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Deflazacort

Deflazacort is a synthetic glucocorticoid prodrug approved for treating Duchenne muscular dystrophy (DMD) in patients aged 2 years and older.^[1] Administered orally, it undergoes rapid metabolism to its active form, 21-desacetyldeflazacort, which mediates anti-inflammatory and immunosuppressive effects through glucocorticoid receptor binding, thereby slowing muscle degeneration and preserving strength in DMD.^[2]^[3] Unlike some other corticosteroids such as prednisone, deflazacort demonstrates a more favorable therapeutic index, with clinical evidence indicating comparable efficacy in maintaining motor function but reduced risks of certain side effects, including excessive weight gain and cushingoid features.^[4]^[5] First approved by the U.S. Food and Drug Administration in 2017 as Emflaza, it received orphan drug designation due to DMD's rarity, enabling expedited review based on pivotal trials showing delayed functional decline over placebo and active comparators.^[6]^[7] 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 osteoporosis and growth suppression.^[8]^[9]

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.^[10]^[11] 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.^[12] 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.^[12]^[13] This regimen stems from clinical data demonstrating efficacy in slowing disease progression, as evidenced by the phase 3 ACT-DMD trial, which showed preservation of motor function and delayed deterioration in ambulatory patients.^[14] Empirical evidence from controlled trials indicates that deflazacort treatment preserves pulmonary function, as measured by forced vital capacity, and delays loss of ambulation compared to untreated progression, with ambulation extended by approximately 1.4 to 2.5 years in treated cohorts.^[15] It also reduces the risk of scoliosis development by stabilizing spinal alignment through maintained muscle support, thereby lowering the incidence of severe deformities requiring surgical intervention.^[16]^[17] Real-world observational data from long-term cohorts support these benefits, showing that sustained deflazacort use correlates with prolonged survival—up to 15 years in some glucocorticoid-treated groups versus shorter timelines without—and enhanced quality of life metrics, including sustained independent mobility and respiratory stability, attributable to reduced inflammatory damage to muscle fibers over time.^[18]^[19] These outcomes reflect causal mechanisms where deflazacort's glucocorticoid activity interrupts the cycle of muscle necrosis and fibrosis central to DMD pathology.^[20]

Other Inflammatory and Autoimmune Conditions

Deflazacort, approved for medical use in Europe in 1985, has been employed internationally for treating inflammatory conditions such as allergic asthma and rheumatoid arthritis, as well as allergic disorders, primarily due to its potent immunosuppressive and anti-inflammatory effects comparable to those of other glucocorticoids like prednisolone.^[21]^[5] In these applications, it is administered orally to mitigate symptoms associated with immune-mediated inflammation, with dosing typically adjusted based on disease severity and patient response.^[22] Clinical studies have indicated efficacy in nephrotic syndrome, where deflazacort has shown benefits in both adults and children for reducing proteinuria and inflammation, often with a profile suggesting fewer metabolic disturbances than prednisone in comparative assessments.^[23] Similarly, its use extends to other autoimmune conditions like systemic lupus erythematosus through immunosuppressive mechanisms that dampen aberrant immune responses, though such applications remain off-label in regions without specific regulatory endorsement.^[24]^[5] In markets favoring chronic glucocorticoid therapy, deflazacort is selected for its relatively advantageous metabolic effects, including lesser impacts on calcium homeostasis—potentially lowering osteoporosis risk—and glucose metabolism compared to alternatives like betamethasone or prednisone, which supports prolonged use in autoimmune management without excessive disruption to bone and endocrine function.^[25]^[5] This profile arises from its pharmacodynamic properties as an oxazoline derivative of prednisolone, yielding a therapeutic index that balances efficacy with reduced adverse metabolic shifts during extended treatment.^[4]^[23]

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).^[26] 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.^[22] ^[27] 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.^[1] 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 (NF-κB) pathway by tethering NF-κB 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.^[28] It also induces the expression of annexin-1 (lipocortin-1), which inhibits phospholipase A2 activity, reducing the release of arachidonic acid and subsequent production of prostaglandins and leukotrienes.^[22] These actions collectively mediate the immunosuppressive and anti-inflammatory properties characteristic of glucocorticoids.^[1] 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.^[28] 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.^[22]

