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Patisiran
Clinical data
Trade namesOnpattro
Other namesALN-18328
AHFS/Drugs.comMonograph
License data
Pregnancy
category
Routes of
administration		Intravenous
ATC code
Legal status
Legal status
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CAS Number
DrugBank
UNII
KEGG
Chemical and physical data
FormulaC412H520N148O290P40
Molar mass13424.388 g·mol−1

Patisiran, sold under the brand name Onpattro, is a medication used for the treatment of polyneuropathy in people with hereditary transthyretin-mediated amyloidosis,[7] a fatal rare disease that is estimated to affect 50,000 people worldwide.[8][9]

It is the first small interfering RNA-based drug approved by the U.S. Food and Drug Administration (FDA) and the first drug approved by the FDA to treat this condition.[8] It is a gene silencing drug that interferes with the production of an abnormal form of transthyretin.[10] Patisiran utilizes a novel approach to target and reduce production of the TTR protein in the liver via the RNAi pathway.[11]

Patisiran was developed and is marketed by Alnylam.[12] The FDA considers it to be a first-in-class medication.[13]

History

[edit]

Patisiran was granted orphan drug status, fast track designation, priority review and breakthrough therapy designation due to its novel mechanism and the rarity of the condition it treats.[14][15] It was approved for medical use in the United States and in the European Union in August 2018.[16][17] The per-patient cost is between US$451,430 and US$677,145 per year, depending on the number of vials needed.[18]

[19][20]

Formulation

[edit]

The siRNA active component of Patisiran is formulated into lipid nanoparticles, which protect the RNA and facilitate its delivery to target tissues. The lipid nanoparticle formulation includes buffer components, as well as the lipid components DLin-MC3-DMA, Distearoylphosphatidylcholine, cholesterol, and the PEGylated lipid DMG-PEG 2000.[21]

Society and culture

[edit]

Economics

[edit]

As of 2020, there were 1050 people globally receiving patisiran, generating $65.5M in net-revenues for Alnylam Pharmaceuticals.[22][23]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Patisiran

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from Grokipedia
Patisiran is a small interfering ribonucleic acid (siRNA) therapeutic agent indicated for the treatment of associated with hereditary -mediated (hATTR) in adults. Marketed under the brand name Onpattro, it represents the first approved (RNAi) medication, targeting the root cause of hATTR by reducing the production of (TTR) protein. Developed by , patisiran is formulated as a lipid complex for targeted delivery to hepatocytes in the liver. The mechanism of action involves sequence-specific degradation of both mutant and wild-type TTR mRNA through (RISC), resulting in decreased serum TTR levels by approximately 80% and reduced amyloid deposition in tissues. This inhibition slows the progression of peripheral nerve damage and improves quality of life in patients with stage 1 or 2 . Patisiran received accelerated approval from the U.S. (FDA) on August 10, 2018, based on its demonstrated efficacy in reducing neuropathy impairment. The (EMA) granted marketing authorization on August 27, 2018, for similar indications. Key evidence supporting patisiran's efficacy comes from the phase 3 APOLLO trial, a randomized, double-blind, -controlled study involving 225 adults with hATTR and , which showed significant improvements in neuropathy scores (mNIS+7: -6.0 vs. +28.0 for ; p<0.001) and quality-of-life measures (Norfolk QoL-DN: -6.7 vs. +14.4; p<0.001) after 18 months of treatment. Long-term open-label extension data through five years confirm sustained benefits on neurological function and safety, with no new signals of concern. Administered intravenously at a dose of 0.3 mg/kg (or 30 mg for patients ≥100 kg) every three weeks, treatment requires premedication with corticosteroids, antihistamines, and acetaminophen to mitigate infusion-related reactions, which occur in about 19% of patients. Common adverse effects include upper respiratory tract infections (29%), infusion-related reactions such as nausea and dyspnea, and reductions in serum vitamin A levels, necessitating daily supplementation. While primarily approved for polyneuropathy, ongoing research explores its role in transthyretin cardiac amyloidosis (ATTR-CM), with studies like APOLLO-B demonstrating improvements in functional capacity. As of 2025, patisiran remains a cornerstone of gene-silencing therapy for hATTR amyloidosis, alongside newer agents like vutrisiran.

