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US & EU Melanoma Therapeutics Market Poised for Robust Expansion, Projected to Grow from US$ 3.89 Billion in 2024 to US$ 8.99 Billion by 2033

01-07-2026 06:19 AM CET | Health & Medicine

Press release from: DataM Intelligence 4market Research LLP

US & EU Melanoma Therapeutics Market

US & EU Melanoma Therapeutics Market

The US & EU Melanoma Therapeutics market reached US$ 3.89 billion in 2024 and is expected to reach US$ 8.99 billion by 2033, growing at a CAGR of 9.8% during the forecast period 2025-2033.

According to DataM Intelligence has published a new research report on "US & EU Melanoma Therapeutics Market Size 2025". The report explores comprehensive and insightful Information about various key factors like Regional Growth, Segmentation, CAGR, Business Revenue Status of Top Key Players and Drivers. The purpose of this report is to provide a telescopic view of the current market size by value and volume, opportunities, and development status.

Melanoma therapeutics refers to the range of medical treatments used to prevent, manage, and treat melanoma, the most aggressive form of skin cancer. These therapies include immunotherapy, targeted therapy, chemotherapy, and combination treatment approaches. Recent advances in immune checkpoint inhibitors and BRAF/MEK inhibitors have significantly improved patient survival rates. The field is increasingly driven by personalized medicine and biomarker-based treatment selection. Ongoing research focuses on improving treatment efficacy, overcoming drug resistance, and enhancing long-term patient outcomes.

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➣ Recent Developments:

United States: Recent Melanoma Therapeutics Developments
✅ In March 2025, the U.S. FDA approved an expanded indication for immune checkpoint inhibitors in advanced melanoma.
The approval strengthens first-line combination immunotherapy adoption across U.S. oncology centers.
It is expected to improve long-term survival outcomes in metastatic melanoma patients.

✅ In February 2025, major U.S. biopharmaceutical companies increased investments in next-generation melanoma pipelines.
Funding focused on personalized cancer vaccines and neoantigen-based immunotherapies.
Several Phase II and Phase III clinical trials entered accelerated enrollment.

✅ In January 2025, U.S. cancer institutes launched AI-driven platforms to optimize melanoma drug response prediction.
These platforms integrate genomic profiling with real-world patient data.
The initiative aims to enhance precision medicine adoption in melanoma care.

Europe: Recent Melanoma Therapeutics Developments
✅ In March 2025, the EMA recommended broader use of combination targeted therapies for BRAF-mutant melanoma.
This aligns treatment regimens across major European oncology networks.
Clinical guidelines now emphasize rapid genetic testing to guide therapy choice.

✅ In February 2025, EU collaborative funding awards supported cross-border melanoma research hubs.
Grants prioritized novel immuno-oncology modalities and tumor microenvironment modulation.
Several pan-European Phase II trials launched under these partnerships.

✅ In January 2025, European healthcare systems expanded reimbursement for adjuvant melanoma therapies.
The policy shift improves patient access to life-extending treatments post-surgery.
Health technology assessments factored in long-term real-world outcome data.

Japan: Recent Melanoma Therapeutics Developments
✅ In March 2025, Japanese regulators supported expanded clinical use of combination immunotherapies for melanoma.
Hospitals began integrating PD-1 inhibitors with targeted therapies for advanced cases.
This marks a shift toward more aggressive first-line melanoma treatment strategies.

✅ In February 2025, leading Japanese pharmaceutical firms announced new R&D investments in rare and aggressive melanoma subtypes.
Research focuses on mucosal and acral melanoma, which are more prevalent in Asian populations.
Collaborations with academic hospitals are accelerating clinical validation.

✅ In January 2025, Japan initiated real-world evidence programs to monitor melanoma treatment effectiveness.
The programs collect long-term safety and efficacy data from oncology centers nationwide.
Insights will guide future regulatory decisions and reimbursement frameworks.

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➣ Top Industry Players:

Merck & Co., Inc., Bristol-Myers Squibb Company., Amgen, Inc., IOVANCE Biotherapeutics, Inc., Novartis AG, F. Hoffmann-La Roche Ltd, Pfizer Inc., Immunocore Holdings plc., Eisai Co., Ltd., Delcath Systems, Inc.

➣ Market Segments:

By Type: Superficial Spreading Melanoma, Nodular Melanoma, Lentigo Maligna Melanoma, Acral Lentiginous Melanoma, Others.

By Therapy: Surgery, Immunotherapy, Targeted Therapy, Chemotherapy, Radiation Therapy, Others.

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Regional Break out:

☞ North America - US, Canada, Mexico

☞ Europe- Germany, Russia, UK, France, Italy, Rest of Europe

☞ Asia Pacific- China, India, Japan, Australia, Rest of Asia Pacific

☞ South America- Brazil, Argentina, Colombia, Rest of South America

☞ Middle East and Africa- Saudi Arabia, UAE, Oman, Bahrain, Qatar, Kuwait, Israel

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✅ Competitive Landscape
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