Pharmacokinetics

Deflazacort, administered orally, is a prodrug rapidly hydrolyzed by ubiquitous plasma esterases to its pharmacologically active metabolite, 21-desacetyldeflazacort (21-desDFZ).^[12] This conversion occurs immediately upon absorption, with the parent compound exhibiting negligible activity.^[1] Absorption of deflazacort is rapid following oral dosing, achieving peak plasma concentrations of 21-desDFZ within 1 to 2 hours post-administration.^[1] The absolute bioavailability has not been precisely quantified, but studies with radiolabeled deflazacort indicate at least 70% absorption in healthy adults.^[1] Food does not significantly alter the extent of absorption but may delay peak concentrations slightly.^[7] The active metabolite 21-desDFZ exhibits moderate protein binding, approximately 40% to plasma proteins.^[12] It is primarily metabolized via cytochrome P450 3A4 (CYP3A4) to one major inactive metabolite (17-keto-deflazacort) and two minor metabolites.^[12] Elimination of 21-desDFZ is biphasic, with a mean terminal half-life of 1.1 to 2.1 hours, facilitating clearance primarily through renal excretion (about 70% of the dose) and to a lesser extent feces (30%).^[1] Approximately 18% of the eliminated dose appears as unchanged 21-desDFZ in urine.^[1] Complete elimination of metabolites occurs within 24 hours, and the short half-life precludes significant accumulation during chronic once-daily dosing.^[25]

Chemical Structure and Relative Potency

Deflazacort is a synthetic glucocorticoid characterized by the insertion of a methyl-oxazoline ring into the chemical structure of prednisolone at the 17,16-d position, resulting in the molecular formula C₂₅H₃₁NO₆ and a molecular weight of 441.52 g/mol.^[4]^[29] This structural modification distinguishes it from traditional corticosteroids like prednisone and prednisolone, altering its pharmacokinetic and pharmacodynamic profile while maintaining potent anti-inflammatory activity.^[25] The relative glucocorticoid potency of deflazacort is approximately 0.7 to 0.8 times that of prednisone on a weight basis, as established through bioassays measuring anti-inflammatory effects, such as granuloma inhibition in animal models.^[30] For instance, equivalence dosing indicates that 0.9 mg/kg/day of deflazacort corresponds to 0.75 mg/kg/day of prednisone, reflecting the need for slightly higher doses of deflazacort to achieve comparable therapeutic effects.^[31] In vitro assessments confirm its immunosuppressive potency aligns closely with prednisolone in suppressing lymphocyte proliferation, though with a potency ratio of about 1:1.3 relative to prednisone in biological response assays.^[32]^[25] Structural differences, including the oxazoline moiety, confer negligible mineralocorticoid receptor activity to deflazacort, in contrast to prednisone's moderate mineralocorticoid effects, which may contribute to reduced sodium retention and associated risks like edema.^[28]^[33] This dissociation supports its use at equivalent glucocorticoid doses with potentially altered side effect profiles, driven by lower affinity for mineralocorticoid pathways rather than differences in lipophilicity.^[5]

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 Duchenne muscular dystrophy (DMD).^[3] Patients received deflazacort at 0.9 mg/kg/day, prednisone 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 placebo group, establishing superiority over placebo in preserving muscle function.^[3] Analysis of data from the ACT-DMD trial, a 48-week multicenter study originally designed to assess ataluren in nonsense mutation DMD but including open-label extensions with deflazacort or prednisone, demonstrated sustained benefits of deflazacort.^[34] In patients receiving deflazacort, the rate of decline in motor function was significantly slower than with prednisone over 48 weeks, as measured by ambulatory decline and forced vital capacity.^[34] 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 median 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.^[35] Additional real-world data from larger cohorts indicate delays ranging from 1.6 to 2.5 years relative to untreated or standard care groups.^[36] In Europe, where deflazacort received marketing authorization in 1985, phase 3 trials from the 1980s and 1990s supported its efficacy in various inflammatory and autoimmune conditions, including rheumatoid arthritis and asthma exacerbations.^[4] Meta-analyses of these randomized controlled studies have confirmed consistent improvements in disease activity scores and symptom control across indications.^[4]

