Chemotherapy induced nausea and vomiting treatment market was valued at USD 3 billion in 2024 and is anticipated to reach USD 5.2 billion by 2032, growing at a CAGR of 6.5 % during the forecast period.
REPORT ATTRIBUTE
DETAILS
Historical Period
2020-2023
Base Year
2024
Forecast Period
2025-2032
Chemotherapy Induced Nausea and Vomiting Treatment Market Size 2024
USD 3 billion
Chemotherapy Induced Nausea and Vomiting Treatment Market, CAGR
6.5%
Chemotherapy Induced Nausea and Vomiting Treatment Market Size 2032
USD 5.2 billion
The chemotherapy-induced nausea and vomiting treatment market is shaped by strong participation from leading companies such as Tesaro, Qilu Pharma, Mundipharma, Heron Therapeutics, Eisai, Roche, Helsinn Holding S.A., ProStrakan, Novartis AG, and Helsinn Holding. These firms compete by expanding fixed-dose combinations, enhancing multi-pathway antiemetic regimens, and securing wider guideline inclusion across oncology centers. Their strategies focus on improving symptom control, reducing treatment interruptions, and supporting both inpatient and outpatient chemotherapy settings. North America leads the global market with a 41% share, supported by advanced oncology infrastructure, strong reimbursement systems, and high adoption of preventive antiemetic protocols.
Market Insights
The market reached USD 3 Billion in 2024 and is projected to hit USD 5.2 Billion by 2032, growing at a 6.5% CAGR.
Demand rises as hospitals increase use of multi-drug antiemetic regimens, especially serotonin antagonists, which hold the dominant share in drug-class segments.
Trends highlight growing adoption of fixed-dose combinations, long-acting formulations, and preventive treatment pathways that reduce therapy interruptions.
Competition intensifies as companies enhance safety profiles and expand oncology partnerships, with major players focusing on simplified dosing and improved tolerability.
North America leads with a 41% share, followed by Europe at 29% and Asia Pacific at 22%, while pharmacological treatment remains the largest segment globally.
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Serotonin receptor antagonists lead this segment with a 44% share, supported by strong use in acute and delayed nausea control. These agents provide fast symptom relief and show high safety levels, which strengthens adoption across oncology centers. Neurokinin-1 antagonists grow due to improved control in highly emetogenic regimens, while dopamine antagonists remain relevant in breakthrough episodes. Corticosteroids support combination protocols and enhance antiemetic effectiveness. Rising multi-drug therapy use and wider availability of guideline-recommended regimens continue to push demand for serotonin-based drugs in first-line treatment.
For instance, Eisai’s palonosetron (marketed as Aloxi) binds to the 5-HT₃ receptor with a half-life of approximately 40 hours, enabling prolonged antiemetic effect even in delayed phases of chemotherapy.
By Patient Type
Adult patients dominate this segment with a 67% share, driven by higher chemotherapy volumes and broader adoption of preventive antiemetic protocols. Adults receive more combination regimens, which increases the need for stronger nausea and vomiting control. Pediatric patients gain steady adoption as dosing guidelines improve, while geriatric patients benefit from safer drug profiles and simplified treatment plans. Growing cancer incidence, wider use of high-intensity therapies, and better supportive-care standards strengthen demand among adult patients.
For instance, in pooled phase III trials involving 1,787 adult patients receiving palonosetron, the complete response (no vomiting, no rescue therapy) rate in the delayed phase (24–120 h) was 57%.
By Treatment Type
Pharmacological treatment holds the dominant position with a 72% share, driven by strong reliance on guideline-backed drug combinations for both acute and delayed symptom control. These therapies deliver predictable outcomes and suit high-risk chemotherapy protocols, which makes them the preferred option for most oncology teams. Prophylactic treatment gains traction as hospitals prioritize prevention to reduce emergency visits and improve patient comfort. Non-pharmacological methods, including relaxation and dietary support, rise slowly but remain supplemental. Strong clinical evidence and wider access to combination antiemetics continue to reinforce the leadership of pharmacological approaches.
