시장보고서
상품코드
2026031

KIMMTRAK : 판매 예측 및 시장 규모(2034년)

KIMMTRAK Sales Forecast, and Market Size Analysis - 2034

발행일: | 리서치사: 구분자 DelveInsight | 페이지 정보: 영문 30 Pages | 배송안내 : 2-10일 (영업일 기준)

    
    
    




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한글목차
영문목차

KIMMTRAK의 성장을 이끄는 주요 요인들

1. 강력한 차별화를 갖춘 일류 TCR 요법

  • KIMMTRAK은 HLA-A*02:01에 존재하는 gp100 펩타이드를 표적으로 하는 최초의 T세포 수용체(TCR) 치료제로, 암 치료제로 승인된 최초의 T세포 수용체(TCR) 치료제입니다.
  • T세포를 재유도하여 종양세포를 사멸시키는 것으로, 체크포인트 억제제를 넘어선 새로운 면역치료제 카테고리를 대표합니다.
  • 강력한 과학적 차별성으로 인해 전이성 포도막 흑색종(mUM) 환자에서 표준 치료제로 빠르게 채택되고 있습니다.

2. 입증된 전체 생존기간(OS) 연장 효과(주요 임상적 요인)

  • KIMMTRAK은 주요 임상 3상 시험(문헌에 게재)에서 다음과 같은 결과를 보여주었습니다.
  • 연구자 선택 치료 대비 유의미한 전체 생존기간 연장
  • mUM에서 OS 개선 효과를 입증한 최초의 치료법
  • 지금까지 mUM의 전체 생존기간(OS) 중앙값은 약 12개월로, 치료 옵션이 제한적이었습니다.
  • 생존기간의 연장(표준 평가변수)은 다음과 같은 사항을 강력하게 뒷받침합니다.
  • 의사 선정
  • 보험 환급 지원
  • 전 세계적으로 급속한 보급

3. 견고하고 일관된 상업적 성장 궤도

  • 2023년 매출액: 약 2억 3,870만 달러
  • 2024년 매출: 약 3억 1,000만 달러(전년 대비 약 30% 증가)
  • 분기별 매출은 계속해서 좋은 모멘텀을 보이고 있다(예: 2024년 4분기 8,410만 달러).

4. 빠른 세계 진출과 접근성 확대

  • 약 39개국에서 승인, 24개국에서 출시 완료(2024년 기준)
  • 2024년에만 14개국에 신규 진출 지속
  • 미국 시장이 주도하는 성장(2024년 매출 2억 2,600만 달러 이상)

5. 전이성 포도막 흑색종에서 높은 미충족 수요가 있습니다.

  • mUM은 희귀하지만 치사율이 높은 암으로 다음과 같은 특징이 있습니다.
  • 기존에는 효과적인 전신 요법이 제한적이었습니다.
  • 예후가 좋지 않고 생존율이 낮음
  • KIMMTRAK은 현재 시판 중인 대부분 시장에서 표준 치료법으로 간주되고 있습니다.

KIMMTRAK의 최근 동향

KIMMTRAK의 순매출은 2025년 6월말 기준 3분기와 1분기에 각각 9,800만 달러와 1억 9,180만 달러로 2024년 동기 대비 각각 30%와 32% 증가하였습니다.

본 보고서는 미국, EU4(독일, 프랑스, 이탈리아, 스페인, 이탈리아, 스페인, 영국, 일본 등 주요 7개국(미국, EU4, 독일, 프랑스, 이탈리아, 스페인, 영국, 일본)의 KIMMTRAK 동향을 조사하여 포도막 흑색종, 악성 흑색종 등 승인된 적응증에 대한 종합적인 인사이트를 제공합니다. 2020년에서 2034년까지 승인된 적응증에서 KIMMTRAK의 현재 사용 현황, 잠재적 적응증에 대한 진입 전망 및 실적에 대한 상세 분석, 승인된 적응증과 잠재적 적응증에서 KIMMTRAK에 대한 상세 설명, KIMMTRAK의 매출 예측, 작용기전(MoA), 투여법, 투여량, 기타 활동에 대한 인사이트. 투여량 및 투여 방법, 규제 마일스톤을 포함한 연구개발, 기타 활동에 대한 인사이트, 미래 시장 평가, SWOT 분석, 애널리스트의 견해, 경쟁 개요, 각 적응증별 다른 신흥 치료법에 대한 개요, 시장을 주도하는 요인에 대한 분석도 수록되어 있습니다.

