Somatostatin analog and uses thereof

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

Reexamination Certificate

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C514S016700, C530S328000, C530S329000

Reexamination Certificate

active

07094753

ABSTRACT:
Claimed is a somatostatin agonist according to formula (I),in-line-formulae description="In-line Formulae" end="lead"?D-Phe-c(Cys-Tyr(I)-D-Trp-Lys-Val-Cys)-Thr-NH2,   (I)in-line-formulae description="In-line Formulae" end="tail"?or a pharmaceutically acceptable salt thereof, and uses thereof.

REFERENCES:
patent: 4853371 (1989-08-01), Coy et al.
patent: 5590656 (1997-01-01), O'Dorisio et al.
Murphy, W.A. et al., “Octapeptide analogs of somatostatin exhibiting greatly enhanced in vivo and in vitro inhibition of growth hormone secretion in the rat,” Biochem. Biophys. Res. Comm., 1985, 132:922-928.
Colao, A. et al., “New medical approaches in pituitary adenomas,” Hormone Research, 2000, 50:76-87.
Ferone, D. et al.,, “In vivo and in vitro effects of octreotide, quinagolide and cabergoline in four hyperprolactinaemic acromegalics: correlation with somatostatin and dopamine D-2 receptor scintigraphy,” Clin. Endocrinology, 2001, 54:469-477.
Saveanu, G. et al., “BIM-23244, a somatostatin receptor subtype 2- and 5-selective analog with enhanced efficacy in suppression growth hormone (GH) from Octreotide-resistant human GH-secreting adenomas,” J. Clin. Endocrinology and Metabolism, 2001, 86:140-145.
Shimon, I. et al., “Somatostatin receptor subtype specificity in human fetal pituitary cultures: differential role of SSTR2 and SSTR5 for growth hormone, thyroid-stimulating hormone, and prolactin regulation,” J. Clin. Investigation, 1997, 99:789-798.

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