Drug General Information (ID: DDIM3AWFU4)
  Drug Name Olanzapine Drug Info Givosiran Drug Info
  Drug Type Small molecule Small interfering RNA
  Therapeutic Class Antipsychotic Agents Metabolic Agents
  Structure

 Mechanism of Olanzapine-Givosiran Interaction (Severity Level: Moderate)
     CYP450 enzyme inhibition Click to Show/Hide Mechanism Graph
Could Not Find 2D Structure
      Drug Name Olanzapine Givosiran
      Mechanism CYP450 1A2 substrate CYP450 1A2 inhibitor
      Key Mechanism Factor 1
Factor Name Cytochrome P450 1A2
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Structure Sequence
MALSQSVPFSATELLLASAIFCLVFWVLKGLRPRVPKGLKSPPEPWGWPLLGHVLTLGKNPHLALSRMSQRYGDVLQIRIGSTPVLVLSRLDTIRQALVRQGDDFKGRPDLYTSTLITDGQSLTFSTDSGPVWAARRRLAQNALNTFSIASDPASSSSCYLEEHVSKEAKALISRLQELMAGPGHFDPYNQVVVSVANVIGAMCFGQHFPESSDEMLSLVKNTHEFVETASSGNPLDFFPILRYLPNPALQRFKAFNQRFLWFLQKTVQEHYQDFDKNSVRDITGALFKHSKKGPRASGNLIPQEKIVNLVNDIFGAGFDTVTTAISWSLMYLVTKPEIQRKIQKELDTVIGRERRPRLSDRPQLPYLEAFILETFRHSSFLPFTIPHSTTRDTTLNGFYIPKKCCVFVNQWQVNHDPELWEDPSEFRPERFLTADGTAINKPLSEKMMLFGMGKRRCIGEVLAKWEIFLFLAILLQQLEFSVPPGVKVDLTPIYGLTMKHARCEHVQARLRFSIN
Gene Name CYP1A2
Uniprot ID CP1A2_HUMAN
KEGG Pathway hsa:1544
Protein Family Cytochrome P450 family
Protein Function
A cytochrome P450 monooxygenase involved in the metabolism of various endogenous substrates, including fatty acids, steroid hormones and vitamins (PubMed:9435160, PubMed:10681376, PubMed:11555828, PubMed:12865317, PubMed:19965576). Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (NADPH--hemoprotein reductase) (PubMed:9435160, PubMed:10681376, PubMed:11555828, PubMed:12865317, PubMed:19965576). Catalyzes the hydroxylation of carbon-hydrogen bonds (PubMed:11555828, PubMed:12865317). Exhibits high catalytic activity for the formation of hydroxyestrogens from estrone (E1) and 17beta-estradiol (E2), namely 2-hydroxy E1 and E2 (PubMed:11555828, PubMed:12865317). Metabolizes cholesterol toward 25-hydroxycholesterol, a physiological regulator of cellular cholesterol homeostasis (PubMed:21576599). May act as a major enzyme for all-trans retinoic acid biosynthesis in the liver. Catalyzes two successive oxidative transformation of all-trans retinol to all-trans retinal and then to the active form all-trans retinoic acid (PubMed:10681376). Primarily catalyzes stereoselective epoxidation of the last double bond of polyunsaturated fatty acids (PUFA), displaying a strong preference for the (R,S) stereoisomer (PubMed:19965576). Catalyzes bisallylic hydroxylation and omega-1 hydroxylation of PUFA (PubMed:9435160). May also participate in eicosanoids metabolism by converting hydroperoxide species into oxo metabolites (lipoxygenase-like reaction, NADPH-independent) (PubMed:21068195). Plays a role in the oxidative metabolism of xenobiotics. Catalyzes the N-hydroxylation of heterocyclic amines and the O-deethylation of phenacetin (PubMed:14725854). Metabolizes caffeine via N3-demethylation (Probable).
    Click to Show/Hide
      Mechanism Description
  • Decreased metabolism of Olanzapine caused by Givosiran mediated inhibition of CYP450 enzyme

Recommended Action
      Management Caution and monitoring are recommended when givosiran is given with drugs that are substrates of CYP450 1A2 and/or 2D6. Concomitant use should generally be avoided with CYP450 1A2 or 2D6 substrates that have a narrow therapeutic range where minimal concentration changes may lead to serious or life-threatening toxicities. If concomitant use is unavoidable, the dosage of the CYP450 1A2 or 2D6 substrate should be reduced according to approved product labeling or clinical response and tolerance. Dosage adjustments as well as clinical and laboratory monitoring should be considered whenever givosiran is added to or withdrawn from therapy with these drugs.

References
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3 Brosen K, Skjelbo E, Rasmussen BB, Poulsen HE, Loft S "Fluvoxamine is a potent inhibitor of cytochrome P4501A2." Biochem Pharmacol 45 (1993): 1211-4. [PMID: 8466541]
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5 Cerner Multum, Inc. "UK Summary of Product Characteristics.".
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8 Desai HD, Seabolt J, Jann MW "Smoking in patients receiving psychotropic medications: a pharmacokinetic perspective." CNS Drugs 15 (2001): 469-94. [PMID: 11524025]
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10 Gossen D, de Suray JM, Vandenhende F, Onkelinx C, Gangji D "Influence of fluoxetine on olanzapine pharmacokinetics." AAPS PharmSci 4 (2002): E11. [PMID: 12102620]
11 Hiemke C, Peled A, Jabarin M, et al. "Fluvoxamine augmentation of olanzapine in chronic schizophrenia: pharmacokinetic interactions and clinical effects." J Clin Psychopharmacol 22 (2002): 502-6. [PMID: 12352274]
12 Letsas KP, Sideris A, Kounas SP, Efremidis M, Korantzopoulos P, Kardaras F "Drug-induced QT interval prolongation after ciprofloxacin administration in a patient receiving olanzapine." Int J Cardiol 109 (2006): 273-4. [PMID: 15935493]
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14 Product Information. Lybalvi (olanzapine-samidorphan). Alkermes, Inc, Cambridge, MA.
15 Product Information. Qelbree (viloxazine). Supernus Pharmaceuticals Inc, Rockville, MD.
16 Product Information. Zyprexa (olanzapine). Lilly, Eli and Company, Indianapolis, IN.
17 Wang CY, Zhang ZJ, Li WB, et al. "The differential effects of steady-state fluvoxamine on the pharmacokinetics of olanzapine and clozapine in healthy volunteers." J Clin Pharmacol 44 (2004): 785-92. [PMID: 15199083]
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