Medical uses

Indications

Patisiran is indicated for the treatment of polyneuropathy in adults with hereditary transthyretin-mediated (hATTR) amyloidosis. hATTR amyloidosis is a rare, autosomal dominant genetic disorder caused by mutations in the transthyretin (TTR) gene, leading to misfolding of the TTR protein and extracellular deposition of amyloid fibrils in various tissues, primarily affecting the peripheral nerves and heart. This results in progressive polyneuropathy characterized by sensory loss, pain, motor weakness, and autonomic dysfunction, as well as cardiomyopathy in many cases. Clinical efficacy for this indication was demonstrated in a phase 3, randomized, double-blind, placebo-controlled trial (APOLLO) involving 225 adults with hATTR amyloidosis and polyneuropathy, where patisiran treatment over 18 months led to significant improvements compared to placebo. Key endpoints included a reduction in the modified Neuropathy Impairment Score plus 7 (mNIS+7) of -6.0 points versus +28.0 points for placebo (p<0.0001), indicating halted progression and reversal of neuropathy impairment; improvement in the Norfolk Quality of Life-Diabetic Neuropathy (QoL-DN) score by -6.7 points versus +14.4 points (p<0.0001), reflecting better quality of life; and enhanced walking speed in the 10-meter walk test by 0.08 m/sec versus a decline of -0.24 m/sec (p<0.0001). Patisiran has no other approved indications, though ongoing research, such as the APOLLO-B phase 3 trial, investigated its potential benefits in hATTR amyloidosis with cardiomyopathy, where it preserved functional capacity over 12 months. In October 2023, the FDA issued a Complete Response Letter denying expanded approval, and as of 2025, no regulatory approval for cardiomyopathy has been granted.

Administration and dosage

Patisiran is administered via intravenous (IV) infusion every 3 weeks to patients with hereditary transthyretin-mediated (hATTR) amyloidosis with polyneuropathy. The recommended dosage is 0.3 mg/kg of actual body weight for patients weighing less than 100 kg, or a fixed dose of 30 mg for those weighing 100 kg or more. Prior to each infusion, premedication is required to mitigate the risk of infusion-related reactions (IRRs). This regimen, administered at least 60 minutes before the start of the infusion, typically includes an intravenous corticosteroid such as dexamethasone 10 mg (which may be reduced to 5 mg after the second dose if tolerated), oral acetaminophen 500 mg, an intravenous H1 receptor blocker such as diphenhydramine 50 mg, and an intravenous H2 receptor blocker such as famotidine 20 mg. Oral alternatives may be used for the H1 and H2 blockers if intravenous administration is not tolerated. For preparation, the patisiran solution must be filtered through a 0.45-micron polyethersulfone (PES) syringe filter and diluted in 200 mL of 0.9% sodium chloride injection using a DEHP-free infusion bag. The mixture should be gently inverted to combine and used immediately, or stored at room temperature (up to 30°C) for no more than 16 hours from the time of dilution. The infusion is delivered over approximately 80 minutes through a dedicated IV line equipped with a 1.2-micron PES in-line filter (DEHP-free), beginning at an initial rate of 1 mL per minute for the first 15 minutes, followed by 3 mL per minute for the remainder. If IRRs occur, the infusion rate should be slowed or interrupted as clinically indicated, with the total duration potentially extended. Patients receiving patisiran require ongoing monitoring, including supplementation with the recommended daily allowance of vitamin A (approximately 2,500 IU for adults) due to the drug's reduction in serum vitamin A levels from decreased transthyretin-mediated retinol transport. Higher supplemental doses should be avoided, as serum levels do not accurately reflect total body vitamin A stores; ophthalmologic evaluation is advised if symptoms of deficiency, such as night blindness, develop. During and after each infusion, patients should be observed for signs of IRRs, and the infusion site monitored for infiltration. No dosage adjustments are necessary for patients with mild hepatic impairment or mild to moderate renal impairment (estimated glomerular filtration rate ≥30 mL/min/1.73 m²). The drug has not been studied in moderate or severe hepatic impairment or severe renal impairment, including end-stage renal disease. In the event of a serious or life-threatening IRR, the infusion must be discontinued immediately and not resumed.

