Ovarian Cancer Pipeline Analysis Report

Ovarian Cancer Pipeline Analysis Report


Ovarian Cancer Drug Pipeline Analysis 2024 The drug pipeline is significantly driven by the increasing prevalence of ovarian cancer, affecting more than 324,603 women worldwide annually. In the United States, about 19,710 new cases are expected to be diagnosed in 2024, with an estimated 238,484 women currently living with the disease, making it a major health concern globally. Key Takeaways • Major companies involved in the ovarian cancer drug pipeline market include Sanofi, AstraZeneca, Seagen Inc., Bristol-Myers Squibb, and GlaxoSmithKline. • The current drug pipeline for ovarian cancer includes promising candidates such as niraparib, olaparib, rucaparib, and bevacizumab, among others. • Regulatory agencies are providing support through expedited pathways for drug approvals and designations, encouraging rapid development and market availability of new therapies. Report Coverage The ovarian cancer drug pipeline analysis provides an overview of recent advancements and ongoing clinical trials. The report highlights progress in targeted therapies and immunotherapies, aiming for improved survival rates and quality of life. It covers innovative approaches such as PARP inhibitors, which target DNA repair pathways, and angiogenesis inhibitors which restrict tumor blood supply. The competitive landscape examines collaborations and strategic partnerships that accelerate R&D. It also discusses regulatory milestones achieved by investigational drugs, highlighting their impact on future treatment paradigms, and promising more effective and personalized treatment options for ovarian cancer patients. Ovarian Cancer Drug Pipeline Outlook Ovarian cancer, a serious condition affecting thousands globally, is characterized by the growth of malignant cells in the ovaries. It often goes undetected until it has spread within the pelvis and abdomen, making it more challenging to treat. Subtypes of ovarian cancer, such as epithelial ovarian carcinomas, account for most cases and require diverse treatment strategies. In 2024, significant advancements in ovarian cancer treatment have been made. The FDA approved Elahere (mirvetuximab soravtansine-gynx) for patients with folate receptor alpha (FRα) positive, platinum-resistant ovarian cancer, providing a new treatment option that has demonstrated improved progression-free survival in clinical trials. Significant advancements in treatment have been made in recent years, particularly with the development of PARP inhibitors like niraparib and olaparib, which offer new options for patients with BRCA mutations. The market is witnessing increased investment in research and development and regulatory approvals for innovative drugs, underscoring a dynamic landscape focused on enhancing patient outcomes. Ovarian Cancer- Pipeline Drug Profiles Recent developments in ovarian cancer treatment have introduced several promising drugs currently in clinical trials: • Docetaxel and Cisplatin: These are cornerstone chemotherapeutic agents used in combination regimens for ovarian cancer. Docetaxel is a taxane that disrupts microtubule function, while cisplatin forms DNA crosslinks, leading to apoptosis. Their combination enhances cytotoxicity against resistant ovarian cancer cells. • Liposomal Doxorubicin: This formulation of doxorubicin encapsulates the drug in liposomes, enhancing delivery to tumor tissues and reducing systemic toxicity. It is particularly effective against recurrent ovarian cancer, offering a favorable safety profile compared to traditional doxorubicin. • Paclitaxel: A microtubule inhibitor that stabilizes tubulin polymerization, paclitaxel is used in combination with platinum-based drugs for first-line treatment. It has a critical role in both primary and maintenance therapy settings. • Olaparib, MEDI4736, Bevacizumab: Olaparib is a PARP inhibitor for BRCA-mutated ovarian cancer, while MEDI4736 (durvalumab) is an immune checkpoint inhibitor targeting PD-L1, and bevacizumab is an anti-angiogenic agent. This combination leverages multiple mechanisms to enhance therapeutic efficacy. Drug Pipeline