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- Q66032331 description "clinical trial" @default.
- Q66032331 description "ensayu clínicu" @default.
- Q66032331 description "klinisch onderzoek" @default.
- Q66032331 description "клінічне випробування" @default.
- Q66032331 name "A Study of MK0217A and Dietary Supplement in Men and Postmenopausal Women With Osteoporosis (0217A-227)" @default.
- Q66032331 name "A Study of MK0217A and Dietary Supplement in Men and Postmenopausal Women With Osteoporosis" @default.
- Q66032331 type Item @default.
- Q66032331 label "A Study of MK0217A and Dietary Supplement in Men and Postmenopausal Women With Osteoporosis (0217A-227)" @default.
- Q66032331 label "A Study of MK0217A and Dietary Supplement in Men and Postmenopausal Women With Osteoporosis" @default.
- Q66032331 prefLabel "A Study of MK0217A and Dietary Supplement in Men and Postmenopausal Women With Osteoporosis (0217A-227)" @default.
- Q66032331 prefLabel "A Study of MK0217A and Dietary Supplement in Men and Postmenopausal Women With Osteoporosis" @default.
- Q66032331 P1050 Q66032331-AB27C698-8B20-4D42-8908-624B54AD2C3D @default.
- Q66032331 P1132 Q66032331-6B30F9B5-BA37-4425-9A17-F6C41C166411 @default.
- Q66032331 P1476 Q66032331-B4067845-B7D2-4CAC-8B16-123E33FA6C71 @default.
- Q66032331 P2899 Q66032331-E00D6F12-BA5A-48FD-B701-FE768011F064 @default.
- Q66032331 P3098 Q66032331-7CC19FB1-E291-4526-86E3-B63F0227C6A4 @default.
- Q66032331 P31 Q66032331-032992A2-5D06-4236-A73C-29B49F25EDA4 @default.
- Q66032331 P4135 Q66032331-AE882006-EDE4-4587-BDB7-746F8A71AD72 @default.
- Q66032331 P4844 Q66032331-78235F6A-9306-4A16-AB86-CDF1C845E234 @default.
- Q66032331 P580 Q66032331-F8BC9417-C55E-4EBF-9854-4BC6F3C37199 @default.
- Q66032331 P582 Q66032331-0B7885DF-CB24-48E4-AC4E-8E6510DF31CB @default.
- Q66032331 P6099 Q66032331-89D74B37-FBBA-40DA-8DD4-794543933444 @default.
- Q66032331 P8363 Q66032331-D361F77F-0368-4061-B274-7FD900B2C1CD @default.
- Q66032331 P1050 Q165328 @default.
- Q66032331 P1132 "+652" @default.
- Q66032331 P1476 "A 15-Week, Double-Blind, Randomized, Active-Controlled, Multi-Center Study With 24-Week Extension to Evaluate the Safety, Tolerability, Efficacy of Alendronate 70 mg Plus Vitamin D3 2800 IU Combination Tablet in Men and Postmenopausal Women With Osteoporosis" @default.
- Q66032331 P2899 "+40" @default.
- Q66032331 P3098 "NCT00092079" @default.
- Q66032331 P31 Q30612 @default.
- Q66032331 P4135 "+90" @default.
- Q66032331 P4844 Q28859601 @default.
- Q66032331 P580 "2004-01-01T00:00:00Z" @default.
- Q66032331 P582 "2004-11-01T00:00:00Z" @default.
- Q66032331 P6099 Q42824827 @default.
- Q66032331 P8363 Q78089383 @default.