Published Date : 2023-09-11
Published Date : 2023-09-11
Updated On : 2024-06-28
Pages : 154
Thelansis’s “Relapsed or Refractory Follicular Lymphoma (r/rFL) Market Outlook, Epidemiology, Competitive Landscape, and Market Forecast Report – 2023 To 2033" covers disease overview, epidemiology, drug utilization, prescription share analysis, competitive landscape, clinical practice, regulatory landscape, patient share, market uptake, market forecast, and key market insights under the potential Relapsed or Refractory Follicular Lymphoma (r/rFL) treatment modalities options for eight major markets (USA, Germany, France, Italy, Spain, UK, Japan, and China).
Follicular lymphoma (FL), often called indolent lymphoma, is the second most prevalent type of non-Hodgkin lymphoma (NHL). Despite treatment, a considerable number of FL patients experience treatment failure, leading to classification as refractory lymphomas. Others initially respond positively but subsequently display signs of recurrent tumor growth, termed relapsed follicular lymphoma. The advanced-stage disease is typically deemed incurable, marked by a protracted pattern of relapse and remission. A notable subset of patients, particularly those with transformed or rapidly progressive disease, face less favorable outcomes. Bone marrow biopsy is typically reserved for individuals presenting with unexplained cytopenias. FL has the potential to progress into a more aggressive form of lymphoma, such as diffuse large B-cell lymphoma. Thus, biopsy remains crucial for diagnosing this transformation upon relapse. The advent of anti-CD20 monoclonal antibodies (mAbs) like rituximab and, more recently, type II anti-CD20 mAbs such as obinutuzumab, has revolutionized FL management, with anti-CD20 antibodies expected to retain prominence in FL treatment strategies. The intricate interplay between FL tumor cells and their distinct immune microenvironment has spurred the development of novel targeted therapies leveraging the immune system's capacity to combat malignant cells.
North America- the United States and Canada
Europe- EU5 (Germany, France, Italy, Spain, and the United Kingdom)
Other countries- Japan & China
This section of the study covers country-specific current clinical practice, the standard of care, and significant limitations around addressing the unmet needs. Retrospective analysis and bench-marking of clinical study outcomes are presented in terms of Pre-treatment & post-treatment clinical and demographic patient characteristics. Essentially, this section will cover the evolution of the current competitive landscape and its impact on the future treatment paradigm.
KOLs across 8 MM markets from the center of Excellence/ Public/ Private hospitals participated in the study. Insights around current treatment landscape, epidemiology, clinical characteristics, future treatment paradigm, and Unmet needs
- Data Inputs with sourcing
- Market Event and Product Event
- Country-specific Forecast Model
- Market uptake and patient share uptake
- Attribute Analysis
- Analog Analysis
- Disease burden and pricing scenario
- Summary and Insights
Optimization of cash flow/ revenue flow concerning all fixed and variable investments throughout the product development process. The rate of return on an investment is a critical indicator to ensure the profitability and break-even of the project.
The competitive landscape includes country-specific approved as well as pipeline therapies. Any asset/product-specific designation or review such as Orphan drug designation, Fast track, Priority Review, Breakthrough Therapy Designation, Rare Pediatric Disease Designation, and Accelerated Approval are tracked and supplemented with analyst commentary.
Detailed clinical trial data analysis and critical product positioning include trial design, primary outcomes, secondary outcomes, dosing and schedules, inclusion and exclusion criteria, recruitment status and essentially covers the reported adverse events. Majorly the trial analysis helps determine the potential of the critical assets and their probable filing and launch date.
This report presents the most important clinical unmet needs in the treatment, according to Thelansis research and analysis. Other essential unmet needs identified through our study include decreased cost burden on patients, improved administration convenience, and improved patient compliance.