Pharmacology

Mechanism of action

Patisiran is a small interfering RNA (siRNA) designed to target transthyretin (TTR) messenger RNA (mRNA) specifically in hepatocytes, the primary site of TTR protein synthesis in the body. As an RNA interference (RNAi) therapeutic, it exploits the natural cellular machinery to silence gene expression by binding to the RNA-induced silencing complex (RISC), which facilitates sequence-specific cleavage and degradation of the target TTR mRNA. This process inhibits the translation of TTR protein, both mutant and wild-type forms, without altering the expression of other proteins. The siRNA component of patisiran is formulated within lipid nanoparticles for targeted delivery to hepatocytes via intravenous administration, enabling efficient uptake through interactions with apolipoprotein E and low-density lipoprotein receptors on liver cells. Once internalized, the siRNA unwinds and incorporates into the RISC complex, where the guide strand directs the endonucleolytic cleavage of TTR mRNA at a conserved sequence in the 3' untranslated region, preventing the production of transthyretin protein. Clinical studies have demonstrated that this mechanism results in a rapid and sustained reduction in serum TTR levels, achieving approximately 80-90% inhibition from baseline within days of dosing and maintaining these reductions over extended periods, such as 18 months in phase 3 trials. By substantially lowering circulating TTR concentrations, patisiran disrupts the pathogenic cascade in hereditary transthyretin-mediated (hATTR) amyloidosis, where misfolded TTR proteins aggregate into amyloid fibrils that deposit in peripheral nerves and organs. This reduction in TTR synthesis prevents further amyloid formation and deposition, thereby stabilizing or improving neurological function in patients with hATTR-associated polyneuropathy. The therapy's high specificity, with over 10,000-fold greater binding affinity for TTR mRNA compared to off-target transcripts, minimizes unintended effects on non-TTR gene products.

Pharmacokinetics

Patisiran is administered intravenously, resulting in immediate bioavailability of 100% upon infusion completion. Peak serum transthyretin (TTR) reduction, reflecting its pharmacodynamic effect, occurs within approximately 2 weeks following administration. The drug's lipid nanoparticles primarily target the liver for hepatocyte uptake, with rapid distribution to hepatic tissues observed in nonclinical studies where over 90% of the dose accumulates in the liver shortly after dosing. The steady-state volume of distribution for patisiran (ALN-18328) is approximately 0.26 L/kg. Patisiran, as a small interfering RNA (siRNA), undergoes metabolism primarily through degradation by nucleases into shorter nucleotide fragments within the RNA-induced silencing complex. The lipid nanoparticle components are cleared via the reticuloendothelial system, with the ionizable lipid (DLin-MC3-DMA) primarily metabolized by hydrolysis to 4-(dimethylamino)butyric acid (DMBA) and the corresponding diol, along with oxidative metabolites such as dioxy-DLin-MC3-DMA. Elimination of intact patisiran occurs minimally through renal excretion, with less than 1% of the dose recovered unchanged in urine. The terminal elimination half-life of patisiran is about 3.2 days, though the pharmacodynamic effect on TTR reduction persists for 2 to 3 months per dose due to sustained hepatic silencing. Nanoparticle components are primarily eliminated via hepatobiliary routes, with fecal excretion accounting for a portion of the dose in preclinical models. Steady-state pharmacokinetics are achieved after approximately 24 weeks of dosing at 0.3 mg/kg every 3 weeks, with an accumulation ratio of about 3.2 for patisiran exposure compared to the first dose; no further accumulation occurs beyond this point.

