PUBLISHER: DelveInsight | PRODUCT CODE: 1886142
PUBLISHER: DelveInsight | PRODUCT CODE: 1886142
DelveInsight's "Hypoactive Sexual Desire Disorder (HSDD) - Market Insight, Epidemiology, and Market Forecast - 2034" report delivers an in-depth understanding of HSDD, historical and forecasted epidemiology as well as the HSDD market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.
The HSDD market report provides current treatment practices, emerging drugs, HSDD share of individual therapies, and current and forecasted HSDD market size from 2020 to 2034, segmented by seven major markets. The report also covers current HSDD treatment practices/algorithms and unmet medical needs to curate the best of the opportunities and assess the underlying potential of the market.
Study Period: 2020-2034
Hypoactive Sexual Desire Disorder (HSDD) Overview
Hypoactive sexual desire disorder is defined in the DSM-IV-TR as a persistent or recurrent absence of sexual fantasies and desire for sexual activity, which causes marked personal distress or interpersonal difficulties. Women can benefit from behavioral and pharmacological interventions. The first barrier to providing this benefit is detection and diagnosis of the disorder. However, the private and personal nature of sexual activity and the potential for feelings of shame, inadequacy, and embarrassment create unique challenges to effective communication about sexual health for both patient and physician. These barriers, combined with lack of awareness of the prevalence and opportunity to treat HSDD on the part of both patient and clinician, are among those responsible for current underdetection and undertreatment. Symptoms of HSDD include decreased spontaneous sexual thoughts or fantasies, decreased responsiveness to stimulation, inability to maintain interest through sex, and loss of desire to initiate sex. Women with HSDD may also avoid situations that could lead to sexual activity.
Hypoactive Sexual Desire Disorder (HSDD) Diagnosis
Hypoactive Sexual Desire Disorder is diagnosed based on a persistent or recurrent lack of sexual desire or thoughts that causes significant distress to the individual and lasts for at least six months. The diagnosis requires ruling out other causes such as medical conditions, medication side effects, psychiatric disorders, or relationship issues. In women, HSDD is now classified under Female Sexual Interest/Arousal Disorder (FSIAD) in the DSM-5, though the term HSDD is still widely used, especially in clinical trials. A detailed sexual and psychosocial history is essential, often supported by validated screening tools such as the Decreased Sexual Desire Screener (DSDS) or the Female Sexual Function Index (FSFI). Clinicians must also assess hormonal status, mental health, and interpersonal factors to determine whether the condition is lifelong or acquired, generalized or situational. Proper diagnosis involves distinguishing HSDD from normal fluctuations in desire and from desire changes secondary to other disorders, ensuring the condition is not better explained by other factors.
Hypoactive Sexual Desire Disorder (HSDD) Treatment
The treatment of Hypoactive Sexual Desire Disorder involves a personalized, multidisciplinary approach that addresses biological, psychological, and relational factors. First-line treatment often includes psychosexual therapy or counseling, particularly when relationship issues, past trauma, or psychological conditions like depression or anxiety contribute to the disorder. Cognitive-behavioral therapy (CBT) and mindfulness-based interventions have also shown benefit in improving sexual desire and reducing distress. Hormonal therapies, such as testosterone supplementation, may be considered off-label in postmenopausal women, though long-term safety and efficacy data are still being evaluated. Treatment plans often combine behavioral strategies, education, and pharmacologic options when appropriate. Lifestyle modifications, such as stress management, regular exercise, and improved sleep, can also support overall sexual health. The choice of therapy depends on individual needs, the underlying cause of HSDD, and whether the patient is pre- or postmenopausal. Regular follow-up is essential to monitor progress and adjust treatment accordingly.
The HSDD epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by the total prevalent cases of HSDD, gender-specific cases of HSDD, age-specific cases of HSDD, and total treated cases of HSDD in the 7MM market covering the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan from 2020 to 2034.