S. no | Asset | Company | Stage |
1 | Epcoritamab | Genmab A/S and AbbVie | Phase 3 |
2 | Abexinostat | Xynomic Pharmaceuticals, Inc. | Phase 2 |
3 | IBI376 | Innovent Biologics (Suzhou) Co. Ltd. | Phase 2 |
4 | Loncastuximab tesirine | ADC Therapeutics S.A. | Phase 2 |
5 | Pralatrexate | Spectrum Pharmaceuticals, Inc | Phase 2 |
6 | PL-001 | Pell Bio-Med Technology Co., Ltd. | Phase 3 |
7 | Odronextamab+Lenalidomide | Regeneron Pharmaceuticals | Phase 2 |
8 | Imvotamab | IGM Biosciences, Inc. | Phase 3 |
9 | Entospletinib and Obinutuzumab | Gilead Sciences | Phase 3 |
10 | CTX112 | CRISPR Therapeutics AG | Phase 2 |
Continued...
KOLs across 8 MM markets from the center of Excellence/ Public/ Private hospitals participated in the study. Insights around current treatment landscape, epidemiology, clinical characteristics, future treatment paradigm, and Unmet needs.
COUNTRY | No. Of KOLs |
USA | 18 |
GERMANY | 4 |
UK | 5 |
SPAIN | 4 |
FRANCE | 4 |
ITALY | 4 |
JAPAN | 5 |
CHINA | 5 |
Data Inputs with sourcing, Market Event, Product Event, Country specific Forecast Model, Market uptake and patient share uptake, Attribute Analysis, Analog Analysis, Disease burden, and pricing scenario, Summary, and Insights.
1. Relapsed or Refractory Follicular Lymphoma (r/rFL) – Key Findings Summary |
1.1. Clinical findings |
1.1.1. Disease overview |
1.1.2. Therapeutic practices |
1.1.3. Future outlook |
1.2. Commercial findings |
1.2.1. Relapsed or Refractory Follicular Lymphoma (r/rFL) market scenario 2023 |
1.2.2. Relapsed or Refractory Follicular Lymphoma (r/rFL) market scenario 2028 |
1.2.3. Relapsed or Refractory Follicular Lymphoma (r/rFL) market scenario 2033 |
2. Relapsed or Refractory Follicular Lymphoma (r/rFL) Overview |
2.1. Disease Introduction |
2.2. Pathophysiology |
2.3. Signs and Symptoms |
2.4. Risk Factors |
2.5. Etiology |
2.6. Classification |
2.7. Pathogenesis |
2.8. Diagnosis |
2.9. Complications |
2.10. Treatment Algorithm |
2.10.1. Treatment in US (guidelines) |
2.10.2. Treatment in EU-5 (guidelines) |
2.10.3. Treatment in Japan (guidelines) |
2.10.4. Treatment in China (guidelines) |
2.11. Treatment Goals for Relapsed or Refractory Follicular Lymphoma (r/rFL) |
2.12. Referral Patterns |
2.12.1. Referral Scenario in US |
2.12.2. Referral Scenario in EU-5 |
2.12.3. Referral Scenario in Japan |
2.12.4. Referral Scenario in China |
2.13. Relapsed or Refractory Follicular Lymphoma (r/rFL) Prognosis |
2.14. Healthcare burden |
2.14.1. Healthcare burden in US |
2.14.2. Healthcare burden in EU-5 |
2.14.3. Healthcare burden in Japan |
2.14.4. Healthcare burden in China |
2.15. Unmet Needs in Relapsed or Refractory Follicular Lymphoma (r/rFL) management |
2.16. Market Opportunity for Relapsed or Refractory Follicular Lymphoma (r/rFL) |
2.17. KOL Comments on current and upcoming/expected treatment practices in Relapsed or Refractory Follicular Lymphoma (r/rFL) |
3. Epidemiology |
3.1. Epidemiology Overview |
3.2. Epidemiology by Geography |
3.2.1. Relapsed or Refractory Follicular Lymphoma (r/rFL) Epidemiology in US (2023-2033) |
3.2.1.1. Incidence of Relapsed or Refractory Follicular Lymphoma (r/rFL) |
3.2.1.2. Diagnosed cases |