Comparative Efficacy with Prednisone

A head-to-head randomized, double-blind, placebo-controlled trial in boys with Duchenne muscular dystrophy (DMD) demonstrated that deflazacort and prednisone produced equivalent improvements in muscle strength over 12 weeks, as measured by quantitative muscle testing, with both superior to placebo.^[37] This short-term equivalence aligns with their similar glucocorticoid potency, where approximately 0.85 mg of deflazacort equates to 1 mg of prednisone in anti-inflammatory effects.^[31] Over longer periods, meta-analyses of multicenter clinical trials have shown deflazacort associated with slower DMD progression compared to prednisone/prednisolone. In a 2018 analysis of placebo-arm data 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 supine and 10-meter walk/run velocity, versus prednisone/prednisolone.^[38]^[34] These findings indicate deflazacort's edge in preserving ambulatory function, with hazard ratios favoring delayed loss of milestones like stair climbing and floor standing by 20-30% over prednisone in pooled 48-week data.^[39] 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 prednisone/prednisolone over 48 weeks, without differences in short-term strength gains.^[14] Real-world retrospective analyses of patient registries have corroborated slower functional decline with deflazacort, particularly in delaying wheelchair dependence, though head-to-head long-term randomized data remain limited.^[40] Overall, while short-term efficacy 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 Duchenne muscular dystrophy (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%), upper respiratory tract infection (12%), cough (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 glucocorticoid 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. Irritability (8%) and sleep disturbances, such as insomnia, were also reported in trial extensions and post-approval data, linked to sustained dosing regimens.^[41]

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.^[31] 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.^[12] 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 prednisone, attributed to glucocorticoid-induced lens opacification through oxidative stress and protein aggregation.^[31] 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.^[12] 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.^[42] 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.^[41]

Comparisons of Side Effect Profiles

Clinical trials and observational studies in Duchenne muscular dystrophy (DMD) patients demonstrate that deflazacort produces less weight gain than prednisone, with mean differences ranging from 2.91 to 4.1 kg over 12 months in comparative analyses.^[43] Similarly, cushingoid features occur at lower rates with deflazacort, as shown in a phase 3 randomized trial where prednisone incidence was significantly higher (p=0.0385), and in pooled person-year data indicating 6% versus 9% for prednisone.^[31] These differences align with deflazacort's lower lipid solubility and reduced sodium retention compared to prednisone.^[44] However, deflazacort is linked to greater risks of bone density loss and fractures, with fracture incidence rates of 1367 per 10,000 person-years versus 748 for prednisone in a large DMD cohort study.^[31] Cataract development also favors prednisone, with deflazacort showing a 2.4-fold higher odds ratio (95% CI 1.3–4.5; p=0.004) in retrospective analyses.^[31] These skeletal and ocular risks may stem from deflazacort's distinct glucocorticoid receptor 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.^[31] Deflazacort may offer advantages in glycemic control, exhibiting less diabetogenic potential than prednisone in insulin-dependent diabetics and healthy subjects, as evidenced by reduced glucose metabolism disruptions in controlled comparisons.^[45]^[5] Overall, no corticosteroid demonstrates uniform superiority in side effect profiles; deflazacort's metabolic benefits are counterbalanced by elevated skeletal and cataract concerns, necessitating individualized risk assessment in long-term use.^[31]^[46]

Contraindications and Drug Interactions

Absolute Contraindications

Deflazacort is contraindicated in patients with known hypersensitivity to the active ingredient or any of the formulation's inactive components.^[47] Hypersensitivity reactions, including anaphylaxis, have been documented in individuals receiving systemic corticosteroid therapy, underscoring the need to avoid administration in such cases to prevent severe allergic responses.^[47] 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.^[48]

