Jump to content

Vutrisiran: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous editNext edit →
Content deleted Content added
VisualWikitext
add CA
Citation bot (talk | contribs)
Bots
5,383,962 edits
Added hdl. | Use this bot. Report bugs. | Suggested by Abductive | Category:Multiple chemicals in Infobox drug | #UCB_Category 189/623
Line 98: Line 98:
}}
}}


'''Vutrisiran''', previously known as (ALN-TTRSC02), sold under the brand name '''Amvuttra''', is a [[medication]] used for the treatment of the [[polyneuropathy]] of [[hereditary transthyretin-mediated amyloidosis|hereditary transthyretin-mediated (hATTR) amyloidosis]] in adults.<ref>{{cite journal | vauthors = Tamargo J, Agewall S, Borghi C, Ceconi C, Cerbai E, Dan GA, Ferdinandy P, Grove EL, Rocca B, Sulzgruber P, Semb AG, Sossalla S, Niessner A, Kaski JC, Dobrev D | display-authors = 6 | title = New pharmacological agents and novel cardiovascular pharmacotherapy strategies in 2022 | journal = European Heart Journal. Cardiovascular Pharmacotherapy | volume = 9 | issue = 4 | pages = 353–370 | date = May 2023 | pmid = 37169875 | pmc = 10236523 | doi = 10.1093/ehjcvp/pvad034 | pmc-embargo-date = May 11, 2024 }}</ref><ref name="Amvuttra FDA label" /><ref name="Alnylam PR 20220613" /> It is a double stranded [[small interfering RNA]] (siRNA) (also called RNA interference, or RNAi therapeutic) that interferes with the expression of the [[transthyretin]] (TTR) gene.<ref name="Aimo_2022">{{cite journal | vauthors = Aimo A, Castiglione V, Rapezzi C, Franzini M, Panichella G, Vergaro G, Gillmore J, Fontana M, Passino C, Emdin M | display-authors = 6 | title = RNA-targeting and gene editing therapies for transthyretin amyloidosis | journal = Nature Reviews. Cardiology | volume = 19 | issue = 10 | pages = 655–667 | date = October 2022 | pmid = 35322226 | doi = 10.1038/s41569-022-00683-z | s2cid = 247623259 | url = https://discovery.ucl.ac.uk/id/eprint/10161200/ }}</ref><ref name="Keam_2022">{{cite journal | vauthors = Keam SJ | title = Vutrisiran: First Approval | journal = Drugs | volume = 82 | issue = 13 | pages = 1419–1425 | date = September 2022 | pmid = 35997942 | doi = 10.1007/s40265-022-01765-5 | s2cid = 251725617 | url = https://figshare.com/articles/online_resource/Vutrisiran_First_Approval/20409192 }}</ref> Transthyretin is a serum protein made in the liver whose major function is transport of vitamin A and thyroxine.<ref name="Luigetti_2020">{{cite journal | vauthors = Luigetti M, Romano A, Di Paolantonio A, Bisogni G, Sabatelli M | title = Diagnosis and Treatment of Hereditary Transthyretin Amyloidosis (hATTR) Polyneuropathy: Current Perspectives on Improving Patient Care | language = English | journal = Therapeutics and Clinical Risk Management | volume = 16 | pages = 109–123 | date = 2020-02-21 | pmid = 32110029 | pmc = 7041433 | doi = 10.2147/TCRM.S219979 | doi-access = free }}</ref><ref name="Al Musaimi_2023">{{cite journal | vauthors = Al Musaimi O, Al Shaer D, Albericio F, de la Torre BG | title = 2022 FDA TIDES (Peptides and Oligonucleotides) Harvest | journal = Pharmaceuticals | volume = 16 | issue = 3 | pages = 336 | date = February 2023 | pmid = 36986436 | pmc = 10056021 | doi = 10.3390/ph16030336 | doi-access = free }}</ref> Rare mutations in the transthyretin gene result in accumulation of large amyloid deposits of misfolded transthyretin molecules most prominently in peripheral nerves and the heart. Patients with hATTR typically present with polyneuropathy or autonomic dysfunction followed by cardiomyopathy which, if untreated, is fatal within 5 to 10 years.<ref name="Al Musaimi_2023" />