Adverse effects

Common adverse reactions

The most common adverse reactions associated with patisiran, observed in the phase 3 APOLLO trial, were infusion-related reactions (IRRs), upper respiratory tract infections, peripheral edema, arthralgia, and abdominal pain, with most events classified as grade 1 or 2 in severity. Infusion-related reactions occurred in 19% of patisiran-treated patients compared to 9% in the placebo group, typically manifesting as mild to moderate symptoms such as flushing (approximately 5%), back pain (approximately 5%), nausea (approximately 4%), and headache (approximately 3%). These reactions were most frequent during the initial infusions, with 79% of cases occurring within the first two doses, and their incidence decreased over time with continued treatment. To mitigate IRRs, patients receive premedication prior to each intravenous infusion of patisiran, including corticosteroids, H1 antihistamines, H2 antihistamines, and acetaminophen, administered approximately 60 minutes before dosing. If symptoms arise during infusion, slowing or interrupting the rate is recommended, and in rare cases of recurrence, permanent discontinuation may be considered. Upper respiratory tract infections were reported in 29% of patisiran patients versus 21% in placebo recipients, generally mild to moderate and not requiring specific intervention beyond standard care. Peripheral edema affected approximately 30% of patisiran-treated patients compared to 22% in the placebo group, presenting as mild to moderate swelling often managed conservatively. Arthralgia occurred in about 11% of patients on patisiran, typically involving joint pain that was self-limiting or responsive to analgesics. Abdominal pain was noted in roughly 10% of cases, frequently linked to IRRs and resolving without long-term sequelae. Overall, discontinuations due to these common adverse reactions were low, affecting approximately 5% of patisiran patients in the APOLLO trial.

Serious adverse reactions

Patisiran administration has been associated with hypersensitivity reactions, including rare cases of anaphylaxis occurring in less than 1% of patients, manifesting as dyspnea, hypotension, and syncope. These severe infusion-related reactions require immediate discontinuation of the infusion and appropriate medical intervention, such as supportive care for anaphylaxis. Premedication with corticosteroids, acetaminophen, and antihistamines is recommended to mitigate the risk of such reactions. Thrombocytopenia has not been identified as a significant risk with patisiran treatment, with no safety signals reported in clinical trials or post-marketing surveillance. Vitamin A deficiency is a notable risk due to patisiran's inhibition of , which transports vitamin A in serum, leading to reduced levels in nearly all patients with normal baseline values. This can result in ocular symptoms such as night blindness, necessitating routine supplementation with the recommended daily allowance of vitamin A and ophthalmologic evaluation if symptoms arise. Post-marketing reports through 2025 have included rare instances of severe infusion-related reactions, such as pronounced hypotension and syncope, as well as occasional liver enzyme elevations that were typically mild and transient. In patients with hereditary ATTR (hATTR) amyloidosis, cardiac events including atrioventricular heart block (incidence 2.7% in trials, with three cases of complete block) have been observed, underscoring the need for cardiac monitoring during treatment. Patisiran carries no black box warnings, and while no Risk Evaluation and Mitigation Strategy (REMS) program is required by the FDA, close monitoring during infusions is essential to manage potential severe reactions.

Contraindications and precautions

Contraindications

Patisiran is contraindicated in patients with a known history of severe hypersensitivity reactions, such as anaphylaxis, to patisiran or to any of the excipients.