3.2.1.3. Treatable Patient Pool |
3.2.1.4. Epidemiology Trends |
3.2.2. Relapsed or Refractory Follicular Lymphoma (r/rFL) Epidemiology in EU-5 (2023-2033) |
3.2.2.1. Incidence of Relapsed or Refractory Follicular Lymphoma (r/rFL) |
3.2.2.2. Diagnosed cases |
3.2.2.3. Treatable Patient Pool |
3.2.2.4. Epidemiology Trends |
3.2.3. Relapsed or Refractory Follicular Lymphoma (r/rFL) Epidemiology in Japan (2023-2033) |
3.2.3.1. Incidence of Relapsed or Refractory Follicular Lymphoma (r/rFL) |
3.2.3.2. Diagnosed cases |
3.2.3.3. Treatable Patient Pool |
3.2.3.4. Epidemiology Trends |
3.2.4. Relapsed or Refractory Follicular Lymphoma (r/rFL) Epidemiology in China (2023-2033) |
3.2.4.1. Incidence of Relapsed or Refractory Follicular Lymphoma (r/rFL) |
3.2.4.2. Diagnosed cases |
3.2.4.3. Treatable Patient Pool |
3.2.4.4. Epidemiology Trends |
3.3. Epidemiology Trends (World-wide) |
4. Market Outlook |
4.1. US Relapsed or Refractory Follicular Lymphoma (r/rFL) Market Forecast 2023-2033 |
4.1.1. Market Progression (Futuristic) |
4.1.2. Market Trends and Expectations |
4.1.2.1. Worst case scenario |
4.1.2.2. Base Case Scenario |
4.1.2.3. Best Case Scenario |
4.1.3. Drivers and Barriers |
4.2. UK Relapsed or Refractory Follicular Lymphoma (r/rFL) Market Forecast 2023-2033 |
4.2.1. Market Progression (Futuristic) |
4.2.2. Market Trends and Expectations |
4.2.2.1. Worst case scenario |
4.2.2.2. Base Case Scenario |
4.2.2.3. Best Case Scenario |
4.2.3. Drivers and Barriers |
4.3. France Relapsed or Refractory Follicular Lymphoma (r/rFL) Market Forecast 2023-2033 |
4.3.1. Market Progression (Futuristic) |
4.3.2. Market Trends and Expectations |
4.3.2.1. Worst case scenario |
4.3.2.2. Base Case Scenario |
4.3.2.3. Best Case Scenario |
4.3.3. Drivers and Barriers |
4.4. Germany Relapsed or Refractory Follicular Lymphoma (r/rFL) Market Forecast 2023-2033 |
4.4.1. Market Progression (Futuristic) |
4.4.2. Market Trends and Expectations |
4.4.2.1. Worst case scenario |
4.4.2.2. Base Case Scenario |
4.4.2.3. Best Case Scenario |
4.4.3. Drivers and Barriers |
4.5. Italy Relapsed or Refractory Follicular Lymphoma (r/rFL) Market Forecast 2023-2033 |
4.5.1. Market Progression (Futuristic) |
4.5.2. Market Trends and Expectations |
4.5.2.1. Worst case scenario |
4.5.2.2. Base Case Scenario |
4.5.2.3. Best Case Scenario |
4.5.3. Drivers and Barriers |
4.6. Spain Relapsed or Refractory Follicular Lymphoma (r/rFL) Market Forecast 2023-2033 |
4.6.1. Market Progression (Futuristic) |
4.6.2. Market Trends and Expectations |
4.6.2.1. Worst case scenario |
4.6.2.2. Base Case Scenario |
4.6.2.3. Best Case Scenario |
4.6.3. Drivers and Barriers |
4.7. Japan Relapsed or Refractory Follicular Lymphoma (r/rFL) Market Forecast 2023-2033 |
4.7.1. Market Progression (Futuristic) |
4.7.2. Market Trends and Expectations |
4.7.2.1. Worst case scenario |
4.7.2.2. Base Case Scenario |
4.7.2.3. Best Case Scenario |
4.7.3. Drivers and Barriers |
4.8. China Relapsed or Refractory Follicular Lymphoma (r/rFL) Market Forecast 2023-2033 |
4.8.1. Market Progression (Futuristic) |
4.8.2. Market Trends and Expectations |
4.8.2.1. Worst case scenario |
4.8.2.2. Base Case Scenario |
