Hubbry Logo
DeflazacortDeflazacortMain
Open search
Deflazacort
Community hub
Deflazacort
logo
8 pages, 0 posts
0 subscribers
Be the first to start a discussion here.
Be the first to start a discussion here.
Deflazacort
Deflazacort
Deflazacort
View on Wikipedia
from Wikipedia

Deflazacort
Clinical data
Trade namesEmflaza, Calcort, others
AHFS/Drugs.comMonograph
Routes of
administration		By mouth
ATC code
Legal status
Legal status
Pharmacokinetic data
Protein binding40%
MetabolismBy plasma esterases, to active metabolite
Elimination half-life1.1–1.9 hours (metabolite)
ExcretionKidney (70%) and fecal (30%)
Identifiers
  • (11β,16β)-21-(Acetyloxy)-11-hydroxy-2′-methyl-5′H-pregna-1,4-dieno[17,16-d]oxazole-3,20-dione
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.034.969 Edit this at Wikidata
Chemical and physical data
FormulaC25H31NO6
Molar mass441.524 g·mol−1
3D model (JSmol)
  • O=C(OCC(=O)[C@]25/N=C(\O[C@@H]5C[C@H]1[C@H]4[C@H]([C@@H](O)C[C@@]12C)[C@]/3(/C=C\C(=O)\C=C\3CC4)C)C)C
  • InChI=1S/C25H31NO6/c1-13-26-25(20(30)12-31-14(2)27)21(32-13)10-18-17-6-5-15-9-16(28)7-8-23(15,3)22(17)19(29)11-24(18,25)4/h7-9,17-19,21-22,29H,5-6,10-12H2,1-4H3/t17-,18-,19-,21+,22+,23-,24-,25+/m0/s1 ☒N
  • Key:FBHSPRKOSMHSIF-GRMWVWQJSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Deflazacort, sold under the brand name Calcort among others, is a glucocorticoid belonging to acetonides or O-isopropylidene derivative.[2] It is used as an anti-inflammatory and was patented in 1969[2] and approved for medical use in 1985.[3] The US Food and Drug Administration considers it to be a first-in-class medication for Duchenne Muscular Dystrophy.[4]

Medical uses

[edit]

The manufacturer lists the following uses for deflazacort:[5]

In the United States, deflazacort is approved for the treatment of duchenne muscular dystrophy in people over the age of two.[6]

Adverse effects

[edit]

Deflazacort carries the risks common to all corticosteroids, including immune suppression, decreased bone density, steroid induced muscle atrophy, myopathy and endocrine insufficiency. In clinical trials, the most common side effects (>10% above placebo) were Cushing's-like appearance, weight gain, and increased appetite.[1]

Pharmacology

[edit]
Main article: Glucocorticoid § Pharmacology

Mechanism of action

[edit]
Further information: Glucocorticoid § Mechanism of action

Deflazacort is an inactive prodrug which is metabolized rapidly to the active drug 21-desacetyldeflazacort.[7]

Relative potency

[edit]

Deflazacort's potency is around 70–90% that of prednisone.[8] A 2017 review found its activity of 7.5 mg of deflazacort is approximately equivalent to 25 mg cortisone, 20 mg hydrocortisone, 5 mg of prednisolone or prednisone, 4 mg of methylprednisolone or triamcinolone, or 0.75 mg of betamethasone or dexamethasone. The review noted that the drug has a high therapeutic index, being used at initial oral doses ranging from 6 to 90 mg, and probably requires a 50% higher dose to induce the same demineralizing effect as prednisolone. Thus it has "a smaller impact on calcium metabolism than any other synthetic corticosteroid, and therefore shows a lower risk of growth rate retardation in children and of osteoporosis" in the elderly, and comparatively small effects on carbohydrate metabolism, sodium retention, and hypokalemia.[9]

History

[edit]

Deflazacort was first introduced in 1969 to treat rheumatoid arthritis, nephritic syndrome, SLE, transplantation, polymyalgia rheumatica, sarcoidosis and juvenile chronic arthritis.[2]

In January 2015, the US Food and Drug Administration (FDA) granted fast track status to Marathon Pharmaceuticals to pursue approval of deflazacort as a potential treatment for Duchenne muscular dystrophy, a rare, "progressive and fatal disease" that affects boys.[10] Although deflazacort was approved by the FDA for use in treatment of Duchenne muscular dystrophy on February 9, 2017,[6][11] Marathon CEO announced on February 13, 2017, that the launch of deflazacort (Emflaza) would be delayed amidst controversy over the steep price Marathon was asking for the drug in the United States - $89,000 per year, which is "roughly 70 times" more than it would cost overseas.[12]

