PUBLISHER: DelveInsight | PRODUCT CODE: 1553385
PUBLISHER: DelveInsight | PRODUCT CODE: 1553385
Report Summary
Postherpetic Neuralgia Overview
Postherpetic neuralgia is a common complication of shingles caused by varicella-zoster virus (VZV) reactivation, which resides latently in the body after a primary varicella infection. The shingles outbreak causes damage to the sensory nerves, which leads to abnormal signals being sent to the brain, resulting in pain. Postherpetic neuralgia is a neuropathic pain syndrome characterized by pain that persists for more than 90 days after the outbreak of herpes zoster. Common symptoms experienced by patients with postherpetic neuralgia include burning, stabbing, shooting, aching, throbbing, itching, or electric shocks on the affected area. Risk factors for postherpetic neuralgia are increasing age and immunosuppression. People who have acute pain and severe rash during shingles also have a higher risk of developing postherpetic neuralgia.
Postherpetic Neuralgia Diagnosis
The diagnosis of postherpetic neuralgia is clinical. A history of herpes zoster and the nature of the pain are critical parameters of a postherpetic neuralgia diagnosis. Thus, obtaining a detailed medical history, including symptoms and vaccination history, is very important. Pain intensity and quality should be assessed using an appropriate pain scale based on the patient's ability to communicate - a numerical rating scale (usually an 11-point scale: from 0, no pain, to 10, severe pain), a visual analog scale, or verbal descriptor scale (e.g., McGill Pain Questionnaire). Postherpetic neuralgia diagnosis does not rely on laboratory evaluations. However, laboratory tests and some targeted imaging may provide a degree of utility. Viral culture or immunofluorescent staining may be used to distinguish herpes simplex from herpes zoster.
Postherpetic Neuralgia Treatment
The treatment of postherpetic neuralgia should be directed at pain control and minimizing treatment-related adverse events. Pain relief is challenging and should include drugs, interventionist procedures, and non-pharmacological adjuvant therapy. Guidelines recommend treatment of postherpetic neuralgia with calcium channel a2-d ligands (gabapentin and pregabalin), tricyclic antidepressants (amitriptyline, nortriptyline, or desipramine), or topical lidocaine patches as first-line drugs; opioids and topical capsaicin patch or cream as second-line treatment options or combination therapies with different mechanisms of action. Some patients with postherpetic neuralgia may have persistent pain despite pharmacological, topical, psychological, and physical therapies. Paravertebral and sympathetic nerve blocks may manage these cases of refractory postherpetic neuralgia.
Further details related to diagnosis and treatment are provided in the report...
As the market is derived using a patient-based model, the postherpetic neuralgia epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by total incident cases of herpes zoster, total incident cases of PHN, gender-specific cases of PHN, age-specific cases of PHN, and total treated cases of PHN in the 7MM covering the United States, EU4 (Germany, France, Italy, and Spain), the United Kingdom, and Japan from 2020 to 2034.
The drug chapter segment of the postherpetic neuralgia report encloses a detailed analysis of postherpetic neuralgia marketed drugs and emerging pipeline drugs. It also helps understand the postherpetic neuralgia pivotal clinical trial details, recent and expected market approvals, patent details, each drug's advantages and disadvantages, the latest news, and recent deals and collaborations.
Marketed Drug
ZTLIDO (topical lidocaine system): 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. The drug received FDA approval in February 2018 for relieving pain associated with postherpetic neuralgia.
TARLIGE (mirogabalin besilate): Daiichi Sankyo
TARLIGE is an analgesic proprietarily discovered by Daiichi Sankyo that works by inhibiting the excessive release of pain-related neurotransmitters in the presynaptic nerve terminal. Mirogabalin exerts an analgesic effect by suppressing calcium current through binding to the a2d subunit, which plays an auxiliary role in the function of voltage-gated calcium channels in the nervous system. Generally, for adults, the initial dose of mirogabalin is 5 mg orally twice daily, and then the dose is gradually increased by 5 mg at intervals of 1 week or longer to 15 mg orally twice daily. The drug was approved for marketing in Japan in January 2019 based on the results of Phase III clinical trials conducted in Asia, including Japan, in patients with diabetic peripheral neuropathic pain (DPNP) and postherpetic neuralgia for peripheral neuropathic pain (PNP).
Emerging Drug
LX9211: Lexicon Pharmaceuticals
LX9211 is a potent, orally delivered, selective small molecule inhibitor of adaptor-associated kinase 1 (AAK1). It was discovered using Lexicon's unique approach to gene science. Preclinical studies of LX9211 demonstrated that mice lacking AAK1 exhibited increased resistance to induced neuropathic pain. LX9211 was identified in a neuroscience drug discovery alliance with Bristol-Myers Squibb, from which Lexicon holds exclusive development and commercialization rights.
The company has completed a Phase II clinical trial (NCT04662281; RELIEF-PHN1) of LX9211 in adults associated with postherpetic neuralgia and has shown clear evidence of an effect. Topline results were announced in December 2022.
IncobotulinumtoxinA (NT 201): Merz Therapeutics
IncobotulinumtoxinA, marketed as XEOMIN, is approved in over 75 countries worldwide to treat patients with upper and lower limb spasticity, cervical dystonia, blepharospasm, glabellar lines, and sialorrhea. The drug effectively treats peripheral cholinergic nerve endings by weakening the contraction of voluntary muscles. It also relieves muscle tone by inhibiting the release of a neurotransmitter called acetylcholine. It is free from complex proteins and has a low risk of neutralizing antibody formation.
Currently, the company is conducting a Phase II (NCT06091020) PaiNT trial to investigate the efficacy and safety of subcutaneous NT 201 injections compared with placebo injections in decreasing pain intensity in adults with moderate to severe chronic peripheral neuropathic pain due to postherpetic neuralgia or peripheral nerve injury.
