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Citations to this article

Efficacy of anti-sclerostin monoclonal antibody BPS804 in adult patients with hypophosphatasia
Lothar Seefried, … , Uwe Junker, Franz Jakob
Lothar Seefried, … , Uwe Junker, Franz Jakob
Published April 24, 2017
Citation Information: J Clin Invest. 2017;127(6):2148-2158. https://doi.org/10.1172/JCI83731.
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Clinical Research and Public Health Bone biology Article has an altmetric score of 6

Efficacy of anti-sclerostin monoclonal antibody BPS804 in adult patients with hypophosphatasia

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Abstract

BACKGROUND. Hypophosphatasia (HPP) is a rare genetic disorder resulting in variable alterations of bone formation and mineralization that are caused by mutations in the ALPL gene, encoding the tissue-nonspecific alkaline phosphatase (ALP) enzyme.

METHODS. In this phase IIA open-label, single-center, intra-patient, dose-escalating study, adult patients with HPP received 3 ascending intravenous doses of 5, 10, and 20 mg/kg BPS804, a fully human anti-sclerostin monoclonal antibody, on days 1, 15, and 29, respectively. Patients were followed for 16 weeks after the last dose. We assessed the pharmacodynamics, pharmacokinetics, preliminary efficacy, and safety of BPS804 administrations at specified intervals during treatment and follow-up.

RESULTS. Eight patients (mean age 47.8 years) were enrolled in the study (6 females, 2 males). BPS804 treatment increased mean ALP and bone-specific ALP enzymatic activity between days 2 and 29. Transient increases in the bone formation markers procollagen type-I N-terminal propeptide (PINP), osteocalcin, and parathyroid hormone as well as a transient decrease in the bone resorption marker C-telopeptide of type I collagen (CTX-1) were observed. Lumbar spine bone mineral density showed a mean increase by day 85 and at end of study. Treatment-associated adverse events were mild and transient.

CONCLUSION. BPS804 treatment was well tolerated and resulted in increases in bone formation biomarkers and bone mineral density, suggesting that sclerostin inhibition could be applied to enhance bone mineral density, stability, and regeneration in non-life-threatening clinical situations in adults with HPP.

TRIAL REGISTRATION. Clinicaltrials.gov NCT01406977.

FUNDING. Novartis Institutes for BioMedical Research, Basel, Switzerland.

Authors

Lothar Seefried, Jasmin Baumann, Sarah Hemsley, Christine Hofmann, Erdmute Kunstmann, Beate Kiese, Yue Huang, Simon Chivers, Marie-Anne Valentin, Babul Borah, Ronenn Roubenoff, Uwe Junker, Franz Jakob

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Year: 2025 2024 2023 2022 2021 2020 2019 2018 Total
Citations: 1 2 2 5 8 8 5 3 34
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Citations to this article (34)

