PUBLISHER: DelveInsight | PRODUCT CODE: 1553390
PUBLISHER: DelveInsight | PRODUCT CODE: 1553390
DelveInsight's "Peripheral Neuropathic Pain (PNP) - Market Insights, Epidemiology, and Market Forecast - 2034" report delivers an in-depth understanding of Peripheral Neuropathic Pain (PNP), historical and forecasted epidemiology as well as the Peripheral Neuropathic Pain (PNP) market trends in the United States, EU4 (Germany, Spain, Italy, and France) and the United Kingdom, and Japan.
Peripheral Neuropathic Pain (PNP) market report provides real-world prescription pattern analysis, emerging drugs, market share of individual therapies, and historical and forecasted 7MM Peripheral Neuropathic Pain (PNP) market size from 2020 to 2034. The report also covers current Peripheral Neuropathic Pain (PNP) treatment practices/algorithms and unmet medical needs to curate the best opportunities and assess the market's underlying potential.
The United States
EU4 (Germany, France, Italy, and Spain) and the United Kingdom
Japan
Peripheral Neuropathic Pain (PNP) Overview, Country-Specific Treatment Guidelines, and Diagnosis
Peripheral neuropathies encompass disorders of peripheral nerve cells and fibers, manifesting secondary to a wide range of pathologies. These nerves include cranial nerves, spinal nerve roots and ganglia, nerve trunks and division, and autonomic nervous system nerves. Several methods are used to classify peripheral neuropathies, including mono-neuropathies, multifocal neuropathies, and polyneuropathies. Some forms of neuropathy involve damage to only one nerve (mononeuropathy). Neuropathy affecting two or more nerves in different areas is called multiple mononeuropathy or mononeuropathy multiplex. Many or most of the nerves are often affected (polyneuropathy).
The variability of symptoms allows distinguishing characteristic clinical phenotypes of peripheral neuropathy that should be recognized in order to stratify the diagnostic workup accordingly. Nerve conduction studies are essential to determine the phenotype (axonal versus demyelinating) and severity. Laboratory tests, including genetic testing, CSF examination, nerve imaging, and nerve biopsy, represent additional clinical tests that can be useful in specific clinical scenarios.
Further details related to country-based variations in diagnosis are provided in the report
Peripheral Neuropathic Pain (PNP) Treatment
Medications such as NSAIDs can relieve mild peripheral neuropathy symptoms, while anti-seizure drugs like gabapentin and pregabalin, as well as topical treatments like lidocaine, can reduce nerve pain. Antidepressants like amitriptyline, nortriptyline, duloxetine, venlafaxine, and desvenlafaxine may also provide relief despite potential side effects. Therapies like scrambler therapy, spinal cord stimulation, plasma exchange, steroids, IV immune globulin, and physical therapy can also help manage symptoms. Surgery may be necessary for neuropathies caused by nerve pressure from tumors.
The Peripheral Neuropathic Pain (PNP) epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented in the 7MM covering the United States, EU4 countries (Germany, France, Italy, and Spain), the United Kingdom, and Japan from 2024 to 2034. The Peripheral Neuropathic Pain (PNP) epidemiology is segmented with detailed insights into Total Cases, Type-specific Cases, and Treated Cases of Peripheral Neuropathic Pain (PNP).
Peripheral Neuropathic Pain (PNP) Drug Chapter
The drug chapter segment of the Peripheral Neuropathic Pain (PNP) report encloses a detailed analysis of Peripheral Neuropathic Pain (PNP) marketed drugs and late-stage (Phase III and Phase II) pipeline drugs. It also deep dives into the Peripheral Neuropathic Pain (PNP) pivotal clinical trial details, recent and expected market approvals, patent details, the latest news, and recent deals and collaborations.
Marketed Drugs
QUTENZA (capsaicin): Grunenthal and Averitas Pharma
QUTENZA (capsaicin) 8% topical system, a non-systemic, non-opioid pain relief delivered in the form of a patch, indicated for treating neuropathic pain associated with postherpetic neuralgia or associated with diabetic peripheral neuropathy (DPN) of the feet in adults. Capsaicin is an agonist for the transient receptor potential vanilloid 1 receptor (TRPV1), an ion channel-receptor complex expressed on nociceptive nerve fibers in the skin. QUTENZA is marketed and distributed by Averitas. Currently, it is being evaluated under a Phase III trial in post-surgical neuropathic pain. The trial is expected to be completed by October 2024, with an estimated enrollment of 408 participants.
