Published Date : 2023-04-19
Published Date : 2023-04-19
Updated On : 2024-03-14
Pages : 154
Thelansis’s “Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia treatment modalities options for eight major markets (USA, Germany, France, Italy, Spain, UK, Japan, and China).
Community-acquired pneumonia (CAP) is an escalating health concern, ranking as the third most frequent cause of hospitalization among adults. Although CAP can affect individuals of all age groups, its incidence and fatality rates are notably higher among the very young and the elderly. The primary contributing factor in infants is the absence of humoral immunity against common pathogens like influenza, RSV, and Streptococcus pneumoniae. Conversely, in the elderly, factors such as a weakened immune system due to aging and the prevalence of concurrent illnesses play pivotal roles. While females have a slightly higher likelihood of contracting CAP, males face a greater risk of mortality from the condition. Typical clinical manifestations of CAP include cough, fever, chills, fatigue, dyspnea, rigors, and pleuritic chest pain. The nature of the cough—whether persistent and dry or productive—depends on the causative pathogen. Additionally, patients may experience accompanying symptoms like headache and myalgia, with certain etiologies, such as legionella, potentially causing gastrointestinal manifestations. Diagnosing pneumonia clinically often involves assessing signs, symptoms, and chest radiographs. However, distinguishing CAP or hospital-acquired pneumonia (HAP) from conditions like congestive heart failure, pulmonary embolism, or chemical aspiration pneumonia can be challenging. Streptococcus pneumoniae and Mycoplasma pneumoniae currently predominate as the most prevalent bacterial agents, particularly beyond the neonatal period. Pneumococcus stands out as the primary pathogen responsible for CAP. It often exhibits resistance to multiple antibiotics, thereby complicating treatment. Other frequently encountered pathogens include atypical organisms like Chlamydophila pneumoniae and Legionella pneumophila, Hemophilus influenzae, enteric Gram-negatives (especially in individuals with chronic ailments and aspiration risk factors), and Staphylococcus aureus. Standard management protocols involve supportive measures and administration of antimicrobial agents in cases of suspected bacterial origin. Current guidelines universally advocate oral Amoxicillin as the preferred medication, with intravenous Penicillin or Ampicillin, which is recommended for fully immunized children requiring parenteral treatment. Clinical complications include tissue necrosis, pleural effusion, empyema, and lung abscess formation. In addition to maintaining universal hygiene standards and sanitary conditions, immunization against Influenza, Streptococcus pneumoniae, Haemophilus influenzae type b, and Bordetella pertussis constitutes the most efficacious strategy for preventing CAP. The prognosis for healthy children with CAP is generally favorable, with complete recovery being the norm. However, a small subset of patients may develop restrictive lung disease and recurrent wheezing as long-term complications.
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 | Delafloxacin and Moxifloxacin | Melinta Therapeutics, Inc. | Phase 3 |
2 | ZEVTERA® (ceftobiprole medocaril) | Basilea Pharmaceutica | Phase 3 |
3 | Omadacycline and Moxifloxacin | Zai Lab (Hong Kong), Ltd. | Phase 3 |
4 | CAL02 | Eagle Pharmaceuticals, Inc. | Phase 2 |
5 | CMTX-101 | Clarametyx Biosciences, Inc. | Phase 1 |
6 | Nemonoxacin | R-Pharm | Phase 3 |
7 | Omadacycline and Moxifloxacin | Paratek Pharmaceuticals Inc | Phase 3 |
KOLs across 8 MM market 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 | 17 |
GERMANY | 4 |
UK | 4 |
SPAIN | 3 |
FRANCE | 2 |
ITALY | 3 |
JAPAN | 3 |
CHINA | 4 |
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. Community-Acquired Bacterial Pneumonia (CABP) – 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. Community-Acquired Bacterial Pneumonia (CABP) market scenario 2023 |
1.2.2. Community-Acquired Bacterial Pneumonia (CABP) market scenario 2028 |
1.2.3. Community-Acquired Bacterial Pneumonia (CABP) market scenario 2033 |
2. Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) |
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. Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) management |
2.16. Market Opportunity for Community-Acquired Bacterial Pneumonia (CABP) |
2.17. KOL Comments on current and upcoming/expected treatment practices in Community-Acquired Bacterial Pneumonia (CABP) |
3. Epidemiology |
3.1. Epidemiology Overview |
3.2. Epidemiology by Geography |
3.2.1. Community-Acquired Bacterial Pneumonia (CABP) Epidemiology in US (2023-2033) |
3.2.1.1. Incidence of Community-Acquired Bacterial Pneumonia (CABP) |
3.2.1.2. Diagnosed cases |
3.2.1.3. Treatable Patient Pool |
3.2.1.4. Epidemiology Trends |
3.2.2. Community-Acquired Bacterial Pneumonia (CABP) Epidemiology in EU-5 (2023-2033) |
3.2.2.1. Incidence of Community-Acquired Bacterial Pneumonia (CABP) |
3.2.2.2. Diagnosed cases |
3.2.2.3. Treatable Patient Pool |
3.2.2.4. Epidemiology Trends |
3.2.3. Community-Acquired Bacterial Pneumonia (CABP) Epidemiology in Japan (2023-2033) |
3.2.3.1. Incidence of Community-Acquired Bacterial Pneumonia (CABP) |
3.2.3.2. Diagnosed cases |
3.2.3.3. Treatable Patient Pool |
3.2.3.4. Epidemiology Trends |
3.2.4. Community-Acquired Bacterial Pneumonia (CABP) Epidemiology in China (2023-2033) |
3.2.4.1. Incidence of Community-Acquired Bacterial Pneumonia (CABP) |
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 Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) |
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 Community-Acquired Bacterial Pneumonia (CABP) 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 Community-Acquired Bacterial Pneumonia (CABP) |
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 Community-Acquired Bacterial Pneumonia (CABP) 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 |