Key Growth Drivers
Growing Use of Highly Emetogenic Chemotherapy Regimens
The rise in highly emetogenic chemotherapy regimens strengthens demand for advanced antiemetic therapies. Oncologists use more aggressive combinations to improve cancer survival, which raises the risk of acute and delayed nausea. This shift drives adoption of multi-class antiemetic protocols that combine serotonin antagonists, NK-1 blockers, corticosteroids, and dopamine antagonists. Hospitals rely on guideline-based regimens to prevent treatment interruptions and improve patient adherence. Wider access to targeted therapies and immuno-oncology drugs also expands supportive-care needs. These trends create sustained demand for reliable nausea-prevention solutions that support treatment continuity and patient comfort across diverse cancer profiles.
For instance, real-world prescribing data information was collected from 45,324 chemotherapy-treated patients across five European countries (France, Germany, Italy, Spain, and the U.K.), which was extrapolated to an estimated 1,394,848 treatments.
Strong Adoption of Prophylactic Treatment Protocols
Preventive antiemetic therapy gains rapid traction as oncology practices shift from reactive to proactive care. Prophylactic protocols lower the risk of severe nausea, reduce emergency visits, and improve therapy tolerance. Healthcare systems integrate standardized antiemetic pathways that support consistent dosing and better clinical outcomes. The focus on patient quality of life and reduced treatment delays drives broader use of first-day and multi-day antiemetic combinations. Growing evidence supporting early intervention encourages oncologists to use serotonin antagonists and NK-1 inhibitors as frontline protection. This move toward preventive care reinforces long-term demand for reliable antiemetic drugs across adult and pediatric populations.
For instance, in multiple-cycle cisplatin chemotherapy, sustained prophylactic use of aprepitant maintained a no emesis + no significant nausea rate of ~59% by the sixth cycle, compared to ~34% in patients on standard antiemetic therapy.
Expanding Oncology Infrastructure and Access to Supportive Care
Growth in cancer centers, infusion clinics, and ambulatory oncology units increases access to structured antiemetic care. More regions adopt modern cancer-treatment protocols that rely on standardized supportive therapies, including antiemetic drugs. Tele-oncology and remote symptom monitoring help clinicians track nausea episodes and adjust therapy sooner. Pharmaceutical companies introduce improved oral formulations that support outpatient use. Public and private investments expand cancer screening and treatment capacity, raising the number of patients receiving chemotherapy. As supportive care becomes a core component of cancer management, demand for consistent and effective nausea-control solutions continues to increase.
Key Trend & Opportunity
Growth of Combination Antiemetic Therapies
Combination therapies gain strong momentum as clinicians adopt multi-pathway control for both acute and delayed nausea. The use of serotonin antagonists with NK-1 inhibitors and corticosteroids becomes standard in many regimens, improving symptom prevention in high-risk patients. New fixed-dose combinations offer simpler dosing and better adherence. Opportunities grow for companies developing long-acting or oral formulations that reduce clinic visits. Research exploring novel receptor targets enhances the pipeline for next-generation therapies. This trend opens room for innovation in personalized antiemetic strategies tailored to chemotherapy intensity and patient-specific risk factors.
For instance, Helsinn’s Akynzeo — a fixed-dose oral combination of 300 mg netupitant (NK-1 antagonist) and 0.5 mg palonosetron — showed a complete response rate (no vomiting, no rescue medication) of 76.9% in the delayed (25–120 h) phase versus 69.5% for palonosetron alone, in a phase III trial of 1,455 patients.
Rising Role of Digital Health and Remote Care Tools
Digital symptom tracking tools support earlier intervention and personalized treatment adjustments. Mobile apps help patients record nausea severity, triggers, and medication use, giving clinicians real-time data. Remote monitoring reduces unplanned hospital visits and supports proactive dose adjustments. Oncology practices adopt AI-based tools that predict nausea risk based on treatment factors, enabling targeted prophylaxis. These capabilities create opportunities for drug makers and digital-health firms to collaborate on integrated care models. Expansion of virtual oncology platforms also increases access to supportive care in rural areas, strengthening market reach for antiemetic therapies.
For instance, the ASyMS system (Advanced Symptom Management System) used in the large eSMART trial across 12 sites in 5 European countries enabled real-time monitoring of 10 chemotherapy-related symptoms (including nausea), with severe alerts (red) sent to clinicians via their dashboard within ~30 minutes.