Precautions and Monitoring

Patients receiving long-term deflazacort therapy, particularly for Duchenne muscular dystrophy (DMD), require regular monitoring for glucocorticoid-induced complications. Bone mineral density should be assessed periodically via dual-energy X-ray absorptiometry (DXA) scans to detect osteoporosis and fracture risk, as corticosteroids decrease bone formation and increase resorption.^[12] ^[49] Ophthalmologic examinations, including intraocular pressure measurement, are recommended if treatment exceeds six weeks to screen for cataracts and glaucoma, with deflazacort associated with elevated cataract risk in DMD patients.^[12] ^[49] In pediatric DMD patients, linear growth and weight should be tracked, as chronic use suppresses growth velocity.^[12] ^[49] 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 surgery to prevent crisis.^[12] ^[49] Live or live-attenuated vaccines should be avoided during immunosuppressive dosing, and pre-treatment immunity to varicella or measles confirmed where possible.^[12] ^[49] Deflazacort, a CYP3A4 substrate, interacts with inhibitors such as ketoconazole or clarithromycin; concomitant use necessitates reducing the dose to one-third of the recommended amount to avoid excessive exposure.^[12] Strong or moderate CYP3A4 inducers should be avoided, as they diminish efficacy.^[12] Nonsteroidal anti-inflammatory drugs like ibuprofen are contraindicated due to heightened gastrointestinal bleeding risk.^[49]

History

Development and Early Research

Deflazacort, an oxazoline 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 anti-inflammatory potency while reducing mineralocorticoid side effects.^[50] This structural modification involved introducing a 16α,17α-d-oxazoline ring to the prednisolone backbone, which preclinical evaluations suggested dissociated glucocorticoid efficacy from sodium-retaining properties more effectively than earlier corticosteroids.^[51] Early pharmacological research in the late 1970s and early 1980s focused on its anti-inflammatory mechanisms, revealing equipotent suppression of inflammation in rodent models compared to dexamethasone or prednisolone, but with diminished effects on collagen synthesis in bone cells and lower electrolyte disturbances.^[52] Preclinical data published during this period highlighted deflazacort's reduced mineralocorticoid activity, as evidenced by minimal impacts on potassium excretion and blood pressure in animal assays, positioning it as a potential alternative for chronic therapy.^[53] Initial human trials in Europe commenced in the mid-1980s, primarily evaluating deflazacort for asthma and rheumatoid arthritis, where it demonstrated comparable efficacy to prednisone in reducing symptoms over short-term (4-6 weeks) and extended (up to 52 weeks) durations, with early signals of favorable tolerability.^[22] These studies, conducted by Guidotti ahead of its 1985 European launch, underscored its role in managing inflammatory conditions while prioritizing metabolic safety.^[21]

Regulatory Approvals and Delays

Deflazacort received its initial regulatory approval in Europe in the early 1980s, with the applicant reporting first approval in 1982, followed by marketing in Italy and several other countries including France, the United Kingdom, Germany, and Spain by the mid-1980s for inflammatory conditions.^[54]^[21] By the 1990s, it had gained broader availability across European nations through national approvals, though not via centralized European Medicines Agency authorization until later formulations in the 2010s.^[55] In the United States, deflazacort lacked prior approval, necessitating a new drug application supported by clinical trials despite decades of international use. The FDA granted orphan drug designation for Duchenne muscular dystrophy (DMD) on September 16, 2010, followed by fast track status in 2014, to facilitate development for this rare condition.^[56]^[54] 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 placebo, reflecting requirements for efficacy data in the orphan indication.^[10]^[57] 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.^[58] Post-2017 U.S. approval remained confined to DMD under orphan drug exclusivity, with label expansion in June 2019 to include patients aged 2 to 5 years following additional pediatric data submission.^[59] 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.^[60]^[61]

Society and Culture

Legal Status and Availability

Deflazacort is classified as a prescription-only medication worldwide and is not designated as a controlled substance under any schedule of the U.S. Controlled Substances Act or equivalent international frameworks.^[62] In the United States, the Food and Drug Administration (FDA) approved deflazacort on February 9, 2017, exclusively for the treatment of Duchenne muscular dystrophy (DMD) in patients aged five years and older, with an expansion in June 2019 to include children aged two to five years.^[6]^[11] 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.^[63]^[64] Outside the United States, deflazacort has been approved for various anti-inflammatory indications since 1985 and is widely available in Europe, Asia, and other regions, often through generic formulations introduced after original patent expirations in the 1990s.^[7] 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.^[65]^[66] While not centrally authorized by the European Medicines Agency (EMA) for DMD, it remains prescribed nationally in European countries for other conditions under established regulatory pathways.^[67]