Therapeutic Assessment This section of the report covers the analysis of Ovarian Cancer drugs based on various segmentations such as: Analysis by Route of Administration • Oral Oral administration is commonly used for PARP inhibitors such as niraparib (Zejula) and olaparib (Lynparza). These drugs offer convenience and improve patient adherence to treatment regimens, as they can be taken at home rather than requiring a visit to a healthcare facility. Olaparib specifically targets DNA repair pathways and is pivotal in maintenance therapy for patients with BRCA mutations, helping to prolong progression-free survival and improve outcomes. • Parenteral Parenteral administration involves delivering drugs intravenously, ensuring rapid delivery and absorption, especially in aggressive cancer types. Bevacizumab (Avastin) is a prime example, administered intravenously to inhibit angiogenesis. By blocking the formation of new blood vessels that tumors need to grow, bevacizumab enhances progression-free survival when used in combination with chemotherapy. • Others Emerging delivery methods such as intraperitoneal chemotherapy are being explored to directly target tumor cells within the abdominal cavity. Intraperitoneal cisplatin is a notable example, allowing high local drug concentrations with reduced systemic toxicity compared to systemic chemotherapy. This method provides direct contact with cancer cells, enhancing therapeutic efficacy and minimizing side effects. Analysis by Phase According to EMR analysis, Phase II clinical trials dominate the ovarian cancer drug pipeline. The number of ovarian cancer drugs currently in Phase 2 clinical trials varies as new trials are continually initiated and completed. However, as of the latest data, there are over 58 ongoing Phase 2 trials for ovarian cancer drugs worldwide. These trials involve a wide range of therapeutic approaches, including targeted therapies, immunotherapies, and combination treatments. • Preclinical Phase: Laboratory and animal studies to assess safety and efficacy. • Phase I: Small-scale human trials focusing on safety and dosage. • Phase II: Larger trials to evaluate efficacy and side effects. • Phase III: Large-scale trials to confirm effectiveness, monitor side effects, and compare with standard treatments. • Phase IV: Post-marketing studies to gather more information on risks, benefits, and optimal use. Analysis by Drug Class • Monoclonal Antibody Monoclonal antibodies are laboratory-produced molecules engineered to serve as substitute antibodies that can restore, enhance, or mimic the immune system's attack on cancer cells. Bevacizumab (Avastin) targets the vascular endothelial growth factor (VEGF), inhibiting angiogenesis, the process of new blood vessel formation that tumors need to grow. Bevacizumab is pivotal in combination therapies for ovarian cancer, as it restricts the tumor's blood supply, helping to slow the progression of the disease. • Recombinant Fusion Proteins Recombinant fusion proteins are engineered to combine functional domains from different proteins, enhancing therapeutic effects. Aflibercept is a fusion protein that acts as a decoy receptor for VEGF, thereby inhibiting blood vessel growth within tumors. This approach helps to cut off the blood supply to the tumor, aiming to starve it and limit its ability to grow and spread. • Small Molecule Small molecules are low-molecular-weight compounds that can penetrate cells easily and disrupt intracellular processes. Olaparib (Lynparza) is a PARP inhibitor that interferes with DNA repair processes in cancer cells, making it particularly effective in treating BRCA-mutated ovarian cancer. By blocking PARP, olaparib induces cell death in cancer cells, which rely on this pathway for survival. • Gene Therapy Gene therapy involves delivering genetic material into cells to correct or alter defective genes responsible for disease development. Although still in the experimental stages for ovarian cancer, gene therapy aims to target oncogenes or restore tumor suppressor genes to inhibit cancer growth and progression. This approach holds the potential for personalized and curative