Increasing Focus on Patient-Centric Care and Quality of Life
Hospitals place stronger emphasis on comfort, symptom relief, and adherence, driving interest in patient-centric antiemetic solutions. Long-acting formulations, non-pharmacological interventions, and simplified dosing schedules align with patient expectations for easier care. Expanded counseling and nutrition support programs improve treatment tolerance. Pharmaceutical companies explore new delivery systems that reduce side effects and enhance convenience. This focus on holistic care opens opportunities for supportive-care innovations that complement chemotherapy protocols. With rising patient awareness and better communication tools, demand for effective nausea-control solutions continues to grow.
Key Challenge
Adverse Effects and Limited Tolerability of Some Antiemetic Drugs
Certain antiemetic classes cause side effects such as constipation, fatigue, or headache, which may limit long-term tolerability. Older dopamine antagonists carry risks of extrapyramidal symptoms, making them less suitable for vulnerable patients. These issues lead clinicians to rely on combination therapies, increasing treatment complexity and overall pill burden. For some patients, managing side effects becomes challenging during multi-day chemotherapy cycles. Limited tolerability can reduce adherence and diminish therapeutic value, especially in outpatient settings. This constraint pushes manufacturers to develop safer formulations while encouraging clinicians to balance efficacy with patient comfort.
High Treatment Costs and Variability in Access
Advanced antiemetic combinations, especially NK-1 inhibitors and newer serotonin antagonists, remain costly for many healthcare systems. Insurance coverage varies, creating gaps in access for patients in low-resource settings. High drug costs can limit use of optimal prophylactic regimens, forcing reliance on older or less effective treatments. Hospitals face budget pressures when adopting standardized multi-drug antiemetic pathways. Cost barriers also affect adherence, particularly for long-term oral therapies used in delayed nausea control. These financial challenges highlight the need for more affordable antiemetic options and expanded reimbursement support to ensure equitable access.
Regional Analysis
North America
North America holds a 41% share, driven by strong oncology infrastructure, high chemotherapy volumes, and early adoption of guideline-based antiemetic protocols. Hospitals use multi-drug regimens that combine serotonin antagonists, NK-1 inhibitors, and corticosteroids to manage acute and delayed nausea. Broad insurance coverage and strong clinical-practice integration reinforce use of prophylactic therapy. The United States leads regional demand due to larger cancer centers and higher uptake of advanced supportive-care drugs. Canada follows with steady adoption in public oncology programs, supported by improved access to fixed-dose antiemetic combinations and standardized care pathways.
Europe
Europe accounts for a 29% share, supported by well-established cancer networks and high adherence to evidence-based antiemetic guidelines. Countries such as Germany, the UK, France, and Italy prioritize preventive therapy to reduce treatment interruptions and hospitalizations. Widespread use of serotonin antagonists and NK-1 blockers strengthens first-line adoption across both inpatient and outpatient care. National cancer programs encourage standardization of supportive-care protocols, improving consistency in treatment outcomes. Rising geriatric populations and expanding chemotherapy access across Eastern Europe further drive regional growth.
Asia Pacific
Asia Pacific captures a 22% share, driven by rising cancer incidence and expanding chemotherapy services in China, India, Japan, and South Korea. Growing investments in cancer hospitals and improved availability of supportive-care drugs support rapid market expansion. Japan maintains strong uptake due to established antiemetic guidelines, while China and India see fast growth as access to multi-drug antiemetic regimens improves. Regional oncology centers increasingly adopt prophylactic protocols to enhance patient comfort and reduce therapy drop-outs. Rising awareness and better reimbursement structures continue to boost demand.
Latin America
Latin America holds a 5% share, supported by expanding oncology capacity in Brazil, Mexico, Argentina, and Chile. Public hospitals adopt more standardized antiemetic regimens as cancer-treatment programs mature. Access to serotonin antagonists grows steadily, while NK-1 inhibitors gain traction in large urban centers with advanced chemotherapy services. Economic constraints limit widespread adoption of premium antiemetic combinations, but rising private healthcare penetration helps close the gap. Improved training and guideline implementation in major cancer institutes continue to support gradual market growth.