4.8.2.3. Best Case Scenario |
4.8.3. Drivers and Barriers |
4.9. Key Expected Milestones (world-wide) Impacting the Market |
5. Competitive Landscape |
5.1. Pipeline Therapies Overview |
5.1.1. Phase III Therapies |
5.1.1.1. Current Status |
5.1.1.2. Trial details, results |
5.1.1.3. Approval Timeline |
5.1.1.4. Likelihood of approval |
5.1.1.5. Expected Product Positioning |
5.1.1.2. All other Phase III Therapies ….. |
5.1.1.3. Attribute Analysis of Phase III molecules |
5.1.2. Phase II and Phase I/II Therapies |
5.1.2.1. Current Status |
5.1.2.2. Trial details, results |
5.1.2.3. Approval Timelines |
5.1.3. List of active Pre-clinical Therapies |
5.1.3.1. Status in Relapsed or Refractory Follicular Lymphoma (r/rFL) |
5.1.3.2. Company positioning |
5.1.3.2. All other pre-clinical therapies |
5.1.4. List of Inactive/discontinued assets |
5.1.4.1. Business impact of discontinuations on current pipeline |
5.1.5. Potential winners from Relapsed or Refractory Follicular Lymphoma (r/rFL) Pipeline |
5.1.5.1. Potential Blockbusters across the pipeline |
6. Regulatory/Approval Scenario |
6.1. Regulatory/Approval Framework in US |
6.1.1. Policy Framework |
6.1.2. Payer Expectations |
6.2. Regulatory/Approval Framework in UK |
6.2.1. Policy Framework |
6.2.2. Payer Expectations |
6.3. Regulatory/Approval Framework in France |
6.3.1. Policy Framework |
6.3.2. Payer Expectations |
6.4. Regulatory/Approval Framework in Germany |
6.4.1. Policy Framework |
6.4.2. Payer Expectations |
6.5. Regulatory/Approval Framework in Italy |
6.5.1. Policy Framework |
6.5.2. Payer Expectations |
6.6. Regulatory/Approval Framework in Spain |
6.6.1. Policy Framework |
6.6.2. Payer Expectations |
6.7. Regulatory/Approval Framework in Japan |
6.7.1. Policy Framework |
6.7.2. Payer Expectations |
6.8. Regulatory/Approval Framework in China |
6.8.1. Policy Framework |
6.8.2. Payer Expectations |
7. Clinical Trial Assessment – Current and Future Paradigm |
7.1. Distribution of Primary Endpoints across trials |
7.2. Distribution of Secondary Endpoints across trials |
7.3. Evolution and acceptance of surrogate endpoints |
7.4. Key Investigator initiated trials |
7.5. Attrition analysis |
7.5.1. Suspended/Discontinued Assets |
7.5.2. Failed Trials, Reasons and Business Impact |
7.5.3. Terminated Trials, Reasons and Business Impact |
7.5.4. Withdrawn Trials, Reasons and Business Impact |
7.6. Trial enrollment scenario and challenges |
7.7. Clinical Trial Guidance (across geographies) |
8. Thelansis Commentary |
8.1. Key Unmet needs in Relapsed or Refractory Follicular Lymphoma (r/rFL) |
8.2. Possible Best-case Clinical Trial Strategies |
8.3. Possible Best Case Targeted Product Profile (TPP) |
8.4. Possible Best-case Market positioning strategies |
8.5. Possible Best-case Market Access Strategies |
8.6. Possible Best-case LCM Strategies |
8.7. Overall View on Relapsed or Refractory Follicular Lymphoma (r/rFL) Market in Dollar Value |
9. Report Methodology |
9.1. Secondary research |
9.2. Primary research |
9.3. Data collation |
9.4. Insight Generation |
10. About Thelansis |
10.1. Our Capabilities |
10.2. Our Services |
10.3. Our Contacts |
10.4. Disclaimer |