treatments. • Peptide Peptide-based therapies utilize short chains of amino acids to interfere with specific biological pathways involved in cancer progression. Cilengitide is a peptide that targets integrins, which are proteins involved in cell adhesion and metastasis. By disrupting these interactions, cilengitide may inhibit cancer cell spread and metastasis, making it a promising candidate for further research. • Polymer Polymeric drug delivery systems are designed to improve the solubility, stability, and bioavailability of therapeutic agents. For example, liposomal doxorubicin encapsulates doxorubicin in liposomes, enhancing drug delivery to tumor sites while reducing systemic toxicity. This formulation improves the therapeutic index of the drug, making it more effective and safer for patients. Ovarian Cancer Drug Clinical Trials Assessment- Competitive Dynamics Here are a few notable participants involved in Ovarian Cancer research and development: These advancements represent significant steps forward in Ovarian Cancer treatment, potentially offering patients more effective and less burdensome options. Sanofi Sanofi, headquartered in Paris, France, is dedicated to developing targeted therapies for ovarian cancer. Their pipeline includes immunotherapies that aim to enhance the body's immune response against tumor cells. One of their notable drugs is SAR439859, an oral selective estrogen receptor degrader (SERD) that targets estrogen receptors in cancer cells, providing a potential treatment option for hormone-driven ovarian cancers. AstraZeneca AstraZeneca, headquartered in Cambridge, UK, is a leader in developing PARP inhibitors for ovarian cancer, with olaparib (Lynparza) being one of their most prominent therapies. Olaparib targets DNA repair mechanisms in cancer cells, particularly effective in BRCA-mutated ovarian cancer, and is part of a personalized treatment approach that improves patient outcomes by exploiting cancer cell vulnerabilities. Seagen Inc. Seagen Inc., based in Bothell, Washington, specializes in antibody-drug conjugates (ADCs) for cancer treatment. Their innovative delivery systems aim to increase drug efficacy while minimizing systemic toxicity. Tisotumab vedotin is an ADC developed by Seagen for the treatment of recurrent or metastatic ovarian cancer, designed to deliver cytotoxic agents directly to cancer cells. Bristol-Myers Squibb Bristol-Myers Squibb, headquartered in New York City, is advancing immunotherapies like nivolumab (Opdivo), which enhance anti-tumor immune responses by blocking immune checkpoint pathways. This approach helps to reinvigorate T-cells, allowing them to effectively target and destroy ovarian cancer cells. Their research aims to integrate immune checkpoint blockade with standard care, improving outcomes for ovarian cancer patients. Other key players in the market include GlaxoSmithKline, Lipomedix Pharmaceuticals Inc., Astellas Pharma Inc., Genentech, Inc., and Bayer AG. Reasons To Purchase This Report The Ovarian Cancer drug pipeline analysis report offers invaluable insights into the latest advancements and future trends in Ovarian Cancer treatment. It provides detailed evaluations of emerging therapies, pipeline assessment, and competitive landscape analysis, enabling informed investment decisions and strategic planning. Key Questions Answered in the Ovarian Cancer Drug Pipeline Analysis Report • What is the current state of the ovarian cancer drug pipeline? • How many companies are currently involved in ovarian cancer drug development? • What is the number of drugs in Phase III and Phase IV trials for ovarian cancer? • Which organisations are at the forefront of ovarian cancer drug research? • What are the effectiveness and safety profiles of the drugs in the ovarian cancer pipeline? • What opportunities and challenges exist in the ovarian cancer clinical trial landscape? • Which companies are leading the major clinical trials for ovarian cancer drugs? • Which regions are involved in clinical trials for ovarian cancer? • What are the recent clinical trial results for ovarian cancer drugs? • What are the emerging trends in ovarian cancer clinical trials?