자주 묻는 질문

  • KIMMTRAK의 주요 특징은 무엇인가요?
  • KIMMTRAK의 전체 생존기간(OS) 연장 효과는 어떻게 입증되었나요?
  • KIMMTRAK의 2023년 매출액은 얼마인가요?
  • KIMMTRAK의 세계 진출 현황은 어떤가요?
  • KIMMTRAK이 전이성 포도막 흑색종에서 충족하는 수요는 무엇인가요?
  • KIMMTRAK의 2024년 매출 예측은 어떻게 되나요?

목차

제1장 보고서 개요

제2장 Emixustat 개요 : 포도막흑색종이나 악성 흑색종등의 승인이 끝난 적응증

제3장 Emixustat : 경쟁 구도(출시 치료제)

제4장 Emixustat : 경쟁 구도(후기 개발 단계 치료제)

제5장 Emixustat : 시장 평가

제6장 Emixustat : SWOT 분석

제7장 애널리스트의 견해

제8장 부록

제9장 DelveInsight의 서비스 내용

제10장 면책사항

제11장 DelveInsight에 대해

제12장 보고서 구입 옵션

LSH 26.05.19

Key Factors Driving KIMMTRAK Growth

1. First-in-class TCR therapy with strong differentiation

  • KIMMTRAK is the first approved T-cell receptor (TCR) therapy for cancer, targeting gp100 peptide presented by HLA-A*02:01.
  • It redirects T cells to kill tumor cells, representing a novel immunotherapy class beyond checkpoint inhibitors.
  • Strong scientific differentiation has enabled rapid adoption as standard of care in eligible metastatic uveal melanoma (mUM) patients.

2. Demonstrated overall survival (OS) benefit (key clinical driver)

  • In the pivotal Phase III trial (published in literature), KIMMTRAK showed:
  • Significant overall survival benefit vs investigator's choice therapy
  • First therapy to demonstrate OS improvement in mUM
  • mUM historically has median OS ~12 months, with limited treatment options.
  • Survival benefit (gold-standard endpoint) strongly drives:
  • Physician preference
  • Reimbursement support
  • Rapid uptake globally

3. Strong and consistent commercial growth trajectory

  • 2023 sales: ~$238.7 million
  • 2024 sales: ~$310 million (~30% YoY growth)
  • Quarterly revenues show continued momentum (e.g., $84.1M in Q4 2024)

4. Rapid global expansion and increasing access

  • Approved in ~39 countries and launched in 24 countries (as of 2024)
  • Continued launches in 14 new countries in 2024 alone
  • Growth driven by US dominance (>$226M in 2024 sales)

5. High unmet need in metastatic uveal melanoma

  • mUM is a rare but highly lethal cancer, with:
  • Limited effective systemic therapies historically
  • Poor prognosis and low survival rates
  • KIMMTRAK is now considered standard of care in most launched markets

KIMMTRAK Recent Developments

KIMMTRAK net product sales were $98.0 million and $191.8 million for the three and six months ended June 2025, respectively, representing increases of 30% and 32% respectively, as compared to the same periods in 2024.

"KIMMTRAK Sales Forecast, and Market Size Analysis - 2034" report provides comprehensive insights of KIMMTRAK for approved indication like Uveal melanoma and Malignant melanoma in the 7MM. A detailed picture of KIMMTRAK's existing usage in approved and anticipated entry and performance in potential indications in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan for the study period 2020 -2034 is provided in this report along with a detailed description of the KIMMTRAK for approved and potential indications. The KIMMTRAK market report provides insights about KIMMTRAK's sales forecast, mechanism of action (MoA), dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of historical and current KIMMTRAK performance, future market assessments inclusive of the KIMMTRAK market forecast analysis for approved and potential indications in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in respective indications. It also provides analysis of KIMMTRAK sales forecasts, along with factors driving its market.