Society and culture

[edit]
[edit]

The US Food and Drug Administration approved deflazacort to treat people aged five years of age and older with Duchenne muscular dystrophy, a rare genetic disorder that causes progressive muscle deterioration and weakness. Emflaza is a corticosteroid that works by decreasing inflammation and reducing the activity of the immune system.[6] NDA 208684 was approved in February 2017, as a Type 1- new molecular entity with orphan status.[13]

Economics

[edit]

Deflazacort is available as an inexpensive generic. For example, in Canada, deflazacort can be purchased for around $1 per tablet.[14]

Brand names

[edit]

Deflazacort is sold in the United States under the brand name Emflaza after PTC Therapeutics, Inc. acquired all rights to Emflaza in March 2017.[15] Deflazacort is sold in the United Kingdom under the trade name Calcort;[8] in Brazil as Cortax, Decortil, Defcort and Deflanil; in India as Moaid, Zenflav, Defolet, DFZ, Decotaz, and DefZot; in Bangladesh as Xalcort; in Panama as Zamen; Spain as Zamene; and in Honduras as Flezacor.

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Deflazacort

View on Grokipedia
from Grokipedia
Deflazacort is a synthetic approved for treating (DMD) in patients aged 2 years and older. Administered orally, it undergoes rapid metabolism to its active form, 21-desacetyldeflazacort, which mediates anti-inflammatory and immunosuppressive effects through binding, thereby slowing muscle degeneration and preserving strength in DMD. Unlike some other corticosteroids such as , deflazacort demonstrates a more favorable , with clinical evidence indicating comparable efficacy in maintaining motor function but reduced risks of certain side effects, including excessive and cushingoid features. First approved by the U.S. in 2017 as Emflaza, it received designation due to DMD's rarity, enabling expedited review based on pivotal trials showing delayed functional decline over and active comparators. Internationally available prior to U.S. approval for various inflammatory conditions, its primary evidence-based application remains in DMD management, where long-term use balances benefits against corticosteroid-related risks like and growth suppression.

Medical Uses

Duchenne Muscular Dystrophy

Deflazacort received FDA approval on February 9, 2017, for the treatment of Duchenne muscular dystrophy (DMD) in patients aged 5 years and older, with the indication expanded on June 7, 2019, to include patients aged 2 years and older. This approval marked deflazacort as the first corticosteroid specifically indicated for DMD in the United States, targeting the progressive muscle degeneration caused by dystrophin deficiency through its glucocorticoid-mediated anti-inflammatory actions that mitigate skeletal muscle breakdown. The recommended dosing regimen for DMD is approximately 0.9 mg/kg/day administered orally once daily, available in tablet or oral suspension formulations, with doses rounded to the nearest practicable amount when using tablets. This regimen stems from demonstrating in slowing progression, as evidenced by the phase 3 ACT-DMD trial, which showed preservation of motor function and delayed deterioration in ambulatory patients. Empirical evidence from controlled trials indicates that deflazacort treatment preserves pulmonary function, as measured by , and delays loss of ambulation compared to untreated progression, with ambulation extended by approximately 1.4 to 2.5 years in treated cohorts. It also reduces the risk of development by stabilizing spinal alignment through maintained muscle support, thereby lowering the incidence of severe deformities requiring surgical intervention. Real-world observational data from long-term cohorts support these benefits, showing that sustained deflazacort use correlates with prolonged —up to 15 years in some glucocorticoid-treated groups versus shorter timelines without—and enhanced metrics, including sustained independent mobility and respiratory stability, attributable to reduced inflammatory damage to muscle fibers over time. These outcomes reflect causal mechanisms where deflazacort's activity interrupts the cycle of muscle and central to DMD .

Other Inflammatory and Autoimmune Conditions

Deflazacort, approved for medical use in in 1985, has been employed internationally for treating inflammatory conditions such as allergic and , as well as allergies, skin and eye disorders, and adjunctive therapy in certain cancers, primarily due to its potent immunosuppressive and anti-inflammatory effects comparable to those of other glucocorticoids like prednisolone. In these applications, it is administered orally to mitigate symptoms associated with immune-mediated inflammation, with dosing typically 6-12 mg daily for adults and 0.5-1 mg/kg/day for children, adjusted based on disease severity and patient response. Clinical studies have indicated efficacy in , where deflazacort has shown benefits in both adults and children for reducing and , often with a profile suggesting fewer metabolic disturbances than in comparative assessments. Similarly, its use extends to other autoimmune conditions like systemic through immunosuppressive mechanisms that dampen aberrant immune responses, though such applications remain off-label in regions without specific regulatory endorsement. In markets favoring chronic therapy, deflazacort is selected for its relatively advantageous metabolic effects, including lesser impacts on calcium —potentially lowering risk—and glucose compared to alternatives like betamethasone or , which supports prolonged use in autoimmune management without excessive disruption to bone and endocrine function. This profile arises from its pharmacodynamic properties as an of prednisolone, yielding a that balances efficacy with reduced adverse metabolic shifts during extended treatment.

