2002•SpineRequires access

Summary Statement: Clinical BMP Programs

D. Greg Anderson, Gunnar B. J. Andersson, Scott D. Boden, Christopher J. Damien, Sohei Ebara, Greg A. Helm, Joseph M. Lane, Bill McKay, Harvinder S. Sandhu, Howard J. Seeherman, John M. Wozney

Open publisher page 4 citations

Abstract

Three osteoinductive bone growth factors have proceeded sufficiently through preclinical studies to generate data from human trials. These osteoinductive factors include recombinant human bone morphogenetic protein-2, recombinant human bone morphogenetic protein-7/osteogenic protein-1, and a bovine extract from a mixture of bone morphogenetic proteins. Each program has its unique challenges with preclinical efficacy, safety, carrier, dose–concentration, and clinical trial design. This article compares and contrasts the programs as they pertain to the use of bone morphogenetic proteins for spine fusion.

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What this paper is about

Three osteoinductive bone growth factors have proceeded sufficiently through preclinical studies to generate data from human trials. These osteoinductive factors include recombinant human bone morphogenetic protein-2, recombinant human bone morphogenetic protein-7/osteogenic protein-1, and a bovine extract from a mixture of bone morphogenetic proteins. Each program has its unique challenges with preclinical efficacy, safety, carrier, dose–concentration, and clinical trial design. This article compares and contrasts the programs as they pertain to the use of bone morphogenetic proteins for spine fusion.

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OpenAlex reports 4 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Three osteoinductive bone growth factors have proceeded sufficiently through preclinical studies to generate data from human trials. These osteoinductive factors include recombinant human bone morphogenetic protein-2, recombinant human bone morphogenetic protein-7/osteogenic protein-1, and a bovine extract from a mixture of bone morphogenetic proteins. Each program has its unique challenges with preclinical efficacy, safety, carrier, dose–concentration, and clinical trial design. This article compares and contrasts the programs as they pertain to the use of bone morphogenetic proteins for spine fusion.

Key concepts: Bone morphogenetic protein, Medicine, Human bone, Recombinant DNA, Bone morphogenetic protein 2, Bone morphogenetic protein 5, Clinical trial, Bone morphogenetic protein 7

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