Spitz IM

No ORCID on file · 12 papers in corpus
review 2010
Contraception ·doi:10.1016/j.contraception.2009.12.012

Administration of mifepristone followed by the prostaglandin, misoprostol, has been used successfully in the medical termination of pregnancy for over 25 years, and the method is registered in 35 countries. Single doses of mifepristone are …

review 2009
Current opinion in obstetrics & gynecology ·doi:10.1097/gco.0b013e32832e07e8

PURPOSE OF REVIEW: In view of the spate of recent publications related to mifepristone and some second generation progesterone receptor modulators (PRMs), this appears to be an opportune time to view the clinical status of these compounds. …

review 2006
Current opinion in investigational drugs (London, England : 2000) ·doi:10.1002/9783527623297.ch7

Since the discovery of the progesterone receptor antagonist mifepristone, numerous additional compounds, which display a spectrum of biological actions ranging from full antagonist to those with mixed agonist/antagonist activity, have been …

review 2005
Human Reproduction Update ·doi:10.1093/humupd/dmi002

Since the discovery of the antiprogestin mifepristone, hundreds of similar compounds have been synthesized, which can be grouped in a large family of progesterone receptor ligands. This family includes pure agonists such as progesterone its…

article 2003
Human Reproduction ·doi:10.1093/humrep/deg179

BACKGROUND: The levonorgestrel-releasing intra-uterine system (LNg-IUS) has been used to control menorrhagia, but irregular bleeding during the first 3 months of use was the most notable side effect. Endometrial angiogenesis is believed to …

review 2003
Expert opinion on investigational drugs ·doi:10.1517/13543784.12.10.1693

Since the discovery of the antiprogestin RU 486 (mifepristone), other compounds have been synthesised that function as pure progesterone antagonists or progesterone receptor modulators. The latter are mixed agonists-antagonists. Mifepriston…

review 2003
Steroids ·doi:10.1016/j.steroids.2003.08.007

Since the original description of the structure of the antiprogestin, mifepristone, was published, numerous related compounds have been synthesized which may function as progesterone antagonists (PAs) or progesterone receptor modulators (PR…

article 2001
Human Reproduction ·doi:10.1093/humrep/16.10.2103

BACKGROUND: The levonorgestrel-releasing intrauterine system (LNg-IUS) has been shown to be effective in the management of menorrhagia. In order to evaluate the effects of LNg-IUS on endometrial proliferation and apoptosis, proliferating ce…

case-report 2001
Clinical endocrinology ·doi:10.1046/j.1365-2265.2001.01026.x

Mifepristone (RU486) is a potent antiprogestagen, and at high doses it also acts as an antiglucocorticoid drug. Mifepristone, administered as a single 600 mg dose, is commonly employed to induce medical abortion in conjunction with prostagl…

review 2000
Steroids ·doi:10.1016/s0039-128x(00)00194-x

Both progesterone receptor modulators (PRMs) as well as pure progesterone antagonists (PAs) have numerous proven and potential therapeutic applications in female health care. Mifepristone, a PRM with only marginal agonistic activity, togeth…

review 1998
Human Reproduction Update ·doi:10.1093/humupd/4.5.584

Considerable progress has been made in elucidating the mechanism of action of antiprogestins. The biological response to a progesterone antagonist depends on many factors. The usual effect is that of an antagonist, but progesterone agnostic…

review 1996
Annual review of pharmacology and toxicology ·doi:10.1146/annurev.pa.36.040196.000403

Antiprogestins are characterized by substitutions at the 11 beta and 17 alpha positions of the steroid ring system and bind strongly to both progesterone and glucocorticoid receptors. Although they function predominantly as antiprogestins a…