Pharmacology

Pharmacodynamics

Deflazacort functions as an inactive ester prodrug that undergoes rapid hydrolysis by plasma esterases to its primary active metabolite, 21-desacetyl deflazacort (21-desDFZ). This metabolite exerts glucocorticoid activity by binding to cytoplasmic glucocorticoid receptors (GR), with an affinity lower than that of prednisolone but sufficient to form a steroid-receptor complex. Upon binding, the complex translocates to the nucleus, where it dimerizes and interacts with glucocorticoid response elements (GREs) on DNA to regulate transcription of target genes. The pharmacodynamic effects primarily involve transrepression of pro-inflammatory pathways and transactivation of anti-inflammatory genes. Specifically, the GR-21-desDFZ complex inhibits the nuclear factor kappa B () pathway by tethering and preventing its binding to promoter regions, thereby suppressing transcription of genes encoding pro-inflammatory cytokines such as interleukin-1, interleukin-6, and tumor necrosis factor-alpha. It also induces the expression of annexin-1 (lipocortin-1), which inhibits activity, reducing the release of and subsequent production of prostaglandins and leukotrienes. These actions collectively mediate the immunosuppressive and anti-inflammatory properties characteristic of glucocorticoids. In skeletal muscle contexts, such as Duchenne muscular dystrophy, the mechanism contributes to reduced inflammation and proteolysis by downregulating matrix metalloproteinases and other catabolic signals, without direct anabolic effects on muscle protein synthesis. Compared to prednisolone, 21-desDFZ demonstrates equivalent anti-inflammatory potency in vivo despite lower receptor binding affinity in vitro, attributed to differences in metabolic handling and tissue-specific effects.

Pharmacokinetics

Deflazacort, administered orally, is a rapidly hydrolyzed by ubiquitous plasma esterases to its pharmacologically , 21-desacetyldeflazacort (21-desDFZ). This conversion occurs immediately upon absorption, with the parent compound exhibiting negligible activity. Absorption of deflazacort is rapid following oral dosing, achieving peak plasma concentrations of 21-desDFZ within 1 to 2 hours post-administration. The absolute has not been precisely quantified, but studies with radiolabeled deflazacort indicate at least 70% absorption in healthy adults. does not significantly alter the extent of absorption but may delay peak concentrations slightly. The active metabolite 21-desDFZ exhibits moderate protein binding, approximately 40% to plasma proteins. It is primarily metabolized via 3A4 () to one major inactive (17-keto-deflazacort) and two minor metabolites. Elimination of 21-desDFZ is biphasic, with a mean terminal of 1.1 to 2.1 hours, facilitating clearance primarily through renal (about 70% of the dose) and to a lesser extent feces (30%). Approximately 18% of the eliminated dose appears as unchanged 21-desDFZ in . Complete elimination of metabolites occurs within 24 hours, and the short precludes significant accumulation during chronic once-daily dosing.

Chemical Structure and Relative Potency

Deflazacort is a synthetic characterized by the insertion of a methyl-oxazoline ring into the of prednisolone at the 17,16-d position, resulting in the molecular formula C25H31NO6 and a molecular weight of 441.52 g/mol. This structural modification distinguishes it from traditional corticosteroids like and prednisolone, altering its pharmacokinetic and pharmacodynamic profile while maintaining potent anti-inflammatory activity. The relative potency of deflazacort is approximately 0.7 to 0.8 times that of on a weight basis, as established through bioassays measuring effects, such as inhibition in animal models. For instance, equivalence dosing indicates that 0.9 mg/kg/day of deflazacort corresponds to 0.75 mg/kg/day of , reflecting the need for slightly higher doses of deflazacort to achieve comparable therapeutic effects. assessments confirm its immunosuppressive potency aligns closely with prednisolone in suppressing proliferation, though with a potency ratio of about 1:1.3 relative to in biological response assays. Structural differences, including the oxazoline moiety, confer negligible activity to deflazacort, in contrast to prednisone's moderate effects, which may contribute to reduced sodium retention and associated risks like . This dissociation supports its use at equivalent doses with potentially altered side effect profiles, driven by lower affinity for pathways rather than differences in lipophilicity.