Title and authors Publication Year
Medical Management of Hypophosphatasia: Review of Data on Asfotase Alfa
Dahir KM, Dunbar NS
Current Osteoporosis Reports 2025
Τhe story of sclerostin inhibition: the past, the present, and the future.
Anastasilakis AD, Tsourdi E
Hormones (Athens, Greece) 2024
Monoclonal antibody anti-sclerostin for treatment of pelvic insufficiency fractures in adult hypophosphatasia: A case report
Schwab PE, Dessain A, Milby J
2024
Hypophosphatasia: from birth to adulthood
Reis FS, Lazaretti-Castro M
Archives of Endocrinology and Metabolism 2023
Musculoskeletal and neurocognitive clinical significance of adult hypophosphatasia
Kim SM, Korkmaz F, Sims S, Ryu V, Yuen T, Zaidi M
Osteoporosis and Sarcopenia 2023
The Role of Sclerostin in Bone Diseases
E Vasiliadis, D Evangelopoulos, A Kaspiris, I Benetos, C Vlachos, S Pneumaticos
Journal of Clinical Medicine 2022
Role of Wnt signaling and sclerostin in bone and as therapeutic targets in skeletal disorders.
Marini F, Giusti F, Palmini G, Brandi ML
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2022
Proposing a clinical algorithm for better diagnosis of hypophosphatasia in resource-limiting situations.
Sadhukhan S, Mehta P, Rajender S, Gupta SK, Chattopadhyay N
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2022
Gene Therapy Using Recombinant AAV Type 8 Vector Encoding TNAP‐D10 Improves the Skeletal Phenotypes in Murine Models of Osteomalacia
Amadeu de Oliveira F, Mohamed FF, Kinoshita Y, Narisawa S, Farquharson C, Miyake K, Foster BL, Millan JL
JBMR Plus 2022
Wnt signaling: Essential roles in osteoblast differentiation, bone metabolism and therapeutic implications for bone and skeletal disorders
Vlashi R, Zhang X, Wu M, Chen G
Genes & Diseases 2022
Sclerostin and Osteocalcin: Candidate Bone-Produced Hormones
JS Wang, CM Mazur, MN Wein
Frontiers in Endocrinology 2021
New therapeutic options for bone diseases
R Kocijan, J Haschka, J Feurstein, J Zwerina
Wiener Medizinische Wochenschrift 2021
TNAP as a New Player in Chronic Inflammatory Conditions and Metabolism
S Graser, D Liedtke, F Jakob
International journal of molecular sciences 2021
Osteoporosis Treatment with Anti-Sclerostin Antibodies—Mechanisms of Action and Clinical Application
M Rauner, H Taipaleenmäki, E Tsourdi, EM Winter
Journal of Clinical Medicine 2021
Hypophosphatasia: A Unique Disorder of Bone Mineralization
JM Villa-Suárez, C García-Fontana, F Andújar-Vera, S González-Salvatierra, T de Haro-Muñoz, V Contreras-Bolívar, B García-Fontana, M Muñoz-Torres
International journal of molecular sciences 2021
Hypophosphatasia
S Tournis, M Yavropoulou, S Polyzos, A Doulgeraki
Journal of Clinical Medicine 2021
Gene Therapy Using Adeno‐Associated Virus Serotype 8 Encoding TNAP‐D10 Improves the Skeletal and Dentoalveolar Phenotypes in Alpl −/− Mice
Kinoshita Y, Mohamed FF, Amadeu de Oliveira F, Narisawa S, Miyake K, Foster BL, Millán JL
Journal of Bone and Mineral Research 2021
Bilateral atypical femoral fractures during denosumab therapy in a patient with adult-onset hypophosphatasia
Warren AM, Ebeling PR, Grill V, Seeman E, Sztal-Mazer S
Endocrinology, diabetes & metabolism case reports 2021
Ionomycin ameliorates hypophosphatasia via rescuing alkaline phosphatase deficiency-mediated L-type Ca2+ channel internalization in mesenchymal stem cells
B Li, X He, Z Dong, K Xuan, W Sun, L Gao, S Liu, W Liu, C Hu, Y Zhao, S Shi, Y Jin
Bone Research 2020
Phage Display Derived Monoclonal Antibodies: From Bench to Bedside
MA Alfaleh, HO Alsaab, AB Mahmoud, AA Alkayyal, ML Jones, SM Mahler, AM Hashem
Frontiers in immunology 2020
Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics
J Bovijn, K Krebs, CY Chen, R Boxall, JC Censin, T Ferreira, SL Pulit, CA Glastonbury, S Laber, IY Millwood, K Lin, L Li, Z Chen, L Milani, GD Smith, RG Walters, R Mägi, BM Neale, CM Lindgren, MV Holmes
Science Translational Medicine 2020
Bone mineral density and fracture risk in adult patients with hypophosphatasia
F Genest, L Claußen, D Rak, L Seefried
Osteoporosis International 2020
Anti-Sclerostin Antibodies in Osteoporosis and Other Bone Diseases
S Fabre, T Funck-Brentano, M Cohen-Solal
Journal of Clinical Medicine 2020
Adult hypophosphatasia with a novel ALPL mutation: Report of an Indian kindred
Bhadada SK, Pal R, Dhiman V, Alonso N, Ralston SH, Kaur S, Gupta R
Bone Reports 2020
Hypophosphatasia: Current Literature for Pathophysiology, Clinical Manifestations, Diagnosis, and Treatment
Bangura A, Wright L, Shuler T
Cureus 2020
Adult hypophosphatasia manifests in a marathon runner
Fanous N, Barb D
BMJ case reports 2020
The Regulation of Bone Metabolism and Disorders by Wnt Signaling
K Maeda, Y Kobayashi, M Koide, S Uehara, M Okamoto, A Ishihara, T Kayama, M Saito, K Marumo
International journal of molecular sciences 2019
Therapeutic Enzymes: Function and Clinical Implications
N Labrou
2019
Outcome of Teriparatide Treatment on Fracture Healing Complications and Symptomatic Bone Marrow Edema in Four Adult Patients With Hypophosphatasia: FRACTURE HEALING COMPLICATIONS AND TEIPARATIDE IN HPP
T Schmidt, T Rolvien, C Linke, NM Jandl, R Oheim, M Amling, F Barvencik
JBMR Plus 2019
Romosozumab: a novel bone anabolic treatment option for osteoporosis?
K Kerschan-Schindl
Wiener Medizinische Wochenschrift 2019
The evolving therapeutic landscape of genetic skeletal disorders
AH Sabir, T Cole
Orphanet Journal of Rare Diseases 2019
Abnormal bone turnover in individuals with low serum alkaline phosphatase
L López-Delgado, L Riancho-Zarrabeitia, MT García-Unzueta, JA Tenorio, M García-Hoyos, P Lapunzina, C Valero, JA Riancho
Osteoporosis International 2018
Profile of asfotase alfa in the treatment of hypophosphatasia: design, development, and place in therapy
SA Bowden, BL Foster
Drug design, development and therapy 2018
Hypophosphatasia: From Diagnosis to Treatment.
Simon S, Resch H, Klaushofer K, Roschger P, Zwerina J, Kocijan R
Current Rheumatology Reports 2018

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