'''Vutrisiran''', previously known as (ALN-TTRSC02), sold under the brand name '''Amvuttra''', is a [[medication]] used for the treatment of the [[polyneuropathy]] of [[hereditary transthyretin-mediated amyloidosis|hereditary transthyretin-mediated (hATTR) amyloidosis]] in adults.<ref>{{cite journal | vauthors = Tamargo J, Agewall S, Borghi C, Ceconi C, Cerbai E, Dan GA, Ferdinandy P, Grove EL, Rocca B, Sulzgruber P, Semb AG, Sossalla S, Niessner A, Kaski JC, Dobrev D | display-authors = 6 | title = New pharmacological agents and novel cardiovascular pharmacotherapy strategies in 2022 | journal = European Heart Journal. Cardiovascular Pharmacotherapy | volume = 9 | issue = 4 | pages = 353–370 | date = May 2023 | pmid = 37169875 | pmc = 10236523 | doi = 10.1093/ehjcvp/pvad034 | pmc-embargo-date = May 11, 2024 }}</ref><ref name="Amvuttra FDA label" /><ref name="Alnylam PR 20220613" /> It is a double stranded [[small interfering RNA]] (siRNA) (also called RNA interference, or RNAi therapeutic) that interferes with the expression of the [[transthyretin]] (TTR) gene.<ref name="Aimo_2022">{{cite journal | vauthors = Aimo A, Castiglione V, Rapezzi C, Franzini M, Panichella G, Vergaro G, Gillmore J, Fontana M, Passino C, Emdin M | display-authors = 6 | title = RNA-targeting and gene editing therapies for transthyretin amyloidosis | journal = Nature Reviews. Cardiology | volume = 19 | issue = 10 | pages = 655–667 | date = October 2022 | pmid = 35322226 | doi = 10.1038/s41569-022-00683-z | hdl = 11382/558829 | s2cid = 247623259 | url = https://discovery.ucl.ac.uk/id/eprint/10161200/ }}</ref><ref name="Keam_2022">{{cite journal | vauthors = Keam SJ | title = Vutrisiran: First Approval | journal = Drugs | volume = 82 | issue = 13 | pages = 1419–1425 | date = September 2022 | pmid = 35997942 | doi = 10.1007/s40265-022-01765-5 | s2cid = 251725617 | url = https://figshare.com/articles/online_resource/Vutrisiran_First_Approval/20409192 }}</ref> Transthyretin is a serum protein made in the liver whose major function is transport of vitamin A and thyroxine.<ref name="Luigetti_2020">{{cite journal | vauthors = Luigetti M, Romano A, Di Paolantonio A, Bisogni G, Sabatelli M | title = Diagnosis and Treatment of Hereditary Transthyretin Amyloidosis (hATTR) Polyneuropathy: Current Perspectives on Improving Patient Care | language = English | journal = Therapeutics and Clinical Risk Management | volume = 16 | pages = 109–123 | date = 2020-02-21 | pmid = 32110029 | pmc = 7041433 | doi = 10.2147/TCRM.S219979 | doi-access = free }}</ref><ref name="Al Musaimi_2023">{{cite journal | vauthors = Al Musaimi O, Al Shaer D, Albericio F, de la Torre BG | title = 2022 FDA TIDES (Peptides and Oligonucleotides) Harvest | journal = Pharmaceuticals | volume = 16 | issue = 3 | pages = 336 | date = February 2023 | pmid = 36986436 | pmc = 10056021 | doi = 10.3390/ph16030336 | doi-access = free }}</ref> Rare mutations in the transthyretin gene result in accumulation of large amyloid deposits of misfolded transthyretin molecules most prominently in peripheral nerves and the heart. Patients with hATTR typically present with polyneuropathy or autonomic dysfunction followed by cardiomyopathy which, if untreated, is fatal within 5 to 10 years.<ref name="Al Musaimi_2023" />


