Phase 4

Study Design

Study Type:

Interventional

Anticipated Enrollment :

8 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

An Interventional, Prospective Open-Label Study of Immunosuppressive Therapies to Mitigate Immune-Mediated Loss of Therapeutic Response to Asfotase Alfa (STRENSIQ®) for Hypophosphatasia (RESTORE)

Anticipated Study Start Date :

Aug 29, 2023

Anticipated Primary Completion Date :

Aug 27, 2027

Anticipated Study Completion Date :

Aug 27, 2027

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Pediatric participants with HPP Pediatric participants who have been receiving asfotase alfa treatment for their HPP, and who demonstrate immune-mediated LoE.	Drug: methotrexate Methotrexate will be administered SC or orally weekly for 104 weeks. Drug: rituximab Rituximab will be administered intravenously (IV) continuously weekly, for up to 74 weeks. Drug: bortezomib Bortezomib will be administered via IV bolus or SC, as needed. Drug: IVIg IVIg will be administered via IV monthly through initial 74 weeks. Drug: Folic Acid Folic acid will be given orally as long as methotrexate is being dosed.

Arm

Intervention/Treatment

Experimental: Pediatric participants with HPP

Pediatric participants who have been receiving asfotase alfa treatment for their HPP, and who demonstrate immune-mediated LoE.

Drug: methotrexate

Methotrexate will be administered SC or orally weekly for 104 weeks.

Drug: rituximab

Rituximab will be administered intravenously (IV) continuously weekly, for up to 74 weeks.

Drug: bortezomib

Bortezomib will be administered via IV bolus or SC, as needed.

Drug: IVIg

IVIg will be administered via IV monthly through initial 74 weeks.

Drug: Folic Acid

Folic acid will be given orally as long as methotrexate is being dosed.

Outcome Measures

Primary Outcome Measures

Number of Participants Who Achieve Immunosuppressive Therapy (IST) Complete Response at Week 100 [Week 100]

Secondary Outcome Measures

Number Participants with Antidrug Antibodies (ADAs) and Neutralizing Antibodies (NAbs) [Baseline Through Week 100]
ADA and NAb Titer Levels [Baseline Through Week 100]
Serum Concentration of Asofatase Alfa (Measured as Enzyme Activity) [Baseline Through Week 100]
Plasma Concentration of Pyridoxal-5ˈ-Phosphate (PLP) [Baseline Through Week 100]
Plasma Concentration of Inorganic Pyrophosphates (PPi) [Baseline Through Week 100]
Number of Participants with Treatment-emergent Adverse Events and Treatment-emergent Serious Adverse Events [Baseline Through Week 104]

Eligibility Criteria

Criteria

Ages Eligible for Study:

2 Years to 18 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Reoccurrence or worsening of rickets for at least the past 3 months in participants who showed an initial efficacy response to asfotase alfa after at least 6 months of continuous treatment and currently receiving asfotase alfa. RSS will be used to determine severity at Baseline.
Presence of ADAs, with or without NAbs, irrespective of their titers.
Confirmation by the TMB that both the clinical evidence and immunogenicity-mediated association noted above are present.
Female participants of childbearing potential and male participants with partners of childbearing potential must follow protocol-specified contraception guidance as described in Section 10.5.
Participant, or participant's legal guardian, is capable of signing informed consent or assent as described in Section 10.1.3, which includes compliance with the requirements and restrictions listed in the informed consent or assent form and in this protocol.

Exclusion Criteria:

Known history of human immunodeficiency virus (HIV) infection (evidenced by HIV type 1 or type 2 [HIV 1, HIV 2] antibody) or hepatitis B or C viral infection.
Known or suspected history of drug or alcohol abuse or dependence within 1 year prior to Screening.
Inability of the participant, or the participant's legal guardian, to provide informed consent.
Pregnant, breastfeeding, or intending to conceive during the course of the study.
Inability to travel to the clinic for specified visits during the Treatment Period caused by disease per se or logistics (does not apply to external travel restrictions).
The participant is at risk of reactivation or has an active significant viral infection such as hepatitis B, cytomegalovirus, herpes simplex, human polyomavirus (also known as John Cunningham [JC] virus), parvovirus, or Epstein Barr virus.
The participant is at risk of reactivation of tuberculosis or has regular contact (eg, in the household) with individuals who are being actively treated for tuberculosis.
The participant has had or is required to have any live vaccination within 1 month prior to enrollment.