PUBLISHER: DelveInsight | PRODUCT CODE: 1554598
PUBLISHER: DelveInsight | PRODUCT CODE: 1554598
DelveInsight's "NTM Infections - Market Insights, Epidemiology, and Market Forecast - 2034" report delivers an in-depth understanding of NTM Infections, historical and forecasted epidemiology, as well as the NTM Infections market trends in the United States.
The NTM Infections market report provides current treatment practices, emerging drugs, market share of individual therapies, and current and forecasted United States NTM Infections market size from 2020 to 2034. The report also covers NTM infection treatment practices/algorithms and unmet medical needs to curate the best opportunities and assess the market's potential.
NTM infections overview
Nontuberculous mycobacteria (NTM) infections refer to any diseases caused by bacteria belonging to the genus Mycobacterium, excluding those that cause tuberculosis (M. tuberculosis complex) or leprosy/Hansen's disease (M. leprae). According to the American Lung Association, Nontuberculous mycobacteria naturally inhabit soil, water, and dust worldwide. MAC is the predominant type of NTM bacteria in the US, causing the majority of NTM lung disease cases in the country.
There are two forms of NTM lung disease based on disease progression. Nodular bronchiectatic, which is a less progressive NTM disease, affects older women without a smoking history, causing airway inflammation and scarring, leading to recurrent respiratory infections like bronchitis and pneumonia. Cavitary NTM disease, which is more progressive and prevalent in smokers with existing lung conditions, results in lung tissue scarring, fibrosis, and cavity formation, potentially leading to respiratory failure.
Key Symptoms associated with NTM infection include chronic cough, fatigue, weight loss, night sweats, shortness of breath, coughing up blood or excessive mucus, fever, and recurrent respiratory infections. The main risk factors for NTM infection include pre-existing lung disease, quantitatively impaired ciliary function, heterozygosity for mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, breaches in skin or soft tissues, and immunodeficiency conditions.
NTM infections diagnosis
Diagnosing and treating NTM Infections is complex due to variability among NTM species and their clinical presentations, making reliance on symptoms or imaging alone insufficient for accurate diagnosis. Diagnosing NTM Infections involves a combination of medical history review, physical examination, imaging studies (such as chest X-rays or CT scans), and microbiological testing. Microbiological testing may include sputum cultures, bronchoscopy with bronchoalveolar lavage, or lung biopsy to identify the specific NTM species causing the infection.
Further details are provided in the report...
NTM infections treatment
The treatment of NTM infections remains a significant challenge. Current standard therapy for the most common NTM infection, MAC, involves a three-drug regimen taken for approximately 18 months. Effective treatment of NTM infections requires a holistic, patient-centered approach, with close monitoring for drug side effects and adherence. For rapid-growing NTM species like M. abscessus, intravenous antibiotics may be necessary initially.
In some cases, surgery may be recommended to remove localized areas of disease, such as in individuals with bronchiectasis, cavitary disease, or refractory hemoptysis.
Currently, ARIKAYCE is the first and only US FDA-approved medication for the treatment of MAC lung disease as part of a combination antibiotic regimen in adult patients who have limited or no alternative treatment options and is currently being studied in patients with non-refractory MAC infections. Other commonly used antibiotics include macrolides, ethambutol, rifamycins, aminoglycosides, fluoroquinolones, imipenem, and linezolid. However, these regimens are not optimal for efficient and sustained clearance of NTM infection.
As the market is derived using a patient-based forecast model, the NTM Infections epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by total prevalent cases of NTM infections, total diagnosed prevalent cases of NTM infection, gender-specific cases of NTM infections, species-specific cases of NTM infection, type-specific cases of NTM infections, and severity-specific cases of NTM infections in the United States from 2020 to 2034.
The drug chapter segment of the NTM Infections report encloses a detailed analysis of NTM Infections-marketed drugs and mid to late-stage (Phase III and Phase II) pipeline drugs. It also helps understand the NTM Infections 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.
Marketed Drugs
ARIKAYCE (amikacin liposome inhalation suspension): Insmed
ARIKAYCE is the first FDA-approved therapy indicated for the treatment of MAC lung disease as part of a combination antibacterial drug regimen for adult patients with limited or no alternative treatment options. ARIKAYCE is a novel, inhaled, once-daily formulation of amikacin, an established antibiotic historically administered intravenously and associated with severe toxicity to hearing, balance, and kidney function. Insmed's proprietary PULMOVANCE liposomal technology enables the delivery of amikacin directly to the lungs, where lung macrophages take it up, targeting the site of infection. This approach prolongs the release of amikacin in the lungs while limiting systemic exposure. ARIKAYCE is administered once daily using the Lamira Nebulizer System manufactured by PARI Pharma GmbH.
In January 2018, the US FDA approved ARIKAYCE, specifically indicated for the treatment of MAC lung disease in adult patients with limited treatment options.