Vutrisiran was approved for medical use in the United States in June 2022,<ref name="Amvuttra FDA label" /><ref name="Alnylam PR 20220613">{{cite web | title=Alnylam Announces FDA Approval of Amvuttra (vutrisiran), an RNAi Therapeutic for the Treatment of the Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis in Adults | publisher=Alnylam | via=Business Wire | date=13 June 2022 | url=https://www.businesswire.com/news/home/20220603005487/en/Alnylam-Announces-FDA-Approval-of-AMVUTTRA%E2%84%A2-vutrisiran-an-RNAi-Therapeutic-for-the-Treatment-of-the-Polyneuropathy-of-Hereditary-Transthyretin-Mediated-Amyloidosis-in-Adults | access-date=14 June 2022 | archive-date=14 June 2022 | archive-url=https://web.archive.org/web/20220614055318/https://www.businesswire.com/news/home/20220603005487/en/Alnylam-Announces-FDA-Approval-of-AMVUTTRA%E2%84%A2-vutrisiran-an-RNAi-Therapeutic-for-the-Treatment-of-the-Polyneuropathy-of-Hereditary-Transthyretin-Mediated-Amyloidosis-in-Adults | url-status=live }}</ref> and in the European Union in September 2022.<ref name="Amvuttra EPAR" />
Vutrisiran was approved for medical use in the United States in June 2022,<ref name="Amvuttra FDA label" /><ref name="Alnylam PR 20220613">{{cite web | title=Alnylam Announces FDA Approval of Amvuttra (vutrisiran), an RNAi Therapeutic for the Treatment of the Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis in Adults | publisher=Alnylam | via=Business Wire | date=13 June 2022 | url=https://www.businesswire.com/news/home/20220603005487/en/Alnylam-Announces-FDA-Approval-of-AMVUTTRA%E2%84%A2-vutrisiran-an-RNAi-Therapeutic-for-the-Treatment-of-the-Polyneuropathy-of-Hereditary-Transthyretin-Mediated-Amyloidosis-in-Adults | access-date=14 June 2022 | archive-date=14 June 2022 | archive-url=https://web.archive.org/web/20220614055318/https://www.businesswire.com/news/home/20220603005487/en/Alnylam-Announces-FDA-Approval-of-AMVUTTRA%E2%84%A2-vutrisiran-an-RNAi-Therapeutic-for-the-Treatment-of-the-Polyneuropathy-of-Hereditary-Transthyretin-Mediated-Amyloidosis-in-Adults | url-status=live }}</ref> and in the European Union in September 2022.<ref name="Amvuttra EPAR" />

Revision as of 03:26, 22 January 2024

Vutrisiran
Clinical data
Trade namesAmvuttra
Other namesALN-65492
License data
Routes of
administration		Subcutaneous
ATC code
Legal status
Legal status
Identifiers
CAS Number
DrugBank
UNII
KEGG

Vutrisiran, previously known as (ALN-TTRSC02), sold under the brand name Amvuttra, is a medication used for the treatment of the polyneuropathy of hereditary transthyretin-mediated (hATTR) amyloidosis in adults.[4][2][5] It is a double stranded small interfering RNA (siRNA) (also called RNA interference, or RNAi therapeutic) that interferes with the expression of the transthyretin (TTR) gene.[6][7] Transthyretin is a serum protein made in the liver whose major function is transport of vitamin A and thyroxine.[8][9] Rare mutations in the transthyretin gene result in accumulation of large amyloid deposits of misfolded transthyretin molecules most prominently in peripheral nerves and the heart. Patients with hATTR typically present with polyneuropathy or autonomic dysfunction followed by cardiomyopathy which, if untreated, is fatal within 5 to 10 years.[9]

Vutrisiran was approved for medical use in the United States in June 2022,[2][5] and in the European Union in September 2022.[3]

Mechanism of action

Vutrisiran is a gene silencing double-stranded siRNA-GalNAc conjugate that causes degradation of mutant and wild-type TTR mRNA through RNA interference by binding and silencing messenger RNA (mRNA) encoding for disease causing protein (Transthyretin), which results in a reduction of serum TTR protein and TTR protein deposits in tissues.[7][10] Vutrisiran utilises a GalNAc conjugate delivery platform which is an enhanced stabilisation chemistry. This allows subcutaneous administration of smaller doses with longer dosing intervals.[11]