The drug chapter segment of the HSDD report encloses a detailed analysis HSDD marketed and emerging pipeline drugs. It also deep dives into HSDD's pivotal clinical trial details, recent and expected market approvals, patent details, the latest news, and recent deals and collaborations.
Currently, ADDYI (Sprout Pharmaceuticals) and VYLEESI (Cosette Pharmaceuticals) are the only two FDA-approved medications for treating HSDD. key company for their respective drug candidate include Freya Pharma Solutions (Lybrido), among others. The drug chapter also helps understand the HSDD clinical trial details, expressive pharmacological action, agreements and collaborations, approval, and patent details, and the latest news and press releases.
Marketed Drugs
ADDYI (flibanserin): Sprout Pharmaceuticals
ADDYI is a non-hormonal pill for acquired, generalized HSDD for premenopausal women. Flibanserin selectively targets central serotonin postsynaptic receptors, exhibiting both agonistic and antagonistic effects on 5-HT1A and 5-HT2A, respectively.
The US Food and Drug Administration (FDA) has warned Sprout Pharmaceuticals for the second time concerning its promotion of its HSDD drug ADDYI. The agency also sent a warning letter to a company for conducting a clinical investigation without submitting an investigational new drug application (IND).
VYLEESI (bremelanotide injection): Cosette Pharmaceuticals
VYLEESI is a melanocortin receptor agonist indicated for the treatment of premenopausal women with acquired, generalized HSDD as characterized by low sexual desire that causes marked distress or interpersonal difficulty.
In January 2024, Cosette Pharmaceuticals has completed the acquisition of VYLEESI from Palatin Technologies, which includes 5 Orange Book listed patents with protection up to 2041. Palatin and Cosette will ensure continued patient and healthcare professional access to VYLEESI throughout the transition period.
Emerging Drugs
Lybrido: Freya Pharma Solutions
Lybrido focuses on treatment for patients with HSDD, in which low sexual desire results from a central nervous system that is relatively insensitive to sexual cues. In these individuals, exposure to sexual stimuli (internal or external) fails to trigger activation of the brain's sexual excitatory mechanisms. Lybrido contains sildenafil (a phosphodiesterase type 5 inhibitor) with a time-release coating and an outer testosterone shell. A Phase III trial for Lybrido is currently in preparation.
Drug Class Insight
Melanocortin receptor agonist
Melanocortin receptor agonists are a class of drugs that activate melanocortin receptors, particularly the melanocortin-4 receptor (MC4R), which plays a key role in regulating sexual desire through central nervous system pathways. These agents stimulate MC4R in the hypothalamus, enhancing dopaminergic signaling and promoting sexual motivation and arousal. Unlike hormonal treatments, melanocortin agonists act directly on neural circuits involved in sexual behavior, offering a non-hormonal therapeutic approach. The most notable example is bremelanotide (Vyleesi), the first FDA-approved melanocortin receptor agonist for the treatment of acquired, generalized HSDD in premenopausal women. Melanocortin receptor agonists offer a unique, on-demand option for women seeking non-daily, non-hormonal treatment for HSDD, especially those for whom traditional hormone-based therapies are unsuitable.
Serotonin receptor
Serotonin-containing cell bodies are found in the raphe nucleus in the brainstem and in nerve endings distributed diffusely throughout the brain (Julius, 1991). Serotonin has been implicated in sleep, modulation of circadian rhythms, eating, and arousal. Serotonin also has hormone-like effects when released in the bloodstream, regulating smooth muscle contraction and affecting the platelet aggregating and immune systems.
Serotonin receptors are classified into four subtypes: 5-HT1 to 5-HT4, with a further subdivision of the 5-HT1 subtypes. Recall that the 5-HT3 receptor is ionotropic. The other 5-HT receptors exhibit the typical seven transmembrane-spanning segments, and all couple to G proteins to exert their effects. For example, 5-HT1a, 5-HT1b, 5HT1d, and 5HT4 either activate or inhibit adenylyl cyclase. 5-HT1c and 5-HT2 receptors preferentially stimulate activation of phospholipase C to produce increased intracellular levels of diacylglycerol and inositol 1,4,5-trisphosphate.