KIMMTRAK Drug Summary

KIMMTRAK is a prescription bispecific gp100 peptide-HLA-directed CD3 T cell engager developed by Immunocore, FDA-approved on January 2022, and EMA-authorized in 2022 as monotherapy for HLA-A02:01-positive adults with unresectable or metastatic uveal melanoma (mUM), a rare and aggressive eye cancer. It simultaneously binds to the gp100 peptide presented by HLA-A02:01 on tumor cells and CD3 on T cells, redirecting and activating T cells to induce tumor cell killing through immune synapse formation, perforin/granzyme release, and fas/fas ligand-mediated apoptosis, while also promoting broader anti-tumor immunity. Administered intravenously with a step-up dosing regimen (20 mcg Day 1, 30 mcg Day 8, 68 mcg Day 15, then 68 mcg weekly), patients require hospitalization and monitoring for cytokine release syndrome (CRS)-a boxed warning risk-along with other adverse reactions like rash, fever, hypotension, and liver enzyme elevations. The report provides KIMMTRAK's sales, growth barriers and drivers, post usage and approvals in multiple indications.

Scope of the KIMMTRAK Market Report

The report provides insights into:

  • A comprehensive product overview including the KIMMTRAK MoA, description, dosage and administration, research and development activities in approved indications like Uveal melanoma and Malignant melanoma.
  • Elaborated details on KIMMTRAK regulatory milestones and other development activities have been provided in KIMMTRAK market report.
  • The report also highlights KIMMTRAK's cost estimates and regional variations, reported and estimated sales performance, research and development activities in approved and potential indications across the United States, Europe, and Japan.
  • The KIMMTRAK market report also covers the patents information, generic entry and impact on cost cut.
  • The KIMMTRAK market report contains current and forecasted KIMMTRAK sales for approved and potential indications till 2034.
  • Comprehensive coverage of the late-stage emerging therapies for respective indications.
  • The KIMMTRAK market report also features the SWOT analysis with analyst views for KIMMTRAK in approved and potential indications.

Methodology:

The KIMMTRAK market report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by DelveInsight's team of industry experts. Information and data from the secondary sources have been obtained from various printable and nonprintable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.

KIMMTRAK Analytical Perspective by DelveInsight

  • In-depth KIMMTRAK Market Assessment

This KIMMTRAK sales market forecast report provides a detailed market assessment of KIMMTRAK for approved indication like Uveal melanoma and Malignant melanoma in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. This segment of the report provides current and forecasted KIMMTRAK sales data uptil 2034.

  • KIMMTRAK Clinical Assessment

The KIMMTRAK market report provides the clinical trials information of KIMMTRAK for approved and potential indications covering trial interventions, trial conditions, trial status, start and completion dates.

KIMMTRAK Competitive Landscape

The report provides Insights on competitors and marketed products within the domain, along with a summary of emerging products and their respective launch dates, posing significant competition in the market.

KIMMTRAK Market Potential & Revenue Forecast

  • Projected market size for the KIMMTRAK and its key indications
  • Estimated KIMMTRAK sales potential (KIMMTRAK peak sales forecasts)
  • KIMMTRAK Pricing strategies and reimbursement landscape

KIMMTRAK Competitive Intelligence

  • Number of competing drugs in development (pipeline analysis)
  • KIMMTRAK Market positioning compared to existing treatments
  • KIMMTRAK Strengths & weaknesses relative to competitors

KIMMTRAK Regulatory & Commercial Milestones

  • KIMMTRAK Key regulatory approvals & expected launch timelines
  • Commercial partnerships, licensing deals, and M&A activity

