Calliditas Therapeutics Presents Additional Data Analyses from the Phase 3 NeflgArd trial of Nefecon in Primary IgA Nephropathy at the ISN World Congress of Nephrology 2024
- Consistent improvement in estimated glomerular filtrate rate (eGFR) with Nefecon treatment compared to placebo.
- 30% reduction in UPCR with Nefecon sustained over 2 years, leading to lower risk of kidney failure.
- Significantly delayed time to kidney function decline events with Nefecon compared to placebo.
- Positive quality of life outcomes with no meaningful differences between Nefecon and placebo groups.
- Favorable response to Nefecon treatment in Asian and White patient populations with reduced UPCR and delays in kidney function decline events.
- Nefecon demonstrated efficacy and tolerability across different racial and ethnic groups.
- Safety information highlighted contraindications, warnings, precautions, and potential adverse reactions associated with TARPEYO use.
- None.
Insights
The analysis of the Phase 3 NeflgArd trial data for Nefecon in treating primary IgA nephropathy (IgAN) can be indicative of this therapy's efficacy. Nefecon, which is a formulation of budesonide, shows promise in mitigating the decline of kidney function as suggested by the eGFR rates and UPCR levels in patients. Looking closer, the sustained improvement in eGFR, particularly in patients with lower baseline UPCR, aligns with the RaDaR treatment target and could signify a leap forward in managing IgAN.
Considering the chronic nature of IgAN and the lack of effective treatments, this drug has the potential to become a significant therapeutic option. Nefecon's consistent performance across various patient demographics offers a wider market appeal. However, the reported results need to be weighed against the backdrop of potential hypercorticism and immunosuppression risks associated with long-term corticosteroid use.
From a financial perspective, the positive outcomes from the NeflgArd trial may potentially lead to increased market penetration and sales for Calliditas Therapeutics, especially considering the current lack of competing treatments for IgAN. Furthermore, the clinical success across diverse racial and ethnic backgrounds may allow for broader global market adoption.
However, it is also important to analyze the company's capacity to manage the commercialization process, any pending patent issues and the scalability of production in line with the projected demand. The cost-efficiency and reimbursement policies will also be a factor in the drug's market success, influencing investor confidence and the stock's performance.
Given the chronic nature of IgA nephropathy and the limited treatment options available, there is likely a substantial unmet need in the market which Nefecon could address. The drug's demonstrated ability to improve eGFR rates and lower UPCR may position it as a preferred option for clinicians and patients alike, influencing market dynamics in the nephrology sector.
Gauging the market response to Nefecon will require monitoring competitor activity, patent landscapes and the progression of reimbursement strategies. Long-term market adoption will depend on the balance between therapeutic efficacy and the managed risk profile of the drug.
"We were pleased to share additional analyses from the 2-year Phase 3 NeflgArd trial of Nefecon in IgAN at this year's World Congress of Nephrology," said Richard Philipson, Chief Medical Officer of Calliditas. "These additional data further reinforce the impact of Nefecon across the entire study population, irrespective of baseline UPCR levels or patient's racial and ethnic backgrounds."
Poster presentation details are below and will be available on the Presentations and Publications page on the Calliditas' corporate website following the meeting.
Poster Presentation Analyses:
Poster Title: "Nefecon treatment provides kidney benefits for patients with IgAN that extend to those with low levels of UPCR: A sub-analysis of the phase III NefIgArd trial"
An extended analysis of patients with baseline UPCR levels above and below 0.8 g/g was performed to further explore the potential benefits of Nefecon. In the full analysis involving 364 patients regardless of baseline UPCR, Nefecon treatment consistently improved the estimated glomerular filtrate rate (eGFR) over the 2-year study period compared to placebo. 72 patients with a baseline UPCR <0.8 g/g experienced sustained eGFR improvement (p=0.0026), which persisted for up to 18 months after treatment initiation, even after the treatment cessation at month 9. Those patients also achieved an eGFR slope of -0.25 mL/min/1.73 m2 per year, indicating that Nefecon treatment may support them in reaching the RaDaR treatment target of an eGFR decline of <1 mL/min/1.73 m2 per year. This objective is pivotal in mitigating the risk of kidney failure in their lifetime.
