Hypophosphatasia Clinical Trials
53 clinical trials for Hypophosphatasia across international registries, including 12 currently recruiting participants. Compare status, phase, eligibility criteria and locations.
- Prospective, Longitudinal, Observational Registry of Adult Patients With Hypophosphatasia (REG-HYPO) — RECRUITING
- A Study to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ALE1 in Healthy Adults and Adults With Hypophosphatasia in Order to Identify Suitable Doses of ALE1 — RECRUITING · PHASE1
- The Effect of Monoallelic Variants in the ALPL Gene on the Natural Course of Hypophosphatasia in Russia — RECRUITING
- A Phase 3, Randomized, Double-blinded, Placebo-controlled, Multicenter Study to Evaluate Efficacy and Safety of ALXN1850 Versus Placebo Administered Subcutaneously in Pediatric (2 to < 12 years of age) Participants with Hypophosphatasia Who Have Not Received Previous Treatment with Asfotase Alfa — RECRUITING · PHASE3
- Natural History Study of Patients With Hypophosphatasia (HPP) — RECRUITING
- Registry of Patients With Hypophosphatasia — RECRUITING
- A Prospective Sub-Study of the Global Hypophosphatasia Registry — RECRUITING
- Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford — RECRUITING
- Characteristics of Hypophosphatasia in Adult Patients in Rheumatology and Their Value in Developing an Algorithm to HPP-diagnosis - the COHIR Multi-center Study — RECRUITING
- A PHASE 3, RANDOMIZED, OPEN-LABEL,
PARALLEL-ARM, ACTIVE-CONTROLLED, MULTICENTER STUDY TO EVALUATE SAFETY AND
EFFICACY OF ALXN1850 VERSUS ASFOTASE ALFA ADMINISTERED
SUBCUTANEOUSLY IN PEDIATRIC PARTICIPANTS (2 TO < 12 YEARS OF AGE) WITH
HYPOPHOSPHATASIA (HPP) PREVIOUSLY TREATED WITH ASFOTASE ALFA — RECRUITING · PHASE3
- A PHASE 3, RANDOMIZED, DOUBLE-BLINDED, PLACEBO-CONTROLLED, MULTICENTER STUDY
TO EVALUATE EFFICACY AND SAFETY OF ALXN1850 VERSUS PLACEBO ADMINISTERED
SUBCUTANEOUSLY IN PEDIATRIC (2 TO < 12 YEARS OF AGE) PARTICIPANTS WITH
HYPOPHOSPHATASIA WHO HAVE NOT RECEIVED PREVIOUS TREATMENT WITH ASFOTASE
ALFA — RECRUITING · PHASE3
- A PHASE 3, RANDOMIZED, DOUBLE-BLINDED,
PLACEBO-CONTROLLED, MULTICENTER STUDY TO EVALUATE EFFICACY AND SAFETY OF
ALXN1850 (RECOMBINANT ALKALINE PHOSPHATASE) ADMINISTERED SUBCUTANEOUSLY IN
ADOLESCENT (12 TO < 18 YEARS OF AGE) AND ADULT PARTICIPANTS WITH
HYPOPHOSPHATASIA WHO HAVE NOT PREVIOUSLY BEEN TREATED WITH ASFOTASE ALFA — RECRUITING · PHASE3
- Safety and Efficacy Study of Asfotase Alfa in Adolescents and Adults With Hypophosphatasia (HPP) — OTHER · PHASE2
- Access Program for Asfotase Alfa — COMPLETED · PHASE4
- A Randomised, Placebo-Controlled, Double-Blind, Single-Ascending Dose and Multiple-Ascending Dose First-In-Human Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Orally Administered ALE1 With or Without Food in Healthy Adult Participants and Adult Patients With Hypophosphatasia — NOT_YET_RECRUITING · PHASE2
- Early Check: Expanded Screening in Newborns — ACTIVE_NOT_RECRUITING
- Phase 3 Study of ALXN1850 Versus Placebo in Adolescent and Adult Participants With HPP Who Have Not Previously Been Treated With Asfotase Alfa — ACTIVE_NOT_RECRUITING · PHASE3
- Phase 3 Study of ALXN1850 in Treatment-Naïve Pediatric Participants With HPP — ACTIVE_NOT_RECRUITING · PHASE3
- United States Hypophosphatasia Molecular Research Center — COMPLETED
- Phase 3 Study of ALXN1850 in Pediatric Participants With HPP Previously Treated With Asfotase Alfa — ACTIVE_NOT_RECRUITING · PHASE3
- Mitigate Immune-Mediated Loss of Therapeutic Response to Asfotase Alfa (STRENSIQ®) for Hypophosphatasia — WITHDRAWN · PHASE4