Clinical Evidence

Key Clinical Trials

A phase 3, randomized, double-blind, placebo-controlled trial conducted between 1991 and 1995 evaluated deflazacort's efficacy in 196 ambulatory boys aged 5-15 years with (DMD). Patients received deflazacort at 0.9 mg/kg/day, at 0.75 mg/kg/day, or placebo for 12 weeks, with the primary outcome being change in a weighted muscle strength score. Deflazacort treatment resulted in a 23.3% improvement in muscle strength compared to a 6.3% decline in the group, establishing superiority over placebo in preserving muscle function. Analysis of data from the ACT-DMD trial, a 48-week multicenter study originally designed to assess in DMD but including open-label extensions with deflazacort or , demonstrated sustained benefits of deflazacort. In patients receiving deflazacort, the rate of decline in motor function was significantly slower than with over 48 weeks, as measured by ambulatory decline and forced . Long-term observational studies in DMD cohorts have shown deflazacort delays loss of ambulation compared to untreated patients. In a prospective study of 54 boys treated with deflazacort for up to 5 years, the age at loss of ambulation was 11.8 years, versus 10.5 years in historical untreated controls, representing a delay of approximately 1.3 years. Additional real-world data from larger cohorts indicate delays ranging from 1.6 to 2.5 years relative to untreated or standard care groups. In , where deflazacort received marketing authorization in , phase 3 trials from the and supported its efficacy in various inflammatory and autoimmune conditions, including and exacerbations. Meta-analyses of these randomized controlled studies have confirmed consistent improvements in disease activity scores and symptom control across indications.

Comparative Efficacy with Prednisone

A head-to-head randomized, double-blind, placebo-controlled trial in boys with (DMD) demonstrated that deflazacort and produced equivalent improvements in muscle strength over 12 weeks, as measured by quantitative muscle testing, with both superior to . This short-term equivalence aligns with their similar potency, where approximately 0.85 mg of deflazacort equates to 1 mg of in effects. Over longer periods, meta-analyses of multicenter clinical trials have shown deflazacort associated with slower DMD progression compared to /prednisolone. In a 2018 of placebo-arm from trials including the ACT DMD study, deflazacort treatment resulted in significantly reduced rates of decline over 48 weeks on key motor function metrics, such as time to rise from and 10-meter walk/run velocity, versus /prednisolone. These findings indicate deflazacort's edge in preserving ambulatory function, with hazard ratios favoring delayed loss of milestones like and floor standing by 20-30% over in pooled 48-week . Post-hoc comparisons from the ACT DMD trial further support deflazacort's benefits in maintaining motor milestones, including reduced risk of losing the ability to stand unaided, relative to /prednisolone over 48 weeks, without differences in short-term strength gains. Real-world retrospective analyses of patient registries have corroborated slower functional decline with deflazacort, particularly in delaying dependence, though head-to-head long-term randomized data remain limited. Overall, while short-term is comparable, evidence points to deflazacort's superior impact on long-term disease trajectory in DMD.

Safety and Adverse Effects

Common Adverse Effects

In clinical trials for (DMD), deflazacort at 0.9 mg/kg/day was associated with adverse reactions occurring in ≥10% of patients over 12 weeks, including Cushingoid appearance (33%), increased weight (20%), increased appetite (14%), (12%), (12%), and pollakiuria (12%). Over 52 weeks of exposure, the incidence of weight increase rose to 28% and Cushingoid appearance to 60%, reflecting cumulative effects of chronic therapy. Other common effects (≥5% and >placebo) included nasopharyngitis (10%), hirsutism (10%), and central obesity (10%), with immunosuppression contributing to infection rates comparable to those seen with other corticosteroids like prednisone. Hyperglycemia, leading to elevated blood sugar levels, is also associated with deflazacort use, consistent with glucocorticoid class effects. Irritability (8%), indicative of mood changes, and sleep disturbances, such as insomnia, were also reported in trial extensions and post-approval data, linked to sustained dosing regimens.

Serious Risks and Long-Term Concerns

Prolonged use of deflazacort, a glucocorticoid, is associated with osteoporosis due to its interference with bone metabolism, leading to reduced bone mineral density and heightened fracture risk, as evidenced by longitudinal data in Duchenne muscular dystrophy (DMD) patients showing fracture rates of 1367 per 10,000 person-years in daily deflazacort cohorts. This class effect stems from glucocorticoids' promotion of osteoclast activity and inhibition of osteoblast function, necessitating monitoring of bone density via dual-energy X-ray absorptiometry in long-term users. Cataract formation represents another serious long-term concern, with retrospective analyses of 596 DMD patients indicating an elevated incidence linked to deflazacort compared to alternatives like , attributed to glucocorticoid-induced lens opacification through and . In pediatric populations, deflazacort contributes to linear growth suppression by disrupting growth hormone-insulin-like growth factor-1 axis signaling, resulting in height deficits that persist despite dose adjustments. Adrenal insufficiency arises from hypothalamic-pituitary-adrenal axis suppression after extended exposure exceeding two weeks at high doses, mandating gradual tapering protocols to mitigate acute withdrawal risks such as hypotension and crisis during stress. Cardiovascular morbidity, including hypertension, is exacerbated by deflazacort's mineralocorticoid activity promoting sodium retention and vascular stiffness, with DMD-specific cohorts demonstrating sustained blood pressure elevations correlating with prolonged therapy duration.