Special populations

Patisiran requires no dosage adjustment in elderly patients aged 65 years and older, as clinical studies showed no overall differences in safety or efficacy compared to younger adults, although greater sensitivity cannot be ruled out in some individuals. Hereditary transthyretin-mediated (hATTR) amyloidosis often presents with late onset in the elderly, where comorbidities such as cardiovascular disease and renal dysfunction are more prevalent, necessitating careful monitoring during treatment. In patients with renal impairment, no dosage adjustment is needed for mild (eGFR 60–89 mL/min/1.73 m²) or moderate (eGFR 30–59 mL/min/1.73 m²) impairment, based on pharmacokinetic data indicating similar exposure to . has not been studied in severe renal impairment (eGFR <30 mL/min/1.73 m²) or end-stage renal disease, though long-term use has been associated with preservation of kidney function in patients with hATTR amyloidosis and . For hepatic impairment, no dosage adjustment is required in mild cases (total bilirubin ≤ upper limit of normal with AST > upper limit of normal, or total bilirubin 1–1.5 times upper limit of normal with any AST level). Patisiran has not been studied in moderate or severe hepatic impairment, and use is not recommended unless the potential benefit outweighs the risk. Patisiran is not approved for use in pediatric patients, and its safety and efficacy have not been established in individuals under 18 years of age, with no available data from clinical studies. Based on its mechanism of action and findings from animal reproduction studies, patisiran may cause embryo-fetal harm when administered to pregnant individuals. In animal studies, intravenous patisiran during organogenesis resulted in post-implantation loss, decreased fetal body weights, and skeletal variations in rats at doses ≥3 times the recommended human dose. There are no adequate data in pregnant women. Patisiran should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Females of reproductive potential should use effective contraception during treatment and for at least 3 months after the last dose. Males of reproductive potential should use effective contraception, including a condom, during treatment and for at least 3 months after the last dose if their partner is of childbearing potential or pregnant. A pregnancy exposure registry is available to monitor pregnancy outcomes in women exposed to patisiran during pregnancy; healthcare providers are encouraged to report by calling 1-877-256-9526 or visiting https://mothertobaby.org/ongoing-study/patisiran/.[](https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/210922s012lbl.pdf)[](https://www.ema.europa.eu/en/documents/product-information/onpattro-epar-product-information_en.pdf)[](https://pdf.hres.ca/dpd_pm/00052462.PDF) It is unknown if patisiran is excreted in human . Lipid nanoparticle components were detected in from lactating rats. Because of the potential for serious adverse reactions in a breastfed , is not recommended during treatment with patisiran and for 12 weeks after the last dose, or patisiran should be discontinued based on consideration of benefits of to the and benefits of treatment to the mother. No clinically significant drug interactions are expected with patisiran, as it is not an inhibitor or inducer of cytochrome P450 (CYP) enzymes or transporters at therapeutic doses. However, patisiran has been shown to be a time-dependent inhibitor of CYP2B6 in vitro; the net effect in vivo is unknown, and caution is advised when co-administered with CYP2B6 substrates (e.g., bupropion, efavirenz). Patisiran's efficacy has been demonstrated across various transthyretin (TTR) mutations, including the common Val30Met variant, with consistent reductions in serum TTR levels regardless of mutation type. As patisiran silences both mutant and wild-type TTR mRNA, patients require monitoring for potential effects of wild-type TTR reduction, such as , with supplementation recommended at the daily allowance.

History

Development

Patisiran was developed by , a company founded in 2002 to pioneer (RNAi) therapeutics, with initial efforts targeting (TTR) for hereditary ATTR beginning around 2003 following consultations with clinical experts such as Philip Hawkins. The program focused on (siRNA) molecules to silence the TTR gene and reduce mutant TTR protein production in the liver. Within a year of initiation, Alnylam achieved scalable manufacturing of the siRNA candidate, marking a key advancement in translating RNAi technology from concept to therapeutic development. Pre-clinical studies demonstrated the efficacy of patisiran (initially designated ALN-TTR02) in animal models. In transgenic mice expressing the human V30M TTR variant (hTTR V30M HSF1±), a single dose resulted in greater than 85% knockdown of hepatic TTR mRNA and serum TTR protein levels. Repeat dosing in these mice reduced TTR deposits by 70–80% in tissues including the , , colon, , and , with deposit regression correlating directly with the extent of serum TTR reduction. Studies in cynomolgus monkeys achieved up to 96% maximal serum TTR knockdown with repeat dosing every four weeks, confirming robust hepatic silencing without significant off-target effects. A major challenge in early development was efficient delivery of the siRNA to hepatocytes, as naked RNAi molecules degrade rapidly and exhibit poor cellular uptake; this was addressed by encapsulating patisiran in nanoparticles (LNPs) optimized for liver-specific targeting, which improved stability, biodistribution, and knockdown efficiency following initial setbacks with a prior conjugate-based candidate (ALN-TTR01). Key milestones included the initiation of the Phase 1 clinical trial for patisiran in healthy volunteers in , validating the transition from pre-clinical success to human testing. In 2014, Alnylam expanded its collaboration with (via ), securing up to $700 million in funding and co-development rights to accelerate patisiran's commercialization for rare diseases. In April 2019, Alnylam and concluded the research and option phase of their alliance, with Alnylam regaining full global development and commercialization rights to patisiran.

