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2064061

IMV-102 : 판매 예측 및 시장 규모(2034년)

IMV-102 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

IMV-102의 성장을 이끄는 주요 요인

1. 복잡한 CAR-T 제조 공정을 불필요하게 만들 가능성

IMV-102의 주요 성장 요인은 생체 내(in vivo) CAR-T 접근법에 있습니다. 이는 기존의 CAR-T 치료에서 필요한 백혈구 분리법, 집중 생산, 장기간에 걸친 제조 과정을 피하는 것을 목표로 하고 있습니다.

Carvykti나 Abecma와 같은 현재의 BCMA 표적 CAR-T 치료법은 수 주간이 소요되는 맞춤형 제조 과정이 필요합니다. IMV-102는 환자의 체내에서 직접 CAR-T 세포를 생성하는 것을 목표로 하고 있으며, 이로 인해 치료 지연 시간을 단축하고 치료 접근성을 높일 수 있을 것으로 기대됩니다. Immunofoco에 따르면 iMAGIC 플랫폼은 기존 CAR-T 치료법과 관련된 확장성 및 제조상의 제약을 해결하기 위해 특별히 설계된 것입니다.

2. 다발성골수종에서 BCMA 표적 치료의 유효성

BCMA는 다발성골수종에서 효능이 가장 잘 입증된 표적 중 하나입니다. 승인된 BCMA 표적 치료법은 다제내성 환자에서도 깊고 지속적인 치료 효과를 보이고 있습니다.

예를 들어 다음과 같은 결과가 보고되고 있습니다.

  • Carvykti는 주요 시험에서 95%를 넘는 전체 변환 효율을 달성했습니다.
  • Abecma는 재발성·난치성 다발성골수종 환자에서 유의미한 생존 이점을 보여주었습니다.

이러한 치료법의 성공은 IMV-102의 생물학적 근거와 관련된 위험을 대폭 줄여줍니다. 왜냐하면 IMV-102는 동일한 BCMA를 표적으로 삼으면서도 전달 효율과 제조 효율의 향상을 목표로 하고 있기 때문입니다.

3. 대규모이며 성장 중인 다발성골수종 시장

다발성골수종은 치료법이 크게 발전했음에도 불구하고 여전히 완치가 어려운 형질세포 악성 종양입니다.

공개된 역학 연구에 따르면

  • 전 세계에서 매년 18만 건 이상의 다발성골수종 신규 환자가 진단되고 있습니다.
  • 환자는 대개 여러 단계의 치료를 거친 후, 결국 난치성 질환으로 진행됩니다.

환자들이 기존 치료법을 거치면서 병세가 진행됨에 따라 BCMA를 표적으로 하는 고효능 치료법에 대한 수요는 계속해서 증가하고 있습니다. IMV-102는 임상적 유효성이 확인될 경우, 이처럼 확대되고 있는 치료 체계에 임베디드될 가능성이 있습니다.

4. 기존 CAR-T 치료법에 비해 비용 및 접근성 측면에서 갖는 잠재적 우위

CAR-T 요법의 상업적 도입은 종종 다음과 같은 요인들로 인해 제약을 받습니다.

  • 제조 과정의 복잡성
  • 전문 치료 센터의 부족
  • 고액의 치료비
  • 생산 능력의 제약

효과적인 생체내 CAR-T 접근법은 제조 비용을 대폭 절감하고 환자의 접근성을 확대할 가능성이 있습니다. 이는 생체내 세포 치료 분야 전체에 있으며, 가장 중요한 상업적 기회 중 하나가 될 것입니다. IMV-102가 이미 승인된 BCMA CAR-T 요법과 동등한 효능을 보여주면서 치료 과정을 간소화할 수 있다면, 의미 있는 경쟁적 차별화를 실현할 가능성이 있습니다.