Comparisons of Side Effect Profiles

Clinical trials and observational studies in (DMD) patients demonstrate that deflazacort produces less weight gain than , with mean differences ranging from 2.91 to 4.1 kg over 12 months in comparative analyses. Similarly, cushingoid features occur at lower rates with deflazacort, as shown in a phase 3 randomized trial where incidence was significantly higher (p=0.0385), and in pooled person-year data indicating 6% versus 9% for . These differences align with deflazacort's lower and reduced sodium retention compared to . However, deflazacort is linked to greater risks of loss and , with fracture incidence rates of 1367 per 10,000 person-years versus 748 for in a large DMD . development also favors prednisone, with deflazacort showing a 2.4-fold higher (95% CI 1.3–4.5; p=0.004) in retrospective analyses. These skeletal and ocular risks may stem from deflazacort's distinct interactions, though direct causal mechanisms remain under investigation beyond empirical associations. Infection risks appear equivalent between the two, with no significant differences reported in DMD trial safety data. Deflazacort may offer advantages in glycemic control, exhibiting less diabetogenic potential than in insulin-dependent diabetics and healthy subjects, as evidenced by reduced glucose metabolism disruptions in controlled comparisons. Overall, no demonstrates uniform superiority in side effect profiles; deflazacort's metabolic benefits are counterbalanced by elevated skeletal and concerns, necessitating individualized in long-term use.

Contraindications and Drug Interactions

Absolute Contraindications

Deflazacort is contraindicated in patients with known to the or any of the formulation's inactive components. reactions, including , have been documented in individuals receiving systemic therapy, underscoring the need to avoid administration in such cases to prevent severe allergic responses. This restriction is specified in the product's U.S. prescribing information, reflecting direct evidence of elevated risk from clinical observations and post-marketing reports.

Precautions and Monitoring

Patients receiving long-term deflazacort therapy, particularly for (DMD), require regular monitoring for glucocorticoid-induced complications. Bone mineral density should be assessed periodically via (DXA) scans to detect and fracture risk, as corticosteroids decrease bone formation and increase resorption. Ophthalmologic examinations, including measurement, are recommended if treatment exceeds six weeks to screen for and , with deflazacort associated with elevated cataract risk in DMD patients. In pediatric DMD patients, linear growth and weight should be tracked, as chronic use suppresses growth velocity. To mitigate adrenal suppression, deflazacort doses must be tapered gradually after more than a few days of use, with stress-dose adjustments during illness or to prevent . Live or live-attenuated vaccines should be avoided during immunosuppressive dosing, and pre-treatment immunity to varicella or confirmed where possible. Deflazacort should be used only under medical supervision. Deflazacort should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus, as corticosteroids cross the placenta and may cause adverse developmental outcomes. Caution is advised during breastfeeding, as deflazacort appears in human milk and could suppress growth or cause other effects in the infant; the benefits of breastfeeding should be weighed against the mother's clinical need. Deflazacort, a substrate, interacts with inhibitors such as or ; concomitant use necessitates reducing the dose to one-third of the recommended amount to avoid excessive exposure. Strong or moderate inducers should be avoided, as they diminish efficacy. Nonsteroidal anti-inflammatory drugs like ibuprofen are contraindicated due to heightened risk.

History

Development and Early Research

Deflazacort, an derivative of prednisolone, was first synthesized in 1967 by Italian chemists Giorgio Nathansohn, Giorgio Winters, and Emilio Testa as part of a series of nitrogen-containing steroids aimed at enhancing potency while reducing side effects. This structural modification involved introducing a 16α,17α-d-oxazoline ring to the prednisolone backbone, which preclinical evaluations suggested dissociated efficacy from sodium-retaining properties more effectively than earlier corticosteroids. Early pharmacological research in the late and early focused on its mechanisms, revealing equipotent suppression of in models compared to dexamethasone or prednisolone, but with diminished effects on synthesis in cells and lower disturbances. Preclinical data published during this period highlighted deflazacort's reduced activity, as evidenced by minimal impacts on excretion and in animal assays, positioning it as a potential alternative for chronic . Initial human trials in commenced in the mid-1980s, primarily evaluating deflazacort for and , where it demonstrated comparable efficacy to in reducing symptoms over short-term (4-6 weeks) and extended (up to 52 weeks) durations, with early signals of favorable tolerability. These studies, conducted by Guidotti ahead of its 1985 European launch, underscored its role in managing inflammatory conditions while prioritizing metabolic safety.