The therapeutic landscape for HSDD still relies chiefly on behavioral interventions and a pair of centrally acting agents-flibanserin (a daily 5-HT1A agonist/5-HT2A antagonist) and bremelanotide (melanocortin-4 receptor agonist)-both approved only for pre-menopausal women. Although these drugs can improve desire, their modest efficacy, required lifestyle adjustments (night-time dosing for flibanserin; injections for bremelanotide) and notable adverse-effect profiles mean that many patients discontinue or never start pharmacologic therapy. Hormonal approaches (e.g., off-label transdermal testosterone or intranasal oxytocin) offer alternatives for post-menopausal women, yet long-term safety and regulatory acceptance remain unsettled, underscoring the need for newer, more durable solutions.
Encouragingly, pipeline activity is shifting toward multimodal, precision treatments that address both neurochemical imbalance and inhibitory pathways underlying low desire. Late-stage candidates include Lybrido. Three Phase II studies (two for Lybridos and one for Lybrido) have been conducted by company at 16 research sites in the United States. The efficacy and safety of various doses of testosterone, sildenafil, buspirone and combination therapies (testosterone + sildenafil, testosterone + buspirone) were tested in 497 women with HSDD to determine the change in satisfying sexual events (SSEs) over a period of eight weeks.
Despite the advances, only two medications have regulatory approval, and none yet address post-menopausal or male HSDD comprehensively. As awareness for HSDD is growing and as its psychological and relational impact becomes clearer, continued investment in mechanistically targeted trials is essential to deliver safer, more effective, and more inclusive treatments for the millions of individuals affected by HSDD.
This section focuses on the uptake rate of potential drugs expected to be launched in the market during 2025-2034. The landscape of HSDD treatment has experienced a profound transformation with the uptake of novel medicines. These innovative therapies are redefining standards of care.
Hypoactive Sexual Desire Disorder (HSDD) Pipeline Development Activities
The report provides insights into different therapeutic candidates in Phase III, and Phase II stage. It also analyzes key players involved in developing targeted therapeutics.
Pipeline Development Activities
The report covers detailed information on collaborations, acquisitions and mergers, licensing, and patent details for HSDD emerging therapies.
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. Some of the leaders like MD, Professor and Vice Chair of the Department of Rheumatology and Director, PhD, and others. Their opinion helps to understand and validate current and emerging therapies and treatment patterns or HSDD 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 15+ KOLs to gather insights; however, interviews were conducted with 5+ KOLs in the 7MM. Centers such as the Washington University School of Medicine, University Medical Center Hamburg-Eppendorf, and University Graduate School of Medicine etc. were contacted. Their opinion helps understand and validate HSDD epidemiology and market trends.
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 approved and emerging therapies based on relevant attributes such as safety, efficacy, frequency of administration, designation, route of administration, and order of entry. Scoring is given based on these parameters to analyze the effectiveness of therapy.
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 may be referred to as the negotiation of a price between a manufacturer and a payer that allows the manufacturer access to the market. It is provided to reduce the high costs and make the essential drugs affordable. Health technology assessment (HTA) plays an important role in reimbursement decision-making and recommending the use of a drug. These recommendations vary widely throughout the seven major markets, even for the same drug. In the US healthcare system, both Public and Private health insurance coverage are included. Also, Medicare and Medicaid are the largest government-funded programs in the US. The major healthcare programs, including Medicare, Medicaid, Health Insurance Program (CHIP), and the state and federal health insurance marketplaces, are overseen by the Centers for Medicare & Medicaid Services (CMS). Other than these, Pharmacy Benefit Managers (PBMs) and third-party organizations that provide services and educational programs to aid patients are also present.
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.