IMV-102의 최근 동향

2026년 4월, Immunofoco는 자사의 생체내 BCMA 표적 CAR-T 후보물질인 IMV-102에 관한 새로운 전임상 데이터를 2026년 AACR 연간 총회에서 발표했습니다. 이 데이터는 IMV-102가 다발성골수종 모델에서 강력하고 지속적인 항종양 활성을 보였음을 입증하며, 기존 CAR-T 요법의 주요 한계를 극복할 가능성이 있음을 보여주었습니다.

이 보고서는 주요 7개국(미국, EU 4개국(독일, 프랑스, 이탈리아, 스페인), 영국, 일본)에서 IMV-102의 동향을 조사하여, 다발성골수종 등 잠재적 적응증에 대한 포괄적인 인사이트를 제공합니다.

이 보고서에서는 2020-2034년 승인된 적응증에 대한 기존 사용 현황, 시장 진입 전망, 시장 실적에 대한 상세한 분석과 더불어, 잠재적 적응증에 대한 IMV-102의 상세한 설명이 제공됩니다. 또한 IMV-102의 매출 전망, 작용 기전(MoA), 투여량 및 투여 방법, 규제 관련 마일스톤을 포함한 연구개발 및 기타 활동에 대한 인사이트, 향후 시장 평가, SWOT 분석, 애널리스트의 견해, 경쟁 구도, 각 적응증별 기타 신흥 치료제에 대한 개요, 시장을 촉진하는 요인에 대해서도 분석하고 있습니다.

자주 묻는 질문

  • IMV-102의 주요 성장 요인은 무엇인가요?
  • BCMA 표적 치료의 유효성은 어떻게 입증되었나요?
  • 다발성골수종 시장의 규모는 어떻게 되나요?
  • IMV-102가 기존 CAR-T 치료법에 비해 갖는 잠재적 우위는 무엇인가요?
  • IMV-102의 최근 동향은 무엇인가요?

목차

제1장 리포트 개요

제2장 IMV-102의 개요 : 다발성골수종 등의 잠재적 적응증

제3장 IMV-102 : 경쟁 구도(출시 치료제)

제4장 IMV-102 : 경쟁 구도(후기 개발 단계 신규 치료제)

제5장 IMV-102 : 시장 평가

제6장 IMV-102 : SWOT 분석

제7장 애널리스트의 견해

제8장 부록

제9장 DelveInsight의 서비스 내용

제10장 면책사항

제11장 DelveInsight 소개

제12장 리포트 구입 옵션

KSA 26.06.26

Key Factors Driving IMV-102 Growth

1. Potential to Eliminate Complex CAR-T Manufacturing

A major growth driver for IMV-102 is it's in vivo CAR-T approach, which seeks to bypass leukapheresis, centralized manufacturing, and lengthy production timelines required by conventional CAR-T therapies.

Current BCMA CAR-T therapies such as Carvykti and Abecma require individualized manufacturing that can take several weeks. IMV-102 aims to generate CAR-T cells directly within the patient, potentially reducing treatment delays and improving accessibility. According to Immunofoco, the iMAGIC platform was specifically designed to address scalability and manufacturing limitations associated with traditional CAR-T therapy.

2. Validation of the BCMA Target in Multiple Myeloma

BCMA has become one of the most validated targets in multiple myeloma. Approved BCMA-directed therapies have demonstrated deep and durable responses in heavily pretreated patients.

For example:

  • Carvykti achieved overall response rates exceeding 95% in pivotal studies.
  • Abecma demonstrated meaningful survival benefits in relapsed/refractory multiple myeloma.

The success of these therapies significantly de-risks the biological rationale for IMV-102 because it utilizes the same BCMA target while attempting to improve delivery and manufacturing efficiency.

3. Large and Growing Multiple Myeloma Market

Multiple myeloma remains an incurable plasma-cell malignancy despite major therapeutic advances.

According to published epidemiological studies:

  • More than 180,000 new multiple myeloma cases are diagnosed globally each year.
  • Patients typically receive multiple lines of therapy and eventually develop refractory disease.