Regulatory Approvals and Delays

Deflazacort received its initial regulatory approval in in the early 1980s, with the applicant reporting first approval in 1982, followed by marketing in and several other countries including , the , , and by the mid-1980s for inflammatory conditions. By the , it had gained broader availability across European nations through national approvals, though not via centralized authorization until later formulations in the . In the United States, deflazacort lacked prior approval, necessitating a supported by clinical trials despite decades of international use. The FDA granted designation for (DMD) on September 16, 2010, followed by fast track status in 2014, to facilitate development for this rare condition. Approval as Emflaza for DMD treatment in patients aged 5 years and older occurred on February 9, 2017, based on a phase 3 trial demonstrating delayed motor decline compared to , reflecting requirements for efficacy data in the orphan indication. This timeline spanned over three decades from initial European approvals, attributable to the need for U.S.-specific pivotal trials absent from earlier foreign dossiers. Post-2017 U.S. approval remained confined to DMD under exclusivity, with label expansion in June 2019 to include patients aged 2 to 5 years following additional pediatric data submission. Internationally, deflazacort was widely accessible as a generic for various indications outside the U.S. well before 2017, often at lower costs, enabling patient importation while U.S. regulatory hurdles persisted.

Society and Culture

Deflazacort is classified as a prescription-only medication worldwide and is not designated as a under any schedule of the U.S. or equivalent international frameworks. In the United States, the (FDA) approved deflazacort on February 9, 2017, exclusively for the treatment of (DMD) in patients aged five years and older, with an expansion in June 2019 to include children aged two to five years. Prior to this approval, deflazacort lacked U.S. regulatory authorization, resulting in import restrictions for unapproved drugs; however, some DMD patients obtained it through personal importation from overseas sources despite FDA oversight on such imports. Outside the , deflazacort has been approved for various indications since 1985 and is widely available in , , and other regions, often through generic formulations introduced after original expirations in the 1990s. In contrast to the U.S. market's branded exclusivity post-2017 approval, generics have long been accessible internationally, supporting broader utilization for approved uses. While not centrally authorized by the (EMA) for DMD, it remains prescribed nationally in European countries for other conditions under established regulatory pathways.

Economics and Pricing Controversies

Upon FDA approval of Emflaza (deflazacort) on February 9, 2017, for , Marathon Pharmaceuticals established an annual U.S. list price of $89,000, a markup exceeding 5,000% relative to generic deflazacort's international cost of $1,000–$1,600 per year, which U.S. patients had previously imported for . This pricing, enabled by seven-year exclusivity under the Orphan Drug Act despite the molecule's decades-long availability abroad with minimal U.S.-specific development by Marathon, ignited backlash from patient groups, clinicians, and policymakers who argued it prioritized profit extraction over accessibility for a affecting roughly 15,000 U.S. males. Critics, including Senators and , condemned the strategy in a March 2017 letter to Marathon, labeling it "unconscionable" and citing the firm's acquisition of licensing rights from an Italian developer rather than substantial original R&D investment, which raised questions about the orphan incentives' distortion toward windfall gains rather than innovation for unmet needs. Marathon paused the launch amid the outcry, resigned from the Pharmaceutical Research and Manufacturers of America (PhRMA) in April 2017, and sold Emflaza rights to three months later for $140 million upfront plus royalties exceeding 20%, yielding rapid returns that fueled debates on exclusivity-driven profiteering. Defenders of the model invoked the need to offset regulatory compliance costs, including bioequivalence studies and pediatric trials required for approval, asserting that without high pricing, firms would avoid rare disease markets lacking economies of scale. PTC subsequently tiered pricing by weight, e.g., $35,000 annually for a 25 kg patient, but retained elevated costs relative to generics abroad, perpetuating access barriers until orphan exclusivity lapsed around 2024, after which FDA approvals for generic deflazacort formulations—such as Zydus Lifesciences' oral suspension in October 2025—began enabling competition and prospective price reductions. The episode exemplified tensions in orphan drug economics, where incentives intended to spur development can incentivize strategic U.S. entry for established compounds, prompting calls for reforms to balance R&D recovery against patient affordability without empirical evidence linking such markups to broader therapeutic advances.