Poster Title: "eGFR decline in patients with IgAN treated with Nefecon or placebo: Results from the 2-year NefIgArd Phase 3 trial"
During the 9-month treatment period, Nefecon showed a
Poster Title: Nefecon effect on quality of life in patients with IgAN: SF-36 results from the Phase 3 NefIgArd trial"
The 2-year results of quality of life (QoL) analyses based on 36-Item Short Form Survey (SF-36) assessments at 9 and 24 months revealed no meaningful differences in any QoL domain between Nefecon and placebo groups after 9 months of treatment. These SF-36 scores remained consistent after 15 months of off-drug observational follow-up further supporting the benefit/risk profile of Nefecon.
Poster Title: "Nefecon treatment response in Asian and White patient populations with immunoglobulin A nephropathy: A 2-year analysis of the Phase 3 NefIgArd trial"
The responses to Nefecon treatment from the full 2-year NefIgArd trial were assessed in patients identifying as Asian (n=83) or White (n=275). Regardless of race and ethnicity, Nefecon showed a favorable change in eGFR compared to placebo of 5.5 mL/min/1.73 m2 in Asian patients and 4.8 mL/min/1.73 m2 in White patients. Nefecon also demonstrated greater reductions in UPCR at 9 and 24 months with notable delays in kidney function decline events. These effects were consistent across races and ethnicities. Additionally, Nefecon significantly reduced the rate of microhematuria in both Asian and White patients. Overall, these findings highlight Nefecon's efficacy and tolerability across different racial and ethnic groups.
Indication
TARPEYO is indicated to reduce the loss of kidney function in adults with primary immunoglobulin A nephropathy (IgAN) who are at risk for disease progression.
Important Safety Information
Contraindications: TARPEYO is contraindicated in patients with hypersensitivity to budesonide or any of the ingredients of TARPEYO. Serious hypersensitivity reactions, including anaphylaxis, have occurred with other budesonide formulations.
Warnings and Precautions
Hypercorticism and adrenal axis suppression: When corticosteroids are used chronically, systemic effects such as hypercorticism and adrenal suppression may occur. Corticosteroids can reduce the response of the hypothalamus-pituitary-adrenal (HPA) axis to stress. In situations where patients are subject to surgery or other stress situations, supplementation with a systemic corticosteroid is recommended. When discontinuing therapy or switching between corticosteroids, monitor for signs of adrenal axis suppression.
Patients with moderate to severe hepatic impairment (Child-Pugh Class B and C respectively) could be at an increased risk of hypercorticism and adrenal axis suppression due to an increased systemic exposure to oral budesonide. Avoid use in patients with severe hepatic impairment (Child-Pugh Class C). Monitor for increased signs and/or symptoms of hypercorticism in patients with moderate hepatic impairment (Child-Pugh Class B).
Risks of immunosuppression: Patients who are on drugs that suppress the immune system are more susceptible to infection than healthy individuals. Chickenpox and measles, for example, can have a more serious or even fatal course in susceptible patients or patients on immunosuppressive doses of corticosteroids. Avoid corticosteroid therapy in patients with active or quiescent tuberculosis infection; untreated fungal, bacterial, systemic viral, or parasitic infections, or ocular herpes simplex. Avoid exposure to active, easily transmitted infections (e.g., chicken pox, measles). Corticosteroid therapy may decrease the immune response to some vaccines.
Other corticosteroid effects: TARPEYO is a systemically available corticosteroid and is expected to cause related adverse reactions. Monitor patients with hypertension, prediabetes, diabetes mellitus, osteoporosis, peptic ulcer, glaucoma or cataracts, or with a family history of diabetes or glaucoma, or with any other condition where corticosteroids may have unwanted effects.