Economics and Pricing Controversies

Upon FDA approval of Emflaza (deflazacort) on February 9, 2017, for Duchenne muscular dystrophy, 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 off-label use.^[68]^[69] This pricing, enabled by seven-year orphan drug 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 rare disease affecting roughly 15,000 U.S. males.^[6]^[61] Critics, including Senators Bernie Sanders and Elijah Cummings, 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.^[70] 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 PTC Therapeutics three months later for $140 million upfront plus royalties exceeding 20%, yielding rapid returns that fueled debates on exclusivity-driven profiteering.^[71]^[72] 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.^[73] 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.^[74]^[75] 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).^[12]^[13] The oral suspension formulation facilitates precise dosing for pediatric patients with Duchenne muscular dystrophy (DMD), who require weight-based administration around 0.9 mg/kg/day.^[76] Tablets may be administered whole or crushed and mixed with applesauce for patients unable to swallow them intact.^[77] 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.^[1]^[78] These tablet formulations are standard for anti-inflammatory and immunosuppressive uses, with dosing adjusted based on condition severity, typically ranging from 0.25 to 1.5 mg/kg/day.^[78] Oral suspensions are less commonly branded internationally but may be compounded or available generically for pediatric needs.^[79] 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 drug has been approved since the 1980s.^[1] 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.^[80]