Drug Class Insights
FDA-approved treatments for postherpetic neuralgia (PHN) include analgesics, anticonvulsants, and topical solutions. Antiiconvulsants such as Gabapentin, Pregabalin are commonly used to treat neuropathic pain that work by stabilizing electrical activity in the nerves and reducing abnormal signalling. Tricyclic Antidepressants like Amitriptyline, Nortriptyline modulate pain signals in the central nervous system. Opioids (e.g., oxycodone, morphine), strong pain relievers may be prescribed for severe postherpetic neuralgia pain. However, due to the risk of dependence and other side effects, they are typically used cautiously and for short durations. Topical therapies, such as the lidocaine patch or the capsaicin patch, can reduce pain in PHN without significant systemic effects, a characteristic that may be beneficial in the elderly population. The lidocaine medicated plaster represents a simple and safe therapy that can be used since the onset of the first PHN symptoms.
Postherpetic neuralgia is associated with significant loss of function and reduced quality of life, particularly in the elderly, and is highly resistant to treatment. Since postherpetic neuralgia is often resistant to pharmacologic treatments, a multimodal analgesic treatment strategy is often used to balance the efficacy and tolerability of the medication regimen, the side effects of which can be limiting and compromise the quality of life and patient compliance. Postherpetic neuralgia has no cure, and patients rely on palliative treatments to reduce pain duration and severity. The market for postherpetic neuralgia treatments has undergone significant changes in recent years, driven by advances in the understanding of neuropathic pain and the development of new treatment options. Previously, the treatment options were limited and were based mainly on oral medications such as NSAIDs, opioids, tricyclic antidepressants, and anticonvulsants. These medications had limited efficacy in treating postherpetic neuralgia and were associated with significant side effects. In recent years, there has been a shift toward using topical medications to treat postherpetic neuralgia. Current treatment of postherpetic neuralgia most often consists of oral gabapentin and prescription lidocaine patches (first-line), and refractory cases may be prescribed opioids to address persistent pain.
The first-line use of opioids in treating neuropathic pain (including postherpetic neuralgia) remains controversial. The CDC in the United States advises healthcare professionals to limit opioid prescriptions strictly to cancer-related conditions and a select few other severe health issues. Regarding topical lidocaine therapy for postherpetic neuralgia, a patch version has been approved in the United States, Europe, and Australia, and its use is recommended in the treatment guidelines of the International Association for the Study of Pain. ZTlido, a proprietary 1.8% lidocaine topical system developed by Scilex Holding, gained FDA approval in 2018. In Japan, topical lidocaine therapy for postherpetic neuralgia has not been approved, but lidocaine topical preparations containing gels are being prepared as in-hospital preparations for postherpetic neuralgia.
The market is expected to change in the coming years, driven by the increasing incidence of shingles and the aging population. One of the major trends in the market is the increasing use of non-opioid pain medications. The emerging pipeline for postherpetic neuralgia in the 7MM is relatively limited, focusing on drugs being approved for neuropathic pain based on clinical trials involving postherpetic neuralgia and diabetic peripheral neuropathic pain.
Detailed market assessment will be provided in the final report
Key Findings
As per DelveInsight's estimates, the potential drugs that can mark a significant change in the forecast period include ZTLIDO (lidocaine topical system), TARLIGE (mirogabalin besilate), LX9211, and others.
This section focuses on the uptake rate of potential drugs expected to be launched in the market during 2020-2034. A fast acceptance can be seen with ZTlido, being designed as a lighter, thinner product with superior adhesion relative to LIDODERM (lidocaine patch 5%) while providing a bioequivalent delivery of lidocaine in an efficient drug delivery system. The product lowers doses while raising efficacy with expected increase in sales in the coming years.
Further detailed analysis of therapies drug uptake will be provided in the final report ...
Postherpetic Neuralgia Pipeline Development Activities
The report provides insights into different therapeutic candidates in Phase III and Phase II. 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 postherpetic neuralgia emerging therapy.
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 postherpetic neuralgia evolving treatment landscape, patient reliance on conventional therapies, patient's therapy switching acceptability, and drug uptake, along with challenges related to accessibility, include Medical/scientific writers; Neurologist; Dermatologists; and Professors; MD, FACS, Chair of the Department of The Pain Relief Foundation, Universities, and others.
Delveinsight's analysts connected with 30+ KOLs to gather insights; however, interviews were conducted with 10+ KOLs in the 7MM. Centers such as the Pain Relief Foundation, Nihon University School of Medicine, the Royal Marsden Hospital, Keck Hospital of USC, etc. were contacted. Their opinion helps understand and validate current and emerging therapy treatment patterns or postherpetic neuralgia market trends. 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 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.
Market Access and Reimbursement
Reimbursement is a crucial factor affecting the drug's market access. Often, the decision to reimburse comes down to the price of the drug relative to the benefit it produces in treated patients. To reduce the healthcare burden of these high-cost therapies, payers and other industry insiders are considering many payment models. Currently, ZTlido is covered for more than 200 million lives in the United States, with ongoing efforts to expand coverage. As of January 2023, the company has successfully secured coverage for ZTlido with major entities such as CVS Caremark/Aetna Commercial, Cigna HealthCare (commercial and Medicare plans), Express Scripts (commercial and most Medicare plans), United Healthcare Commercial, Optum Rx Select Commercial, Anthem BCBS, BCBS Louisiana and Kansas, Lifetime/Excellus BCBS, MedImpact, CareFirst, Elixir Commercial, and Medicaid in California, Florida, Idaho, and North Dakota.
The report further provides detailed insights on the country-wise accessibility and reimbursement scenarios, cost-effectiveness scenario of approved 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.