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Malignant Pleural Effusion represents a serious complication of advanced malignancies, affecting nearly 1 million individuals globally each year, with an estimated incidence of around 70 cases per 100,000 population annually. Up to 20% of cancer patients in the United States and Europe develop MPE, most commonly secondary to lung and breast cancers. According to malignant pleural effusion pipeline analysis by Expert Market Research, expanding immunotherapy combinations and targeted pleural-directed interventions are expected to reshape future treatment strategies.
Major companies involved in the malignant pleural effusion pipeline analysis include Suzhou Maximum Bio-tech Co., Ltd., Jemincare, and others.
Leading drugs currently in the pipeline include MT027 Cell Suspension and others.
A key market driver for the malignant pleural effusion (MPE) treatment pipeline is the rising adoption of pleural-space-direct delivery platforms that enable targeted therapy and fluid management, potentially reducing repeated invasive procedures, a significant unmet need in MPE care.
The malignant pleural effusion Pipeline Analysis Report by Expert Market Research gives comprehensive insights into malignant pleural effusion therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for malignant pleural effusion. The malignant pleural effusion report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The malignant pleural effusion pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with malignant pleural effusion treatment guidelines to ensure optimal care practices.
The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to malignant pleural effusion.

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Malignant pleural effusion (MPE), defined as fluid accumulation in the pleural space due to metastatic or primary pleural cancers, typically receives palliative treatment such as thoracentesis, pleurodesis or indwelling catheters, while systemic therapy targets the underlying malignancy.
Malignant pleural mesothelioma treatment is undergoing meaningful evolution as immunotherapy reshapes frontline management strategies. A notable milestone was the September 2024 U.S. FDA approval of Pembrolizumab (with pemetrexed and platinum chemotherapy) as first-line therapy for unresectable advanced or metastatic MPM, potentially improving control of effusion-causing tumors. This regulatory development bolsters confidence in ongoing pleural oncology research and supports greater investment in effusion-targeted therapeutics.
Malignant Pleural Effusion (MPE) affects nearly 1 million people globally each year, highlighting its severe worldwide burden. Incidence estimates indicate that approximately 70 per 100,000 people develop MPE annually, reflecting its strong association with advanced malignancies. Across Europe and the United States, up to 20% of cancer patients progress to MPE, with lung and breast cancers contributing to over half of reported cases. Globally, MPE is widely recognized as a marker of late-stage disease, often correlating with reduced survival outcomes. These epidemiological patterns underscore the pressing need for earlier detection, improved therapeutic approaches, and strengthened supportive care strategies to address this growing global challenge effectively.
This section of the report covers the analysis of malignant pleural effusion drug candidates based on several segmentations, including:
By Phase
The pipeline assessment report covers 50+ drug analyses based on phase:
By Drug Class
The malignant pleural effusion pipeline analysis report covers 50+ drug analyses based on drug classes:
By Route of Administration
The pipeline assessment report covers 50+ drug analyses based on the route of administration:
The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase I covers a major share of the total malignant pleural effusion clinical trials. Early Phase I represents about 18.8% of ongoing studies, while phase I accounts for 50%, indicating strong exploratory activity. Phase II contributes 31.3%, forming a major share of malignant pleural effusion clinical trials, while Phases III and IV currently show minimal representation, highlighting the limited presence of late-stage development and the early-stage nature of the pipeline.
The drug molecule categories covered under the malignant pleural effusion pipeline analysis include oligonucleotides, peptides, and small molecules. The malignant pleural effusion report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for malignant pleural effusion. For instance, in May 2019, the U.S. Food and Drug Administration approved the NovoTTF-100L System (Novocure) used with pemetrexed and platinum-based chemotherapy for unresectable, locally advanced or metastatic malignant pleural mesothelioma, the first new mesothelioma-therapy approval in over 15 years.
The EMR report for the malignant pleural effusion pipeline covers the profile of key companies involved in clinical trials and their drugs under development. It provides a detailed malignant pleural effusion therapeutic assessment, analyzing the competitive dynamics of the clinical trial landscape. Below is the list of a few players involved in malignant pleural effusion clinical trials:
This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging drugs for malignant pleural effusion. It includes product description, trial ID, study type, drug class, mode of administration, and recruitment status of malignant pleural effusion drug candidates.
M701 Pleural Infusion is an investigational biologic therapy developed by Wuhan YZY Biopharma Co., Ltd., designed to modulate the tumor-immune interface within the pleural cavity. It aims to suppress malignant cell proliferation and reduce recurrent effusion by enhancing localized immune activity. By acting directly in the pleural space, the therapy seeks to improve fluid control and symptom relief in malignant pleural effusion. Wuhan YZY Biopharma is an emerging biotechnology company focused on immunotherapies and innovative biologics for oncology indications.
MT027 Cells Suspension is a cell-based therapeutic candidate from Suzhou Maximum Bio-tech Co., Ltd., developed to target the immunological mechanisms driving malignant pleural effusion. The therapy utilizes modified engineered immune cells to inhibit tumor-driven inflammation and reduce pleural fluid accumulation. By enhancing antitumor cytotoxicity locally, MT027 aims to manage effusion recurrence and improve patient outcomes. Suzhou Maximum Bio-tech is a biotechnology company advancing novel cell therapies, with a focus on translational research and early-stage oncology programs.
*Please note that this is only a partial list; the complete list of drugs will be available in the full report.*
The Malignant Pleural Effusion Pipeline Analysis Report provides a strategic overview of the latest and future landscape of treatments for malignant pleural effusion. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into malignant pleural effusion collaborations, regulatory environments, and potential growth opportunities.
Malignant Pleural Effusion (MPE) Epidemiology Forecast
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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