As patients progress through existing treatments, demand for highly effective BCMA-directed therapies continues to increase. IMV-102 could potentially participate in this expanding treatment landscape if clinical efficacy is confirmed.

4. Potential Cost and Access Advantages Over Conventional CAR-T

Commercial adoption of CAR-T therapy is often constrained by:

  • Manufacturing complexity.
  • Specialized treatment centers.
  • High treatment costs.
  • Limited production capacity.

An effective in vivo CAR-T approach could significantly lower manufacturing costs and increase patient access. This represents one of the most important commercial opportunities for the entire in vivo cell therapy field. If IMV-102 can demonstrate efficacy comparable to approved BCMA CAR-T therapies while simplifying treatment logistics, it may achieve meaningful competitive differentiation.

IMV-102 Recent Developments

In April 2026, Immunofoco announced the presentation of new preclinical data for its in vivo BCMA-targeting CAR-T candidate, IMV102, at the AACR Annual Meeting 2026. The data demonstrate that IMV102 achieved potent and durable anti-tumor activity in multiple myeloma models, highlighting its potential to address key limitations of conventional CAR-T therapies.

"IMV-102 Sales Forecast, and Market Size Analysis - 2034" report provides comprehensive insights of IMV-102 for potential indication like Multiple myeloma in the 7MM. A detailed picture of IMV-102's existing usage in 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 IMV-102 for potential indications. The IMV-102 market report provides insights about IMV-102'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 IMV-102 performance, future market assessments inclusive of the IMV-102 market forecast analysis for 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 IMV-102 sales forecasts, along with factors driving its market.

IMV-102 Drug Summary

IMV-102 is an investigational in vivo BCMA-targeted CAR-T therapy being developed by Immunofoco for the treatment of relapsed/refractory multiple myeloma and potentially other B-cell-mediated diseases. Unlike conventional ex vivo CAR-T therapies that require collection, genetic modification, and reinfusion of a patient's T cells, IMV-102 utilizes Immunofoco's proprietary iMAGIC platform, a lentiviral vector-based system designed to generate BCMA-directed CAR-T cells directly within the patient's body. The therapy selectively targets and transduces T cells in vivo, enabling them to recognize and eliminate BCMA-expressing malignant plasma cells while potentially reducing the manufacturing complexity, treatment delays, and costs associated with traditional CAR-T products. Preclinical studies have demonstrated efficient and selective T-cell transduction, potent cytotoxic activity against BCMA-positive multiple myeloma cells, durable tumor control in xenograft models, and a favorable safety profile with minimal off-target effects. IMV-102 has advanced into early clinical development, including an investigator-initiated study in patients with relapsed/refractory multiple myeloma, where its safety, pharmacokinetics, and preliminary antitumor efficacy are being evaluated. The report provides IMV-102's sales, growth barriers and drivers, post usage and approvals in multiple indications.

Scope of the IMV-102 Market Report

The report provides insights into:

  • A comprehensive product overview including the IMV-102 MoA, description, dosage and administration, research and development activities in potential indication like Multiple myeloma.
  • Elaborated details on IMV-102 regulatory milestones and other development activities have been provided in IMV-102 market report.
  • The report also highlights IMV-102's cost estimates and regional variations, reported and estimated sales performance, research and development activities in potential indications across the United States, Europe, and Japan.
  • The IMV-102 market report also covers the patents information, generic entry and impact on cost cut.
  • The IMV-102 market report contains current and forecasted IMV-102 sales for potential indications till 2034.
  • Comprehensive coverage of the late-stage emerging therapies for respective indications.
  • The IMV-102 market report also features the SWOT analysis with analyst views for IMV-102 in potential indications.

Methodology:

The IMV-102 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.

IMV-102 Analytical Perspective by DelveInsight

  • In-depth IMV-102 Market Assessment

This IMV-102 sales market forecast report provides a detailed market assessment of IMV-102 for potential indication like Multiple myeloma 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 IMV-102 sales data uptil 2034.