History

The U.S. Food and Drug Administration (FDA) granted the application for vutrisiran orphan drug designation.[12]

Society and culture

On 21 July 2022, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product Amvuttra, intended for treatment of hereditary transthyretin-mediated (hATTR) amyloidosis.[13] Amvuttra was designated as an orphan medicinal product on 25 May 2018.[13] The applicant for this medicinal product is Alnylam Netherlands B.V.[13] Vutrisiran was approved for medical use in the European Union in September 2022.[3][14] Vutrisiran is also under regulatory review for the treatment of polyneuropathy of hATTR amyloidosis in adults in Japan and Brazil, and is being investigated in amyloidosis with cardiomyopathy in the ongoing phase 3, HELIOS-B trial.[7]

Names

Vutrisiran is the international nonproprietary name (INN).[15]

Dosage and administration

Vutrisiran sodium is available in solution in a single-dose prefilled syringe of 25 mg/0.5 mL under the brand name Amvuttra.[16] The recommended dosage of vutrisiran sodium is 25 mg administered by subcutaneous injection once every 3 months.[7]

Efficacy and trials

Preclinical: In preclinical studies involving nonhuman primates, single SC doses of vutrisiran 0.3 and 1 mg/kg achieved mean maximum TTR reductions of 55% and 96%, respectively, with serum TTR reductions persisting beyond 4 months for the 1 mg/kg dose. In the same study, monthly doses of 1 and 3 mg/kg maintained a reduction of TTR levels at 96%, relative to baseline. These potent and durable pharmacodynamic properties of vutrisiran, together with an acceptable safety profile, prompted further evaluation in a phase I clinical study.[17]

Clinical trials:

A phase 1 clinical trial (NCT02797847) was completed in January 2018, in which vutrisiran was evaluated to determine the safety, tolerability, pharmacokinetics, and pharmacodynamics in 80 healthy volunteers.[17][18] It was a randomized, single blind, placebo- controlled study.[6] Participants were randomized 6:2 to receive a single subcutaneous dose of vutrisiran (5 – 300 mg) or placebo (normal saline).[18] Vutrisiran was found to be well tolerated, established a good safety profile and elicited rapid robust and durable TTR reduction.[17][19] Vutrisiran achieved a dose-dependent TTR knockdown; a single 25 mg subcutaneous dose resulted in a maximum TTR reduction of 80%, which was sustained for 90 days.[11] Based on these results, the company launched two Phase 3 trials: HELIOS-A and HELIOS-B.[18]

HELIOS-A (NCT03759379) was a phase 3, global, open-label study comparing the efficacy and safety of vutrisiran to patisiran. 164 ATTRv amyloidosis patients were randomized 3:1 to subcutaneous vutrisiran 25 mg every 3 months or patisiran 0.3 mg/kg IV infusion every 3 weeks for 18 months’ treatment period to be followed by a lengthier extension period.[18][19] The study used the placebo arm of the APOLLO study (NCT01960348) as an external comparator for the primary and most other efficacy end points.[8] The primary endpoints of the study are the change from baseline in modified Neuropathy Impairment Score mNIS+7 and Norfolk Quality of Life-Diabetic Neuropathy QOL-DN score. Secondary endpoints include measures of mobility, BMI, disability, and serum TTR.[18] Vutrisiran met the primary endpoints at 9 months, which were maintained through 18 month.[20] It also met all secondary efficacy endpoints.[19] Additionally, patients in HELIOS-A showed improvement across exploratory cardiac end points.[20] Vutrisiran treatment resulted in rapid (≤3 weeks) and sustained reduction in serum TTR levels over 18 months, similar to what was observed in the patisiran group. Following 18 months of vutrisiran treatment, steady-state mean (SD) peak and trough serum TTR reductions from baseline were 87.6% and 81.0%, respectively. The fluctuation between median steady-state peak and trough values was lower with vutrisiran compared with patisiran, which was reflected in the reduced variability in TTR reduction (smaller standard error) observed at most time points with vutrisiran. Serum TTR reduction with vutrisiran was also similar across all patient subgroups. As expected from previous studies, serum vitamin A levels were reduced in parallel with reductions in serum TTR levels in both treatment groups.[19] The extent of the reduction in TTR was not affected by TTR genotype (45.1% of participants were V30M and 54.9% had 1 of 24 other mutations), or patient age, sex, body weight or race.[7] A subcutaneous dose of 25 mg vutrisiran every 3 months caused similar or greater efficacy than patisiran given as IV infusion three times a week.[18] Vutrisiran significantly improved multiple disease-relevant outcomes versus placebo, with an acceptable safety profile.[19] These findings from HELIOS-A resulted in FDA and EMA approval of vutrisiran for treatment of ATTRv-PN.[11] The ongoing extension period of HELIOS-A will assess long-term safety and efficacy with continued Q3M vutrisiran treatment, or an alternative every 6 months dosing regimen.[19] The estimated completion date is May 2024.[21]

