PUBLISHER: DelveInsight | PRODUCT CODE: 1415504
PUBLISHER: DelveInsight | PRODUCT CODE: 1415504
DelveInsight's "Acute Kidney Injury-Market Insights, Epidemiology and Market Forecast-2032" report delivers an in-depth understanding of the AKI, historical and forecasted epidemiology as well as the AKI market trends in the United States, EU4 (Germany, France, Italy, and Spain), and the United Kingdom, and Japan.
AKI market report provides current treatment practices, emerging drugs, and market share of the individual therapies, current and forecasted 7MM AKI market size from 2019 to 2032. The report also covers current AKI treatment practices/algorithms, and unmet medical needs to curate the best of the opportunities and assesses the underlying potential of the market.
Study Period: 2019-2032.
AKI is commonly defined as an abrupt decline in renal function, clinically manifesting as a reversible acute increase in nitrogen waste products measured by blood urea nitrogen (BUN) and serum creatinine levels over hours to weeks. Signs and symptoms of AKI include nausea, vomiting, weakness, dizziness, and, pain in the lower back. Some patients are asymptomatic (no noticeable symptoms) and others may have generalized non-specific (not specific to kidneys) symptoms.
The history and physical examination are important in determining the etiology of AKI. The history can identify nephrotoxic medications or a systemic illness contributing to impaired renal function. The physical examination should focus on evaluating intravascular volume status. Skin rashes may indicate an underlying condition (e.g., systemic lupus erythematosus, atheroembolism/vasculitis) or exposure (e.g., drug rash suggesting acute interstitial necrosis) leading to acute kidney injury. The diagnosis of AKI is traditionally based on a rise in serum creatinine and/or a fall in urine output. The laboratory assessment includes the measurement of serum creatinine level, urinalysis, renal biopsy, urine electrolytes, and others.
The therapeutic strategies for AKI based on the KDIGO guidelines and bundles of care are limited and mostly supportive. The clinical approach should begin with hemodynamic stabilization, the early identification of AKI complications, its cause, and its treatment. Hemodynamic stabilization is of critical significance because autoregulation mechanisms are impaired in AKI. The treatment for AKI depends on the cause of the condition. Most people need to stay in the hospital during treatment and until the recovery of the kidneys. Some possible treatments apart from temporary hemodialysis include medicines to control the amounts of vitamins and minerals in the blood, and treatments to keep the right amount of fluid in the blood. There is no approved treatment for AKI, the current treatment practices use conventional therapies (vasopressor, diuretics, statins, and others) and Renal Replacement Therapies (RRT).
The disease epidemiology covered in the report provides historical as well as forecasted epidemiology segmented by Total Incident Population of AKI in Hospitalized Patients, Mortality Adjusted Incident Population of AKI in Hospitalized Patients, Stage-specific Incident Population of AKI, and, Age-specific Incident Population of AKI in the 7MM covering the United States, EU4 (Germany, France, Italy, and Spain), and the United Kingdom, and Japan from 2019 to 2032.
The drug chapter segment of the AKI report encloses a detailed analysis of AKI emerging (Phase-III and Phase II and Phase I/II) pipeline drugs. It also helps to understand the AKI clinical trial details, expressive pharmacological action, agreements and collaborations, approval and patent details, advantages and disadvantages of each included drug, and the latest news and press releases.
RBT-1 by Renibus Therapeutics is an investigational drug that upregulates anti-inflammatory, antioxidant, and iron-scavenging pathways, activating a cytoprotective preconditioning response to reduce the risk of postoperative complications and improve patient outcomes following cardiothoracic surgery. The RBT-1-mediated pharmacologic preconditioning is thought to induce broad organ protection, thereby mitigating the risks of postoperative complications and improving both short- and long-term outcomes. In July 2023, Renibus Therapeutics announced that the US FDA granted Breakthrough Therapy Designation to RBT-1 for the reduction in risk of postoperative complications in patients undergoing cardiothoracic surgery and confirmed its alignment with the company's planned Phase III pivotal trial. In October 2023, Renibus Therapeutics announced that the first patient had been dosed in the pivotal Phase III PROTECT trial of RBT-1. Top-line results are expected in mid-2025. NDA filing is anticipated by early 2026.
Ocelot Bio's lead asset, OCE-205, is a therapeutic peptide with a differentiated mechanism of action that has the potential to improve outcomes for patients with complications of end-stage liver disease (ESLD). OCE-205's innovation emanates from its design as a mixed agonist-antagonist peptide selective for the vasopressin 1a (V1a) receptor with no vasopressin 2 (v2) receptor activity at drug concentrations well above those used in treating ESLD. In August 2022, Ocelot Bio announced that the US FDA granted ODD to OCE-205 for the treatment of hepatorenal syndrome. Ocelot Bio has completed the enrolment of patients in a Phase II clinical trial of OCE-205 in hepatorenal syndrome with acute kidney injury (HRS-AKI).