Clinical trials

The initial clinical evaluation of patisiran in patients with hereditary -mediated (hATTR) amyloidosis occurred in a phase 2 open-label dose-escalation study involving 29 patients with , confirming its safety profile and demonstrating robust serum (TTR) reduction with a mean of 80% at the 0.3 mg/kg dose administered intravenously every three or four weeks. No serious adverse events related to the drug were reported, with mild infusion-related reactions being the most common side effect. The pivotal phase 3 APOLLO trial, conducted from 2013 to 2017, enrolled 225 adults with hATTR and , randomizing them 2:1 to patisiran (0.3 mg/kg every three weeks) or for 18 months. The trial met its primary endpoint, showing a least-squares mean change from baseline in the modified Neurologic Impairment Score plus 7 (mNIS+7) of -6.0 points with patisiran versus +28.0 points with (difference, -34.0; 95% CI, -42.9 to -25.2; P<0.001), indicating halted or reversed neuropathy progression. Secondary endpoints were also achieved, including improvement in as measured by the Norfolk Quality of Life-Diabetic Neuropathy (QOL-DN) score (-6.7 vs. +14.4; difference, -21.1; P<0.001) and speed (+0.08 m/s vs. -0.24 m/s; difference, +0.31 m/s; P<0.001). revealed adverse events in 97% of participants, primarily mild-to-moderate infusion-related reactions (19% in the patisiran group), with no significant differences in serious events compared to . Long-term efficacy was assessed in the global open-label extension (OLE) study, enrolling 211 patients from APOLLO and earlier phase 2 trials, with data extending up to five years of continuous patisiran treatment. Neuropathy stabilization was sustained, with 65% of patients showing stable or improved disability scores at five years and a mean mNIS+7 change of +10.9 from baseline, reflecting modest progression compared to natural disease history. Quality of life improvements persisted, as evidenced by a mean Norfolk QOL-DN change of +4.1 and Rasch-built Overall Disability Scale change of -3.7, alongside nutritional gains (mean modified increase of +46.4). The safety profile remained consistent, with infusion-related reactions in 16.1% and 19.4% overall mortality, lower in early-treated groups; 22.3% discontinued due to adverse events. In addition to polyneuropathy-focused trials, the phase 3 APOLLO-B study evaluated patisiran in 360 patients with cardiac amyloidosis (ATTR-CM), including both hereditary and wild-type forms, over 12 months. It met its primary endpoint of change in six-minute walk test distance, with a median difference of +14.7 meters favoring patisiran over (95% CI, 0.7 to 28.7; P=0.02), alongside benefits in measures. No dedicated pediatric trials have been conducted for patisiran.