The FDA has designated ARIKAYCE as an orphan drug and a QIDP for NTM lung disease. Insmed is also conducting a Phase III clinical trial of ARIKAYCE in adult patients with newly diagnosed NTM lung infections caused by MAC.
Emerging Drugs
Epetraborole: AN2 Therapeutics
Epetraborole (EBO), developed by AN2 Therapeutics, is a novel, once-daily, orally administered investigational treatment for patients with chronic NTM lung disease. Epetraborole is a boron-containing small molecule inhibitor of bacterial leucyl-tRNA synthetase, or LeuRS, an enzyme that catalyzes the attachment of leucine to transfer RNA, or tRNA, molecules, an essential step in protein synthesis. Epetraborole forms a complex with a tRNALEU molecule, trapping the terminal ribonucleotide of tRNALEU in the editing site of the enzyme, which prevents the synthetic site from attaching leucine to tRNALEU thus shutting down tRNA leucylation and leading to a block in protein synthesis.
Currently, the drug is in Phase II/III of clinical development for the treatment of patients with NTM lung disease.
AN2 Therapeutics intends to expand the indication targeted by epetraborole by pursuing development in other mycobacterial diseases, including treatment-naive MAC lung disease. AN2 Therapeutics also intends to conduct trials in which they plan to incorporate epetraborole as part of first-line combination treatment for treatment-naive patients with NTM lung disease and M. abscessus lung infections.
MNKD-101 (Clofazimine Inhalation Suspension): Mannkind Corporation
MNKD-101, a nebulized formulation of clofazimine, is being developed for the treatment of severe chronic and recurrent pulmonary infections, including NTM lung disease. An orally inhaled formulation of clofazimine is anticipated to offer several clinical advantages over the current solid oral dosage form of this drug. MNKD-101 has been designated as both an orphan drug and a qualified infectious disease product by the US FDA for the treatment of pulmonary NTM infections. Mannkind is also assessing the feasibility of developing a dry-powder formulation of clofazimine using Mannkind's technosphere formulation technology. MNKD-101 is designated with fast-track designation by the US FDA for the treatment of NTM lung infections.
Mannkind intends to commence a Phase III registration study of MNKD-101 in the US in the second quarter of 2024.
SPR720 (Fobrepodacin): Spero Therapeutics
SPR720, developed by Spero Therapeutics, is a broad-spectrum oral antibiotic designed to treat NTM pulmonary disease. SPR720 employs a novel mechanism and has no known cross-resistance with marketed antibiotics. SPR720 has demonstrated a broad spectrum of activity in preclinical studies against the most common organisms causing NTM infections, including M. avium complex, or MAC, M. kansasii, and M. abscessus. SPR720 is applicable to both nonrefractory and refractory patients.
In September 2020, SPR720 received FTD for the treatment of adult patients with NTM pulmonary disease.
In March 2020, the US FDA granted ODD for SPR720 for the treatment of NTM infections.
In February 2019, Spero Therapeutics was granted QIDP designation for SPR720 capsule for oral use for the treatment of lung infections caused by NTM.
SPR720 is designated with QIDP, fast-track, and orphan drug designation by the US FDA. Currently, the drug is in Phase II of clinical development for the treatment of NTM pulmonary disease.
Drug Class Insights
Current standard therapy for the most common NTM infection, MAC, involves a three-drug regimen taken for approximately 18 months. However, the rates of culture conversion with this approach are only 45-70%, and relapse or reinfection rates can be as high as 60%. Effective treatment of NTM infections requires a holistic, patient-centered approach, with close monitoring for drug side effects and adherence.
Commonly used antibiotics for the treatment of NTM infections include macrolides, ethambutol, rifamycins, aminoglycosides, fluoroquinolones, imipenem, and linezolid. However, these regimens are not optimal for efficient and sustained clearance of NTM infection. Therefore, the treatment of NTM infections relies on repurposed and combination antibiotic regimens, as there is a lack of novel drugs approved for these mycobacterial diseases, highlighting the urgent need for new therapeutic options.
Continued in report...
Treatment for NTM infections is challenging and requires prolonged, multidrug regimens that are often tailored to the specific NTM species and the site of infection. The management of these infections is complicated by the intrinsic resistance of many NTM species to standard antibiotics, necessitating the use of specialized and often costly medications. Consequently, NTM infections represent a significant and growing market within the pharmaceutical and healthcare industries, with ongoing research efforts focused on developing more effective diagnostic tools and novel therapeutics to improve patient outcomes.
Antibiotics: Doctors often use a combination of antibiotics "off-label," meaning they are approved for other conditions but demonstrate effectiveness against specific NTM strains. Common antibiotics used include macrolides (azithromycin, clarithromycin), rifamycins (rifampin, rifabutin), fluoroquinolones (ciprofloxacin), aminoglycosides (amikacin, streptomycin), and ethambutol.