A study whose results are awaited is the phase III HELIOS-B (NCT04153149) randomized, double-blind, placebo-controlled trial, in which 6 patients with TTR-related amyloid heart disease, both wild-type and mutated forms, are enrolled to evaluate the possible effects of the drug in terms of cardiac involvement.[11][18][22] The estimated completion date is June 2025. Patients are randomized on a 1:1 basis to receive 25 mg of vutrisiran or placebo administered as a subcutaneous injection once every 3 months for up to 36 months. The primary end point will evaluate the efficacy of vutrisiran in the composite outcome of reducing all-cause mortality and recurrent cardiovascular hospitalization.[21] Secondary endpoints include measures of functional exercise capacity, self-perception of health status, and cardiac structure and function.[18]

Safety

Vutrisiran is well tolerated and has an acceptable safety profile. In contrast to patisiran, patients do not require premedication, although all patients require vitamin A supplementation. The majority of adverse events in the phase 1 trial of vutrisiran were mild, and included nasopharyngitis, headache, diarrhoea and nausea, and injection site reactions.[11] HELIOS-A trial also reported encouraging safety and tolerability, with the majority of adverse events being mild or moderate 10 and no drug- related discontinuations or deaths occurred.[20] Only two serious adverse events were attributed to vutrisiran—dyslipidaemia and urinary tract infection.[11] AEs occurring in (≥ 10%) of patients receiving vutrisiran included falls, pain in extremity, diarrhea, peripheral edema, urinary tract infection, arthralgia, and dizziness; all of which, except pain in extremity and arthralgia, occurred at a similar or lower rate than in the external placebo group. There were no cardiac AEs related to vutrisiran in the safety population. Five patients (4.1%) who received vutrisiran reported mild and transient injection site reactions (ISRs). There were no safety signals regarding liver function tests, haematology, or renal function related to vutrisiran. Four vutrisiran recipients (3.3%) developed antidrug antibodies (ADAs) that were low and transient with no evidence of an effect on clinical efficacy, safety, pharmacokinetics or pharmacodynamic parameters.[19] No clinically significant changes in laboratory measures, vital signs, physical examinations, or electrocardiogram were noted.[17]

Adverse effects

Vutrisiran is generally well tolerated but side effects can include injection site reactions, fatigue, arthralgia, dyspnea, diarrhea and musculoskeletal pains.[9][16] Vutrisiran treatment leads to decreased Vitamin A levels and supplementation at the recommended daily allowance of vitamin A is advised. Patients should be referred to an ophthalmologist if ocular symptoms suggestive of vitamin A deficiency (e.g. night blindness) develop.[7]