Middle East & Africa
The Middle East & Africa region accounts for a 3% share, shaped by uneven access to cancer treatment across markets. Gulf countries, including the UAE, Saudi Arabia, and Qatar, lead adoption due to advanced oncology centers and strong investment in supportive care. North African countries experience moderate growth as access to essential antiemetics improves. Limited reimbursement and infrastructure challenges restrict use of high-cost NK-1 inhibitors in several African regions. However, ongoing healthcare modernization and expansion of cancer screening programs gradually increase uptake of essential nausea-control therapies.
Market Segmentations
By Drug Class
Serotonin Receptor Antagonists
Neurokinin-1 Antagonists
Dopamine Antagonists
Corticosteroids
By Patient Type
Adult Patients
Pediatric Patients
Geriatric Patients
By Treatment
Pharmacological Treatment
Non-Pharmacological Treatment
Prophylactic Treatment
By Geography
North America
U.S.
Canada
Mexico
Europe
Germany
France
U.K.
Italy
Spain
Rest of Europe
Asia Pacific
China
Japan
India
South Korea
South-east Asia
Rest of Asia Pacific
Latin America
Brazil
Argentina
Rest of Latin America
Middle East & Africa
GCC Countries
South Africa
Rest of the Middle East and Africa
Competitive Landscape
The competitive landscape of the chemotherapy-induced nausea and vomiting treatment market features a mix of global pharmaceutical leaders and specialized supportive-care developers. Companies focus on improving multi-pathway antiemetic regimens that combine serotonin antagonists, NK-1 inhibitors, dopamine antagonists, and corticosteroids to enhance control of both acute and delayed nausea. Leading players invest in fixed-dose combinations, long-acting formulations, and oral therapies that support outpatient chemotherapy. Firms such as Helsinn, Eisai, Novartis, Roche, and Heron Therapeutics strengthen their positions through clinical data, streamlined dosing profiles, and expanded label indications. Partnerships with oncology networks and guideline updates further shape competitive strategies, while emerging players from Asia intensify price competition. Overall, companies aim to deliver safer, more predictable, and more convenient antiemetic solutions that align with evolving cancer-care protocols.
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In September 2025, Eisai A phase IV STOP-CINV study reported that IV Akynzeo (fosnetupitant 235 mg + palonosetron 0.25 mg), a fixed NK1/5-HT3 combination co-marketed in various regions by partners including Eisai, achieved complete response rates of 84.27 % in the acute phase, 93.26 % in the delayed phase, and 96.07 % in the extended phase for CINV prevention in 178 Indian patients receiving highly or moderately emetogenic chemotherapy, with no new safety signals identified.
In October 2024, Heron Therapeutics Heron Therapeutics reaffirmed that it had ample U.S. supply of its CINV portfolio products CINVANTI (aprepitant injectable emulsion) and SUSTOL (extended-release granisetron) for chemotherapy-induced nausea and vomiting prevention, highlighting that these ready-to-administer formulations do not require dilution with IV fluids and can help maintain antiemetic care during an anticipated national IV fluid shortage linked to Hurricane Helene
Report Coverage
The research report offers an in-depth analysis based on Drug Class, Patient Type, Treatment Type and Geography. It details leading market players, providing an overview of their business, product offerings, investments, revenue streams, and key applications. Additionally, the report includes insights into the competitive environment, SWOT analysis, current market trends, as well as the primary drivers and constraints. Furthermore, it discusses various factors that have driven market expansion in recent years. The report also explores market dynamics, regulatory scenarios, and technological advancements that are shaping the industry. It assesses the impact of external factors and global economic changes on market growth. Lastly, it provides strategic recommendations for new entrants and established companies to navigate the complexities of the market.
Future Outlook
Demand for multi-pathway antiemetic combinations will rise as chemotherapy intensity increases.
Prophylactic treatment protocols will become standard in most oncology centers to prevent symptom escalation.
Long-acting and fixed-dose formulations will gain wider adoption for better adherence and convenience.
Digital monitoring tools will support earlier intervention and improve treatment personalization.
Emerging biologics and novel receptor-targeted agents will expand options for resistant nausea cases.
Outpatient chemotherapy growth will drive demand for safe and easy-to-administer oral therapies.