APX-115 is a potent small-molecule inhibitor of NADPH-oxidase (NOX) isozymes developed by AptaBio Therapeutics. The NADPH-oxidase (NOX) enzymes represent a family of seven membrane enzymes, which catalyze NADPH-dependent generation of superoxide and secondary reactive oxygen species (ROS), which can cause tissue damage and modification of cell function. The company is currently conducting a Phase II trial of APX-115 in patients with contrast-induced (CI)-AKI. In January 2023, the US FDA approved the Phase II clinical trial plan of APX-115 for CI-AKI. Patient recruitment began in October 2023. The trial is anticipated to be completed by the end of 2024.
Note: Detailed emerging therapies assessment will be provided in the final report.
Patients suffering from AKI are often prescribed diuretics, with loop diuretics being the most commonly recommended class of dialectics. Furosemide, which is a potent loop diuretic, is frequently used in different stages of AKI since it offers the possibility of eliminating large amounts of electrolytes and water as long as the kidneys are capable of filtration.
A robust pipeline with a novel mechanism of action and increasing incidence are major market drivers of the AKI market. Additionally, the AKI pipeline is also expected to change the current dynamics of the market, which presently comprises biologics and molecules with new mechanisms of action.
Currently, there are no targeted pharmacotherapies approved for the treatment of AKI. At present, the therapeutic market size of AKI is mainly dominated by the use of RRT and off-label drugs, which include various classes such as ACE inhibitors, ARBs, Diuretics, and NSAIDs.
Various comorbidities like cardiovascular disease, hypertension, diabetes mellitus, pre-existing CKD, renal recovery, and others increase the risk of AKI in these patients. As mentioned earlier, the current market of AKI is majorly dependent on RRT and conventional therapies like NSAIDs, ACE inhibitors, ARBs, diuretics, etc. However, this might change in the future, as there are various emerging therapies in the pipeline targeting AKI caused by comorbidities like sepsis, cardiac surgery, delayed graft function, and others. The pipeline of AKI possesses novel candidates targeting HRS-AKI, post cardiac surgery, and AKI due to sepsis are diversifying the treatment options that can reduce the current unmet need in AKI. The current emerging pipeline consists of key players including Renibus Therapeutics (RBT-1), Ocelot Bio (OCE-205), AM-Pharma (Ilofotase alfa), Guard Therapeutics (RMC-035), and others who are developing their products to address the patient population and reduce mortality rates in hospital settings. Overall, the AKI therapeutics market is further expected to increase in the forecast period (2023-2032).
This section focuses on the rate of uptake of the potential drugs expected to be launched in the market during the study period 2019-2032. The analysis covers AKI market uptake by drugs; patient uptake by therapies; and sales of each drug. For example- AM-Pharma's therapeutic candidate is a proprietary recombinant human Alkaline Phosphatase (Ilofotase alfa) constructed from two naturally occurring human isoforms of the AP enzyme.
The report provides insights into different therapeutic candidates in Phase III, Phase II, and Phase I/II stage. It also analyzes key players involved in developing targeted therapeutics.
The report covers detailed information on collaborations, acquisitions and mergers, licensing, and patent details for AKI emerging therapies.
To keep up with current market trends, we take KOLs and SMEs' opinions working in the domain through primary research to fill the data gaps and validate our secondary research. Some of the leaders like MD, Professor and Vice Chair Department of Critical Care Medicine and Director, Center for Critical Care Nephrology, PhD, and others. Their opinion helps to understand and validate current and emerging therapies and treatment patterns or AKI market trends. This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the market and the unmet needs.
DelveInsight's analysts connected with 30+ KOLs to gather insights; however, interviews were conducted with 10+ KOLs in the 7MM. Centers such as the Center for Kidney Diseases, Department of Rheumatology, Department of Nephrology, etc., were contacted. Their opinion helps understand and validate AKI epidemiology and market trends.
We perform Qualitative and market Intelligence analysis using various approaches, such as SWOT analysis and Analyst views. In the SWOT analysis, strengths, weaknesses, opportunities, and threats in terms of disease diagnosis, patient awareness, patient burden, competitive landscape, cost-effectiveness, and geographical accessibility of therapies are provided. These pointers are based on the Analyst's discretion and assessment of the patient burden, cost analysis, and existing and evolving treatment landscape.
The analyst analyzes multiple emerging therapies based on relevant attributes such as safety, efficacy, frequency of administration, route of administration, and order of entry.
In efficacy, the trial's primary and secondary outcome measures are evaluated.
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 January 2017, the Centers for Medicare and Medicaid Services published that end-stage renal disease (ESRD) facilities will be able to furnish dialysis services to AKI patients. The provision provides Medicare coverage and payment to both hospital-based and freestanding ESRD facilities for renal dialysis services furnished to beneficiaries with AKI. Medicare will pay ESRD facilities for dialysis treatment using the ESRD Prospective Payment System (PPS) base rate adjusted by the wage index. In addition to the dialysis treatment, the ESRD PPS base rate pays ESRD facilities for the items and services that are renal dialysis services, and there will be no separate payment for those services. Specifically, this includes renal dialysis drugs, biologicals, laboratory services, and supplies that are included in the ESRD PPS base rate when furnished by an ESRD facility to an individual with AKI.