Regulatory approvals

Patisiran, marketed as Onpattro, received approval from the U.S. (FDA) on August 10, 2018, for the treatment of the of hereditary transthyretin-mediated (hATTR) in adults, becoming the first (siRNA) therapeutic approved by the agency. Prior to approval, it was granted designation by the FDA on June 14, 2012, for the treatment of transthyretin-mediated , as well as designation in 2017 to expedite development for this . The approval was supported by data from the pivotal APOLLO phase 3 trial demonstrating efficacy in reducing neuropathy impairment. In Europe, the (EMA) granted marketing authorization for patisiran on August 27, 2018, valid throughout the for the treatment of hATTR with stage 1 or 2 in adult patients. The EMA had previously designated patisiran as an orphan medicine on April 15, 2011, recognizing its potential for treating the rare condition of transthyretin . Patisiran has also been approved in several other regions, including by the Ministry of Health, Labour and Welfare in June 2019 for hATTR amyloidosis with , Canada by in July 2019 for the same indication, and by the in November 2022 for hereditary transthyretin-mediated amyloidosis. As of 2025, patisiran is approved in over 30 countries worldwide for the treatment of hATTR amyloidosis with , though indications may vary by region. No label expansions have been approved for patisiran as of 2025, including for associated with ATTR ; the FDA issued a complete response letter denying a supplemental for this indication in 2023, citing insufficient evidence from the APOLLO-B trial despite meeting its primary endpoint. Ongoing regulatory reviews for broader indications, such as , remain unresolved, with no further approvals granted.

Chemistry and formulation

Chemical structure

Patisiran is a synthetic double-stranded (siRNA) composed of a and an antisense strand, each containing 21 and forming a 19-base-pair duplex with 2-nucleotide 3' deoxythymidine (dT-dT) overhangs on both strands. The sequence is 5'-GUUACCAAGAGUAUUCCAUDT-3', and the antisense strand sequence is 5'-AUGGAAUACUCUUGGUUACDT-3'. To enhance stability against degradation and improve pharmacokinetic properties, the siRNA incorporates site-specific chemical modifications, including 2'-O-methyl substitutions on sugars at various positions (denoted by lowercase letters in sequence notation: sense strand GuAAccAAGAGuAuuccAudTdT; antisense strand AUGGAAuACUCUUGGUuACdTdT) and phosphorothioate linkages at the 5' end of the and both the 5' and 3' ends of the antisense strand. The molecular weight of the patisiran siRNA duplex is approximately 13,424 Da in its free acid form and 14,304 Da as the sodium salt, accounting for 40 sodium ions across the two strands.

Formulation details

Patisiran is formulated as a (LNP) encapsulation system designed for intravenous administration, enabling targeted delivery of the (siRNA) to hepatocytes. The LNP consists of the ionizable lipid DLin-MC3-DMA, the helper lipid (DSPC), , and the polyethylene glycol (PEG)-lipid PEG2000-C-DMG, which collectively form a stable complex around the patisiran sodium salt equivalent to 10 mg patisiran per vial. This composition is suspended in a solution with a of approximately 7.0, containing no preservatives. The commercial product is supplied as a 10 mg/5 mL (2 mg/mL) sterile solution in single-dose vials for dilution prior to . For preparation, the concentrate is filtered through a 0.45 μm polyethersulfone (PES) syringe filter and diluted in 200 mL of 0.9% injection using a DEHP-free bag, followed by gentle inversion to mix; the diluted solution remains stable for up to 16 hours at (up to 30°C). Unopened vials should be refrigerated at 2°C to 8°C and protected from light, with a of 24 months from the date of manufacture, though they may be stored at (up to 25°C) for up to 14 days without impacting stability. Manufacturing of patisiran involves compounding the siRNA into LNPs at in , followed by sterile filling into Type I glass vials at Ajinomoto Althea, Inc. in , , using and final sterile filtration through a 0.2 μm PES filter to ensure sterility. The LNP formulation provides key advantages for therapeutic efficacy, including hepatic targeting through apolipoprotein E-mediated uptake by hepatocytes and facilitated endosomal escape via the pH-sensitive ionization of DLin-MC3-DMA in the acidic endosomal environment, which promotes osmotic swelling and rupture to release the siRNA into the .