Brand Names and Formulations

Deflazacort is marketed under the brand name Emflaza in the United States, available as immediate-release oral tablets in strengths of 6 mg, 18 mg, 30 mg, and 36 mg, and as an oral suspension containing 22.75 mg/mL (equivalent to 18 mg/mL of deflazacort after accounting for inactive ingredients). The oral suspension formulation facilitates precise dosing for pediatric patients with (DMD), who require weight-based administration around 0.9 mg/kg/day. Tablets may be administered whole or crushed and mixed with for patients unable to swallow them intact. Internationally, deflazacort is commonly sold under brand names such as Calcort and Enflazacort, primarily as oral tablets in various strengths including 1 mg, 6 mg, and 30 mg, depending on the market and manufacturer. These tablet formulations are standard for and immunosuppressive uses, with dosing adjusted based on condition severity, typically ranging from 0.25 to 1.5 mg/kg/day. Oral suspensions are less commonly branded internationally but may be compounded or available generically for pediatric needs. Generic versions of deflazacort tablets and suspensions have been available in non-U.S. markets following patent expiration, enabling broader access in regions where the has been approved since the . In the U.S., generic oral suspension was approved in June 2024, mirroring the Emflaza suspension concentration of 22.75 mg/mL for DMD treatment in patients aged 5 years and older.

