PUBLISHER: DelveInsight | PRODUCT CODE: 1553403
PUBLISHER: DelveInsight | PRODUCT CODE: 1553403
DelveInsight's "Idiopathic Membranous Nephropathy (IMN) - Market Insights, Epidemiology and Market Forecast - 2034" report delivers an in-depth understanding of Idiopathic Membranous Nephropathy (IMN), historical and forecasted epidemiology as well as the Idiopathic Membranous Nephropathy (IMN) market trends in the United States, EU4 (Germany, Spain, Italy, and France) and the United Kingdom, and Japan.
Idiopathic Membranous Nephropathy (IMN) market report provides real-world prescription pattern analysis, emerging drugs, market share of individual therapies, and historical and forecasted 7MM Idiopathic Membranous Nephropathy (IMN) market size from 2020 to 2034. The report also covers current Idiopathic Membranous Nephropathy (IMN) treatment practices/algorithms and unmet medical needs to curate the best opportunities and assess the market's underlying potential.
Idiopathic Membranous Nephropathy (IMN) Overview
Idiopathic Membranous Nephropathy (IMN) is a prevalent form of glomerular disease primarily associated with nephrotic syndrome. It is characterized by the immune system's attack on the glomeruli, leading to significant proteinuria, edema, and potential progression to renal failure. The condition is termed "idiopathic" when no identifiable secondary cause is found, although it can also arise from various underlying conditions, including autoimmune diseases and infections. IMN typically affects adults, particularly middle-aged men, and presents with symptoms such as frothy urine, swelling in the legs and abdomen, and weight gain due to fluid retention.
The diagnosis of IMN involves a combination of clinical evaluation and laboratory tests. Initial assessments typically include urine analysis to detect proteinuria, which is often in the nephrotic range (>3.5 g/day). Blood tests are conducted to evaluate kidney function and check for hypoalbuminemia and dyslipidemia, common in nephrotic syndrome. A definitive diagnosis is usually confirmed through a kidney biopsy, which reveals characteristic changes in the glomeruli, such as immune complex deposition along the capillary walls. Additionally, serological tests for specific antibodies, such as those against the phospholipase A2 receptor (PLA2R), can help differentiate primary IMN from secondary forms, guiding further management strategies.
Further details related to country-based variations in diagnosis are provided in the report
Idiopathic Membranous Nephropathy (IMN) Treatment
Currently, there is no specific cure for IMN, and treatment primarily focuses on managing symptoms and preventing disease progression. Supportive care includes the use of diuretics to manage edema and angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers (ARBs) to reduce proteinuria and protect kidney function. In cases where supportive measures are insufficient, immunosuppressive therapies may be initiated. These include corticosteroids, cyclophosphamide, and newer agents like rituximab, which targets B cells implicated in the autoimmune response. However, the effectiveness of these treatments can vary, and they may carry significant side effects. Recent studies suggest that targeting B cells may offer a promising therapeutic approach, potentially improving outcomes in patients with IMN.
The Idiopathic Membranous Nephropathy (IMN) epidemiology chapter in the report provides historical as well as forecasted in the 7MM covering the United States, EU4 countries (Germany, France, Italy, and Spain), the United Kingdom, and Japan from 2024 to 2034. The Idiopathic Membranous Nephropathy (IMN) epidemiology is segmented with detailed insights into total prevalent cases, antigen-specific cases, total treated cases of Idiopathic Membranous Nephropathy (IMN).
Idiopathic Membranous Nephropathy (IMN) Drug Chapter
The drug chapter segment of the Idiopathic Membranous Nephropathy (IMN) report encloses a detailed analysis of Idiopathic Membranous Nephropathy (IMN) marketed drugs and late-stage (Phase III and Phase II) pipeline drugs. It also deep dives into the Idiopathic Membranous Nephropathy (IMN) pivotal clinical trial details, recent and expected market approvals, patent details, the latest news, and recent deals and collaborations.
Emerging Drugs
GAZYVA (obinutuzumab): Hoffmann-La Roche
GAZYVA (obinutuzumab) is a humanized and glycoengineered type II anti-CD20 monoclonal antibody with superior in vitro B-cell cytotoxicity than rituximab. Obinutuzumab is directed at a different epitope on CD20 than that recognized by rituximab and can evoke a greater B-cell apoptotic response.