Pharmacokinetics

Plasma concentration profiles of vutrisiran showed rapid absorption and elimination from systemic circulation. There was a dose-proportional increase in peak plasma concentrations Cmax and a slightly greater than dose-proportional increase in AUC∞ inf and AUC last after a single subcutaneous dose across the dose range studied in the phase 1 trial in healthy volunteers.[7][17] However, accumulation was not evident after repeated administration of vutrisiran 25 mg every 3 months in patients with hATTR amyloidosis. Plasma concentrations of vutrisiran were detectable at 10 minutes after SC administration and peak plasma concentrations were seen at a median 4 h after SC administration of a 25 mg single dose in healthy volunteers.[7] Plasma half-life was (4.2–7.5 hours).[17] The apparent volume of distribution of vutrisiran is estimated to be 10.1 L. Vutrisiran is 80% plasma protein bound; however, plasma protein binding is concentration dependent and decreases with increasing concentrations. Vutrisiran distributes mainly to the liver after subcutaneous administration.[7] The plasma clearance of siRNA is primarily influenced by ASGPR-facilitated uptake into the liver where the siRNAs are gradually metabolized by endonucleases and exonucleases to short nucleotide fragments of varying sizes.[7][17] After a 25 mg single dose SC vutrisiran in healthy volunteers, the median elimination half-life was 5.2 h and the median apparent clearance was 21.4 L/h. The primary pathway for excretion of vutrisiran is via the kidneys, although the fraction of renal clearance to total clearance was 15.5–27.5% after a single 5–300 mg subcutaneous dose in healthy volunteers, indicating that renal excretion is a minor route of elimination.[7] Across the dose levels tested, mean renal CLR of vutrisiran ranged from 4.45 to 5.74 L/hour (mean, 5 L/hour) after a single subcutaneous dose in healthy volunteers and the percentage of vutrisiran dose excreted unchanged in urine through 24 hours ranged between 15–25% and increased slightly with increasing dose, with a majority excreted within the first 12 hours after administration.[7][17] Age, sex, bodyweight, race, and mild or moderate kidney impairment or mild hepatic impairment do not have clinically significant effects on vutrisiran pharmacokinetics. In vitro, vutrisiran was neither a substrate nor inhibitor of cytochrome P450 enzymes and is not expected to cause drug- drug interaction by inducing CYP enzymes. Vutrisiran is not expected to modulate drug transporter activities.[7]