Adverse reactions: In clinical studies, the most common adverse reactions with TARPEYO (occurring in ≥
Drug interactions: Budesonide is a substrate for CYP3A4. Avoid use with potent CYP3A4 inhibitors, such as ketoconazole, itraconazole, ritonavir, indinavir, saquinavir, erythromycin, and cyclosporine. Avoid ingestion of grapefruit juice with TARPEYO. Intake of grapefruit juice, which inhibits CYP3A4 activity, can increase the systemic exposure to budesonide.
Use in specific populations
Pregnancy: The available data from published case series, epidemiological studies, and reviews with oral budesonide use in pregnant women have not identified a drug-associated risk of major birth defects, miscarriage, or other adverse maternal or fetal outcomes. There are risks to the mother and fetus associated with IgAN. Infants exposed to in-utero corticosteroids, including budesonide, are at risk for hypoadrenalism.
Please see Full Prescribing Information.
About TARPEYO
TARPEYO is an oral 4mg delayed release formulation of budesonide, designed to remain intact until it reaches the ileum. Each capsule contains coated beads of budesonide that target mucosal B-cells present in the ileum, including the Peyer's patches, which are responsible for the production of galactose-deficient IgA1 antibodies (Gd-Ag1) causing IgA nephropathy.
About the NeflgArd Study
NefIgArd was a global, Phase 3, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of TARPEYO 16 mg once daily vs placebo in adult patients with primary IgAN (N=364) as an addition to optimized RASi therapy. Patients were randomized 1:1 to receive 16 mg/day oral capsules of TARPEYO or matching placebo for 9 months, followed by a 15-month observational follow-up period without the study drug.
The primary efficacy endpoint was time-weighted average of eGFR over 2 years. The time-weighted average of eGFR over 2 years showed a statistically significant treatment benefit with TARPEYO versus placebo (difference 5•05 mL/min per 1•73 m² [
The favorable effect of TARPEYO on eGFR was seen by Month 3 (the earliest assessment) and did not appear to increase in magnitude over two years. At the end of Year 2, there was a 5.9 mL/min/1.73 m2 difference in the mean change from baseline in eGFR between TARPEYO and placebo (
The most common adverse reactions with TARPEYO (occurring in ≥
About Primary Immunoglobulin A Nephropathy
Primary immunoglobulin A nephropathy (IgA nephropathy or IgAN or Berger's Disease) is a rare, progressive, chronic autoimmune disease that attacks the kidneys and occurs when galactose-deficient IgA1 is recognized by autoantibodies, creating IgA1 immune complexes that become deposited in the glomerular mesangium of the kidney.This deposition in the kidney can lead to progressive kidney damage and potentially a clinical course resulting in end- stage renal disease. IgAN most often develops between late teens and late 30s.
For further information, please contact:
Åsa Hillsten, Head of IR & Sustainability, Calliditas
Tel : +46 76 403 35 43, Email : asa.hillsten@calliditas.com
The information was sent for publication, through the agency of the contact persons set out above, on April 18, 2023, at 13.00 p.m. CET.
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FAQ
What additional data analyses were presented by Calliditas Therapeutics at the ISN World Congress of Nephrology 2024?
What was the main focus of the extended analysis of patients with baseline UPCR levels above and below 0.8 g/g?
What was the percentage of patients with a confirmed 30% reduction in eGFR or kidney failure in the Nefecon arm compared to placebo?
What were the results of the quality of life (QoL) analyses based on SF-36 assessments in patients with IgAN?
How did Nefecon treatment response vary in Asian and White patient populations with IgAN?
What are the contraindications associated with TARPEYO use?
What are the risks of immunosuppression related to TARPEYO use?
What are the most common adverse reactions associated with TARPEYO treatment?
What drug interactions should be avoided with TARPEYO?
What are the pregnancy considerations for TARPEYO use?
What was the main takeaway from the data analyses presented by Calliditas Therapeutics?
