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Erschienen in: Drugs in R&D 1/2005

01.01.2005 | Adis R&D Profile

Lasofoxifene

CP 336156, CP-336156

Erschienen in: Drugs in R&D | Ausgabe 1/2005

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Excerpt

Lasofoxifene [CP 336156] is a potent, nonsteroidal, tissue-selective estrogen receptor modulator (SERM). It has the bone-sparing and cardioprotective effects of estrogen, but lacks estrogen’s uterine cancer risk. Lasofoxifene is under development with Ligand Pharmaceuticals and Pfizer (formerly Parke-Davis) for the prevention of postmenopausal osteoporosis and breast cancer. …
Literatur
1.
Zurück zum Zitat Ligand Pharmaceuticals, Royalty Pharma. Ligand, Royalty Pharma Amend SERM Royalty Agreement; Royalty Pharma Accelerates and Increases Royalty Purchase to $32.5 Million as Substitute for Final Two Options. Media Release: 9 Nov 2004. Available from URL: http://www.ligand.com Ligand Pharmaceuticals, Royalty Pharma. Ligand, Royalty Pharma Amend SERM Royalty Agreement; Royalty Pharma Accelerates and Increases Royalty Purchase to $32.5 Million as Substitute for Final Two Options. Media Release: 9 Nov 2004. Available from URL: http://​www.​ligand.​com
2.
Zurück zum Zitat Ligand Pharmaceuticals Incorporated. Ligand Earns Milestone as Pfizer Submits NDA for Lasofoxifene for Osteoporosis; First of Three Phase III SERM Products Advancing Prospects of Future Royalties. Media Release: 16 Sep 2004. Available from URL: http://www.ligand.com Ligand Pharmaceuticals Incorporated. Ligand Earns Milestone as Pfizer Submits NDA for Lasofoxifene for Osteoporosis; First of Three Phase III SERM Products Advancing Prospects of Future Royalties. Media Release: 16 Sep 2004. Available from URL: http://​www.​ligand.​com
3.
Zurück zum Zitat Pfizer Inc. Pfizer Sees Strong Prospects from the Industry’s Premier R&D Pipeline and Expanding New Product Opportunities. Media Release: 30 Nov 2004. Available from URL: http://www.pfizer.com Pfizer Inc. Pfizer Sees Strong Prospects from the Industry’s Premier R&D Pipeline and Expanding New Product Opportunities. Media Release: 30 Nov 2004. Available from URL: http://​www.​pfizer.​com
4.
Zurück zum Zitat Rosati RL, Jardine PDS, Cameron KO. Discovery and sar of a potent non-steroidal estrogen agonist, CP-336,156. 212th American Chemical Society National Meeting 212: abstr. 205, 25 Aug 1996 Rosati RL, Jardine PDS, Cameron KO. Discovery and sar of a potent non-steroidal estrogen agonist, CP-336,156. 212th American Chemical Society National Meeting 212: abstr. 205, 25 Aug 1996
5.
Zurück zum Zitat Pfizer cancer treatment portfolio has four candidates nearing clinic. FDC Reports — Pink Sheet — Prescription Pharmaceuticals and Biotechnology 60: 19, 16 Nov 1998 Pfizer cancer treatment portfolio has four candidates nearing clinic. FDC Reports — Pink Sheet — Prescription Pharmaceuticals and Biotechnology 60: 19, 16 Nov 1998
6.
Zurück zum Zitat McClung M, Weiss S, Moffett AH, et al. A study of lasofoxifene, a next generation SERM, versus raloxifene, in preventing bone loss in postmenopausal women. Arthritis and Rheumatism 50 (Suppl.): 669, No. 9, Sep 2004 McClung M, Weiss S, Moffett AH, et al. A study of lasofoxifene, a next generation SERM, versus raloxifene, in preventing bone loss in postmenopausal women. Arthritis and Rheumatism 50 (Suppl.): 669, No. 9, Sep 2004
7.
Zurück zum Zitat Ke HZ, Oi H, Crawford DT. A new selective estrogen receptor modulator, CP-336,156, preserves bone mass and bone strength, decreases total serum cholesterol without causing prostate hypertrophy in a model of male osteoporosis. Bone 23 (Suppl.): 183, No. 5, 1998 Ke HZ, Oi H, Crawford DT. A new selective estrogen receptor modulator, CP-336,156, preserves bone mass and bone strength, decreases total serum cholesterol without causing prostate hypertrophy in a model of male osteoporosis. Bone 23 (Suppl.): 183, No. 5, 1998
8.
Zurück zum Zitat Rosati RL, Da Silva Jardine P, Cameron KO. Discovery and preclinical pharmacology of a novel, potent, nonsteroidal estrogen receptor agonist/antagonist, CP-336156, a diaryltetrahydronaphthalene. Journal of Medicinal Chemistry 41: 2928–2931, 30 Jul 1998PubMedCrossRef Rosati RL, Da Silva Jardine P, Cameron KO. Discovery and preclinical pharmacology of a novel, potent, nonsteroidal estrogen receptor agonist/antagonist, CP-336156, a diaryltetrahydronaphthalene. Journal of Medicinal Chemistry 41: 2928–2931, 30 Jul 1998PubMedCrossRef
9.
Zurück zum Zitat Ke HZ, Li M, Pan LC, et al. Combined administration of a growth hormone secretagogue and a new selective estrogen receptor modulator increases bone and muscle mass and decreases total serum cholesterol in ovariectomized rats. Bone 23 (Suppl.): 390, No. 5, 1998 Ke HZ, Li M, Pan LC, et al. Combined administration of a growth hormone secretagogue and a new selective estrogen receptor modulator increases bone and muscle mass and decreases total serum cholesterol in ovariectomized rats. Bone 23 (Suppl.): 390, No. 5, 1998
10.
Zurück zum Zitat Ke HZ, Qi H, Chidsey-Frink KL. et al. Effects of different dose regimens of lasofoxifene (CP-336,156) in preventing bone loss in ovariectomized rats. Journal of Bone and Mineral Research 15 (Suppl. 1): 310 (plus poster), Sep 2000 Ke HZ, Qi H, Chidsey-Frink KL. et al. Effects of different dose regimens of lasofoxifene (CP-336,156) in preventing bone loss in ovariectomized rats. Journal of Bone and Mineral Research 15 (Suppl. 1): 310 (plus poster), Sep 2000
11.
Zurück zum Zitat Cole HW, Adrian MD, Shetler PK, et al. Comparative pharmacology of high potency selective estrogen receptor modulators (SERMs): LY353381 HCL and CP336,156. Journal of Bone and Mineral Research 12: 349, 1997CrossRef Cole HW, Adrian MD, Shetler PK, et al. Comparative pharmacology of high potency selective estrogen receptor modulators (SERMs): LY353381 HCL and CP336,156. Journal of Bone and Mineral Research 12: 349, 1997CrossRef
12.
Zurück zum Zitat Bell J. SERMs: benefits for bone and breast (ASBMR 2000). Scientific Meetings News: 2 Oct 2000 Bell J. SERMs: benefits for bone and breast (ASBMR 2000). Scientific Meetings News: 2 Oct 2000
Metadaten
Titel
Lasofoxifene
CP 336156, CP-336156
Publikationsdatum
01.01.2005
Verlag
Springer International Publishing
Erschienen in
Drugs in R&D / Ausgabe 1/2005
Print ISSN: 1174-5886
Elektronische ISSN: 1179-6901
DOI
https://doi.org/10.2165/00126839-200506010-00008

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