  • IMV-102 Clinical Assessment

The IMV-102 market report provides the clinical trials information of IMV-102 for potential indications covering trial interventions, trial conditions, trial status, start and completion dates.

IMV-102 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.

IMV-102 Market Potential & Revenue Forecast

  • Projected market size for the IMV-102 and its key indications
  • Estimated IMV-102 sales potential (IMV-102 peak sales forecasts)
  • IMV-102 Pricing strategies and reimbursement landscape

IMV-102 Competitive Intelligence

  • Number of competing drugs in development (pipeline analysis)
  • IMV-102 Market positioning compared to existing treatments
  • IMV-102 Strengths & weaknesses relative to competitors

IMV-102 Regulatory & Commercial Milestones

  • IMV-102 Key regulatory approvals & expected launch timelines
  • Commercial partnerships, licensing deals, and M&A activity

IMV-102 Clinical Differentiation

  • IMV-102 Efficacy & safety advantages over existing drugs
  • IMV-102 Unique selling points

IMV-102 Market Report Highlights

  • In the coming years, the IMV-102 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 IMV-102 companies are developing therapies that focus on novel approaches to treat/improve the disease condition, assess challenges, and seek opportunities that could influence IMV-102's dominance.
  • Other emerging products for Multiple myeloma are expected to give tough market competition to IMV-102 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 IMV-102 in potential indications.
  • Analyse IMV-102 cost, pricing trends and market positioning to support strategic decision-making in the immunology landscape.
  • Our in-depth analysis of the forecasted IMV-102 sales data uptil 2034 will support the clients in decision-making process regarding their therapeutic portfolio by identifying the overall scenario of IMV-102 in potential indications.

Key Questions:

  • What is the class of therapy, route of administration and mechanism of action of IMV-102? How strong is IMV-102's clinical and commercial performance?
  • What is IMV-102's clinical trial status in each individual indications such as Multiple myeloma and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the IMV-102 Manufacturers?
  • What are the key designations that have been granted to IMV-102 for potential indications? How are they going to impact IMV-102's penetration in various geographies?
  • What is the current and forecasted IMV-102 market scenario for potential indications? What are the key assumptions behind the forecast?
  • What are the current and forecasted sales of IMV-102 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 IMV-102 for potential indications?
  • Which are the late-stage emerging therapies under development for the treatment of potential indications?
  • How cost-effective is IMV-102? What is the duration of therapy and what are the geographical variations in cost per patient?

Table of Contents

1. Report Introduction

2. IMV-102 Overview in potential indication like Multiple myeloma

  • 2.1. Product Detail
  • 2.2. IMV-102 Clinical Development
    • 2.2.1. IMV-102 Clinical studies
    • 2.2.2. IMV-102 Clinical trials information
    • 2.2.3. Safety and efficacy
  • 2.3. Other Developmental Activities
  • 2.4. Product Profile

3. IMV-102 Competitive Landscape (Marketed Therapies)

4. Competitive Landscape (Late-stage Emerging IMV-102 Therapies)

5. IMV-102 Market Assessment

  • 5.1. IMV-102 Market Outlook in potential indications
  • 5.2. 7MM Analysis
    • 5.2.1. IMV-102 Market Size in the 7MM for potential indications
  • 5.3. Country-wise Market Analysis
    • 5.3.1. IMV-102 Market Size in the United States for potential indications
    • 5.3.2. IMV-102 Market Size in Germany for potential indications
    • 5.3.3. IMV-102 Market Size in France for potential indications
    • 5.3.4. IMV-102 Market Size in Italy for potential indications
    • 5.3.5. IMV-102 Market Size in Spain for potential indications
    • 5.3.6. IMV-102 Market Size in the United Kingdom for potential indications
    • 5.3.7. IMV-102 Market Size in Japan for potential indications

6. IMV-102 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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