Precision-based antiemetic strategies will strengthen as clinicians integrate patient risk scoring.
Lower-cost generics will increase access in developing regions and broaden market penetration.
Collaborations between oncology networks and drug manufacturers will accelerate guideline inclusion.
Supportive-care integration will remain central to improving patient quality of life and treatment continuity.
Introduction
1.1. Report Description
1.2. Purpose of the Report
1.3. USP & Key Offerings
1.4. Key Benefits for Stakeholders
1.5. Target Audience
1.6. Report Scope
1.7. Regional Scope
Scope and Methodology
2.1. Objectives of the Study
2.2. Stakeholders
2.3. Data Sources
2.3.1. Primary Sources
2.3.2. Secondary Sources
2.4. Market Estimation
2.4.1. Bottom-Up Approach
2.4.2. Top-Down Approach
2.5. Forecasting Methodology
Executive Summary
Introduction
4.1. Overview
4.2. Key Industry Trends
Global Chemotherapy Induced Nausea and Vomiting Treatment Market
5.1. Market Overview
5.2. Market Performance
5.3. Impact of COVID-19
5.4. Market Forecast
Market Breakup by Region
9.1. North America
9.1.1. United States
9.1.2. Canada
9.2. Asia-Pacific
9.2.1. China
9.2.2. Japan
9.2.3. India
9.2.4. South Korea
9.2.5. Australia
9.2.6. Indonesia
9.2.7. Others
9.3. Europe
9.3.1. Germany
9.3.2. France
9.3.3. United Kingdom
9.3.4. Italy
9.3.5. Spain
9.3.6. Russia
9.3.7. Others
9.4. Latin America
9.4.1. Brazil
9.4.2. Mexico
9.4.3. Others
9.5. Middle East and Africa
9.5.1. Market Trends
9.5.2. Market Breakup by Country
9.5.3. Market Forecast
Porter’s Five Forces Analysis
12.1. Overview
12.2. Bargaining Power of Buyers
12.3. Bargaining Power of Suppliers
12.4. Degree of Competition
12.5. Threat of New Entrants
12.6. Threat of Substitutes
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Frequently Asked Question
What is the current market size for the Chemotherapy-Induced Nausea and Vomiting Treatment Market, and what is its projected size in 2032?
The market was valued at USD 3 billion in 2024 and is projected to reach USD 5.2 billion by 2032.
At what Compound Annual Growth Rate is the Chemotherapy-Induced Nausea and Vomiting Treatment Market projected to grow between 2025 and 2032?
The market is expected to expand at a 6.5% CAGR during the forecast period.
Which administration route segment governs the market demand for Chemotherapy-Induced Nausea and Vomiting Therapeutics ?
Oral medications are frequently in more demand than intravenous (IV) medications
Who are the major players in the global Chemotherapy-Induced Nausea and Vomiting Therapeutics Market?
The top players include Kyowa Kirin, Inc., Pfizer Inc., AbbVie Inc. (Allergan plc), GlaxoSmithKline plc., Merck & Co., Inc., Bausch Health Companies Inc.
What are the major market drivers of the Chemotherapy-Induced Nausea and Vomiting Therapeutics industry?
The primary market drivers are rising cancer and chemotherapy treatment prevalence, rising demand for efficient CINV therapies, and advancements in research and development.
What are the major market restraints of the Chemotherapy-Induced Nausea and Vomiting Therapeutics industry?
The market’s main obstacles are variability in patient responses to antiemetic drugs, the high cost of CINV treatments, and limited access to healthcare resources in certain countries.
What are the major market opportunities of the Chemotherapy-Induced Nausea and Vomiting Therapeutics industry?
The primary opportunity in the market is the focus on customized treatment, the introduction of new and more effective antiemetic drugs, and ongoing research and development initiatives.
Who are the leading companies in the Chemotherapy-Induced Nausea and Vomiting Treatment Market?
Key players include Tesaro, Qilu Pharma, Mundipharma, Heron Therapeutics, Eisai, Roche, Helsinn Holding S.A., ProStrakan, Novartis AG, and Helsinn Holding.
About Author
Shweta Bisht
Healthcare & Biotech Analyst
Shweta is a healthcare and biotech researcher with strong analytical skills in chemical and agri domains.
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