References

  1. ^ "Notice: Multiple additions to the Prescription Drug List (PDL) [2023-12-22]". Health Canada. 22 December 2023. Retrieved 3 January 2024.
  2. ^ a b c "Amvuttra- vutrisiran injection". DailyMed. 21 June 2022. Archived from the original on 3 July 2022. Retrieved 3 July 2022.
  3. ^ a b c "Amvuttra EPAR". European Medicines Agency. 18 July 2022. Retrieved 13 October 2022. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  4. ^ Tamargo J, Agewall S, Borghi C, Ceconi C, Cerbai E, Dan GA, et al. (May 2023). "New pharmacological agents and novel cardiovascular pharmacotherapy strategies in 2022". European Heart Journal. Cardiovascular Pharmacotherapy. 9 (4): 353–370. doi:10.1093/ehjcvp/pvad034. PMC 10236523. PMID 37169875.{{cite journal}}: CS1 maint: PMC embargo expired (link)
  5. ^ a b "Alnylam Announces FDA Approval of Amvuttra (vutrisiran), an RNAi Therapeutic for the Treatment of the Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis in Adults". Alnylam. 13 June 2022. Archived from the original on 14 June 2022. Retrieved 14 June 2022 – via Business Wire.
  6. ^ a b Aimo A, Castiglione V, Rapezzi C, Franzini M, Panichella G, Vergaro G, et al. (October 2022). "RNA-targeting and gene editing therapies for transthyretin amyloidosis". Nature Reviews. Cardiology. 19 (10): 655–667. doi:10.1038/s41569-022-00683-z. hdl:11382/558829. PMID 35322226. S2CID 247623259.
  7. ^ a b c d e f g h i j k l m Keam SJ (September 2022). "Vutrisiran: First Approval". Drugs. 82 (13): 1419–1425. doi:10.1007/s40265-022-01765-5. PMID 35997942. S2CID 251725617.
  8. ^ a b Luigetti M, Romano A, Di Paolantonio A, Bisogni G, Sabatelli M (21 February 2020). "Diagnosis and Treatment of Hereditary Transthyretin Amyloidosis (hATTR) Polyneuropathy: Current Perspectives on Improving Patient Care". Therapeutics and Clinical Risk Management. 16: 109–123. doi:10.2147/TCRM.S219979. PMC 7041433. PMID 32110029.
  9. ^ a b c Al Musaimi O, Al Shaer D, Albericio F, de la Torre BG (February 2023). "2022 FDA TIDES (Peptides and Oligonucleotides) Harvest". Pharmaceuticals. 16 (3): 336. doi:10.3390/ph16030336. PMC 10056021. PMID 36986436.
  10. ^ "Vutrisiran Sodium". American Journal of Health-System Pharmacy. 79 (19): 1617–1618. September 2022. doi:10.1093/ajhp/zxac195. PMID 35904362.
  11. ^ a b c d e f Ioannou A, Fontana M, Gillmore JD (March 2023). "RNA Targeting and Gene Editing Strategies for Transthyretin Amyloidosis". BioDrugs. 37 (2): 127–142. doi:10.1007/s40259-023-00577-7. PMC 9933836. PMID 36795354.
  12. ^ "Vutrisiran Orphan Drug Designations and Approvals". U.S. Food and Drug Administration (FDA). 25 May 2018. Archived from the original on 14 June 2022. Retrieved 14 June 2022.
  13. ^ a b c "Amvuttra: Pending EC decision". European Medicines Agency. 21 July 2022. Archived from the original on 28 July 2022. Retrieved 30 July 2022. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  14. ^ "Amvuttra Product information". Union Register of medicinal products. Retrieved 3 March 2023.
  15. ^ World Health Organization (2019). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 81". WHO Drug Information. 33 (1). hdl:10665/330896.
  16. ^ a b LiverTox: Clinical and Research Information on Drug-Induced Liver Injury. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases. 2012. PMID 31643176.
  17. ^ a b c d e f g h Habtemariam BA, Karsten V, Attarwala H, Goel V, Melch M, Clausen VA, et al. (February 2021). "Single-Dose Pharmacokinetics and Pharmacodynamics of Transthyretin Targeting N-acetylgalactosamine-Small Interfering Ribonucleic Acid Conjugate, Vutrisiran, in Healthy Subjects". Clinical Pharmacology and Therapeutics. 109 (2): 372–382. doi:10.1002/cpt.1974. PMID 32599652. S2CID 220271638.
  18. ^ a b c d e f g h Zhang MM, Bahal R, Rasmussen TP, Manautou JE, Zhong XB (July 2021). "The growth of siRNA-based therapeutics: Updated clinical studies". Biochemical Pharmacology. 189: 114432. doi:10.1016/j.bcp.2021.114432. PMC 8187268. PMID 33513339.
  19. ^ a b c d e f g Adams D, Tournev IL, Taylor MS, Coelho T, Planté-Bordeneuve V, Berk JL, et al. (March 2023). "Efficacy and safety of vutrisiran for patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy: a randomized clinical trial". Amyloid. 30 (1): 18–26. doi:10.1080/13506129.2022.2091985. PMID 35875890. S2CID 251033186.
  20. ^ a b c Maurer MS (December 2022). "Overview of Current and Emerging Therapies for Amyloid Transthyretin Cardiomyopathy". The American Journal of Cardiology. 185 (Suppl 1): S23–S34. doi:10.1016/j.amjcard.2022.10.014. PMID 36371281. S2CID 253476162.
  21. ^ a b Yadav JD, Othee H, Chan KA, Man DC, Belliveau PP, Towle J (December 2021). "Transthyretin Amyloid Cardiomyopathy-Current and Future Therapies". The Annals of Pharmacotherapy. 55 (12): 1502–1514. doi:10.1177/10600280211000351. PMID 33685242. S2CID 232160553.
  22. ^ Cantone A, Sanguettoli F, Dal Passo B, Serenelli M, Rapezzi C (November 2022). "The treatment of amyloidosis is being refined". European Heart Journal Supplements. 24 (Suppl I): I131–I138. doi:10.1093/eurheartjsupp/suac104. PMC 9653129. PMID 36380794.
Retrieved from "https://en.wikipedia.org/enwiki/w/index.php?title=Vutrisiran&oldid=1197836956"