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Apr 7, 1987 · In conclusion, the relative antiinflammatory potency of deflazacort and prednisone lies between 0.83 and 0.66 on a weight basis (1.02 and 0.82 ...
[31]
Comparing Deflazacort and Prednisone in Duchenne Muscular ...
Jun 14, 2022 · There is some evidence that long-term deflazacort increases the likelihood of cataracts. A retrospective review of 596 patients with DMD ...
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In vitro immunosuppressive potency of deflazacort, a new bone ...
Deflazacort and the 21-deacetyl metabolite were as potent as prednisolone and hydrocortisone in suppressing PHA stimulated lymphocytes in a dose dependent way, ...
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Deflazacort Tablets vs. Other Corticosteroids - Bionova
Jul 26, 2024 · Some potential advantages of Deflazacort over other corticosteroids include its reduced mineralocorticoid activity, potentially lower risk ...
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Deflazacort vs prednisone treatment for Duchenne muscular dystrophy
Patients receiving deflazacort were found to experience significantly slower rates of decline over 48 weeks than those receiving prednisone/prednisolone on ...
[35]
Deflazacort in Duchenne dystrophy: study of long-term effect - PubMed
Our treated patients lost their ambulation at a median age of 11.8 years vs. 10.5 years in the placebo group. Side effects were mild, consisting of moderate ...
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[PDF] Real-world outcomes of long-term prednisone and deflazacort use ...
Our finding of a near similar 2-year delay in the time to loss of ambulation with deflazacort compared with prednisone treatment in a single large care center, ...
[37]
Efficacy and safety of deflazacort vs prednisone and placebo for ...
This study provides Class I evidence that for boys with DMD, daily use of either DFZ and PRED is effective in preserving muscle strength over a 12-week period.
[38]
Meta-Analysis of Deflazacort vs Prednisone/Prednisolone in ...
Apr 10, 2018 · Deflazacort appeared to be more effective than prednisone/prednisolone in delaying progression of DMD. Study Supported by: PTC Therapeutics, Inc.
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Meta-analyses of deflazacort versus prednisone/prednisolone in ...
Oct 25, 2021 · Conclusion: Deflazacort provides clinically meaningful delays in loss of physical milestones over 48 weeks compared with prednisone/prednisolone ...
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Study Summaries - EMFLAZA® (deflazacort)
Long-term effects of glucocorticoids on function, quality of life, and survival in patients with Duchenne muscular dystrophy: a prospective cohort study. Lancet ...
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Safety & Side Effects - EMFLAZA® (deflazacort)
The most common side effects of EMFLAZA include facial puffiness or Cushingoid appearance, weight increased, increased appetite, upper respiratory tract ...
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Management of Adrenal Insufficiency Risk After Long-term Systemic ...
Jan 2, 2019 · Chronic GC therapy causes adrenal suppression in patients with DMD, therefore, clinicians must have high index of suspicion for AI and GC stress ...
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[PDF] OHSU Drug Effectiveness Review Project Summary Report
Overall, there is insufficient evidence to evaluate differences in adverse effects between deflazacort and other oral corticosteroids. Evidence is limited by.<|separator|>
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Comparing Deflazacort and Prednisone in Duchenne Muscular ...
Jun 14, 2022 · The mean cumulative failure rate reduced by 28% in deflazacort-treated versus prednisone/prednisolone-treated patients over the study duration ( ...<|separator|>
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Deflazacort vs prednisone. Effect on blood glucose control in insulin ...
Recent reports have indicated that deflazacort is less diabetogenic than prednisone in healthy subjects. Ten insulin-treated diabetics who required steroid ...Missing: infection risk
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A review of the literature compares prednisone and deflazacort in ...
Sep 22, 2022 · Deflazacort increased the risk of bone loss, cataract and slowed growth more than prednisone/prednisolone. Prednisone, on the other hand ...Missing: mineral density meta-
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[PDF] HIGHLIGHTS OF PRESCRIBING INFORMATION - accessdata.fda.gov
Toxic epidermal necrolysis has been reported with the use of deflazacort with symptoms beginning within 8 weeks of starting treatment. Discontinue at the first ...
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[PDF] HIGHLIGHTS OF PRESCRIBING INFORMATION - Emflaza
Common adverse reactions (≥ 5% of deflazacort-treated patients) that occurred over 52 weeks of exposure to deflazacort 0.9 mg/kg/day in Study 1 and at a higher ...
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[PDF] Corticosteroids in Duchenne Muscular Dystrophy (DMD)
CS can be beneficial for people with DMD. Our clinical guidance recommends that CS should be given daily as this gives the greatest benefits on muscle ...Missing: precautions | Show results with:precautions
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Steroids Possessing Nitrogen Atoms. III. Synthesis of New Highly ...
Effect of therapy with a new glucocorticoid, deflazacort, on linear growth and growth hormone secretion after renal transplantation. The Journal of ...
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DEFLAZACORT VERSUS OTHER GLUCOCORTICOIDS - LWW
A new glucocorticoid deflazacort was introduced in 1969; it is a D-ring substituted steroid, otherwise similar to cortisol. It is a synthetic oxazoline ...
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Comparative study of deflazacort, a new synthetic corticosteroid, and ...
In this study, we have compared the effects of deflazacort with those of dexamethasone on the synthesis of collagen in various rat bone cell populations and ...
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Effects of prednisone and deflazacort on mineral metabolism and ...
The effects of two different glucocorticoids, prednisone and deflazacort, (an oxazoline derivative of prednisolone) on bone metabolism were analyzed in 10.Missing: mineralocorticoid | Show results with:mineralocorticoid
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[PDF] 208684Orig1s000 208685Orig1s000 - accessdata.fda.gov