In November 2018, Grunenthal extended its commercial footprint to the US, acquiring Averitas Pharma. Averitas Pharma will commercialize the pain patch QUTENZA for Grunenthal in the US. Grunenthal had recently acquired the remaining global rights from Acorda Therapeutics.
ZTLIDO (lidocaine): Scilex Pharmaceuticals
ZTLIDO is a topical lidocaine system (1.8%) approved for relieving pain associated with postherpetic neuralgia. ZTLIDO is designed as a lighter, thinner product with improved adhesion relative to LIDODERM (lidocaine patch 5%) while providing a bioequivalent delivery of lidocaine in an efficient drug delivery system. Lidocaine is a local amide anesthetic; it blocks sodium ion channels required for initiating and conducting neuronal impulses.
Patients are advised to apply ZTLIDO to intact skin to cover the most painful area and to apply the prescribed number of topical systems (maximum of three) only once for up to 12 h within 24 h (12 h on and 12 h off). Smaller areas of treatment are recommended in patients who are debilitated or have impaired elimination. Achieve this by cutting ZTLIDO with scissors into a smaller size before removing the release liner.
Emerging Drugs
SEMDEXA (SP-102): Scilex Holding Company
SP-102 is a preservative-free, surfactant-free, and particulate-free, novel epidural steroid injection (ESI) formulation of 10 mg dexamethasone sodium phosphate in a viscous gel solution for subacute lumbosacral radicular pain (Sciatica). Its extended local effect provides durable pain relief and significant improvement in functioning from a single injection with rapid onset.
Recently, the company has completed a pivotal Phase III (NCT03372161) Corticosteroid Lumbar Epidural Analgesia ("CLEAR") trial, which was designed to evaluate the safety and efficacy of SP-102 in Lumbosacral Radiculopathy ( or Sciatica).
In November 2023, Scilex Holding Company announced a positive Type C meeting with the US FDA. The company has reached an agreement with the FDA on the path forward to advance the clinical development of SP-102 and on the requirements to file a New Drug Application.
Adezunap (AP707): Apurano Pharmaceuticals
Apurano Pharmaceuticals' investigational drug AP707, featuring the THC-focused active ingredient adezunap, has received EMA approval for DISCOVER approval studies. Utilizing the patented PuranoTec manufacturing process, cannabis flower undergoes processing to create an aqueous nanodispersion of cannabinoids, primarily ?-9-THC. Administered as a sublingual mouth spray, this dispersion allows for rapid and efficient absorption through the oral mucosa, facilitated by a water-soluble shell termed the smart coating. These SmartLipids, encapsulating lipophilic cannabinoids, remain stable in aqueous environments and can directly enter the bloodstream due to their small particle size (<250 nm).
Currently, two Phase III clinical trials, NCT06072573 and NCT06071975, to evaluate the efficacy and tolerability of AP707 in patients with chronic pain due to diabetic polyneuropathy are recruiting participants. Additionally, two other Phase III trials, NCT06071936 and NCT06071988, are recruiting participants to evaluate the efficacy and tolerability of AP707 in patients with chronic pain due to traumatic or post-operative peripheral neuropathy.
Adezunap is expected to have a low uptake in the 7MM due to legal hurdles, public stigma, business constraints from being labeled high-risk, and quality control issues related to cannabidiol in emerging markets. These challenges hinder its market acceptance and manufacturing quality.
Among EU4 and the UK, the highest revenue was generated by NSAIDs, ~USD 600 million in 2023.
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...
Peripheral Neuropathic Pain (PNP) 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 Peripheral Neuropathic Pain (PNP) 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 40+ KOLs to gather insights; however, interviews were conducted with 25+ KOLs in the 7MM. Centers such as Keck Hospital of USC, Harvard Medical School, Robert Koch Institute, Rouen University Hospital, University Hospital Munster, etc., were contacted. Their opinion helps understand and validate current and emerging treatment patterns of Peripheral Neuropathic Pain (PNP). 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; for instance, Change in Average Daily Pain Score (ADPS), one of the most important primary outcome measures Change in API on 11-point Numerical Rating Scale (NRS) and ADPS.
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.