Currently, the drug is in Phase III of development. Roche plans to file a regulatory application for obinutuzumab as a treatment option for membranous nephropathy in or after 2025.
SNP-ACTH (1-39) Gel: Cerium Pharmaceuticals
Cerium has formulated a synthetic porcine ACTH drug substance into a subcutaneous injectable drug product (SNP-ACTH [1-39] Gel). Similar to other synthetic long-acting ACTH products containing highly purified synthetic ACTH peptides, a quantifiable number of ACTH molecules present in a long-acting synthetic ACTH drug product is a clear advantage for optimizing the dosing required to achieve strong response rates in PMN.
The Company has completed its preclinical studies confirming the safety and potency of SNP-ACTH (1-39) Gel and a Phase I clinical trial in healthy subjects, further demonstrating its safety and tolerability. Cerium has engaged with the FDA on its Phase III trial design and outcome measures for a prospective, randomized superiority trial to determine if SNP-ACTH (1-39) Gel is superior to rituximab in inducing a durable remission of proteinuria as a first-line immunosuppressive treatment of moderate to high-risk PMN patients. Cerium is currently enrolling patients in its Phase III clinical trial.
Key players, such as Hoffmann-La Roche, HI-Bio, Cerium Pharmaceuticals, BeiGene and others are evaluating their lead candidates in different stages of clinical development, respectively. They aim to investigate their products for the treatment of Idiopathic Membranous Nephropathy (IMN).
This section focuses on the uptake rate of potential drugs expected to be launched in the market during 2024-2034, which depends on the competitive landscape, safety, and efficacy data along with order of entry. It is important to understand that the key players evaluating their novel therapies in the pivotal and confirmatory trials should remain vigilant when selecting appropriate comparators to stand the greatest chance of a positive opinion from regulatory bodies, leading to approval, smooth launch, and rapid uptake.
Further detailed analysis of emerging therapies drug uptake in the report...
Idiopathic Membranous Nephropathy (IMN) Activities
The report provides insights into different therapeutic candidates in Phase III and Phase II stages. It also analyzes key players involved in developing targeted therapeutics.
Pipeline Development Activities
The report covers information on collaborations, acquisitions and mergers, licensing, and patent details for Idiopathic Membranous Nephropathy (IMN) emerging therapies.
KOL Views
To keep up with the real-world scenario in current and emerging market trends, we take opinions from Key Industry leaders working in the domain through primary research to fill the data gaps and validate our secondary research. Industry Experts were contacted for insights on the evolving treatment landscape, patient reliance on conventional therapies, patient therapy switching acceptability, and drug uptake along with challenges related to accessibility.
DelveInsight's analysts connected with 25+ KOLs to gather insights; however, interviews were conducted with 10+ KOLs in the 7MM. Centers such as University of Minnesota, UCL Centre for Nephrology, University of Washington, Hospital Gregorio Maranon, etc., were contacted. Their opinion helps understand and validate current and emerging treatment patterns of Idiopathic Membranous Nephropathy (IMN). This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the market and the unmet needs.
Qualitative Analysis
We perform Qualitative and market Intelligence analysis using various approaches, such as SWOT analysis and Conjoint Analysis. In the SWOT analysis, strengths, weaknesses, opportunities, and threats in terms of gaps in disease diagnosis, patient awareness, physician acceptability, competitive landscape, cost-effectiveness, and geographical accessibility of therapies are provided.
Conjoint Analysis analyzes multiple approved and emerging therapies based on relevant attributes such as safety, efficacy, frequency of administration, route of administration, and order of entry. Scoring is given based on these parameters to analyze the effectiveness of therapy.
In efficacy, the trial's primary and secondary outcome measures are evaluated, one of the most important primary outcome measures is change in urinary protein and change in anti-phospholipase A2 receptor (PLA2R) auto-antibody.
Further, the therapies' safety is evaluated wherein the acceptability, tolerability, and adverse events are majorly observed, and it sets a clear understanding of the side effects posed by the drug in the trials. In addition, the scoring is also based on the probability of success, and the addressable patient pool for each therapy. According to these parameters, the final weightage score and the ranking of the emerging therapies are decided.
Market Access and Reimbursement
The report further provides detailed insights on the country-wise accessibility and reimbursement scenarios, cost-effectiveness scenario of currently used therapies, programs making accessibility easier and out-of-pocket costs more affordable, insights on patients insured under federal or state government prescription drug programs, etc.