1 Preface
1.1 Introduction
1.2 Objectives of the Study
1.3 Research Methodology and Assumptions
2 Executive Summary
3 Overview of Ovarian Cancer
3.1 Signs and Symptoms
3.2 Causes
3.3 Risk Factors
3.4 Types of Ovarian Cancer
3.5 Diagnosis
3.6 Treatment
4 Patient Profile
4.1 Patient Profile Overview
4.2 Patient Psychology and Emotional Impact Factors
4.3 Risk Assessment and Treatment Success Rate
5 Ovarian Cancer: Epidemiology Snapshot
5.1 Ovarian Cancer Incidence by Key Markets
5.2 Ovarian Cancer– Patients Seeking Treatment in Key Markets
6 Ovarian Cancer: Market Dynamics
6.1 Market Drivers and Constraints
6.2 SWOT Analysis
7 Ovarian Cancer: Key Facts Covered
7.1 Top Countries Contributing to Clinical Trials in Asia-Pacific
7.2 Top Countries Contributing to Clinical Trials in Europe
7.3 Top Countries Contributing to Clinical Trials in North America
7.4 Top Countries Contributing to Clinical Trials in Other Regions
8 Ovarian Cancer, Drug Pipeline Assessment
8.1 Assessment by Treatment Type
8.2 Assessment by Route of Administration
8.3 Assessment by Drug Class
9 EMR Drug Pipeline Comparative Analysis
9.1 List of Ovarian Cancer Pipeline Drugs
9.1.1 By Company
9.1.2 By Phase
9.1.3 By Indication
9.1.4 By Trial Status
9.1.5 By Funder Type
9.2 EMR Attribute Scoring Analysis of Pipeline Drugs (Top Drugs)
10 Ovarian Cancer Drug Pipeline - Late-Stage Products (Phase III and IV) (Top Drugs)
10.1 Comparative Analysis for Late-Stage Drugs
10.1.1 Study Type
10.1.2 Recruitment Status
10.1.3 Company
10.1.4 Funder Type
10.2 Product Level Analysis*
10.2.1 Olaparib
10.2.1.1 Product Description
10.2.1.2 Trial ID
10.2.1.3 Sponsor Name
10.2.1.4 Study Type
10.2.1.5 Drug Class
10.2.1.6 Eligibility Criteria
10.2.1.7 Study Record Dates
10.2.1.7.1 First Submitted
10.2.1.7.2 First Posted
10.2.1.7.3 Last Update Posted
10.2.1.7.4 Last Verified
10.2.1.8 Indication
10.2.1.9 Study Design
10.2.1.10 Recruitment Status
10.2.1.11 Enrollment (Estimated)
10.2.1.12 Location Countries
10.2.1.13 Recent Results
10.2.2 Caelyx
10.2.3 Pegylated Liposomal Doxorubicin hydrochloride
10.2.4 Niraparib
10.2.5 Other Drug
11 Ovarian Cancer Drug Pipeline - Mid-Stage Products (Phase II) (Top Drugs)
11.1 Comparative Analysis for Mid-Stage Drugs
11.1.1 Study Type
11.1.2 Recruitment Status
11.1.3 Company
11.1.4 Funder Type
11.2 Product Level Analysis*
11.2.1 Bevacizumab
11.2.1.1 Product Description
11.2.1.2 Trial ID
11.2.1.3 Sponsor Name
11.2.1.4 Study Type
11.2.1.5 Drug Class
11.2.1.6 Eligibility Criteria
11.2.1.7 Study Record Dates
11.2.1.7.1 First Submitted
11.2.1.7.2 First Posted
11.2.1.7.3 Last Update Posted
11.2.1.7.4 Last Verified
11.2.1.8 Indication
11.2.1.9 Study Design
11.2.1.10 Recruitment Status
11.2.1.11 Enrollment (Estimated)
11.2.1.12 Location Countries
11.2.1.13 Recent Results
11.2.2 DCVAC/OvCa
11.2.3 Aflibercept
11.2.4 Dostarlimab
11.2.5 Other Drugs
12 Ovarian Cancer Drug Pipeline - Early-Stage Products (Phase I) (Top Drugs)
12.1 Comparative Analysis for Early-Stage Drugs
12.1.1 Study Type
12.1.2 Recruitment Status
12.1.3 Company
12.1.4 Funder Type
