First-in-Human Testing of a Wirelessly Controlled Drug Delivery Microchip

被引:313
作者
Farra, Robert [1 ]
Sheppard, Norman F., Jr. [1 ]
McCabe, Laura [1 ]
Neer, Robert M. [2 ]
Anderson, James M. [3 ]
Santini, John T., Jr. [4 ]
Cima, Michael J. [5 ]
Langer, Robert [6 ]
机构
[1] MicroCHIPS Inc, Waltham, MA 02451 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Endocrine Unit, Boston, MA 02114 USA
[3] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[4] Demand Therapeut Inc, Tyngsboro, MA 01879 USA
[5] MIT, Dept Mat Sci & Engn, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[6] MIT, Dept Chem Engn, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
关键词
PARATHYROID-HORMONE; 1-34; MULTI-RESERVOIR ARRAY; IN-VITRO RELEASE; BONE; OSTEOPOROSIS; FRACTURES; DEVICE;
D O I
10.1126/scitranslmed.3003276
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The first clinical trial of an implantable microchip-based drug delivery device is discussed. Human parathyroid hormone fragment (1-34) [hPTH(1-34)] was delivered from the device in vivo. hPTH(1-34) is the only approved anabolic osteoporosis treatment, but requires daily injections, making patient compliance an obstacle to effective treatment. Furthermore, a net increase in bone mineral density requires intermittent or pulsatile hPTH(1-34) delivery, a challenge for implantable drug delivery products. The microchip-based devices, containing discrete doses of lyophilized hPTH(1-34), were implanted in eight osteoporotic postmenopausal women for 4 months and wirelessly programmed to release doses from the device once daily for up to 20 days. A computer-based programmer, operating in the Medical Implant Communications Service band, established a bidirectional wireless communication link with the implant to program the dosing schedule and receive implant status confirming proper operation. Each woman subsequently received hPTH(1-34) injections in escalating doses. The pharmacokinetics, safety, tolerability, and bioequivalence of hPTH(1-34) were assessed. Device dosing produced similar pharmacokinetics to multiple injections and had lower coefficients of variation. Bone marker evaluation indicated that daily release from the device increased bone formation. There were no toxic or adverse events due to the device or drug, and patients stated that the implant did not affect quality of life.
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页数:10
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