Nov 15, 2016 · Deflazacort is likely to be used in the outpatient and inpatient settings. As an orally administered drug, deflazacort will primarily be ...
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[PDF] ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS
EU/1/13/902/003. 9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION. Date of first authorisation: 31 July 2014. Date of latest renewal: 16 June 2017.
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Search Orphan Drug Designations and Approvals - FDA
Generic Name: deflazacort. Date Designated: 09/16/2010. Orphan Designation: Treatment of Duchenne muscular dystrophy. Orphan Designation Status: Designated.
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[PDF] 208684Orig1s000 208685Orig1s000 - accessdata.fda.gov
Feb 15, 2017 · Deflazacort (EMFLAZA) is an inactive, ester pro-drug which is metabolized rapidly to the active drug 21-desacetyldeflazacort (21-. desDFZ).
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The Effectiveness and Value of Deflazacort and Exon-Skipping ... - NIH
Deflazacort was first licensed for use overseas in the 1980s and was approved in February 2017 for treatment of DMD in the United States.
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PTC Receives FDA Approval for Expansion of EMFLAZA ...
Jun 7, 2019 · Emflaza was first approved by the FDA in February 2017 for the treatment of Duchenne in patients 5-years and older. Read the Press Release from ...
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How to prevent the next Marathon Pharmaceuticals - PMC
Jan 17, 2018 · Deflazacort, a synthetic corticosteroid originally developed by Merrell Dow Pharmaceuticals, has been available since the 1990s outside the U.S. ...
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Duchenne Drug Delayed After Outrage Over Price - NPR
Feb 14, 2017 · For years, many American patients have imported deflazacort, the generic version of Emflaza, for about $1,200 a year. But because the medicine ...
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Deflazacort Uses, Side Effects & Warnings - Drugs.com
Jul 10, 2025 · Deflazacort may cause serious side effects. Call your doctor at once if ... Long-term use of steroids may lead to bone loss (osteoporosis) ...
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[PDF] Deflazacort, Eteplirsen, and Golodirsen for Duchenne Muscular ...
deflazacort was not approved for use in the US until 2017. Prior to that ... For prednisone, since numerous generic forms are available in the US.
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Marathon charges $89,000 a year for new new muscular dystrophy ...
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FDA approves rare disease deflazacort at exorbitant price
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PTC's Emflaza to face generics this month post Aurobindo FDA nod
Feb 12, 2024 · Aurobindo plans to launch generic deflazacort tablets at various dosage strengths this month, the company said in a release.
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[PDF] Agamree - European Medicines Agency - Europa.eu
Oct 12, 2023 · Thus, neither prednisone nor deflazacort are approved for the treatment of DMD in Europe. For a subpopulation of DMD patients, in which ...
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Marathon Pharmaceuticals criticized for outrageous pricing of drug
Feb 13, 2017 · Stung by criticism of its plan to charge a whopping $89,000 a year in the U.S. for a muscular dystrophy drug that costs less than $1,500 ...Missing: controversy | Show results with:controversy
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$$89000 Orphan Drug Gets A New Owner — And Likely A New Price
Mar 16, 2017 · For years, many American patients have imported the generic version at a cost averaging from $1,000 to $1,600 annually. The cost typically was ...Missing: abroad | Show results with:abroad
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[PDF] United States Senate
Mar 3, 2017 · Deflazacort, like many steroids, has numerous medical applications. However, no company has sought FDA approval of this drug until Marathon's ...<|control11|><|separator|>
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Marathon Pharmaceutical Drops Out Of PhRMA Following Drug ...
Apr 21, 2017 · The news of Marathon's resignation comes after the company was widely criticized this year for the $89,000 price tag for Emflaza, a drug for ...
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Marathon, under heavy fire for Emflaza pricing, makes surprise deal ...
Mar 16, 2017 · Marathon Pharma sold its controversial Emflaza drug to PTC Therapeutics in a deal potentially worth more than $190 million.
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Marathon presses pause on Emflaza launch after pricing pushback
Feb 13, 2017 · The controversy over Marathon's pricing of Emflaza has echoes of previous pricing firestorms which have sparked scrutiny over industry practices ...<|separator|>
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New price for muscular dystrophy drug draws criticism - CNBC
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Zydus Lifesciences gets FDA approval for Deflazacort oral suspension
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Dosing & How to Take EMFLAZA® (deflazacort)
EMFLAZA is available in tablet and liquid forms and can be taken with or without food. Recommended dosing is approximately 0.9 mg/kg/day for both formulations.
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Dosing & Administration - EMFLAZA® (deflazacort)
Contraindications: EMFLAZA is contraindicated in patients with a hypersensitivity to deflazacort or any of the inactive ingredients in EMFLAZA.
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[PDF] Calcort 6mg Tablets Deflazacort Important things you need to know ...
You must take this medicine regularly to get maximum benefit from it. Calcort can be used to: • Treat inflammation including asthma, arthritis and allergies. • ...Missing: international | Show results with:international
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Deflazacort: Side Effects, Uses, Dosage, Interactions, Warnings
Blood and lymphatic system disorders: Leukocytosis · Cardiac disorder: Heart failure · Eye disorders: Chorioretinopathy, corneal or scleral thinning ...Missing: absolute | Show results with:absolute
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Cranbury Pharmaceuticals Receives U.S. FDA Approval for First ...
Jun 12, 2024 · Deflazacort oral suspension is indicated to treat patients five years of age and older for Duchenne muscular dystrophy, a rare disease with limited treatment ...