KIMMTRAK Clinical Differentiation

  • KIMMTRAK Efficacy & safety advantages over existing drugs
  • KIMMTRAK Unique selling points

KIMMTRAK Market Report Highlights

  • In the coming years, the KIMMTRAK market scenario is set to change due to strong adoption, increased prescriptions and broader uptake in multiple immunological indications; which would expand the size of the market.
  • The KIMMTRAK companies are developing therapies that focus on novel approaches to treat/improve the disease condition, assess challenges, and seek opportunities that could influence KIMMTRAK's dominance.
  • Other emerging products for Uveal melanoma and Malignant melanoma are expected to give tough market competition to KIMMTRAK and launch of late-stage emerging therapies in the near future will significantly impact the market.
  • A detailed description of regulatory milestones, and developmental activities, provide the current development scenario of KIMMTRAK in approved and potential indications.
  • Analyse KIMMTRAK cost, pricing trends and market positioning to support strategic decision-making in the immunology landscape.
  • Our in-depth analysis of the forecasted KIMMTRAK sales data uptil 2034 will support the clients in decision-making process regarding their therapeutic portfolio by identifying the overall scenario of KIMMTRAK in approved and potential indications.

Key Questions:

  • What is the class of therapy, route of administration and mechanism of action of KIMMTRAK? How strong is KIMMTRAK's clinical and commercial performance?
  • What is KIMMTRAK's clinical trial status in each individual indications such as Uveal melanoma and Malignant melanoma and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the KIMMTRAK Manufacturers?
  • What are the key designations that have been granted to KIMMTRAK for approved and potential indications? How are they going to impact KIMMTRAK's penetration in various geographies?
  • What is the current and forecasted KIMMTRAK market scenario for approved and potential indications? What are the key assumptions behind the forecast?
  • What are the current and forecasted sales of KIMMTRAK in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain) and the United Kingdom, and Japan?
  • What are the other emerging products available and how are these giving competition to KIMMTRAK for approved and potential indications?
  • Which are the late-stage emerging therapies under development for the treatment of approved and potential indications?
  • How cost-effective is KIMMTRAK? What is the duration of therapy and what are the geographical variations in cost per patient?

Table of Contents

1. Report Introduction

2. KIMMTRAK Overview in approved indications like Uveal melanoma and Malignant melanoma

  • 2.1. Product Detail
  • 2.2. KIMMTRAK Clinical Development
    • 2.2.1. KIMMTRAK Clinical studies
    • 2.2.2. KIMMTRAK Clinical trials information
    • 2.2.3. Safety and efficacy
  • 2.3. Other Developmental Activities
  • 2.4. Product Profile

3. KIMMTRAK Competitive Landscape (Marketed Therapies)

4. Competitive Landscape (Late-stage Emerging KIMMTRAK Therapies)

5. KIMMTRAK Market Assessment

  • 5.1. KIMMTRAK Market Outlook in approved and potential indications
  • 5.2. 7MM Analysis
    • 5.2.1. KIMMTRAK Market Size in the 7MM for approved and potential indications
  • 5.3. Country-wise Market Analysis
    • 5.3.1. KIMMTRAK Market Size in the United States for approved and potential indications
    • 5.3.2. KIMMTRAK Market Size in Germany for approved and potential indications
    • 5.3.3. KIMMTRAK Market Size in France for approved and potential indications
    • 5.3.4. KIMMTRAK Market Size in Italy for approved and potential indications
    • 5.3.5. KIMMTRAK Market Size in Spain for approved and potential indications
    • 5.3.6. KIMMTRAK Market Size in the United Kingdom for approved and potential indications
    • 5.3.7. KIMMTRAK Market Size in Japan for approved and potential indications

6. KIMMTRAK SWOT Analysis

7. Analysts' Views

8. Appendix

  • 8.1. Bibliography
  • 8.2. Report Methodology

9. DelveInsight Capabilities

10. Disclaimer

11. About DelveInsight

12. Report Purchase Options

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