Upacicalcet

Upacicalcet
Clinical data
Trade names	Upasita
Legal status
Legal status	Rx in Japan;
Identifiers
	IUPAC name (2S)-2-Amino-3-[(3-chloro-2-methyl-5-sulfophenyl)carbamoylamino]propanoic acid;
CAS Number	1333218-50-0;
PubChem CID	53374467;
ChemSpider	71115962;
UNII	5C1222PBE2;
KEGG	D11564;
Chemical and physical data
Formula	C11H14ClN3O6S
Molar mass	351.76 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC1=C(C=C(C=C1Cl)S(=O)(=O)O)NC(=O)NC[C@@H](C(=O)O)N;
	InChI InChI=1S/C11H14ClN3O6S/c1-5-7(12)2-6(22(19,20)21)3-9(5)15-11(18)14-4-8(13)10(16)17/h2-3,8H,4,13H2,1H3,(H,16,17)(H2,14,15,18)(H,19,20,21)/t8-/m0/s1; Key:LHEYGVSDVBEYQF-QMMMGPOBSA-N;

Upacicalcet is a drug used to treat secondary hyperparathyroidism (SHPT) - a disease of the parathyroid gland - in dialysis patients.^[1] It was approved as Upasita in Japan in June 2021.^[2] The drug is given intravenously. The active ingredient is used in the form of its sodium salt.

Mechanism of action[edit]

Upacicalcet is a calcimimetic, a substance which acts at the calcium sensing receptor of parathyroid cells and thereby inhibiting parathyroid hormone secretion. Parathyroid hormone regulates the calcium concentration in the blood plasma to maintain calcium homeostasis in the body tissues ("calcium balance").

Clinical studies[edit]

Efficacy and safety were investigated in a multicenter, randomized, double-blind, placebo-controlled phase 3 study in 154 SHPT patients. Upacicalcet or placebo was given three times a week at the end of hemodialysis. The doses were then adjusted every three weeks during the 24-week treatment period in order to maintain the serum level of intact parathyroid hormone (iPTH) in the concentration range recommended by the Japanese guideline. The primary endpoint was the percentage of patients who achieved mean iPTH levels of 60–240 pg/ml by weeks 22–24.^[3]

The primary endpoint for upacicalcet was significantly higher than for placebo (67.0% vs. 8.0%). Upacicalcet significantly reduced the iPTH and cCa values (corrected calcium levels) compared to placebo. No statistically significant difference between the groups was observed for serum phosphate, but it tended to decrease in that in the upacicalcet group. Hypocalcemia did not occur in either group.^[3]

References[edit]

^ Hoy SM (September 2021). "Upacicalcet: First Approval". Drugs. 81 (13): 1593–1596. doi:10.1007/s40265-021-01578-y. PMID 34390486. S2CID 237005126.
^ "Announcement of Marketing Authorization Approval in Japan and Co-promotion Agreement of UPASITA® IV Injection Syringe for the Treatment of Secondary Hyperparathyroidism in Dialysis Patients" (Press release). Sanwa Kagaku Kenkyusho Co. and Kissei Pharmaceutical Co. June 23, 2021. Retrieved December 11, 2021.
^ ^a ^b Akizawa T, Honda D, Taniguchi M, Koiwa F (2020). "Efficacy and safety of upacicalcet in hemodialysis patients with secondary hyperparathyroidism: a phase 3 study".

[1] Hoy SM (September 2021). "Upacicalcet: First Approval". Drugs. 81 (13): 1593–1596. doi:10.1007/s40265-021-01578-y. PMID 34390486. S2CID 237005126.

[2] "Announcement of Marketing Authorization Approval in Japan and Co-promotion Agreement of UPASITA® IV Injection Syringe for the Treatment of Secondary Hyperparathyroidism in Dialysis Patients" (Press release). Sanwa Kagaku Kenkyusho Co. and Kissei Pharmaceutical Co. June 23, 2021. Retrieved December 11, 2021.

[Akizawa-3] Akizawa T, Honda D, Taniguchi M, Koiwa F (2020). "Efficacy and safety of upacicalcet in hemodialysis patients with secondary hyperparathyroidism: a phase 3 study".

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