- A Phase 3, Randomized, Double-blinded, Placebo-controlled, Multicenter Study to Evaluate Efficacy and Safety of ALXN1850 (Recombinant Alkaline Phosphatase) Administered Subcutaneously in Adolescent (12 to < 18 years of age) and Adult Participants with Hypophosphatasia Who Have Not Previously Been Treated with Asfotase Alfa (Hickory) — TERMINATED · PHASE3
- Pilot Trial of Single Dose Ilofotase Alfa in Hypophosphatasia — COMPLETED · PHASE1
- Study of ALXN1850 in Participants With Hypophosphatasia (HPP) — COMPLETED · PHASE1
- An Interventional, Prospective Open-Label Study of Immunosuppressive Therapies to Mitigate Immune-Mediated Loss of Therapeutic Response to Asfotase Alfa (STRENSIQ®) for Hypophosphatasia (RESTORE) — OTHER · PHASE4
- Patient Reported Outcomes in Adults With Pediatric-onset Hypophosphatasia Treated With Strensiq® (Asfotase Alfa) — COMPLETED
- A Phase 3, Randomized, Open-label, Parallel-arm, Active-controlled, Multicenter Study to Evaluate Safety and Efficacy of ALXN1850 Versus Asfotase Alfa Administered Subcutaneously in Pediatric Participants (2 to < 12 years of age) with Hypophosphatasia (HPP) Previously Treated with Asfotase Alfa (Chestnut) — OTHER · PHASE3
- Characteristics of Hypophosphatasia in Adult Patients in Rheumatology — OTHER
- Characterisation of Adult-Onset Hypophosphatasia — COMPLETED
- Safety and Efficacy Study of ENB-0040 in Juvenile Patients With Hypophosphatasia (HPP) — WITHDRAWN · PHASE2
- Circulating miRNAs and Bone Microstructure in Adults With Hypophosphatasia — OTHER
- The PORTRAIT Study — OTHER
- Dose Escalation Study to Evaluate the Safety and Tolerability of Multiple Infusions of BPS804 in Adults With Hypophosphatasia (HPP) — COMPLETED · PHASE2
- Evaluate and Monitor Physical Performance of Adults Treated With Asfotase Alfa for Hypophosphatasia — COMPLETED
- Unraveling Genetics of HypoPhosPhatasia (HPP Genetics) — COMPLETED
- Evaluation of Bone Architecture and Bone Strength in Adults With Hypophosphatasia (HPP) — OTHER
- Relieving Burden of Hypophosphatasia in Adults With Functional Impairment Due to Chronic Disease — WITHDRAWN · PHASE4
- Pharmacokinetic and Dose Response Study of Asfotase Alfa in Adult Patients With Pediatric-Onset Hypophosphatasia (HPP) — COMPLETED · PHASE2
- A Retrospective Study of the Natural History of Patients With Severe Perinatal and Infantile Hypophosphatasia (HPP) — COMPLETED
- Safety and Efficacy Study of Asfotase Alfa in Severely Affected Infants With Hypophosphatasia (HPP) — COMPLETED · PHASE1
- Safety and Efficacy of Asfotase Alfa in Juvenile Patients With Hypophosphatasia (HPP) — COMPLETED · PHASE2
- Retrospective, Non-interventional Natural History of Patients With Juvenile-onset Hypophosphatasia (HPP) — COMPLETED
- Safety Study of Human Recombinant Tissue Non-Specific Alkaline Phosphatase Fusion Protein Asfotase Alfa in Adults With Hypophosphatasia (HPP) — COMPLETED · PHASE1
- Expanded Access Program for Asfotase Alfa Treatment for Patients With Infantile- or Juvenile-onset Hypophosphatasia (HPP) — OTHER
- Extension Study of Protocol ENB-002-08 - Study of Asfotase Alfa in Infants and Young Children With Hypophosphatasia (HPP) — COMPLETED · PHASE2
- Extension Study of Protocol ENB-006-09 - Study of Asfotase Alfa in Children With Hypophosphatasia (HPP) — COMPLETED · PHASE2
- Non-interventional Substudy of ALX-HPP-502 to Assess Natural History of Patients With Juvenile-onset HPP Who Served as Historical Controls in ENB-006-09 — COMPLETED
- Safety and Efficacy Study of Asfotase Alfa in Adolescents and Adults With Hypophosphatasia (HPP) — COMPLETED · PHASE2
- Open-Label Study of Asfotase Alfa in Infants and Children ≤ 5 Years of Age With Hypophosphatasia (HPP) — COMPLETED · PHASE2
- Health Burden of Hypophosphatasia — COMPLETED
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