References

  1. https://go.drugbank.com/drugs/DB11921
  2. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/208684%2C208685Orig1s000SumR.pdf
  3. https://pmc.ncbi.nlm.nih.gov/articles/PMC5109941/
  4. https://bmcpharmacoltoxicol.biomedcentral.com/articles/10.1186/s40360-016-0111-8
  5. https://pmc.ncbi.nlm.nih.gov/articles/PMC2763756/
  6. https://www.accessdata.fda.gov/scripts/opdlisting/oopd/detailedIndex.cfm?cfgridkey=403413
  7. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/208684%2C208685Orig1s000ClinPharmR.pdf
  8. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/208684%2C208685Orig1s000PharmR.pdf
  9. https://link.springer.com/article/10.2165/00003495-199550020-00008
  10. https://www.drugs.com/history/emflaza.html
  11. https://ir.ptcbio.com/news-releases/news-release-details/ptc-therapeutics-receives-fda-approval-expansion-emflazar
  12. https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/208684s000%2C208685s000lbl.pdf
  13. https://reference.medscape.com/drug/emflaza-deflazacort-1000120
  14. https://pmc.ncbi.nlm.nih.gov/articles/PMC6767037/
  15. https://publications.aap.org/aapnews/news/10374/Guideline-reviews-corticosteroids-for-patients
  16. https://pubmed.ncbi.nlm.nih.gov/33204350/
  17. https://becarispublishing.com/doi/10.2217/cer-2019-0170
  18. https://pubmed.ncbi.nlm.nih.gov/31922454/
  19. https://hcp.emflaza.com/efficacy/long-term-outcomes
  20. https://www.jmcp.org/doi/10.18553/jmcp.2020.26.4.361
  21. https://newdrugapprovals.org/2017/02/17/deflazacort/
  22. https://www.apollohospitals.com/medicines/deflazacort
  23. https://pubmed.ncbi.nlm.nih.gov/8521761/
  24. https://link.springer.com/article/10.1007/BF02877711
  25. https://effectivehealthcare.ahrq.gov/get-involved/nominated-topics/safety-and-efficacy-of-deflazacort-in-comparison-with-that-of-prednisolone-in-systemic-autoimmune-rheumatic-diseases
  26. https://pmc.ncbi.nlm.nih.gov/articles/PMC5216559/
  27. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=77d7525d-89c9-4fde-a6a8-0a463fd6cfeb
  28. https://www.sciencedirect.com/science/article/abs/pii/0014299981901151
  29. https://academic.oup.com/hmg/article/33/3/211/7306829
  30. https://pubchem.ncbi.nlm.nih.gov/compound/Deflazacort
  31. https://link.springer.com/article/10.1007/BF02556669
  32. https://pmc.ncbi.nlm.nih.gov/articles/PMC9398085/
  33. https://bpspubs.onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-2125.1986.tb05165.x
  34. https://www.bionova.co.in/Articles/deflazacort-tablets/
  35. https://pmc.ncbi.nlm.nih.gov/articles/PMC6973289/
  36. https://pubmed.ncbi.nlm.nih.gov/8170484/
  37. https://ctap-duchenne.org/wp-content/uploads/2020/09/outcomes-prednisone-deflazacort-DMD-2020.pdf
  38. https://www.neurology.org/doi/10.1212/WNL.0000000000003217
  39. https://www.neurology.org/doi/10.1212/WNL.90.15_supplement.P2.325
  40. https://becarispublishing.com/doi/10.2217/cer-2021-0018
  41. https://hcp.emflaza.com/study-summaries
  42. https://www.emflaza.com/safety
  43. https://pmc.ncbi.nlm.nih.gov/articles/PMC6398538/
  44. https://www.oregon.gov/oha/HPA/DSI-HERC/MeetingDocuments/VbBS-Materials-Handout-8-10-2017.pdf
  45. https://journals.sagepub.com/doi/10.3233/JND-210776
  46. https://pubmed.ncbi.nlm.nih.gov/3827456/
  47. https://www.institut-myologie.org/en/2022/09/22/a-review-of-the-literature-compares-prednisone-and-deflazacort-in-dmd-and-favours-the-latter-in-the-short-term-while-in-the-long-term-their-effects-are-similar/
  48. https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/208684s005%2C208685s005lbl.pdf
  49. https://www.emflaza.com/prescribing-information.pdf
  50. https://www.duchenneuk.org/wp-content/uploads/2025/08/DMDCare-Corticosteroid-Guidance.pdf
  51. https://pubs.acs.org/doi/10.1021/jm00317a009
  52. https://journals.lww.com/ijd/fulltext/2008/53040/deflazacort_versus_other_glucocorticoids__a.2.aspx
  53. https://pubmed.ncbi.nlm.nih.gov/6430498/
  54. https://link.springer.com/article/10.1007/BF02405325
  55. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/208684%2C208685Orig1s000RiskR.pdf
  56. https://ec.europa.eu/health/documents/community-register/2018/20180719141517/anx_141517_en.pdf
  57. https://www.accessdata.fda.gov/scripts/opdlisting/oopd/detailedIndex.cfm?cfgridkey=315110
  58. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/208684%2C208685Orig1s000MedR.pdf
  59. https://pmc.ncbi.nlm.nih.gov/articles/PMC10391264/
  60. https://www.parentprojectmd.org/ptc-receives-fda-approval-for-expansion-of-emflaza-deflazacort-labeling-to-include-patients-2-5-years-of-age/
  61. https://pmc.ncbi.nlm.nih.gov/articles/PMC5865197/
  62. https://www.npr.org/sections/health-shots/2017/02/14/515046376/duchenne-drug-delayed-after-outrage-over-price
  63. https://www.drugs.com/mtm/deflazacort.html
  64. https://icer.org/wp-content/uploads/2020/10/ICER_DMD-Final-Report_081519-2-1.pdf
  65. https://www.cnbc.com/2017/02/13/marathon-charges-89000-a-year-for-new-new-muscular-dystrophy-drug.html
  66. https://gabionline.net/generics/news/FDA-approves-rare-disease-deflazacort-at-exorbitant-price
  67. https://www.fiercepharma.com/pharma/ptcs-emflaza-face-generics-month-after-aurobindos-final-fda-nod
  68. https://www.ema.europa.eu/en/documents/assessment-report/agamree-epar-public-assessment-report_en.pdf
  69. https://www.cnbc.com/2017/02/13/marathon-pharmaceuticals-criticized-for-outrageous-pricing-of-drug.html
  70. https://kffhealthnews.org/news/89000-orphan-drug-gets-a-new-owner-and-likely-a-new-price/
  71. https://www.help.senate.gov/imo/media/doc/2017.03.02%2520Letter%2520to%2520Marathon%2520re-DMD%2520drug.pdf
  72. https://kffhealthnews.org/news/marathon-pharmaceutical-drops-out-of-phrma-following-drug-price-controversy/
  73. https://www.fiercepharma.com/pharma/marathon-under-heavy-fire-for-emflaza-pricing-makes-surprise-deal-to-sell-drug-for-140m-plus
  74. https://www.biopharmadive.com/news/marathon-deflazacort-sanders-cummings-price-letter/436080/
  75. https://www.cnbc.com/2017/05/08/new-price-for-muscular-dystrophy-drug-draws-criticism.html
  76. https://www.linkedin.com/posts/harshal-jain_pharmanews-healthcareinnovation-usfdaapprovals-activity-7381252207997804544-uaHi
  77. https://www.emflaza.com/dosing
  78. https://hcp.emflaza.com/dosing-administration
  79. https://www.medicines.org.uk/emc/files/pil.13999.pdf
  80. https://www.rxlist.com/deflazacort/generic-drug.htm
  81. https://www.trispharma.com/cranbury-pharmaceuticals-receives-u-s-fda-approval-for-first-generic-version-of-emflaza-oral-suspension-deflazacort-for-duchenne-muscular-dystrophy/
Add your contribution
Related Hubs
User Avatar
No comments yet.