Society and culture

Economics

Patisiran, marketed as Onpattro, was launched in the United States in 2018 with an annual of approximately $450,000 per . As of 2025, the annual cost remains around $450,000 in the , varying slightly based on weight and dosing requirements. This high pricing reflects its status as an for the rare hereditary transthyretin-mediated . In the , patisiran infusions are typically covered under Medicare Part B, as self-administration is not feasible, facilitating access for eligible . Alnylam Pharmaceuticals offers the Alnylam Assist Assistance Program, which provides the drug at no cost to uninsured or underinsured meeting financial eligibility criteria. An analysis by the Institute for Clinical and Economic Review (ICER) estimated patisiran's cost-effectiveness at a net price of $345,000 annually (after discounts) as yielding an of approximately $500,000 per gained compared to best supportive care, a figure influenced by the rarity of the disease and limited patient population. This has prompted discussions on models, with Alnylam committing to outcomes-based rebates tied to clinical benefits. In the , annual pricing for patisiran is lower, estimated at around €370,000 per patient, as reported in pharmacoeconomic studies. No generic versions are available, as key patents protecting patisiran are set to expire no earlier than 2032. Patisiran is marketed globally under the brand name Onpattro, with no generic versions available as of 2025. It holds prescription-only status in major markets, including the (Rx-only), (Rx-only), (Rx-only), and (Schedule 4). As a biologic therapeutic, it is not subject to scheduling. Onpattro is widely available in developed regions following regulatory approvals, including the since 2018, the since 2018, since 2019, and since 2019, with approvals in over 30 countries overall. In low- and middle-income countries, access remains limited, primarily through programs for eligible patients with hereditary transthyretin-mediated . The drug benefits from exclusivity in , granting seven years of market protection from its 2018 approval, which expired on August 10, 2025. Broader protections, including term extensions, extend exclusivity until at least 2032, delaying potential generic entry. No major controversies surround Onpattro's , though access barriers persist in developing regions due to regulatory and distribution challenges.

References

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  21. https://www.renalandurologynews.com/news/patisiran-preserves-kidney-function-in-hereditary-amyloidosis-patients/
  22. https://www.nature.com/articles/d41586-019-03070-w
  23. https://pmc.ncbi.nlm.nih.gov/articles/PMC4898164/
  24. https://www.bloomberg.com/news/articles/2014-01-13/sanofi-pays-700-million-for-alnylam-drugs-and-12-percent-stake
  25. https://investors.alnylam.com/press-release?id=23656
  26. https://accp1.onlinelibrary.wiley.com/doi/10.1002/jcph.1553
  27. https://jamanetwork.com/journals/jamaneurology/fullarticle/2828606
  28. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2018/210922Orig1s000Approv.pdf
  29. https://www.accessdata.fda.gov/scripts/opdlisting/oopd/detailedIndex.cfm?cfgridkey=371112
  30. https://www.ema.europa.eu/en/medicines/human/orphan-designations/eu-3-11-857
  31. https://investors.alnylam.com/press-release?id=23886
  32. https://www.clinicaltrialsarena.com/marketdata/onpattro-for-hereditary-transthyretin-mediated-amyloidosis/
  33. https://www.tga.gov.au/resources/artg/380813
  34. https://www.rarediseaseadvisor.com/therapies/onpattro-patisiran-2/
  35. https://pmc.ncbi.nlm.nih.gov/articles/PMC12379670/
  36. https://patents.google.com/patent/EP3185957B1/en
  37. https://www.mdpi.com/1422-0067/23/16/8875
  38. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2018/210922Orig1s000ChemR.pdf
  39. https://pmc.ncbi.nlm.nih.gov/articles/PMC7606409/
  40. https://www.drugs.com/availability/generic-onpattro.html
  41. https://dhpp.hpfb-dgpsa.ca/review-documents/resource/RDS00567
  42. https://clinicaltrials.gov/study/NCT02939820
  43. https://www.drugpatentwatch.com/p/tradename/ONPATTRO
  44. https://www.alnylam.com/medical-professional-resources/early-access-program
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