The treatment of NTM infections is intricate and highly dependent on the specific NTM species, infection site, and patient health status. For pulmonary NTM disease, the regimen varies: MAC typically requires a combination of macrolides (such as clarithromycin or azithromycin), rifamycins (rifampin or rifabutin), and ethambutol, often for at least 12 months post-culture conversion. Mycobacterium kansasii infections are treated with rifampin, isoniazid (with pyridoxine), and ethambutol for a similar duration. More resistant species like M. abscessus necessitate an intensive initial phase using intravenous amikacin and imipenem or cefoxitin, followed by a continuation phase with oral macrolides and possibly inhaled amikacin, often extending treatment over several months to years. For skin and soft tissue infections, especially those caused by rapidly growing mycobacteria (RGM) like M. abscessus and M. fortuitum, treatment is guided by susceptibility testing and may include combinations of clarithromycin, amikacin, cefoxitin, and imipenem, alongside necessary surgical interventions.
ARIKAYCE (amikacin liposome inhalation suspension) stands as the only FDA-approved drug specifically targeting NTM infections. However, its approval is limited to the treatment of refractory MAC lung infections in adults. This means it is only used for patients whose NTM infection has not responded to conventional treatment.
Key players including AN2 Therapeutics, Mannkind Corporation, and Spero Therapeutics, among others are evaluating their lead candidates in different stages of clinical development. They aim to investigate their products to treat NTM Infections.
This section focuses on the uptake rate of potential drugs expected to be launched in the market during 2020-2034. For example, Epetraborole is expected to enter the US market by 2026 and is projected to have a medium uptake during the forecast period.
Further detailed analysis of emerging therapies drug uptake in the report...
NTM Infections Pipeline Development Activities
The report provides insights into different therapeutic candidates in Phase III, Phase II, and Phase I. 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 emerging therapies for NTM Infections.
KOL Views
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. Industry Experts contacted for insights on NTM infections evolving treatment landscape, patient reliance on conventional therapies, patient therapy switching acceptability, and drug uptake, along with challenges related to accessibility, including Medical/scientific writers, Medical Professionals, Professors, Directors, and Others.
DelveInsight's analysts connected with 30+ KOLs to gather insights; however, interviews were conducted with 15+ KOLs in the US. Centers like Regis University, Oregon Health & Science University, Massachusetts General Hospital, Medical University of South Carolina, and Washington University School of Medicine, among others were contacted. Their opinion helps understand and validate current and emerging therapy treatment patterns or NTM Infections market trends. This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the market and the unmet needs.
Physician's View
According to our primary research analysis, NTM infections are becoming increasingly prevalent, particularly among individuals aged 65 and above in the United States, underscoring the urgent need for expanded research and improved clinical strategies to effectively address and mitigate the impact of these infections in this vulnerable demographic. Managing NTM lung disease generally necessitates a complex regimen of multiple antibiotics, customized according to the specific NTM species and drug susceptibility test results. Despite these measures, achieving successful treatment outcomes remains challenging, often requiring prolonged therapy that carries a significant risk of toxicity. This highlights the critical importance of developing novel therapeutic approaches and enhancing our understanding of NTM infections to improve patient outcomes and quality of life for older adults.
The current pipeline includes promising therapies such as AN2 therapeutics' Epetraborole, Mannkind's MNKD-101, and Spero Therapeutics' SPR720, among others. The entry of these drugs will provide various options tailored to patient-specific needs based on the severity and type of the condition.
Qualitative Analysis
We perform Qualitative and market Intelligence analysis using various approaches, such as SWOT and Conjoint Analysis. 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.
Conjoint Analysis analyzes multiple 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.
To analyze the effectiveness of these therapies, have calculated their attributed analysis by giving them scores based on their ability to improve atrial and ventricular dimension/function and ability to regulate heart rate.
Further, the therapies' safety is evaluated wherein the adverse events are majorly observed, and it sets a clear understanding of the side effects posed by the drug in the trials, which directly affects the safety of the molecule in the upcoming trials. 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 route of administration, order of entry and designation, 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 current treatment regime for NTM Infections in the US has high costs of treatment that affect the affordability and access of drugs to patients. Several organizations in the US are working to provide support to NTM Infections patients and spread awareness, including the ARIKAYCE copay savings program.
Arikayce Copay savings program
Insurance covers ARIKAYCE for most people; savings and financial support resources are also available for eligible patients.
For people with commercial or private insurance
Patients may be eligible for a copay as low as USD 0 for ARIKAYCE. If patients have commercial or private insurance, they may be able to save on out-of-pocket costs with the ARIKAYCE copay savings program.
For people with government insurance
Extra Help is designed to help people who are on Medicare with a limited income. The program provides a range of financial assistance for prescription drug costs. Benefits may include:
Further details will be provided in the report.
The report provides detailed insights on the country-wise accessibility and reimbursement scenarios, cost-effectiveness scenarios, programs making accessibility easier and out-of-pocket costs more affordable, insights on patients insured under federal or state government prescription drug programs, etc.
NTM Infections report insights
NTM Infections report key strengths
NTM Infections report assessment
Market Insights
Epidemiology Insights
Current Treatment Scenario, Marketed Drugs, and Emerging Therapies