12.2 Product Level Analysis*
12.2.1 Carboplatin
12.2.1.1 Product Description
12.2.1.2 Trial ID
12.2.1.3 Sponsor Name
12.2.1.4 Study Type
12.2.1.5 Drug Class
12.2.1.6 Eligibility Criteria
12.2.1.7 Study Record Dates
12.2.1.7.1 First Submitted
12.2.1.7.2 First Posted
12.2.1.7.3 Last Update Posted
12.2.1.7.4 Last Verified
12.2.1.8 Indication
12.2.1.9 Study Design
12.2.1.10 Recruitment Status
12.2.1.11 Enrollment (Estimated)
12.2.1.12 Location Countries
12.2.2 GRN-300
12.2.3 Pazopanib
12.2.4 Pazopanib
12.2.5 Other Drugs
13 Ovarian Cancer Drug Pipeline - Preclinical and Discovery Stage Products (Top Drugs)
13.1 Comparative Analysis for Preclinical and Discovery Stage Drugs
13.1.1 Study Type
13.1.2 Recruitment Status
13.1.3 Company
13.1.4 Funder Type
13.2 Product Level Analysis*
13.2.1 SZ011 CAR-NK
13.2.1.1 Product Description
13.2.1.2 Trial ID
13.2.1.3 Sponsor Name
13.2.1.4 Study Type
13.2.1.5 Drug Class
13.2.1.6 Eligibility Criteria
13.2.1.7 Study Record Dates
13.2.1.7.1 First Submitted
13.2.1.7.2 First Posted
13.2.1.7.3 Last Update Posted
13.2.1.7.4 Last Verified
13.2.1.8 Indication
13.2.1.9 Study Design
13.2.1.10 Recruitment Status
13.2.1.11 Enrollment (Estimated)
13.2.1.12 Location Countries
13.2.2 Anti-Mesothelin Car NK Cells
13.2.3 Anti-MESO CAR-T cells
13.2.4 Pembrolizumab
13.2.5 Other Drugs
14 Ovarian Cancer, Key Drug Pipeline Companies
14.1 Sanofi
14.1.1 Company Snapshot
14.1.2 Pipeline Product Portfolio
14.1.3 Financial Analysis
14.1.4 Recent News and Developments
14.2 AstraZeneca
14.2.1 Company Snapshot
14.2.2 Pipeline Product Portfolio
14.2.3 Financial Analysis
14.2.4 Recent News and Developments
14.3 Seagen Inc.
14.3.1 Company Snapshot
14.3.2 Pipeline Product Portfolio
14.3.3 Financial Analysis
14.3.4 Recent News and Developments
14.4 Bristol-Myers Squibb
14.4.1 Company Snapshot
14.4.2 Pipeline Product Portfolio
14.4.3 Financial Analysis
14.4.4 Recent News and Developments
14.5 GlaxoSmithKline
14.5.1 Company Snapshot
14.5.2 Pipeline Product Portfolio
14.5.3 Financial Analysis
14.5.4 Recent News and Developments
14.6 Lipomedix Pharmaceuticals Inc.
14.6.1 Company Snapshot
14.6.2 Pipeline Product Portfolio
14.6.3 Financial Analysis
14.6.4 Recent News and Developments
14.7 Astellas Pharma Inc.
14.7.1 Company Snapshot
14.7.2 Pipeline Product Portfolio
14.7.3 Financial Analysis
14.7.4 Recent News and Developments
14.8 Genentech, Inc.
14.8.1 Company Snapshot
14.8.2 Pipeline Product Portfolio
14.8.3 Financial Analysis
14.8.4 Recent News and Developments
14.9 Bayer AG
14.9.1 Company Snapshot
14.9.2 Pipeline Product Portfolio
14.9.3 Financial Analysis
14.9.4 Recent News and Developments
15 Regulatory Framework for Drug Approval, By Region
16 Terminated or Suspended Pipeline Products
*Complete list of drugs covered will be provided in the report.
The EMR team aims to provide comprehensive coverage of the Top Drugs for each Phase, considering factors such as the company's financial standing, geographic presence, and market position to ensure thorough analysis in this section.

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